diff --git a/OMEGA.bib b/OMEGA.bib index 4deb5f4..70e6096 100644 --- a/OMEGA.bib +++ b/OMEGA.bib @@ -5,13 +5,12 @@ Date-Modified = {2018-09-18 20:50:58 +0000}, Doi = {10.1016/j.neuron.2008.08.006}, Journal = {Neuron}, - Journal-Full = {Neuron}, - Mesh = {Animals; Basic Helix-Loop-Helix Transcription Factors; Body Patterning; Cell Differentiation; Cell Movement; Efferent Pathways; Mice; Mice, Knockout; Mice, Transgenic; Mitosis; Motor Cortex; Neocortex; Neurons; Pyramidal Tracts; Somatosensory Cortex; Stem Cells; Telencephalon; Transcriptional Activation}, + keywords = {Animals; Basic Helix-Loop-Helix Transcription Factors; Body Patterning; Cell Differentiation; Cell Movement; Efferent Pathways; Mice; Mice, Knockout; Mice, Transgenic; Mitosis; Motor Cortex; Neocortex; Neurons; Pyramidal Tracts; Somatosensory Cortex; Stem Cells; Telencephalon; Transcriptional Activation}, Month = {Oct}, Number = {2}, Pages = {258-72}, Pmc = {PMC2643370}, - pubmed = {18957218}, + pmid = {18957218}, Pst = {ppublish}, Title = {Bhlhb5 regulates the postmitotic acquisition of area identities in layers II-V of the developing neocortex}, Volume = {60}, @@ -30,7 +29,7 @@ Month = {Oct}, Number = {10}, Pages = {655-69}, - pubmed = {25234264}, + pmid = {25234264}, Pst = {ppublish}, Title = {Functional organization of the hippocampal longitudinal axis}, Volume = {15}, @@ -48,7 +47,7 @@ Number = {11}, Pages = {1434-1447}, Pmc = {PMC5943637}, - pubmed = {29073641}, + pmid = {29073641}, Pst = {ppublish}, Title = {Viewpoints: how the hippocampus contributes to memory, navigation and cognition}, Volume = {20}, @@ -66,7 +65,7 @@ Month = {Oct}, Number = {11}, Pages = {1465-1473}, - pubmed = {29073639}, + pmid = {29073639}, Pst = {aheadofprint}, Title = {Our sense of direction: progress, controversies and challenges}, Volume = {20}, @@ -85,7 +84,7 @@ Month = {Oct}, Number = {11}, Pages = {1448-1464}, - pubmed = {29073644}, + pmid = {29073644}, Pst = {ppublish}, Title = {Spatial representation in the hippocampal formation: a history}, Volume = {20}, @@ -105,7 +104,7 @@ Mesh = {Action Potentials; Animals; Animals, Genetically Modified; Brain; Brain Mapping; Cell Nucleus; Cells, Cultured; Eye Movements; Fluorescence; HEK293 Cells; Humans; Nerve Tissue Proteins; Neural Pathways; Neurons; Nuclear Proteins; Rats; Transfection; Zebrafish; Zebrafish Proteins}, Pages = {138}, Pmc = {PMC4244806}, - pubmed = {25505384}, + pmid = {25505384}, Pst = {epublish}, Title = {Prolonged, brain-wide expression of nuclear-localized GCaMP3 for functional circuit mapping}, Volume = {8}, @@ -122,7 +121,7 @@ Journal-Full = {The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry}, Keywords = {action observation; basal ganglia; development; grasping; social cognition}, Month = {Jan}, - pubmed = {26747293}, + pmid = {26747293}, Pst = {aheadofprint}, Title = {The Extended Mirror Neuron Network: Anatomy, Origin, and Functions}, Year = {2016}, @@ -140,7 +139,7 @@ Month = {Jul}, Pages = {12043}, Pmc = {PMC4498233}, - pubmed = {26159124}, + pmid = {26159124}, Pst = {epublish}, Title = {Rapid fusion between mesenchymal stem cells and cardiomyocytes yields electrically active, non-contractile hybrid cells}, Volume = {5}, @@ -180,7 +179,7 @@ Number = {4}, Pages = {979-84}, Pmc = {PMC5457904}, - pubmed = {26967229}, + pmid = {26967229}, Pst = {ppublish}, Title = {Microbes and Alzheimer's Disease}, Volume = {51}, @@ -240,7 +239,7 @@ Number = {35}, Pages = {12667-72}, Pmc = {PMC4156754}, - pubmed = {25136099}, + pmid = {25136099}, Pst = {ppublish}, Title = {Gyrification from constrained cortical expansion}, Volume = {111}, @@ -260,7 +259,7 @@ Number = {11}, Pages = {1860-1896}, Pmc = {PMC4917295}, - pubmed = {26492141}, + pmid = {26492141}, Pst = {ppublish}, Title = {Whole-body tissue stabilization and selective extractions via tissue-hydrogel hybrids for high-resolution intact circuit mapping and phenotyping}, Volume = {10}, @@ -280,7 +279,7 @@ Month = {Aug}, Pages = {193-207}, Pmc = {PMC4975678}, - pubmed = {27393829}, + pmid = {27393829}, Pst = {ppublish}, Title = {Extracting structural and functional features of widely distributed biological circuits with single cell resolution via tissue clearing and delivery vectors}, Volume = {40}, @@ -301,7 +300,7 @@ Month = {Jun}, Number = {6}, Pages = {1205-1219.e8}, - pubmed = {28602690}, + pmid = {28602690}, Pst = {ppublish}, Title = {Dorsal Raphe Dopamine Neurons Modulate Arousal and Promote Wakefulness by Salient Stimuli}, Volume = {94}, @@ -321,7 +320,7 @@ Number = {4}, Pages = {683-695.e15}, Pmc = {PMC5810594}, - pubmed = {29425490}, + pmid = {29425490}, Pst = {ppublish}, Title = {Fast-Spiking Interneurons Supply Feedforward Control of Bursting, Calcium, and Plasticity for Efficient Learning}, Volume = {172}, @@ -342,7 +341,7 @@ Number = {7463}, Pages = {458-62}, Pmc = {PMC5283693}, - pubmed = {23913275}, + pmid = {23913275}, Pst = {ppublish}, Title = {Oxytocin enhances hippocampal spike transmission by modulating fast-spiking interneurons}, Volume = {500}, @@ -363,7 +362,7 @@ Number = {2}, Pages = {341-356.e6}, Pmc = {PMC5754189}, - pubmed = {28689984}, + pmid = {28689984}, Pst = {ppublish}, Title = {Local Cues Establish and Maintain Region-Specific Phenotypes of Basal Ganglia Microglia}, Volume = {95}, @@ -385,7 +384,7 @@ Number = {4}, Pages = {792-804}, Pmc = {PMC4775740}, - pubmed = {26871636}, + pmid = {26871636}, Pst = {ppublish}, Title = {Multiplexed Intact-Tissue Transcriptional Analysis at Cellular Resolution}, Volume = {164}, @@ -406,7 +405,7 @@ Number = {4}, Pages = {537-49}, Pmc = {PMC2796273}, - pubmed = {19945395}, + pmid = {19945395}, Pst = {ppublish}, Title = {Endocannabinoid signaling is required for development and critical period plasticity of the whisker map in somatosensory cortex}, Volume = {64}, @@ -426,7 +425,7 @@ Number = {6}, Pages = {1253-67}, Pmc = {PMC4688126}, - pubmed = {26671462}, + pmid = {26671462}, Pst = {ppublish}, Title = {Three Types of Cortical Layer 5 Neurons That Differ in Brain-wide Connectivity and Function}, Volume = {88}, @@ -447,7 +446,7 @@ Number = {6106}, Pages = {536-40}, Pmc = {PMC5297939}, - pubmed = {23042292}, + pmid = {23042292}, Pst = {ppublish}, Title = {Elfn1 regulates target-specific release probability at CA1-interneuron synapses}, Volume = {338}, @@ -467,7 +466,7 @@ Month = {09}, Number = {7672}, Pages = {345-350}, - pubmed = {28902833}, + pmid = {28902833}, Pst = {ppublish}, Title = {Rabies screen reveals GPe control of cocaine-triggered plasticity}, Volume = {549}, @@ -488,7 +487,7 @@ Number = {10}, Pages = {3600-11}, Pmc = {PMC2838193}, - pubmed = {20219994}, + pmid = {20219994}, Pst = {ppublish}, Title = {Excitability and synaptic communication within the oligodendrocyte lineage}, Volume = {30}, @@ -508,7 +507,7 @@ Number = {1}, Pages = {35-51}, Pmc = {PMC3711516}, - pubmed = {23283320}, + pmid = {23283320}, Pst = {ppublish}, Title = {Transsynaptic tracing with vesicular stomatitis virus reveals novel retinal circuitry}, Volume = {33}, @@ -528,7 +527,7 @@ Number = {16}, Pages = {6800-8}, Pmc = {PMC3865506}, - pubmed = {23595739}, + pmid = {23595739}, Pst = {ppublish}, Title = {Restoration of retinal structure and function after selective photocoagulation}, Volume = {33}, @@ -548,7 +547,7 @@ Month = {Dec}, Number = {12}, Pages = {3216-27}, - pubmed = {25180257}, + pmid = {25180257}, Pst = {ppublish}, Title = {Tuning properties of avian and frog bitter taste receptors dynamically fit gene repertoire sizes}, Volume = {31}, @@ -567,7 +566,7 @@ Month = {May}, Number = {21}, Pages = {5584-92}, - pubmed = {17522303}, + pmid = {17522303}, Pst = {ppublish}, Title = {Characterization of ligands for fish taste receptors}, Volume = {27}, @@ -586,7 +585,7 @@ Month = {Dec}, Number = {12}, Pages = {1647-1657}, - pubmed = {27749825}, + pmid = {27749825}, Pst = {ppublish}, Title = {Layer 4 fast-spiking interneurons filter thalamocortical signals during active somatosensation}, Volume = {19}, @@ -605,7 +604,7 @@ Month = {Dec}, Number = {49}, Pages = {13468-80}, - pubmed = {18057205}, + pmid = {18057205}, Pst = {ppublish}, Title = {Light-evoked calcium responses of isolated melanopsin-expressing retinal ganglion cells}, Volume = {27}, @@ -626,7 +625,7 @@ Number = {1}, Pages = {49-57}, Pmc = {PMC4389678}, - pubmed = {24411938}, + pmid = {24411938}, Pst = {ppublish}, Title = {Aerobic glycolysis in the human brain is associated with development and neotenous gene expression}, Volume = {19}, @@ -648,7 +647,7 @@ Month = {May}, Number = {4}, Pages = {883-901}, - pubmed = {25996133}, + pmid = {25996133}, Pst = {ppublish}, Title = {A cellular perspective on brain energy metabolism and functional imaging}, Volume = {86}, @@ -669,7 +668,7 @@ Month = {Aug}, Number = {6}, Pages = {397-445}, - pubmed = {15313334}, + pmid = {15313334}, Pst = {ppublish}, Title = {Energy metabolism in mammalian brain during development}, Volume = {73}, @@ -690,7 +689,7 @@ Number = {7667}, Pages = {330-333}, Pmc = {PMC5805144}, - pubmed = {28792937}, + pmid = {28792937}, Pst = {ppublish}, Title = {Rewiring the taste system}, Volume = {548}, @@ -742,7 +741,7 @@ Number = {10}, Pages = {587-97}, Pmc = {PMC3900881}, - pubmed = {23968694}, + pmid = {23968694}, Pst = {ppublish}, Title = {Sugar for the brain: the role of glucose in physiological and pathological brain function}, Volume = {36}, @@ -762,7 +761,7 @@ Number = {7223}, Pages = {745-9}, Pmc = {PMC4097022}, - pubmed = {18971930}, + pmid = {18971930}, Pst = {ppublish}, Title = {Brain metabolism dictates the polarity of astrocyte control over arterioles}, Volume = {456}, @@ -792,7 +791,7 @@ Month = {May}, Number = {10}, Pages = {1533-9}, - pubmed = {22606999}, + pmid = {22606999}, Pst = {ppublish}, Title = {Patterning of pre-thalamic somatosensory pathways}, Volume = {35}, @@ -813,7 +812,7 @@ Number = {5}, Pages = {996-1006}, Pmc = {PMC3328343}, - pubmed = {21799210}, + pmid = {21799210}, Pst = {ppublish}, Title = {RORβ induces barrel-like neuronal clusters in the developing neocortex}, Volume = {22}, @@ -833,7 +832,7 @@ Month = {Apr}, Number = {1-2}, Pages = {37-49}, - pubmed = {8734042}, + pmid = {8734042}, Pst = {ppublish}, Title = {Interareal synchronization in the visual cortex}, Volume = {76}, @@ -850,7 +849,7 @@ Mesh = {Animals; Biotin; Brain Mapping; Corpus Callosum; Dextrans; Female; Fluorescent Dyes; Lysine; Neural Pathways; Neurons; Rats; Rats, Long-Evans; Visual Cortex; Visual Perception}, Number = {1}, Pages = {35-52}, - pubmed = {11226668}, + pmid = {11226668}, Pst = {ppublish}, Title = {Intra- and inter-areal connections between the primary visual cortex V1 and the area immediately surrounding V1 in the rat}, Volume = {102}, @@ -869,7 +868,7 @@ Month = {Dec}, Number = {6}, Pages = {1477-90}, - pubmed = {24360548}, + pmid = {24360548}, Pst = {ppublish}, Title = {Membrane potential dynamics of neocortical projection neurons driving target-specific signals}, Volume = {80}, @@ -889,7 +888,7 @@ Month = {Apr}, Number = {1}, Pages = {28-48}, - pubmed = {23583106}, + pmid = {23583106}, Pst = {ppublish}, Title = {Synaptic computation and sensory processing in neocortical layer 2/3}, Volume = {78}, @@ -908,7 +907,7 @@ Month = {Jun}, Number = {6}, Pages = {443-52}, - pubmed = {12042879}, + pmid = {12042879}, Pst = {ppublish}, Title = {Cross-modal plasticity: where and how?}, Volume = {3}, @@ -925,7 +924,7 @@ Journal-Full = {Brain : a journal of neurology}, Keywords = {TREM2; chronic traumatic encephalopathy; concussion; tau protein; traumatic brain injury}, Month = {Jan}, - pubmed = {29360998}, + pmid = {29360998}, Pst = {aheadofprint}, Title = {Concussion, microvascular injury, and early tauopathy in young athletes after impact head injury and an impact concussion mouse model}, Year = {2018}, @@ -942,7 +941,7 @@ Month = {Sep}, Number = {1}, Pages = {31-43}, - pubmed = {12367504}, + pmid = {12367504}, Pst = {ppublish}, Title = {Changing requirements for Gbx2 in development of the cerebellum and maintenance of the mid/hindbrain organizer}, Volume = {36}, @@ -959,7 +958,7 @@ Journal-Full = {Cerebellum (London, England)}, Keywords = {C57BL/6; Cerebellar development; Knock-out mice; Transgenic mice}, Month = {Oct}, - pubmed = {29043563}, + pmid = {29043563}, Pst = {aheadofprint}, Title = {Malformation of the Posterior Cerebellar Vermis Is a Common Neuroanatomical Phenotype of Genetically Engineered Mice on the C57BL/6 Background}, Year = {2017}, @@ -976,7 +975,7 @@ Mesh = {Animals; Animals, Newborn; Brain; Immunoenzyme Techniques; Macrophages; Neuroglia; Rats}, Number = {1}, Pages = {85-95}, - pubmed = {6339067}, + pmid = {6339067}, Pst = {ppublish}, Title = {Morphological studies on neuroglia. VII. Distribution of "brain macrophages" in brains of neonatal and adult rats, as determined by means of immunohistochemistry}, Volume = {229}, @@ -993,7 +992,7 @@ Month = {Jul}, Number = {1-2}, Pages = {15-20}, - pubmed = {3412636}, + pmid = {3412636}, Pst = {ppublish}, Title = {Layer VII of rodent cerebral cortex}, Volume = {90}, @@ -1010,7 +1009,7 @@ Mesh = {Animals; Ganglia, Invertebrate; Motor Neurons; Nephropidae; Nervous System Physiological Phenomena; Periodicity; Stomach}, Month = {Nov}, Pages = {35-50}, - pubmed = {9928300}, + pmid = {9928300}, Pst = {ppublish}, Title = {Basic principles for generating motor output in the stomatogastric ganglion}, Volume = {860}, @@ -1029,7 +1028,7 @@ Number = {2}, Pages = {357-74}, Pmc = {PMC1350459}, - pubmed = {4727085}, + pmid = {4727085}, Pst = {ppublish}, Title = {Long-lasting potentiation of synaptic transmission in the dentate area of the unanaestetized rabbit following stimulation of the perforant path}, Volume = {232}, @@ -1047,7 +1046,7 @@ Number = {2}, Pages = {331-56}, Pmc = {PMC1350458}, - pubmed = {4727084}, + pmid = {4727084}, Pst = {ppublish}, Title = {Long-lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path}, Volume = {232}, @@ -1064,7 +1063,7 @@ Number = {1}, Pages = {18-46}, Pmc = {PMC1420503}, - pubmed = {16993247}, + pmid = {16993247}, Pst = {ppublish}, Title = {On the nature of the fundamental activity of the nervous centres; together with an analysis of the conditioning of rhythmic activity in progression, and a theory of the evolution of function in the nervous system}, Volume = {48}, @@ -1083,7 +1082,7 @@ Method. In the present experiments the mode of evoking the rhythmic reflex has b Number = {3}, Pages = {196-214}, Pmc = {PMC1420464}, - pubmed = {16993214}, + pmid = {16993214}, Pst = {ppublish}, Title = {Further observations on the production of reflex stepping by combination of reflex excitation with reflex inhibition}, Volume = {47}, @@ -1103,7 +1102,7 @@ Method. In the present experiments the mode of evoking the rhythmic reflex has b Month = {Sep}, Number = {9}, Pages = {991-3}, - pubmed = {18725901}, + pmid = {18725901}, Pst = {ppublish}, Title = {Finding coherence in spontaneous oscillations}, Volume = {11}, @@ -1125,7 +1124,7 @@ Method. In the present experiments the mode of evoking the rhythmic reflex has b Number = {1}, Pages = {e1004032}, Pmc = {PMC4304787}, - pubmed = {25615592}, + pmid = {25615592}, Pst = {epublish}, Title = {Laminar and dorsoventral molecular organization of the medial entorhinal cortex revealed by large-scale anatomical analysis of gene expression}, Volume = {11}, @@ -1147,7 +1146,7 @@ RESULTS: NERs and connectivity extractors are evaluated against a manually annot Number = {10}, Pages = {1640-7}, Pmc = {PMC4426844}, - pubmed = {25609795}, + pmid = {25609795}, Pst = {ppublish}, Title = {Large-scale extraction of brain connectivity from the neuroscientific literature}, Volume = {31}, @@ -1166,7 +1165,7 @@ RESULTS: NERs and connectivity extractors are evaluated against a manually annot Mesh = {Animals; Atlases as Topic; Brain; Brain Mapping; Humans; Informatics; Mice; Mice, Inbred C57BL}, Month = {Feb}, Pages = {4-17}, - pubmed = {25536338}, + pmid = {25536338}, Pst = {ppublish}, Title = {Neuroinformatics of the Allen Mouse Brain Connectivity Atlas}, Volume = {73}, @@ -1185,7 +1184,7 @@ RESULTS: NERs and connectivity extractors are evaluated against a manually annot Month = {Jan}, Number = {1}, Pages = {33-44}, - pubmed = {11182079}, + pmid = {11182079}, Pst = {ppublish}, Title = {Traveling electrical waves in cortex: insights from phase dynamics and speculation on a computational role}, Volume = {29}, @@ -1207,7 +1206,7 @@ CONCLUSIONS/SIGNIFICANCE: Since the retinotopic map was functionally refined to Number = {3}, Pages = {e9925}, Pmc = {PMC2848025}, - pubmed = {20369001}, + pmid = {20369001}, Pst = {epublish}, Title = {The refinement of ipsilateral eye retinotopic maps is increased by removing the dominant contralateral eye in adult mice}, Volume = {5}, @@ -1227,7 +1226,7 @@ CONCLUSIONS/SIGNIFICANCE: Since the retinotopic map was functionally refined to Number = {2}, Pages = {855-61}, Pmc = {PMC2657065}, - pubmed = {19052109}, + pmid = {19052109}, Pst = {ppublish}, Title = {Ipsilateral eye cortical maps are uniquely sensitive to binocular plasticity}, Volume = {101}, @@ -1248,7 +1247,7 @@ CONCLUSIONS/SIGNIFICANCE: Since the retinotopic map was functionally refined to Number = {7}, Pages = {816-23}, Pmc = {PMC4963006}, - pubmed = {23799474}, + pmid = {23799474}, Pst = {ppublish}, Title = {Optogenetic pharmacology for control of native neuronal signaling proteins}, Volume = {16}, @@ -1268,7 +1267,7 @@ CONCLUSIONS/SIGNIFICANCE: Since the retinotopic map was functionally refined to Number = {23}, Pages = {8661-6}, Pmc = {PMC4060653}, - pubmed = {24912150}, + pmid = {24912150}, Pst = {ppublish}, Title = {Encoding and storage of spatial information in the retrosplenial cortex}, Volume = {111}, @@ -1287,7 +1286,7 @@ CONCLUSIONS/SIGNIFICANCE: Since the retinotopic map was functionally refined to Mesh = {Animals; Hippocampus; Image Processing, Computer-Assisted; Imaging, Three-Dimensional; Mice; Mice, Inbred C57BL; Neurons; Zebrafish}, Pages = {29}, Pmc = {PMC3982072}, - pubmed = {24772066}, + pmid = {24772066}, Pst = {epublish}, Title = {Simultaneous imaging of neural activity in three dimensions}, Volume = {8}, @@ -1307,7 +1306,7 @@ CONCLUSIONS/SIGNIFICANCE: Since the retinotopic map was functionally refined to Month = {Sep}, Number = {9}, Pages = {941-50}, - pubmed = {25068736}, + pmid = {25068736}, Pst = {ppublish}, Title = {Mapping brain activity at scale with cluster computing}, Volume = {11}, @@ -1332,7 +1331,7 @@ Conclusions and Relevance: In a convenience sample of deceased football players Month = {07}, Number = {4}, Pages = {360-370}, - pubmed = {28742910}, + pmid = {28742910}, Pst = {ppublish}, Title = {Clinicopathological Evaluation of Chronic Traumatic Encephalopathy in Players of American Football}, Volume = {318}, @@ -1352,7 +1351,7 @@ Conclusions and Relevance: In a convenience sample of deceased football players Number = {1}, Pages = {29-51}, Pmc = {PMC4255282}, - pubmed = {24366527}, + pmid = {24366527}, Pst = {ppublish}, Title = {The neuropathology of sport}, Volume = {127}, @@ -1372,7 +1371,7 @@ Conclusions and Relevance: In a convenience sample of deceased football players Number = {5}, Pages = {1589-601}, Pmc = {PMC3517995}, - pubmed = {22302801}, + pmid = {22302801}, Pst = {ppublish}, Title = {Changing microcircuits in the subplate of the developing cortex}, Volume = {32}, @@ -1394,7 +1393,7 @@ INTERPRETATION: These results suggest a major role of the normotopic cortex over Month = {Sep}, Number = {3}, Pages = {428-42}, - pubmed = {25074818}, + pmid = {25074818}, Pst = {ppublish}, Title = {Normotopic cortex is the major contributor to epilepsy in experimental double cortex}, Volume = {76}, @@ -1414,7 +1413,7 @@ INTERPRETATION: These results suggest a major role of the normotopic cortex over Month = {Sep}, Number = {9}, Pages = {1377-91}, - pubmed = {24807023}, + pmid = {24807023}, Pst = {ppublish}, Title = {The glia/neuron ratio: how it varies uniformly across brain structures and species and what that means for brain physiology and evolution}, Volume = {62}, @@ -1432,7 +1431,7 @@ INTERPRETATION: These results suggest a major role of the normotopic cortex over Keywords = {gamma synchronization; olfactory bulb; olfactory consciousness; olfactory cortex; orbitofrontal cortex; tufted and mitral cells}, Pages = {743}, Pmc = {PMC3797617}, - pubmed = {24137148}, + pmid = {24137148}, Pst = {epublish}, Title = {Olfactory consciousness and gamma oscillation couplings across the olfactory bulb, olfactory cortex, and orbitofrontal cortex}, Volume = {4}, @@ -1451,7 +1450,7 @@ INTERPRETATION: These results suggest a major role of the normotopic cortex over Mesh = {Animals; Brain Mapping; Choice Behavior; Functional Neuroimaging; Memory; Mice; Optogenetics; Parietal Lobe; Sensorimotor Cortex; Visual Cortex; Visual Perception}, Month = {08}, Pmc = {PMC4974053}, - pubmed = {27490481}, + pmid = {27490481}, Pst = {epublish}, Title = {Distinct roles of visual, parietal, and frontal motor cortices in memory-guided sensorimotor decisions}, Volume = {5}, @@ -1471,7 +1470,7 @@ INTERPRETATION: These results suggest a major role of the normotopic cortex over Month = {Dec}, Pages = {e10774}, Pmc = {PMC4749564}, - pubmed = {26633811}, + pmid = {26633811}, Pst = {epublish}, Title = {Cortex commands the performance of skilled movement}, Volume = {4}, @@ -1492,7 +1491,7 @@ INTERPRETATION: These results suggest a major role of the normotopic cortex over Number = {42}, Pages = {10707-10722}, Pmc = {PMC5083002}, - pubmed = {27798125}, + pmid = {27798125}, Pst = {ppublish}, Title = {Reconnecting Eye to Brain}, Volume = {36}, @@ -1512,7 +1511,7 @@ INTERPRETATION: These results suggest a major role of the normotopic cortex over Number = {6}, Pages = {1181-1192}, Pmc = {PMC4635400}, - pubmed = {26402602}, + pmid = {26402602}, Pst = {ppublish}, Title = {Inhibitory Actions Unified by Network Integration}, Volume = {87}, @@ -1536,7 +1535,7 @@ CONCLUSIONS: We demonstrate techniques for the large-scale simultaneous interrog Mesh = {Animals; Artifacts; Auditory Perception; Cerebral Cortex; Computer-Aided Design; Electric Impedance; Electrocorticography; Electrodes, Implanted; Equipment Design; Evoked Potentials; Macaca mulatta; Male; Mice, Transgenic; Neural Inhibition; Neurons; Optogenetics; Photic Stimulation; Rats, Long-Evans; Tin Compounds}, Month = {Dec}, Pages = {220-31}, - pubmed = {26296286}, + pmid = {26296286}, Pst = {ppublish}, Title = {Strategies for optical control and simultaneous electrical readout of extended cortical circuits}, Volume = {256}, @@ -1555,7 +1554,7 @@ CONCLUSIONS: We demonstrate techniques for the large-scale simultaneous interrog Mesh = {Adolescent; Counseling; Humans; Marijuana Abuse; Marijuana Smoking; Parents; Pediatricians; Physician's Role}, Month = {Mar}, Number = {3}, - pubmed = {28242859}, + pmid = {28242859}, Pst = {ppublish}, Title = {Counseling Parents and Teens About Marijuana Use in the Era of Legalization of Marijuana}, Volume = {139}, @@ -1574,7 +1573,7 @@ CONCLUSIONS: We demonstrate techniques for the large-scale simultaneous interrog Mesh = {Animals; Cerebral Cortex; Flavoproteins; Mice; Neuronal Plasticity; Photobleaching; Spectrometry, Fluorescence}, Month = {May}, Pages = {3-9}, - pubmed = {19393002}, + pmid = {19393002}, Pst = {ppublish}, Title = {Transcranial flavoprotein fluorescence imaging of mouse cortical activity and plasticity}, Volume = {109 Suppl 1}, @@ -1592,7 +1591,7 @@ CONCLUSIONS: We demonstrate techniques for the large-scale simultaneous interrog Month = {Oct}, Pages = {13210}, Pmc = {PMC5078743}, - pubmed = {27767032}, + pmid = {27767032}, Pst = {epublish}, Title = {Mixed functional microarchitectures for orientation selectivity in the mouse primary visual cortex}, Volume = {7}, @@ -1610,7 +1609,7 @@ CONCLUSIONS: We demonstrate techniques for the large-scale simultaneous interrog Mesh = {Action Potentials; Animals; Animals, Newborn; GABA Agents; Mice; Neocortex; Nerve Net; Neural Inhibition; Neurons; Occipital Lobe; Patch-Clamp Techniques; Receptors, GABA-A; Synaptic Transmission; gamma-Aminobutyric Acid}, Month = {Jul}, Pages = {7750}, - pubmed = {26177896}, + pmid = {26177896}, Pst = {epublish}, Title = {GABA depolarizes immature neurons and inhibits network activity in the neonatal neocortex in vivo}, Volume = {6}, @@ -1629,7 +1628,7 @@ CONCLUSIONS: We demonstrate techniques for the large-scale simultaneous interrog Month = {Apr}, Pages = {6887}, Pmc = {PMC4423212}, - pubmed = {25904499}, + pmid = {25904499}, Pst = {epublish}, Title = {Nkx2.1-derived astrocytes and neurons together with Slit2 are indispensable for anterior commissure formation}, Volume = {6}, @@ -1648,7 +1647,7 @@ CONCLUSIONS: We demonstrate techniques for the large-scale simultaneous interrog Month = {Apr}, Pages = {3708}, Pmc = {PMC3997811}, - pubmed = {24739528}, + pmid = {24739528}, Pst = {epublish}, Title = {Unc5C and DCC act downstream of Ctip2 and Satb2 and contribute to corpus callosum formation}, Volume = {5}, @@ -1669,7 +1668,7 @@ DISCUSSION: Our case studies highlight that not all athletes with history of rep Keywords = {chronic traumatic encephalopathy; dementia; neurodegenerative disease; professional athletes; repetitive brain injury}, Pages = {222}, Pmc = {PMC3662898}, - pubmed = {23745112}, + pmid = {23745112}, Pst = {epublish}, Title = {Absence of chronic traumatic encephalopathy in retired football players with multiple concussions and neurological symptomatology}, Volume = {7}, @@ -1687,7 +1686,7 @@ DISCUSSION: Our case studies highlight that not all athletes with history of rep Keywords = {cortex; mouse; neuroscience; topographic map; visual map}, Month = {Jan}, Pmc = {PMC5218535}, - pubmed = {28059700}, + pmid = {28059700}, Pst = {epublish}, Title = {An extended retinotopic map of mouse cortex}, Volume = {6}, @@ -1706,7 +1705,7 @@ DISCUSSION: Our case studies highlight that not all athletes with history of rep Mesh = {Animals; Apoptosis; Body Size; DNA Repair; Elephants; Evolution, Molecular; Gene Dosage; Gene Expression Profiling; Genes, p53; Protein Biosynthesis; Signal Transduction; Transcription, Genetic}, Month = {09}, Pmc = {PMC5061548}, - pubmed = {27642012}, + pmid = {27642012}, Pst = {epublish}, Title = {TP53 copy number expansion is associated with the evolution of increased body size and an enhanced DNA damage response in elephants}, Volume = {5}, @@ -1728,7 +1727,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Month = {May}, Number = {5}, Pages = {433-43}, - pubmed = {15195792}, + pmid = {15195792}, Pst = {ppublish}, Title = {Cumulative effects of concussion in amateur athletes}, Volume = {18}, @@ -1748,7 +1747,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Month = {Jan}, Number = {2}, Pages = {302-306}, - pubmed = {29229842}, + pmid = {29229842}, Pst = {ppublish}, Title = {Male homosexuality and maternal immune responsivity to the Y-linked protein NLGN4Y}, Volume = {115}, @@ -1768,7 +1767,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Number = {1}, Pages = {221-230.e4}, Pmc = {PMC5754239}, - pubmed = {29249289}, + pmid = {29249289}, Pst = {ppublish}, Title = {Old Brains Come Uncoupled in Sleep: Slow Wave-Spindle Synchrony, Brain Atrophy, and Forgetting}, Volume = {97}, @@ -1789,7 +1788,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Number = {5}, Pages = {716-724}, Pmc = {PMC4846490}, - pubmed = {26928064}, + pmid = {26928064}, Pst = {ppublish}, Title = {Early hyperactivity and precocious maturation of corticostriatal circuits in Shank3B(-/-) mice}, Volume = {19}, @@ -1809,7 +1808,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Number = {7}, Pages = {503-13}, Pmc = {PMC3447364}, - pubmed = {20559337}, + pmid = {20559337}, Pst = {ppublish}, Title = {The habenula: from stress evasion to value-based decision-making}, Volume = {11}, @@ -1828,7 +1827,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Number = {3}, Pages = {507-18}, Pmc = {PMC2132923}, - pubmed = {9971745}, + pmid = {9971745}, Pst = {ppublish}, Title = {Neurotransmitter secretion along growing nerve processes: comparison with synaptic vesicle exocytosis}, Volume = {144}, @@ -1847,7 +1846,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Number = {3}, Pages = {398-414}, Pmc = {PMC4651208}, - pubmed = {16320250}, + pmid = {16320250}, Pst = {ppublish}, Title = {Development of layer-specific axonal arborizations in mouse primary somatosensory cortex}, Volume = {494}, @@ -1866,7 +1865,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Number = {3}, Pages = {507-18}, Pmc = {PMC2132923}, - pubmed = {9971745}, + pmid = {9971745}, Pst = {ppublish}, Title = {Neurotransmitter secretion along growing nerve processes: comparison with synaptic vesicle exocytosis}, Volume = {144}, @@ -1886,7 +1885,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Number = {21}, Pages = {7191-201}, Pmc = {PMC3466079}, - pubmed = {22623663}, + pmid = {22623663}, Pst = {ppublish}, Title = {Fibroblast growth factor 8 organizes the neocortical area map and regulates sensory map topography}, Volume = {32}, @@ -1905,7 +1904,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Month = {Dec}, Number = {6}, Pages = {1051-61}, - pubmed = {12495621}, + pmid = {12495621}, Pst = {ppublish}, Title = {Paracrine intercellular communication by a Ca2+- and SNARE-independent release of GABA and glutamate prior to synapse formation}, Volume = {36}, @@ -1926,7 +1925,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Number = {1688}, Pages = {20150115}, Pmc = {PMC4785901}, - pubmed = {26833836}, + pmid = {26833836}, Pst = {ppublish}, Title = {Hypothalamic control of the male neonatal testosterone surge}, Volume = {371}, @@ -1963,7 +1962,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Number = {3}, Pages = {206-20}, Pmc = {PMC4756920}, - pubmed = {17299456}, + pmid = {17299456}, Pst = {ppublish}, Title = {Cell adhesion molecules: signalling functions at the synapse}, Volume = {8}, @@ -1985,7 +1984,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Number = {2}, Pages = {358-71}, Pmc = {PMC4815281}, - pubmed = {23818057}, + pmid = {23818057}, Pst = {ppublish}, Title = {Estrogen receptor β expression in the mouse forebrain: age and sex differences}, Volume = {522}, @@ -2025,7 +2024,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Number = {4}, Pages = {499-501}, Pmc = {PMC3226785}, - pubmed = {22099452}, + pmid = {22099452}, Pst = {ppublish}, Title = {Mapping genetic influences on cortical regionalization}, Volume = {72}, @@ -2044,7 +2043,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Month = {Apr}, Number = {15}, Pages = {6476-91}, - pubmed = {23575846}, + pmid = {23575846}, Pst = {ppublish}, Title = {Separate Ca2+ sources are buffered by distinct Ca2+ handling systems in aplysia neuroendocrine cells}, Volume = {33}, @@ -2062,7 +2061,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Keywords = {anterior commissure; axon guidance; commissural plate; comparative neuroanatomy; corpus callosum; hippocampal commissure}, Pages = {497}, Pmc = {PMC4094842}, - pubmed = {25071525}, + pmid = {25071525}, Pst = {epublish}, Title = {Evolution and development of interhemispheric connections in the vertebrate forebrain}, Volume = {8}, @@ -2080,7 +2079,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Keywords = {action potentials; calcium; calcium sensing receptor; excitability; ion channels; nervous system; synaptic transmission}, Pages = {116}, Pmc = {PMC4811949}, - pubmed = {27065884}, + pmid = {27065884}, Pst = {epublish}, Title = {Calcium-Sensing Receptor: A Key Target for Extracellular Calcium Signaling in Neurons}, Volume = {7}, @@ -2100,7 +2099,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Number = {2}, Pages = {261-77}, Pmc = {PMC4873772}, - pubmed = {27100196}, + pmid = {27100196}, Pst = {ppublish}, Title = {Ctip1 Controls Acquisition of Sensory Area Identity and Establishment of Sensory Input Fields in the Developing Neocortex}, Volume = {90}, @@ -2122,7 +2121,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Number = {3}, Pages = {609-29}, Pmc = {PMC4706819}, - pubmed = {26304102}, + pmid = {26304102}, Pst = {ppublish}, Title = {Transcriptional and epigenetic mechanisms of early cortical development: An examination of how Pax6 coordinates cortical development}, Volume = {524}, @@ -2141,7 +2140,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Keywords = {Transcriptomics; computational biology; developmental biology; human; mouse; stem cells; systems biology}, Month = {Mar}, Pmc = {PMC5352226}, - pubmed = {28296636}, + pmid = {28296636}, Pst = {epublish}, Title = {Discovering sparse transcription factor codes for cell states and state transitions during development}, Volume = {6}, @@ -2160,7 +2159,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Mesh = {Animals; Biological Evolution; Brain Mapping; Nerve Tissue Proteins; Neurons; Visual Cortex; Visual Pathways}, Pages = {79}, Pmc = {PMC4081835}, - pubmed = {25071460}, + pmid = {25071460}, Pst = {epublish}, Title = {Mapping arealisation of the visual cortex of non-primate species: lessons for development and evolution}, Volume = {8}, @@ -2179,7 +2178,7 @@ CONCLUSIONS: This study provides preliminary evidence to suggest that athletes w Month = {Aug}, Number = {35}, Pages = {13938-9}, - pubmed = {23986230}, + pmid = {23986230}, Pst = {ppublish}, Title = {Thalamic afferents and neocortical arealization: an ongoing journey}, Volume = {33}, @@ -2201,7 +2200,7 @@ SUMMARY: These recent studies have revealed interwoven links between thalamic an Month = {Apr}, Number = {2}, Pages = {142-8}, - pubmed = {24553463}, + pmid = {24553463}, Pst = {ppublish}, Title = {Nurturing the cortex's thalamic nature}, Volume = {27}, @@ -2218,7 +2217,7 @@ SUMMARY: These recent studies have revealed interwoven links between thalamic an Month = {Jul}, Pages = {16042}, Pmc = {PMC5500875}, - pubmed = {28671189}, + pmid = {28671189}, Pst = {epublish}, Title = {Fate and freedom in developing neocortical circuits}, Volume = {8}, @@ -2237,7 +2236,7 @@ SUMMARY: These recent studies have revealed interwoven links between thalamic an Month = {Oct}, Number = {7623}, Pages = {96-98}, - pubmed = {27669022}, + pmid = {27669022}, Pst = {ppublish}, Title = {A cross-modal genetic framework for the development and plasticity of sensory pathways}, Volume = {538}, @@ -2259,7 +2258,7 @@ SUMMARY: These recent studies have revealed interwoven links between thalamic an Number = {3}, Pages = {536-49}, Pmc = {PMC4742537}, - pubmed = {26844833}, + pmid = {26844833}, Pst = {ppublish}, Title = {A Transient Translaminar GABAergic Interneuron Circuit Connects Thalamocortical Recipient Layers in Neonatal Somatosensory Cortex}, Volume = {89}, @@ -2280,7 +2279,7 @@ SUMMARY: These recent studies have revealed interwoven links between thalamic an Number = {3}, Pages = {632-43}, Pmc = {PMC4529541}, - pubmed = {26247867}, + pmid = {26247867}, Pst = {ppublish}, Title = {Modularity in the Organization of Mouse Primary Visual Cortex}, Volume = {87}, @@ -2301,7 +2300,7 @@ SUMMARY: These recent studies have revealed interwoven links between thalamic an Number = {6137}, Pages = {1239-42}, Pmc = {PMC3851411}, - pubmed = {23744949}, + pmid = {23744949}, Pst = {ppublish}, Title = {Geniculocortical input drives genetic distinctions between primary and higher-order visual areas}, Volume = {340}, @@ -2323,7 +2322,7 @@ SUMMARY: These recent studies have revealed interwoven links between thalamic an Number = {3}, Pages = {503-15}, Pmc = {PMC4431637}, - pubmed = {25635458}, + pmid = {25635458}, Pst = {ppublish}, Title = {Identification of a spinal circuit for light touch and fine motor control}, Volume = {160}, @@ -2344,7 +2343,7 @@ SUMMARY: These recent studies have revealed interwoven links between thalamic an Number = {4}, Pages = {217-32}, Pmc = {PMC4107216}, - pubmed = {24646670}, + pmid = {24646670}, Pst = {ppublish}, Title = {Growth and folding of the mammalian cerebral cortex: from molecules to malformations}, Volume = {15}, @@ -2364,7 +2363,7 @@ SUMMARY: These recent studies have revealed interwoven links between thalamic an Number = {2}, Pages = {170-81}, Pmc = {PMC4889215}, - pubmed = {25622573}, + pmid = {25622573}, Pst = {ppublish}, Title = {The neocortical circuit: themes and variations}, Volume = {18}, @@ -2382,7 +2381,7 @@ SUMMARY: These recent studies have revealed interwoven links between thalamic an Mesh = {Animals; COUP Transcription Factor I; Female; Gene Expression Regulation, Developmental; Male; Mice; Mice, Knockout; Mitosis; Neocortex; Sensory Receptor Cells}, Month = {Dec}, Pages = {5632}, - pubmed = {25476200}, + pmid = {25476200}, Pst = {epublish}, Title = {Postmitotic control of sensory area specification during neocortical development}, Volume = {5}, @@ -2401,7 +2400,7 @@ SUMMARY: These recent studies have revealed interwoven links between thalamic an Mesh = {Animals; Gene Expression Regulation, Developmental; Homeodomain Proteins; Mice, Inbred C57BL; Mice, Transgenic; Transcription Factors; Vision, Ocular; Visual Cortex}, Month = {Dec}, Pmc = {PMC4739755}, - pubmed = {26705332}, + pmid = {26705332}, Pst = {epublish}, Title = {Genetic mechanisms control the linear scaling between related cortical primary and higher order sensory areas}, Volume = {4}, @@ -2422,7 +2421,7 @@ CONCLUSIONS: We demonstrate that interhemispheric connectivity and cortical area Month = {Apr}, Pages = {10}, Pmc = {PMC4412039}, - pubmed = {25879444}, + pmid = {25879444}, Pst = {epublish}, Title = {Formation of functional areas in the cerebral cortex is disrupted in a mouse model of autism spectrum disorder}, Volume = {10}, @@ -2442,7 +2441,7 @@ CONCLUSIONS: We demonstrate that interhemispheric connectivity and cortical area Month = {Aug}, Number = {8}, Pages = {847-81}, - pubmed = {26581033}, + pmid = {26581033}, Pst = {ppublish}, Title = {Tangential migration of glutamatergic neurons and cortical patterning during development: Lessons from Cajal-Retzius cells}, Volume = {76}, @@ -2462,7 +2461,7 @@ CONCLUSIONS: We demonstrate that interhemispheric connectivity and cortical area Number = {19}, Pages = {8442-53}, Pmc = {PMC3732791}, - pubmed = {23658181}, + pmid = {23658181}, Pst = {ppublish}, Title = {Thalamic control of neocortical area formation in mice}, Volume = {33}, @@ -2482,7 +2481,7 @@ CONCLUSIONS: We demonstrate that interhemispheric connectivity and cortical area Number = {18}, Pages = {7652-7}, Pmc = {PMC1863435}, - pubmed = {17442747}, + pmid = {17442747}, Pst = {ppublish}, Title = {Patterning of frontal cortex subdivisions by Fgf17}, Volume = {104}, @@ -2502,7 +2501,7 @@ CONCLUSIONS: We demonstrate that interhemispheric connectivity and cortical area Number = {15}, Pages = {6321-32}, Pmc = {PMC3698850}, - pubmed = {23575831}, + pmid = {23575831}, Pst = {ppublish}, Title = {Lmo4 establishes rostral motor cortex projection neuron subtype diversity}, Volume = {33}, @@ -2522,7 +2521,7 @@ CONCLUSIONS: We demonstrate that interhemispheric connectivity and cortical area Number = {6}, Pages = {712-8}, Pmc = {PMC2791850}, - pubmed = {19446478}, + pmid = {19446478}, Pst = {ppublish}, Title = {Signals from the edges: the cortical hem and antihem in telencephalic development}, Volume = {20}, @@ -2543,7 +2542,7 @@ CONCLUSIONS: We demonstrate that interhemispheric connectivity and cortical area Number = {14}, Pages = {2855-65}, Pmc = {PMC4197624}, - pubmed = {24948604}, + pmid = {24948604}, Pst = {ppublish}, Title = {The cortical hem regulates the size and patterning of neocortex}, Volume = {141}, @@ -2562,7 +2561,7 @@ CONCLUSIONS: We demonstrate that interhemispheric connectivity and cortical area Month = {Sep}, Number = {9}, Pages = {469-76}, - pubmed = {12948657}, + pmid = {12948657}, Pst = {ppublish}, Title = {Forebrain gene expression domains and the evolving prosomeric model}, Volume = {26}, @@ -2583,7 +2582,7 @@ CONCLUSIONS: We demonstrate that interhemispheric connectivity and cortical area Number = {1}, Pages = {90-100}, Pmc = {PMC2677555}, - pubmed = {18524571}, + pmid = {18524571}, Pst = {ppublish}, Title = {Genetic regulation of arealization of the neocortex}, Volume = {18}, @@ -2602,7 +2601,7 @@ SUMMARY: Quantitative mapping of selective OXTR ligand binding during postnatal Keywords = {adrenal gland; autism; autoradiography; experience-dependent plasticity; kidney; neocortex; oronasal cavity; oxytocin}, Pages = {195}, Pmc = {PMC3858721}, - pubmed = {24376405}, + pmid = {24376405}, Pst = {epublish}, Title = {Oxytocin receptor ligand binding in embryonic tissue and postnatal brain development of the C57BL/6J mouse}, Volume = {7}, @@ -2625,7 +2624,7 @@ The results demonstrate that the disappearance of oxytocin from the blood seems Month = {Jul}, Number = {3}, Pages = {425-31}, - pubmed = {5820054}, + pmid = {5820054}, Pst = {ppublish}, Title = {Half-life of oxytocin in blood of pregnant and non-pregnant women}, Volume = {61}, @@ -2643,7 +2642,7 @@ The results demonstrate that the disappearance of oxytocin from the blood seems Number = {2}, Pages = {e0172904}, Pmc = {PMC5325587}, - pubmed = {28235051}, + pmid = {28235051}, Pst = {epublish}, Title = {Oxytocin receptor binding sites in the periphery of the neonatal mouse}, Volume = {12}, @@ -2661,7 +2660,7 @@ The results demonstrate that the disappearance of oxytocin from the blood seems Month = {10}, Number = {6361}, Pages = {369-372}, - pubmed = {29051381}, + pmid = {29051381}, Pst = {ppublish}, Title = {Learning-enhanced coupling between ripple oscillations in association cortices and hippocampus}, Volume = {358}, @@ -2682,7 +2681,7 @@ The results demonstrate that the disappearance of oxytocin from the blood seems Number = {9}, Pages = {e0185541}, Pmc = {PMC5614644}, - pubmed = {28950005}, + pmid = {28950005}, Pst = {epublish}, Title = {CCL11 is increased in the CNS in chronic traumatic encephalopathy but not in Alzheimer's disease}, Volume = {12}, @@ -2702,7 +2701,7 @@ The results demonstrate that the disappearance of oxytocin from the blood seems Mesh = {Animals; Brain Injury, Chronic; Craniocerebral Trauma; Disease Models, Animal; Humans; Mice; Translational Medical Research; tau Proteins}, Month = {Jan}, Pages = {389-404}, - pubmed = {26054886}, + pmid = {26054886}, Pst = {ppublish}, Title = {Repetitive head trauma, chronic traumatic encephalopathy and tau: Challenges in translating from mice to men}, Volume = {275 Pt 3}, @@ -2724,7 +2723,7 @@ The results demonstrate that the disappearance of oxytocin from the blood seems Number = {Pt 1}, Pages = {43-64}, Pmc = {PMC3624697}, - pubmed = {23208308}, + pmid = {23208308}, Pst = {ppublish}, Title = {The spectrum of disease in chronic traumatic encephalopathy}, Volume = {136}, @@ -2745,7 +2744,7 @@ The results demonstrate that the disappearance of oxytocin from the blood seems Number = {4}, Pages = {211-21}, Pmc = {PMC4513655}, - pubmed = {23458973}, + pmid = {23458973}, Pst = {ppublish}, Title = {Chronic neuropathologies of single and repetitive TBI: substrates of dementia?}, Volume = {9}, @@ -2765,7 +2764,7 @@ The results demonstrate that the disappearance of oxytocin from the blood seems Month = {May}, Pages = {21-45}, Pmc = {PMC5367053}, - pubmed = {26772317}, + pmid = {26772317}, Pst = {ppublish}, Title = {Chronic Traumatic Encephalopathy: The Neuropathological Legacy of Traumatic Brain Injury}, Volume = {11}, @@ -2783,7 +2782,7 @@ The results demonstrate that the disappearance of oxytocin from the blood seems Keywords = {chronic traumatic encephalopathy; concussion; football; history; neurodegenerative disorders; traumatic brain injury; concussion}, Mesh = {Biomarkers; Boxing; Brain; Brain Injury, Chronic; Football; History, 20th Century; History, 21st Century; Humans; Neuroimaging; Risk Factors}, Pages = {309-30}, - pubmed = {25581233}, + pmid = {25581233}, Pst = {ppublish}, Title = {Chronic traumatic encephalopathy: historical origins and current perspective}, Volume = {11}, @@ -2804,7 +2803,7 @@ The results demonstrate that the disappearance of oxytocin from the blood seems Number = {1}, Pages = {75-86}, Pmc = {PMC4698281}, - pubmed = {26667418}, + pmid = {26667418}, Pst = {ppublish}, Title = {The first NINDS/NIBIB consensus meeting to define neuropathological criteria for the diagnosis of chronic traumatic encephalopathy}, Volume = {131}, @@ -2823,7 +2822,7 @@ The results demonstrate that the disappearance of oxytocin from the blood seems Month = {Sep}, Number = {1}, Pages = {72-7}, - pubmed = {16083970}, + pmid = {16083970}, Pst = {ppublish}, Title = {Partial nucleotide sequences and expression patterns of frog (Rana pipiens) ephrin-A2 and ephrin-A5 mRNA}, Volume = {159}, @@ -2842,7 +2841,7 @@ The results demonstrate that the disappearance of oxytocin from the blood seems Month = {May}, Number = {17}, Pages = {5388-95}, - pubmed = {15113210}, + pmid = {15113210}, Pst = {ppublish}, Title = {Preparation of protein gradients through the controlled deposition of protein-nanoparticle conjugates onto functionalized surfaces}, Volume = {126}, @@ -2862,7 +2861,7 @@ The results demonstrate that the disappearance of oxytocin from the blood seems Number = {25}, Pages = {8778-83}, Pmc = {PMC2438395}, - pubmed = {18562299}, + pmid = {18562299}, Pst = {ppublish}, Title = {Ephrins as negative regulators of adult neurogenesis in diverse regions of the central nervous system}, Volume = {105}, @@ -2883,7 +2882,7 @@ CONCLUSIONS: Taken together, these data suggest that Isl2+ RGCs comprise a disti Month = {Feb}, Pages = {2}, Pmc = {PMC3937143}, - pubmed = {24495295}, + pmid = {24495295}, Pst = {epublish}, Title = {Dendritic and axonal targeting patterns of a genetically-specified class of retinal ganglion cells that participate in image-forming circuits}, Volume = {9}, @@ -2904,7 +2903,7 @@ CONCLUSIONS: Taken together, these data suggest that Isl2+ RGCs comprise a disti Number = {16}, Pages = {5447-53}, Pmc = {PMC3988404}, - pubmed = {24741035}, + pmid = {24741035}, Pst = {ppublish}, Title = {Tbr2 is required to generate a neural circuit mediating the pupillary light reflex}, Volume = {34}, @@ -2925,7 +2924,7 @@ CONCLUSIONS: Taken together, these data suggest that Isl2+ RGCs comprise a disti Number = {6}, Pages = {584-93}, Pmc = {PMC4437846}, - pubmed = {25649160}, + pmid = {25649160}, Pst = {ppublish}, Title = {Ephrin-As are required for the topographic mapping but not laminar choice of physiologically distinct RGC types}, Volume = {75}, @@ -2945,7 +2944,7 @@ CONCLUSIONS: Taken together, these data suggest that Isl2+ RGCs comprise a disti Number = {6}, Pages = {1261-73}, Pmc = {PMC4583656}, - pubmed = {26402608}, + pmid = {26402608}, Pst = {ppublish}, Title = {Stochastic Interaction between Neural Activity and Molecular Cues in the Formation of Topographic Maps}, Volume = {87}, @@ -2967,7 +2966,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Number = {19}, Pages = {5252-63}, Pmc = {PMC4863061}, - pubmed = {27170123}, + pmid = {27170123}, Pst = {ppublish}, Title = {Corticothalamic Axons Are Essential for Retinal Ganglion Cell Axon Targeting to the Mouse Dorsal Lateral Geniculate Nucleus}, Volume = {36}, @@ -2984,7 +2983,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Journal-Full = {The Journal of comparative neurology}, Keywords = {RRID: AB_10615604; RRID: AB_11143446; RRID: AB_1608077; RRID: AB_2167511; RRID: AB_2301417; RRID: AB_2313614; RRID: AB_231491; RRID: AB_882455; cell fate; retinal ganglion cells; transcription factors}, Month = {Jan}, - pubmed = {28078709}, + pmid = {28078709}, Pst = {aheadofprint}, Title = {Expression of transcription factors divides retinal ganglion cells into distinct classes}, Year = {2017}, @@ -3004,7 +3003,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Number = {35}, Pages = {8428-8443}, Pmc = {PMC5577856}, - pubmed = {28760858}, + pmid = {28760858}, Pst = {ppublish}, Title = {Segregation of Visual Response Properties in the Mouse Superior Colliculus and Their Modulation during Locomotion}, Volume = {37}, @@ -3023,7 +3022,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Month = {May}, Number = {1}, Pages = {30-48}, - pubmed = {19260054}, + pmid = {19260054}, Pst = {ppublish}, Title = {Eph/ephrin gradients in the retinotectal system of Rana pipiens: developmental and adult expression patterns}, Volume = {514}, @@ -3043,7 +3042,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Number = {11}, Pages = {a001768}, Pmc = {PMC2964178}, - pubmed = {20880989}, + pmid = {20880989}, Pst = {ppublish}, Title = {Visual map development: bidirectional signaling, bifunctional guidance molecules, and competition}, Volume = {2}, @@ -3063,7 +3062,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Number = {4}, Pages = {547-63}, Pmc = {PMC3395774}, - pubmed = {21656698}, + pmid = {21656698}, Pst = {ppublish}, Title = {Expression patterns of Ephs and ephrins throughout retinotectal development in Xenopus laevis}, Volume = {72}, @@ -3083,7 +3082,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Number = {4}, Pages = {632-9}, Pmc = {PMC3513360}, - pubmed = {21867880}, + pmid = {21867880}, Pst = {ppublish}, Title = {Cadherin-6 mediates axon-target matching in a non-image-forming visual circuit}, Volume = {71}, @@ -3103,7 +3102,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Number = {1}, Pages = {7-15}, Pmc = {PMC3288406}, - pubmed = {22044886}, + pmid = {22044886}, Pst = {ppublish}, Title = {Eph and ephrin signaling in the formation of topographic maps}, Volume = {23}, @@ -3123,7 +3122,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Number = {47}, Pages = {19060-5}, Pmc = {PMC3223436}, - pubmed = {22065784}, + pmid = {22065784}, Pst = {ppublish}, Title = {Competition is a driving force in topographic mapping}, Volume = {108}, @@ -3143,7 +3142,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Number = {2}, Pages = {174-80}, Pmc = {PMC2726114}, - pubmed = {19481440}, + pmid = {19481440}, Pst = {ppublish}, Title = {Making a visual map: mechanisms and molecules}, Volume = {19}, @@ -3163,7 +3162,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Number = {50}, Pages = {12873-84}, Pmc = {PMC3664553}, - pubmed = {17167078}, + pmid = {17167078}, Pst = {ppublish}, Title = {Ephrin-As and patterned retinal activity act together in the development of topographic maps in the primary visual system}, Volume = {26}, @@ -3182,7 +3181,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Month = {Aug}, Number = {1-2}, Pages = {102-6}, - pubmed = {16002151}, + pmid = {16002151}, Pst = {ppublish}, Title = {Eph/ephrin A- and B-family expression patterns in the leopard frog (Rana utricularia)}, Volume = {158}, @@ -3201,7 +3200,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Month = {Jul}, Number = {2}, Pages = {140-51}, - pubmed = {15924339}, + pmid = {15924339}, Pst = {ppublish}, Title = {Ephrin-A2 and -A5 influence patterning of normal and novel retinal projections to the thalamus: conserved mapping mechanisms in visual and auditory thalamic targets}, Volume = {488}, @@ -3220,7 +3219,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Month = {May}, Number = {5}, Pages = {501-9}, - pubmed = {15107857}, + pmid = {15107857}, Pst = {ppublish}, Title = {Repelling class discrimination: ephrin-A5 binds to and activates EphB2 receptor signaling}, Volume = {7}, @@ -3238,7 +3237,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Month = {Feb}, Number = {2}, Pages = {295-306}, - pubmed = {10719886}, + pmid = {10719886}, Pst = {ppublish}, Title = {Roles for ephrins in positionally selective synaptogenesis between motor neurons and muscle fibers}, Volume = {25}, @@ -3255,7 +3254,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Month = {Mar}, Number = {3}, Pages = {563-74}, - pubmed = {10774725}, + pmid = {10774725}, Pst = {ppublish}, Title = {Genetic analysis of ephrin-A2 and ephrin-A5 shows their requirement in multiple aspects of retinocollicular mapping}, Volume = {25}, @@ -3273,7 +3272,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Month = {Dec}, Number = {4}, Pages = {549-65}, - pubmed = {14624488}, + pmid = {14624488}, Pst = {ppublish}, Title = {Persistence of graded EphA/Ephrin-A expression in the adult frog visual system}, Volume = {467}, @@ -3292,7 +3291,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Month = {Mar}, Number = {10}, Pages = {2542-50}, - pubmed = {15014130}, + pmid = {15014130}, Pst = {ppublish}, Title = {Loss-of-function analysis of EphA receptors in retinotectal mapping}, Volume = {24}, @@ -3309,7 +3308,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Number = {1}, Pages = {38-48}, Pmc = {PMC1465472}, - pubmed = {16992721}, + pmid = {16992721}, Pst = {ppublish}, Title = {The function of the hyaloid canal and some other new points in the mechanism of the accommodation of the eye for distance}, Volume = {31}, @@ -3327,7 +3326,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Month = {Dec}, Number = {6}, Pages = {2055-72}, - pubmed = {3236061}, + pmid = {3236061}, Pst = {ppublish}, Title = {The accessory optic system of rabbit. II. Spatial organization of direction selectivity}, Volume = {60}, @@ -3344,7 +3343,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Month = {Jul}, Number = {1}, Pages = {376-89}, - pubmed = {10899212}, + pmid = {10899212}, Pst = {ppublish}, Title = {Early components of the human vestibulo-ocular response to head rotation: latency and gain}, Volume = {84}, @@ -3361,7 +3360,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Month = {Nov}, Number = {6}, Pages = {395-407}, - pubmed = {14784863}, + pmid = {14784863}, Pst = {ppublish}, Title = {The elementary vestibulo-ocular reflex arc}, Volume = {13}, @@ -3379,7 +3378,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Number = {2}, Pages = {471-98}, Pmc = {PMC1283576}, - pubmed = {857007}, + pmid = {857007}, Pst = {ppublish}, Title = {Eye- and head movements in freely moving rabbits}, Volume = {266}, @@ -3395,7 +3394,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Mesh = {Acoustic Maculae; Animals; Cebidae; Eye Movements; Motion Perception; Neurons, Afferent; Rotation; Saimiri; Semicircular Canals; Vestibular Nerve}, Number = {3}, Pages = {393-402}, - pubmed = {6124447}, + pmid = {6124447}, Pst = {ppublish}, Title = {Eye movements and vestibular-nerve responses produced in the squirrel monkey by rotations about an earth-horizontal axis}, Volume = {46}, @@ -3413,7 +3412,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Month = {Jan}, Number = {1}, Pages = {161-9}, - pubmed = {14715949}, + pmid = {14715949}, Pst = {ppublish}, Title = {Functional and genomic changes in the mouse ocular motor system in response to light deprivation from birth}, Volume = {24}, @@ -3431,7 +3430,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Mesh = {Algorithms; Artifacts; Brain; Humans; Magnetoencephalography; Neural Networks (Computer); Normal Distribution}, Number = {4-5}, Pages = {411-30}, - pubmed = {10946390}, + pmid = {10946390}, Pst = {ppublish}, Title = {Independent component analysis: algorithms and applications}, Volume = {13}, @@ -3448,7 +3447,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Mesh = {Animals; Brain; Cranial Nerves; Eye Abnormalities; Mice}, Month = {Oct}, Pages = {121-39}, - pubmed = {21004976}, + pmid = {21004976}, Pst = {ppublish}, Title = {Studies on an anophthalmic strain of mice; associated cranial nerves and brain centers}, Volume = {83}, @@ -3467,7 +3466,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Month = {Aug}, Number = {32}, Pages = {10667-82}, - pubmed = {20702698}, + pmid = {20702698}, Pst = {ppublish}, Title = {Intralaminar and interlaminar activity within the rodent superior colliculus visualized with voltage imaging}, Volume = {30}, @@ -3485,7 +3484,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Keywords = {anatomy; barrel cortex; basal ganglia; cerebellum; follicle--sinus complex; rhythmic movements; sensorimotor integration; vibrissa}, Pages = {53}, Pmc = {PMC3207327}, - pubmed = {22065951}, + pmid = {22065951}, Pst = {epublish}, Title = {Anatomical pathways involved in generating and sensing rhythmic whisker movements}, Volume = {5}, @@ -3504,7 +3503,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Month = {Feb}, Number = {2}, Pages = {1386-1400}, - pubmed = {26733529}, + pmid = {26733529}, Pst = {ppublish}, Title = {Disrupted Cortical State Regulation in a Rat Model of Fragile X Syndrome}, Volume = {27}, @@ -3523,7 +3522,7 @@ SIGNIFICANCE STATEMENT: The dorsal lateral geniculate nucleus (dLGN) is a sensor Keywords = {EEG; activity depedent development; neuroscience; oscillations; plasticity; rat; retinal waves}, Month = {Oct}, Pmc = {PMC5059135}, - pubmed = {27725086}, + pmid = {27725086}, Pst = {epublish}, Title = {An excitatory cortical feedback loop gates retinal wave transmission in rodent thalamus}, Volume = {5}, @@ -3547,7 +3546,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Number = {48}, Pages = {12259-12275}, Pmc = {PMC5148222}, - pubmed = {27903733}, + pmid = {27903733}, Pst = {ppublish}, Title = {Development of Activity in the Mouse Visual Cortex}, Volume = {36}, @@ -3566,7 +3565,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Keywords = {development; oscillation; retinal wave; spindle-burst; spontaneous activity; synchronization; visual cortex}, Pages = {289}, Pmc = {PMC5611364}, - pubmed = {28979189}, + pmid = {28979189}, Pst = {epublish}, Title = {Uncorrelated Neural Firing in Mouse Visual Cortex during Spontaneous Retinal Waves}, Volume = {11}, @@ -3585,7 +3584,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Sep}, Number = {3}, Pages = {276-88}, - pubmed = {9298765}, + pmid = {9298765}, Pst = {ppublish}, Title = {Supraspinal influence on the development of motor behavior in the fetal lamb}, Volume = {33}, @@ -3604,7 +3603,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Jul}, Number = {7}, Pages = {1510-9}, - pubmed = {21885532}, + pmid = {21885532}, Pst = {ppublish}, Title = {Satb2 is required for dendritic arborization and soma spacing in mouse cerebral cortex}, Volume = {22}, @@ -3623,7 +3622,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Jul}, Number = {3}, Pages = {943-78}, - pubmed = {15987799}, + pmid = {15987799}, Pst = {ppublish}, Title = {Controlling cell behavior electrically: current views and future potential}, Volume = {85}, @@ -3643,7 +3642,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Mar}, Number = {1}, Pages = {77-96}, - pubmed = {3708387}, + pmid = {3708387}, Pst = {ppublish}, Title = {The organization of the rat motor cortex: a microstimulation mapping study}, Volume = {396}, @@ -3662,7 +3661,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Nov}, Number = {32}, Pages = {10411-8}, - pubmed = {14614100}, + pmid = {14614100}, Pst = {ppublish}, Title = {Electrophysiological differentiation of new neurons in the olfactory bulb}, Volume = {23}, @@ -3682,7 +3681,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Dec}, Number = {12}, Pages = {1277-83}, - pubmed = {14625554}, + pmid = {14625554}, Pst = {ppublish}, Title = {RNAi reveals doublecortin is required for radial migration in rat neocortex}, Volume = {6}, @@ -3701,7 +3700,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Mesh = {Animals; Cell Movement; Chlorides; Green Fluorescent Proteins; Humans; Juxtaglomerular Apparatus; Kinetics; Mice; Models, Biological; Neurons; Olfactory Bulb}, Month = {Jan}, Pages = {i119-20}, - pubmed = {15738068}, + pmid = {15738068}, Pst = {ppublish}, Title = {Functional properties of adult-born juxtaglomerular cells in the mammalian olfactory bulb}, Volume = {30 Suppl 1}, @@ -3721,7 +3720,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {May}, Number = {1}, Pages = {5-9}, - pubmed = {16630614}, + pmid = {16630614}, Pst = {ppublish}, Title = {The potential of endogenous neuronal replacement in developing cerebral cortex following hypoxic injury}, Volume = {199}, @@ -3742,7 +3741,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Nov}, Number = {44}, Pages = {11413-22}, - pubmed = {17079670}, + pmid = {17079670}, Pst = {ppublish}, Title = {Fusion of microglia with pyramidal neurons after retroviral infection}, Volume = {26}, @@ -3764,7 +3763,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Number = {1-2}, Pages = {113-23}, Pmc = {PMC2211714}, - pubmed = {17148954}, + pmid = {17148954}, Pst = {ppublish}, Title = {Citron kinase is required for postnatal neurogenesis in the hippocampus}, Volume = {29}, @@ -3785,7 +3784,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Nov}, Number = {48}, Pages = {12851-63}, - pubmed = {19036979}, + pmid = {19036979}, Pst = {ppublish}, Title = {Sequential generation of two distinct synapse-driven network patterns in developing neocortex}, Volume = {28}, @@ -3806,7 +3805,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Jan}, Number = {2}, Pages = {313-27}, - pubmed = {19144832}, + pmid = {19144832}, Pst = {ppublish}, Title = {Abnormal network activity in a targeted genetic model of human double cortex}, Volume = {29}, @@ -3826,7 +3825,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Sep}, Number = {1}, Pages = {98-103}, - pubmed = {12866130}, + pmid = {12866130}, Pst = {ppublish}, Title = {Single-cell study of motor cortex projections to the barrel field in rats}, Volume = {464}, @@ -3846,7 +3845,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Sep}, Number = {4}, Pages = {567-80}, - pubmed = {2822779}, + pmid = {2822779}, Pst = {ppublish}, Title = {Morphology and synaptic connections of crossed corticostriatal neurons in the rat}, Volume = {263}, @@ -3866,7 +3865,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Nov}, Number = {2}, Pages = {233-45}, - pubmed = {1184784}, + pmid = {1184784}, Pst = {ppublish}, Title = {Interhemispheric neocortical connections of the corpus callosum in the normal mouse: a study based on anterograde and retrograde methods}, Volume = {164}, @@ -3887,7 +3886,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Jan}, Number = {1}, Pages = {17-32}, - pubmed = {15612019}, + pmid = {15612019}, Pst = {ppublish}, Title = {Large-scale maintenance of dual projections by callosal and frontal cortical projection neurons in adult mice}, Volume = {482}, @@ -3908,7 +3907,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Number = {11}, Pages = {755-69}, Pmc = {PMC3876965}, - pubmed = {24105342}, + pmid = {24105342}, Pst = {ppublish}, Title = {Molecular logic of neocortical projection neuron specification, development and diversity}, Volume = {14}, @@ -3928,7 +3927,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Jun}, Number = {6}, Pages = {427-37}, - pubmed = {17514196}, + pmid = {17514196}, Pst = {ppublish}, Title = {Neuronal subtype specification in the cerebral cortex}, Volume = {8}, @@ -3948,7 +3947,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Oct}, Number = {10}, Pages = {1277-86}, - pubmed = {17828260}, + pmid = {17828260}, Pst = {ppublish}, Title = {COUP-TFI regulates the balance of cortical patterning between frontal/motor and sensory areas}, Volume = {10}, @@ -3967,7 +3966,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Jan}, Number = {1}, Pages = {85-97}, - pubmed = {11182083}, + pmid = {11182083}, Pst = {ppublish}, Title = {Forward signaling mediated by ephrin-B3 prevents contralateral corticospinal axons from recrossing the spinal cord midline}, Volume = {29}, @@ -3986,7 +3985,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Number = {22}, Pages = {13248-53}, Pmc = {PMC23772}, - pubmed = {9789074}, + pmid = {9789074}, Pst = {ppublish}, Title = {EphA4 (Sek1) receptor tyrosine kinase is required for the development of the corticospinal tract}, Volume = {95}, @@ -4004,7 +4003,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Jan}, Number = {1}, Pages = {73-84}, - pubmed = {11182082}, + pmid = {11182082}, Pst = {ppublish}, Title = {Kinase-dependent and kinase-independent functions of EphA4 receptors in major axon tract formation in vivo}, Volume = {29}, @@ -4023,7 +4022,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Mar}, Number = {6825}, Pages = {174-9}, - pubmed = {11242070}, + pmid = {11242070}, Pst = {ppublish}, Title = {Defining brain wiring patterns and mechanisms through gene trapping in mice}, Volume = {410}, @@ -4044,7 +4043,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Number = {5873}, Pages = {233-6}, Pmc = {PMC3158657}, - pubmed = {18403711}, + pmid = {18403711}, Pst = {ppublish}, Title = {Segregation of axial motor and sensory pathways via heterotypic trans-axonal signaling}, Volume = {320}, @@ -4065,7 +4064,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Number = {29}, Pages = {13129-34}, Pmc = {PMC2919950}, - pubmed = {20615956}, + pmid = {20615956}, Pst = {ppublish}, Title = {Tbr1 regulates regional and laminar identity of postmitotic neurons in developing neocortex}, Volume = {107}, @@ -4084,7 +4083,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Keywords = {CaMKII; Wnt5a; axon branching; axon guidance; axon outgrowth; calcium signaling; corpus callosum; microtubules}, Pages = {62}, Pmc = {PMC3202218}, - pubmed = {22046148}, + pmid = {22046148}, Pst = {epublish}, Title = {Signaling mechanisms in cortical axon growth, guidance, and branching}, Volume = {5}, @@ -4103,7 +4102,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Apr}, Number = {4}, Pages = {287-99}, - pubmed = {17375041}, + pmid = {17375041}, Pst = {ppublish}, Title = {Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity}, Volume = {8}, @@ -4124,7 +4123,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Number = {7}, Pages = {945-50}, Pmc = {PMC2597785}, - pubmed = {17620483}, + pmid = {17620483}, Pst = {ppublish}, Title = {The new neurobiology of autism: cortex, connectivity, and neuronal organization}, Volume = {64}, @@ -4145,7 +4144,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Number = {1}, Pages = {41-50}, Pmc = {PMC3053014}, - pubmed = {21129791}, + pmid = {21129791}, Pst = {ppublish}, Title = {Development, specification, and diversity of callosal projection neurons}, Volume = {34}, @@ -4165,7 +4164,7 @@ SIGNIFICANCE STATEMENT: Cortical activity is an important indicator of long-term Month = {Mar}, Number = {5}, Pages = {1384-94}, - pubmed = {17425565}, + pmid = {17425565}, Pst = {ppublish}, Title = {Axons of callosal neurons bifurcate transiently at the white matter before consolidating an interhemispheric projection}, Volume = {25}, @@ -4188,7 +4187,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Oct}, Number = {10}, Pages = {1728-37}, - pubmed = {22433022}, + pmid = {22433022}, Pst = {ppublish}, Title = {A mouse model for adolescent alcohol abuse: stunted growth and effects in brain}, Volume = {36}, @@ -4208,7 +4207,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Jan}, Number = {1}, Pages = {22-35}, - pubmed = {26656254}, + pmid = {26656254}, Pst = {ppublish}, Title = {Specification of synaptic connectivity by cell surface interactions}, Volume = {17}, @@ -4227,7 +4226,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Apr}, Number = {4}, Pages = {338-51}, - pubmed = {9566953}, + pmid = {9566953}, Pst = {ppublish}, Title = {Cadherin-6 in the developing mouse brain: expression along restricted connection systems and synaptic localization suggest a potential role in neuronal circuitry}, Volume = {211}, @@ -4245,7 +4244,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Dec}, Number = {24}, Pages = {10877-85}, - pubmed = {10594069}, + pmid = {10594069}, Pst = {ppublish}, Title = {Graded and areal expression patterns of regulatory genes and cadherins in embryonic neocortex independent of thalamocortical input}, Volume = {19}, @@ -4263,7 +4262,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Mesh = {Animals; Animals, Newborn; Brain; Cadherins; Cell Differentiation; Cerebellum; Cerebral Cortex; Mice; Mice, Inbred ICR; Neurons; Olivary Nucleus; Thalamus}, Number = {5-6}, Pages = {433-47}, - pubmed = {9361280}, + pmid = {9361280}, Pst = {ppublish}, Title = {Neuronal circuits are subdivided by differential expression of type-II classic cadherins in postnatal mouse brains}, Volume = {9}, @@ -4284,7 +4283,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Number = {24}, Pages = {9857-62}, Pmc = {PMC3116393}, - pubmed = {21613566}, + pmid = {21613566}, Pst = {ppublish}, Title = {Calcium-dependent dynamics of cadherin interactions at cell-cell junctions}, Volume = {108}, @@ -4304,7 +4303,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Nov}, Number = {2}, Pages = {91-100}, - pubmed = {11253370}, + pmid = {11253370}, Pst = {ppublish}, Title = {Cadherins in embryonic and neural morphogenesis}, Volume = {1}, @@ -4324,7 +4323,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Aug}, Number = {8}, Pages = {622-34}, - pubmed = {16025097}, + pmid = {16025097}, Pst = {ppublish}, Title = {Regulation of cadherin-mediated adhesion in morphogenesis}, Volume = {6}, @@ -4343,7 +4342,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Feb}, Number = {3}, Pages = {345-57}, - pubmed = {8608588}, + pmid = {8608588}, Pst = {ppublish}, Title = {Cell adhesion: the molecular basis of tissue architecture and morphogenesis}, Volume = {84}, @@ -4362,7 +4361,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Jan}, Number = {1}, Pages = {75-82}, - pubmed = {19197334}, + pmid = {19197334}, Pst = {ppublish}, Title = {Mechanotransduction at a distance: mechanically coupling the extracellular matrix with the nucleus}, Volume = {10}, @@ -4380,7 +4379,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Apr}, Number = {4}, Pages = {639-55}, - pubmed = {3048970}, + pmid = {3048970}, Pst = {ppublish}, Title = {The cadherins: cell-cell adhesion molecules controlling animal morphogenesis}, Volume = {102}, @@ -4397,7 +4396,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Oct}, Number = {5}, Pages = {555-62}, - pubmed = {11544023}, + pmid = {11544023}, Pst = {ppublish}, Title = {Anoikis mechanisms}, Volume = {13}, @@ -4415,7 +4414,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Jan}, Number = {1 Suppl}, Pages = {S99-105}, - pubmed = {11841621}, + pmid = {11841621}, Pst = {ppublish}, Title = {Emerging targets: molecular mechanisms of cell contact-mediated growth control}, Volume = {61}, @@ -4433,7 +4432,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Keywords = {cannabis; psychophysiology; psychosis; schizophrenia; schizotypy; spice; synthetic cannabinoids}, Pages = {54}, Pmc = {PMC4033190}, - pubmed = {24904437}, + pmid = {24904437}, Pst = {epublish}, Title = {Gone to Pot - A Review of the Association between Cannabis and Psychosis}, Volume = {5}, @@ -4453,7 +4452,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Number = {8}, Pages = {858-67}, Pmc = {PMC2735470}, - pubmed = {17671451}, + pmid = {17671451}, Pst = {ppublish}, Title = {Functional atlas of the integrin adhesome}, Volume = {9}, @@ -4474,7 +4473,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Number = {7280}, Pages = {485-92}, Pmc = {PMC2851742}, - pubmed = {20110992}, + pmid = {20110992}, Pst = {ppublish}, Title = {Cell mechanics and the cytoskeleton}, Volume = {463}, @@ -4493,7 +4492,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Mesh = {Animals; Biopolymers; Calcium; In Vitro Techniques; Microtubule-Associated Proteins; Microtubules; Sea Urchins; Swine; Tubulin}, Number = {2}, Pages = {125-35}, - pubmed = {9015201}, + pmid = {9015201}, Pst = {ppublish}, Title = {How calcium causes microtubule depolymerization}, Volume = {36}, @@ -4513,7 +4512,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Jun}, Number = {6}, Pages = {446-54}, - pubmed = {18464790}, + pmid = {18464790}, Pst = {ppublish}, Title = {Filopodia: molecular architecture and cellular functions}, Volume = {9}, @@ -4532,7 +4531,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Mar}, Number = {1}, Pages = {101-12}, - pubmed = {8815303}, + pmid = {8815303}, Pst = {ppublish}, Title = {Anterograde axonal tracing with the subunit B of cholera toxin: a highly sensitive immunohistochemical protocol for revealing fine axonal morphology in adult and neonatal brains}, Volume = {65}, @@ -4548,7 +4547,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Journal = {Nat Med}, Journal-Full = {Nature medicine}, Month = {May}, - pubmed = {28481360}, + pmid = {28481360}, Pst = {aheadofprint}, Title = {A chronic low dose of Δ(9)-tetrahydrocannabinol (THC) restores cognitive function in old mice}, Year = {2017}, @@ -4567,7 +4566,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Number = {Pt 23}, Pages = {5411-9}, Pmc = {PMC1533994}, - pubmed = {16306220}, + pmid = {16306220}, Pst = {ppublish}, Title = {The axonal transport of mitochondria}, Volume = {118}, @@ -4588,7 +4587,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Number = {Pt 9}, Pages = {2095-104}, Pmc = {PMC3656622}, - pubmed = {22619228}, + pmid = {22619228}, Pst = {ppublish}, Title = {The axonal transport of mitochondria}, Volume = {125}, @@ -4608,7 +4607,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Number = {4}, Pages = {2057-68}, Pmc = {PMC1415296}, - pubmed = {16467387}, + pmid = {16467387}, Pst = {ppublish}, Title = {Kinesin-1 and Dynein are the primary motors for fast transport of mitochondria in Drosophila motor axons}, Volume = {17}, @@ -4629,7 +4628,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Number = {4}, Pages = {541-55}, Pmc = {PMC2670979}, - pubmed = {19249275}, + pmid = {19249275}, Pst = {ppublish}, Title = {Miro1 is a calcium sensor for glutamate receptor-dependent localization of mitochondria at synapses}, Volume = {61}, @@ -4650,7 +4649,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Oct}, Number = {10}, Pages = {682-96}, - pubmed = {19773780}, + pmid = {19773780}, Pst = {ppublish}, Title = {Kinesin superfamily motor proteins and intracellular transport}, Volume = {10}, @@ -4671,7 +4670,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Number = {2}, Pages = {222-8}, Pmc = {PMC3378790}, - pubmed = {22406539}, + pmid = {22406539}, Pst = {ppublish}, Title = {Integrated control of axonemal dynein AAA(+) motors}, Volume = {179}, @@ -4691,7 +4690,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Number = {10}, Pages = {e26626}, Pmc = {PMC3200357}, - pubmed = {22039519}, + pmid = {22039519}, Pst = {ppublish}, Title = {Endo-lysosomal vesicles positive for Rab7 and LAMP1 are terminal vesicles for the transport of dextran}, Volume = {6}, @@ -4711,7 +4710,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Number = {2}, Pages = {292-309}, Pmc = {PMC4269290}, - pubmed = {25374356}, + pmid = {25374356}, Pst = {ppublish}, Title = {Axonal transport: cargo-specific mechanisms of motility and regulation}, Volume = {84}, @@ -4732,7 +4731,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Number = {11}, Pages = {1981-90}, Pmc = {PMC2758274}, - pubmed = {18434421}, + pmid = {18434421}, Pst = {ppublish}, Title = {ISL1 and BRN3B co-regulate the differentiation of murine retinal ganglion cells}, Volume = {135}, @@ -4752,7 +4751,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Jul}, Number = {3}, Pages = {1116-28}, - pubmed = {16545965}, + pmid = {16545965}, Pst = {ppublish}, Title = {User-guided 3D active contour segmentation of anatomical structures: significantly improved efficiency and reliability}, Volume = {31}, @@ -4771,7 +4770,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Jul}, Number = {1}, Pages = {57-69}, - pubmed = {15996548}, + pmid = {15996548}, Pst = {ppublish}, Title = {Opposing gradients of ephrin-As and EphA7 in the superior colliculus are essential for topographic mapping in the mammalian visual system}, Volume = {47}, @@ -4789,7 +4788,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Aug}, Number = {3}, Pages = {359-70}, - pubmed = {7634326}, + pmid = {7634326}, Pst = {ppublish}, Title = {In vitro guidance of retinal ganglion cell axons by RAGS, a 25 kDa tectal protein related to ligands for Eph receptor tyrosine kinases}, Volume = {82}, @@ -4807,7 +4806,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Aug}, Number = {3}, Pages = {371-81}, - pubmed = {7634327}, + pmid = {7634327}, Pst = {ppublish}, Title = {Complementary gradients in expression and binding of ELF-1 and Mek4 in development of the topographic retinotectal projection map}, Volume = {82}, @@ -4824,7 +4823,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Journal-Full = {Annual review of neuroscience}, Mesh = {Animals; Central Nervous System; Ephrin-A2; Ephrin-B1; Ephrin-B3; Membrane Proteins; Receptor Protein-Tyrosine Kinases; Transcription Factors}, Pages = {309-45}, - pubmed = {9530499}, + pmid = {9530499}, Pst = {ppublish}, Title = {The ephrins and Eph receptors in neural development}, Volume = {21}, @@ -4843,7 +4842,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Sep}, Number = {6}, Pages = {601-10}, - pubmed = {10498278}, + pmid = {10498278}, Pst = {ppublish}, Title = {Regional differences in the developing cerebral cortex revealed by ephrin-A5 expression}, Volume = {9}, @@ -4861,7 +4860,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Sep}, Number = {6}, Pages = {586-600}, - pubmed = {10498277}, + pmid = {10498277}, Pst = {ppublish}, Title = {Molecular gradients and compartments in the embryonic primate cerebral cortex}, Volume = {9}, @@ -4880,7 +4879,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Apr}, Number = {4}, Pages = {358-65}, - pubmed = {10725925}, + pmid = {10725925}, Pst = {ppublish}, Title = {A mapping label required for normal scale of body representation in the cortex}, Volume = {3}, @@ -4899,7 +4898,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Oct}, Number = {19}, Pages = {7684-90}, - pubmed = {11567058}, + pmid = {11567058}, Pst = {ppublish}, Title = {Enhanced plasticity of retinothalamic projections in an ephrin-A2/A5 double mutant}, Volume = {21}, @@ -4917,7 +4916,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Aug}, Number = {15}, Pages = {5841-7}, - pubmed = {10908626}, + pmid = {10908626}, Pst = {ppublish}, Title = {Malformation of the functional organization of somatosensory cortex in adult ephrin-A5 knock-out mice revealed by in vivo functional imaging}, Volume = {20}, @@ -4937,7 +4936,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Sep}, Number = {7108}, Pages = {167-72}, - pubmed = {16915236}, + pmid = {16915236}, Pst = {ppublish}, Title = {An RNA gene expressed during cortical development evolved rapidly in humans}, Volume = {443}, @@ -4958,7 +4957,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Number = {1752}, Pages = {20122370}, Pmc = {PMC3574304}, - pubmed = {23235704}, + pmid = {23235704}, Pst = {epublish}, Title = {Experimental demonstration of the growth rate--lifespan trade-off}, Volume = {280}, @@ -4978,7 +4977,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Apr}, Number = {2}, Pages = {365-79}, - pubmed = {24685175}, + pmid = {24685175}, Pst = {ppublish}, Title = {NMDAR-regulated dynamics of layer 4 neuronal dendrites during thalamocortical reorganization in neonates}, Volume = {82}, @@ -4997,7 +4996,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Mesh = {Animals; Axonal Transport; Axons; Brain Mapping; Cerebral Cortex; Humans; Macaca mulatta; Models, Anatomic; Neurons; Prefrontal Cortex; Wheat Germ Agglutinin-Horseradish Peroxidase Conjugate}, Number = {7}, Pages = {635-46}, - pubmed = {9373019}, + pmid = {9373019}, Pst = {ppublish}, Title = {Cortical structure predicts the pattern of corticocortical connections}, Volume = {7}, @@ -5018,7 +5017,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Number = {7}, Pages = {419-29}, Pmc = {PMC4731102}, - pubmed = {26016744}, + pmid = {26016744}, Pst = {ppublish}, Title = {Interoceptive predictions in the brain}, Volume = {16}, @@ -5072,7 +5071,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Nov}, Number = {21}, Pages = {9352-7}, - pubmed = {12417660}, + pmid = {12417660}, Pst = {ppublish}, Title = {Miswiring of limbic thalamocortical projections in the absence of ephrin-A5}, Volume = {22}, @@ -5091,7 +5090,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Month = {Nov}, Number = {1}, Pages = {76-88}, - pubmed = {6294151}, + pmid = {6294151}, Pst = {ppublish}, Title = {The motor cortex of the rat: cytoarchitecture and microstimulation mapping}, Volume = {212}, @@ -5111,7 +5110,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Number = {10}, Pages = {e0140391}, Pmc = {PMC4599918}, - pubmed = {26452243}, + pmid = {26452243}, Pst = {epublish}, Title = {Rapid Changes in Cortical and Subcortical Brain Regions after Early Bilateral Enucleation in the Mouse}, Volume = {10}, @@ -5131,7 +5130,7 @@ CONCLUSIONS: Ethanol treatment significantly reduced the mass of the cerebral co Number = {1456}, Pages = {797-814}, Pmc = {PMC1569485}, - pubmed = {15937013}, + pmid = {15937013}, Pst = {ppublish}, Title = {The importance of being agranular: a comparative account of visual and motor cortex}, Volume = {360}, @@ -5152,7 +5151,7 @@ SIGNIFICANCE STATEMENT: Through our experiments we were able to uncover a clear Month = {Aug}, Number = {32}, Pages = {11196-208}, - pubmed = {26269630}, + pmid = {26269630}, Pst = {ppublish}, Title = {High-Affinity Nicotinic Receptors Modulate Spontaneous Cortical Up States In Vitro}, Volume = {35}, @@ -5172,7 +5171,7 @@ SIGNIFICANCE STATEMENT: Through our experiments we were able to uncover a clear Number = {51}, Pages = {14823-14828}, Pmc = {PMC5187677}, - pubmed = {27911815}, + pmid = {27911815}, Pst = {ppublish}, Title = {Nicotinic receptors in mouse prefrontal cortex modulate ultraslow fluctuations related to conscious processing}, Volume = {113}, @@ -5191,7 +5190,7 @@ SIGNIFICANCE STATEMENT: Through our experiments we were able to uncover a clear Number = {5}, Pages = {e32243}, Pmc = {PMC3362598}, - pubmed = {22666312}, + pmid = {22666312}, Pst = {ppublish}, Title = {The Mice Drawer System (MDS) experiment and the space endurance record-breaking mice}, Volume = {7}, @@ -5211,7 +5210,7 @@ SIGNIFICANCE STATEMENT: Through our experiments we were able to uncover a clear Number = {27}, Pages = {7337-44}, Pmc = {PMC4941493}, - pubmed = {27382147}, + pmid = {27382147}, Pst = {ppublish}, Title = {Inferring cortical function in the mouse visual system through large-scale systems neuroscience}, Volume = {113}, @@ -5231,7 +5230,7 @@ SIGNIFICANCE STATEMENT: Through our experiments we were able to uncover a clear Number = {32}, Pages = {11382-7}, Pmc = {PMC2495013}, - pubmed = {18678899}, + pmid = {18678899}, Pst = {ppublish}, Title = {The Fezf2-Ctip2 genetic pathway regulates the fate choice of subcortical projection neurons in the developing cerebral cortex}, Volume = {105}, @@ -5250,7 +5249,7 @@ SIGNIFICANCE STATEMENT: Through our experiments we were able to uncover a clear Month = {Dec}, Number = {6}, Pages = {3330-40}, - pubmed = {17898147}, + pmid = {17898147}, Pst = {ppublish}, Title = {Layer V neurons in mouse cortex projecting to different targets have distinct physiological properties}, Volume = {98}, @@ -5268,7 +5267,7 @@ SIGNIFICANCE STATEMENT: Through our experiments we were able to uncover a clear Month = {Jan}, Number = {1}, Pages = {39-43}, - pubmed = {11166178}, + pmid = {11166178}, Pst = {ppublish}, Title = {Independent parcellation of the embryonic visual cortex and thalamus revealed by combinatorial Eph/ephrin gene expression}, Volume = {11}, @@ -5288,7 +5287,7 @@ SIGNIFICANCE STATEMENT: Through our experiments we were able to uncover a clear Number = {8}, Pages = {e1001932}, Pmc = {PMC4138028}, - pubmed = {25137065}, + pmid = {25137065}, Pst = {epublish}, Title = {Pyramidal cells make specific connections onto smooth (GABAergic) neurons in mouse visual cortex}, Volume = {12}, @@ -5307,7 +5306,7 @@ SIGNIFICANCE STATEMENT: Through our experiments we were able to uncover a clear Month = {Feb}, Number = {3}, Pages = {364-77}, - pubmed = {18255030}, + pmid = {18255030}, Pst = {ppublish}, Title = {Satb2 regulates callosal projection neuron identity in the developing cerebral cortex}, Volume = {57}, @@ -5329,7 +5328,7 @@ SIGNIFICANCE STATEMENT: Through our experiments we were able to uncover a clear Number = {1456}, Pages = {665-91}, Pmc = {PMC1874231}, - pubmed = {15937007}, + pmid = {15937007}, Pst = {ppublish}, Title = {Brain maps, great and small: lessons from comparative studies of primate visual cortical organization}, Volume = {360}, @@ -5349,7 +5348,7 @@ SIGNIFICANCE STATEMENT: Through our experiments we were able to uncover a clear Number = {3}, Pages = {457-71}, Pmc = {PMC3569744}, - pubmed = {23395373}, + pmid = {23395373}, Pst = {ppublish}, Title = {Contact repulsion controls the dispersion and final distribution of Cajal-Retzius cells}, Volume = {77}, @@ -5368,7 +5367,7 @@ SIGNIFICANCE STATEMENT: Through our experiments we were able to uncover a clear Month = {Aug}, Number = {3}, Pages = {345-8}, - pubmed = {7634322}, + pmid = {7634322}, Pst = {ppublish}, Title = {Eph receptor tyrosine kinases, axon repulsion, and the development of topographic maps}, Volume = {82}, @@ -5387,7 +5386,7 @@ SIGNIFICANCE STATEMENT: Through our experiments we were able to uncover a clear Month = {May}, Number = {20}, Pages = {6677-90}, - pubmed = {19458237}, + pmid = {19458237}, Pst = {ppublish}, Title = {Lewis(x) and alpha2,3-sialyl glycans and their receptors TAG-1, Contactin, and L1 mediate CD24-dependent neurite outgrowth}, Volume = {29}, @@ -5411,7 +5410,7 @@ CONCLUSIONS: The FOXP2-CNTNAP2 pathway provides a mechanistic link between clini Number = {22}, Pages = {2337-45}, Pmc = {PMC2756409}, - pubmed = {18987363}, + pmid = {18987363}, Pst = {ppublish}, Title = {A functional genetic link between distinct developmental language disorders}, Volume = {359}, @@ -5431,7 +5430,7 @@ CONCLUSIONS: The FOXP2-CNTNAP2 pathway provides a mechanistic link between clini Month = {Mar}, Number = {13}, Pages = {1370-7}, - pubmed = {16571880}, + pmid = {16571880}, Pst = {ppublish}, Title = {Recessive symptomatic focal epilepsy and mutant contactin-associated protein-like 2}, Volume = {354}, @@ -5450,7 +5449,7 @@ CONCLUSIONS: The FOXP2-CNTNAP2 pathway provides a mechanistic link between clini Month = {May}, Number = {5}, Pages = {908, 908.e1}, - pubmed = {20510934}, + pmid = {20510934}, Pst = {ppublish}, Title = {SnapShot: Neuroligin-neurexin complexes}, Volume = {141}, @@ -5468,7 +5467,7 @@ CONCLUSIONS: The FOXP2-CNTNAP2 pathway provides a mechanistic link between clini Month = {Oct}, Number = {1}, Pages = {145}, - pubmed = {3655381}, + pmid = {3655381}, Pst = {ppublish}, Title = {Toxicity of light-exposed Hepes media}, Volume = {103}, @@ -5498,7 +5497,7 @@ So peripheral input is functionally influencing the thalamus in their model then Month = {Feb}, Pages = {14172}, Pmc = {PMC5296753}, - pubmed = {28155854}, + pmid = {28155854}, Pst = {epublish}, Title = {Prenatal thalamic waves regulate cortical area size prior to sensory processing}, Volume = {8}, @@ -5515,7 +5514,7 @@ So peripheral input is functionally influencing the thalamus in their model then Mesh = {Animals; Cells, Cultured; Chickens; Microscopy, Electron, Scanning; Neurons; Stress, Mechanical}, Month = {Jun}, Pages = {391-410}, - pubmed = {479327}, + pmid = {479327}, Pst = {ppublish}, Title = {Mechanical tension produced by nerve cells in tissue culture}, Volume = {37}, @@ -5532,7 +5531,7 @@ So peripheral input is functionally influencing the thalamus in their model then Journal-Full = {Annual review of neuroscience}, Mesh = {Animals; Axons; Brain Mapping; Dendrites; Humans; Nerve Net; Neural Pathways; Visual Cortex; Visual Fields; Visual Pathways}, Pages = {369-92}, - pubmed = {15217337}, + pmid = {15217337}, Pst = {ppublish}, Title = {Maps in the brain: what can we learn from them?}, Volume = {27}, @@ -5552,7 +5551,7 @@ So peripheral input is functionally influencing the thalamus in their model then Month = {May}, Number = {4}, Pages = {2096-106}, - pubmed = {22343126}, + pmid = {22343126}, Pst = {ppublish}, Title = {On the use of correlation as a measure of network connectivity}, Volume = {60}, @@ -5571,7 +5570,7 @@ So peripheral input is functionally influencing the thalamus in their model then Month = {Oct}, Number = {4}, Pages = {2296-314}, - pubmed = {22387165}, + pmid = {22387165}, Pst = {ppublish}, Title = {Schizophrenia, neuroimaging and connectomics}, Volume = {62}, @@ -5592,7 +5591,7 @@ So peripheral input is functionally influencing the thalamus in their model then Number = {12}, Pages = {3258-3263}, Pmc = {PMC5373394}, - pubmed = {28193875}, + pmid = {28193875}, Pst = {ppublish}, Title = {Spontaneous expression of mirror self-recognition in monkeys after learning precise visual-proprioceptive association for mirror images}, Volume = {114}, @@ -5611,7 +5610,7 @@ So peripheral input is functionally influencing the thalamus in their model then Number = {2}, Pages = {209-214}, Pmc = {PMC5122474}, - pubmed = {27217150}, + pmid = {27217150}, Pst = {ppublish}, Title = {An epigenetic mechanism links socioeconomic status to changes in depression-related brain function in high-risk adolescents}, Volume = {22}, @@ -5631,7 +5630,7 @@ So peripheral input is functionally influencing the thalamus in their model then Number = {3}, Pages = {342-8}, Pmc = {PMC2944040}, - pubmed = {19234457}, + pmid = {19234457}, Pst = {ppublish}, Title = {Epigenetic regulation of the glucocorticoid receptor in human brain associates with childhood abuse}, Volume = {12}, @@ -5649,7 +5648,7 @@ So peripheral input is functionally influencing the thalamus in their model then Keywords = {Daisy; bouton cluster; canonical microcircuit; cortical column; neuroanatomy}, Pages = {16}, Pmc = {PMC2904586}, - pubmed = {20640245}, + pmid = {20640245}, Pst = {epublish}, Title = {Whose Cortical Column Would that Be?}, Volume = {4}, @@ -5671,7 +5670,7 @@ SIGNIFICANCE STATEMENT: Working memory (WM) is a key component of cognition. Hyp Number = {1}, Pages = {83-96}, Pmc = {PMC5214637}, - pubmed = {28053032}, + pmid = {28053032}, Pst = {ppublish}, Title = {A Spiking Working Memory Model Based on Hebbian Short-Term Potentiation}, Volume = {37}, @@ -5690,7 +5689,7 @@ SIGNIFICANCE STATEMENT: Working memory (WM) is a key component of cognition. Hyp Mesh = {Animals; Cooperative Behavior; Information Systems; Neocortex; Rats; Somatosensory Cortex}, Pages = {44}, Pmc = {PMC4597797}, - pubmed = {26500503}, + pmid = {26500503}, Pst = {epublish}, Title = {The neocortical microcircuit collaboration portal: a resource for rat somatosensory cortex}, Volume = {9}, @@ -5709,7 +5708,7 @@ SIGNIFICANCE STATEMENT: Working memory (WM) is a key component of cognition. Hyp Mesh = {Animals; Excitatory Postsynaptic Potentials; Humans; Motor Cortex; Nerve Net; Neural Pathways; Neurons; Rats}, Pages = {75}, Pmc = {PMC3664775}, - pubmed = {23754982}, + pmid = {23754982}, Pst = {epublish}, Title = {Local connections of excitatory neurons in motor-associated cortical areas of the rat}, Volume = {7}, @@ -5728,7 +5727,7 @@ SIGNIFICANCE STATEMENT: Working memory (WM) is a key component of cognition. Hyp Month = {Mar}, Number = {3}, Pages = {1171-82}, - pubmed = {14602839}, + pmid = {14602839}, Pst = {ppublish}, Title = {Maturation of layer V pyramidal neurons in the rat prefrontal cortex: intrinsic properties and synaptic function}, Volume = {91}, @@ -5748,7 +5747,7 @@ SIGNIFICANCE STATEMENT: Working memory (WM) is a key component of cognition. Hyp Month = {Apr}, Number = {4}, Pages = {533-41}, - pubmed = {27021938}, + pmid = {27021938}, Pst = {ppublish}, Title = {Thalamus plays a central role in ongoing cortical functioning}, Volume = {19}, @@ -5769,7 +5768,7 @@ ABSTRACT: In addition to the primary thalamocortical visual relay in the lateral Number = {7}, Pages = {1911-29}, Pmc = {PMC4818601}, - pubmed = {26842995}, + pmid = {26842995}, Pst = {ppublish}, Title = {Visual input to the mouse lateral posterior and posterior thalamic nuclei: photoreceptive origins and retinotopic order}, Volume = {594}, @@ -5790,7 +5789,7 @@ CONCLUSIONS: These findings suggest that sustained visual input through the pulv Month = {Feb}, Number = {4}, Pages = {424-34}, - pubmed = {25601551}, + pmid = {25601551}, Pst = {ppublish}, Title = {Preservation of vision by the pulvinar following early-life primary visual cortex lesions}, Volume = {25}, @@ -5811,7 +5810,7 @@ CONCLUSIONS: These findings suggest that sustained visual input through the pulv Number = {5}, Pages = {1131-44}, Pmc = {PMC4458710}, - pubmed = {26050033}, + pmid = {26050033}, Pst = {ppublish}, Title = {Neurotransmitter Switching? No Surprise}, Volume = {86}, @@ -5832,7 +5831,7 @@ CONCLUSIONS: These findings suggest that sustained visual input through the pulv Number = {5}, Pages = {1004-16}, Pmc = {PMC4072120}, - pubmed = {24908484}, + pmid = {24908484}, Pst = {ppublish}, Title = {Non-cell-autonomous mechanism of activity-dependent neurotransmitter switching}, Volume = {82}, @@ -5853,7 +5852,7 @@ CONCLUSIONS: These findings suggest that sustained visual input through the pulv Number = {2}, Pages = {270-4}, Pmc = {PMC3864648}, - pubmed = {24139032}, + pmid = {24139032}, Pst = {ppublish}, Title = {The challenge of connecting the dots in the B.R.A.I.N}, Volume = {80}, @@ -5874,7 +5873,7 @@ CONCLUSIONS: These findings suggest that sustained visual input through the pulv Number = {2}, Pages = {321-34}, Pmc = {PMC2913149}, - pubmed = {20670838}, + pmid = {20670838}, Pst = {ppublish}, Title = {Activity-dependent expression of Lmx1b regulates specification of serotonergic neurons modulating swimming behavior}, Volume = {67}, @@ -5893,7 +5892,7 @@ CONCLUSIONS: These findings suggest that sustained visual input through the pulv Month = {Nov}, Number = {5}, Pages = {797-805}, - pubmed = {1742026}, + pmid = {1742026}, Pst = {ppublish}, Title = {Role of calcium and protein kinase C in development of the delayed rectifier potassium current in Xenopus spinal neurons}, Volume = {7}, @@ -5912,7 +5911,7 @@ CONCLUSIONS: These findings suggest that sustained visual input through the pulv Number = {5}, Pages = {989-1003}, Pmc = {PMC4104757}, - pubmed = {24814534}, + pmid = {24814534}, Pst = {ppublish}, Title = {Transcriptional regulation of enhancers active in protodomains of the developing cerebral cortex}, Volume = {82}, @@ -5933,7 +5932,7 @@ CONCLUSIONS: These findings suggest that sustained visual input through the pulv Number = {4}, Pages = {1100-8}, Pmc = {PMC4441766}, - pubmed = {25996137}, + pmid = {25996137}, Pst = {ppublish}, Title = {Cux2-positive radial glial cells generate diverse subtypes of neocortical projection neurons and macroglia}, Volume = {86}, @@ -5955,7 +5954,7 @@ CONCLUSIONS: These findings suggest that sustained visual input through the pulv Number = {4}, Pages = {303-12}, Pmc = {PMC2777887}, - pubmed = {19277053}, + pmid = {19277053}, Pst = {ppublish}, Title = {Prenatal exposure to drugs: effects on brain development and implications for policy and education}, Volume = {10}, @@ -5978,7 +5977,7 @@ CONCLUSIONS: A distinctive pattern of physical abnormalities in infants of mothe Month = {Apr}, Number = {15}, Pages = {1132-8}, - pubmed = {11297704}, + pmid = {11297704}, Pst = {ppublish}, Title = {The teratogenicity of anticonvulsant drugs}, Volume = {344}, @@ -6000,7 +5999,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Month = {Apr}, Number = {4}, Pages = {684-93}, - pubmed = {17437411}, + pmid = {17437411}, Pst = {ppublish}, Title = {Fetal exposure to GABA-acting antiepileptic drugs generates hippocampal and cortical dysplasias}, Volume = {48}, @@ -6021,7 +6020,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Number = {25}, Pages = {11567-72}, Pmc = {PMC2895077}, - pubmed = {20534523}, + pmid = {20534523}, Pst = {ppublish}, Title = {Alterations of cortical pyramidal neurons in mice lacking high-affinity nicotinic receptors}, Volume = {107}, @@ -6039,7 +6038,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Keywords = {cortical modular organization; corticocortical; dendritic bundle; input and recipient matching; thalamocortical}, Pages = {69}, Pmc = {PMC3254062}, - pubmed = {22275884}, + pmid = {22275884}, Pst = {epublish}, Title = {Small-scale module of the rat granular retrosplenial cortex: an example of the minicolumn-like structure of the cerebral cortex}, Volume = {5}, @@ -6057,7 +6056,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Keywords = {GCaMP3; retrosplenial area; transgenic mouse; visual response; wide-field Ca2+ imaging}, Pages = {20}, Pmc = {PMC4458613}, - pubmed = {26106292}, + pmid = {26106292}, Pst = {epublish}, Title = {Wide-field Ca(2+) imaging reveals visually evoked activity in the retrosplenial area}, Volume = {8}, @@ -6075,7 +6074,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Month = {Sep}, Number = {9}, Pages = {3221-32}, - pubmed = {3171676}, + pmid = {3171676}, Pst = {ppublish}, Title = {Organization of adult motor cortex representation patterns following neonatal forelimb nerve injury in rats}, Volume = {8}, @@ -6095,7 +6094,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Number = {4}, Pages = {865-76}, Pmc = {PMC3059888}, - pubmed = {20739477}, + pmid = {20739477}, Pst = {ppublish}, Title = {The organization of the forelimb representation of the C57BL/6 mouse motor cortex as defined by intracortical microstimulation and cytoarchitecture}, Volume = {21}, @@ -6114,7 +6113,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Month = {Dec}, Number = {6}, Pages = {724-38}, - pubmed = {22152301}, + pmid = {22152301}, Pst = {ppublish}, Title = {Brain energy metabolism: focus on astrocyte-neuron metabolic cooperation}, Volume = {14}, @@ -6133,7 +6132,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Number = {16}, Pages = {10237-9}, Pmc = {PMC124895}, - pubmed = {12149485}, + pmid = {12149485}, Pst = {ppublish}, Title = {Appraising the brain's energy budget}, Volume = {99}, @@ -6152,7 +6151,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Month = {Jul}, Number = {7}, Pages = {739-44}, - pubmed = {11426231}, + pmid = {11426231}, Pst = {ppublish}, Title = {Compulsory averaging of crowded orientation signals in human vision}, Volume = {4}, @@ -6171,7 +6170,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Month = {Apr}, Number = {2}, Pages = {117-31}, - pubmed = {8323710}, + pmid = {8323710}, Pst = {ppublish}, Title = {Comparisons of hemi-inattention produced by unilateral lesions of the posterior parietal cortex or medial agranular prefrontal cortex in rats: neglect, extinction, and the role of stimulus distance}, Volume = {54}, @@ -6189,7 +6188,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Month = {Oct}, Number = {5}, Pages = {956-61}, - pubmed = {2803562}, + pmid = {2803562}, Pst = {ppublish}, Title = {Double dissociation of egocentric and allocentric space following medial prefrontal and parietal cortex lesions in the rat}, Volume = {103}, @@ -6206,7 +6205,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Month = {Sep}, Number = {1-2}, Pages = {53-68}, - pubmed = {1449649}, + pmid = {1449649}, Pst = {ppublish}, Title = {Spatial deficits and hemispheric asymmetries in the rat following unilateral and bilateral lesions of posterior parietal or medial agranular cortex}, Volume = {50}, @@ -6224,7 +6223,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Month = {Feb}, Number = {2}, Pages = {187-90}, - pubmed = {3964408}, + pmid = {3964408}, Pst = {ppublish}, Title = {Pineal lesion produces bilateral visual and auditory inattention in the rat}, Volume = {19}, @@ -6241,7 +6240,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Month = {Dec}, Number = {3}, Pages = {227-31}, - pubmed = {3790245}, + pmid = {3790245}, Pst = {ppublish}, Title = {Parietal and frontal eye field neglect in the rat}, Volume = {22}, @@ -6258,7 +6257,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Mesh = {Animals; Cerebral Cortex; Fluorescent Dyes; Hindlimb; Neural Pathways; Parietal Lobe; Rats; Somatosensory Cortex; Stereotaxic Techniques; Stilbamidines; Thalamus; Visual Cortex}, Number = {1}, Pages = {67-84}, - pubmed = {7813654}, + pmid = {7813654}, Pst = {ppublish}, Title = {Rat posterior parietal cortex: topography of corticocortical and thalamic connections}, Volume = {100}, @@ -6276,7 +6275,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Month = {Jul}, Number = {4}, Pages = {871-908}, - pubmed = {808592}, + pmid = {808592}, Pst = {ppublish}, Title = {Posterior parietal association cortex of the monkey: command functions for operations within extrapersonal space}, Volume = {38}, @@ -6293,7 +6292,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Journal-Full = {Annual review of neuroscience}, Mesh = {Animals; Movement; Parietal Lobe; Space Perception}, Pages = {303-30}, - pubmed = {9056716}, + pmid = {9056716}, Pst = {ppublish}, Title = {Multimodal representation of space in the posterior parietal cortex and its use in planning movements}, Volume = {20}, @@ -6313,7 +6312,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Month = {Mar}, Number = {11}, Pages = {2964-70}, - pubmed = {16540574}, + pmid = {16540574}, Pst = {ppublish}, Title = {Lateralization of the human mirror neuron system}, Volume = {26}, @@ -6332,7 +6331,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Month = {Oct}, Pages = {6652}, Pmc = {PMC4200406}, - pubmed = {25323637}, + pmid = {25323637}, Pst = {epublish}, Title = {An experimental task to examine the mirror system in rats}, Volume = {4}, @@ -6350,7 +6349,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Mesh = {Adolescent; Amygdala; Asperger Syndrome; Autistic Disorder; Brain; Brain Mapping; Dominance, Cerebral; Female; Humans; Image Processing, Computer-Assisted; Imaging, Three-Dimensional; Imitative Behavior; Magnetic Resonance Imaging; Male; Nerve Net; Neurons; Orientation; Parietal Lobe; Personal Construct Theory; Psychomotor Performance; Reference Values; Somatosensory Cortex; Temporal Lobe}, Number = {4}, Pages = {610-21}, - pubmed = {16140346}, + pmid = {16140346}, Pst = {ppublish}, Title = {Neural mechanisms of imitation and 'mirror neuron' functioning in autistic spectrum disorder}, Volume = {44}, @@ -6370,7 +6369,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Number = {3}, Pages = {228-37}, Pmc = {PMC2709976}, - pubmed = {17451856}, + pmid = {17451856}, Pst = {ppublish}, Title = {EEG mu rhythm and imitation impairments in individuals with autism spectrum disorder}, Volume = {64}, @@ -6389,7 +6388,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Month = {Dec}, Number = {1}, Pages = {57-68}, - pubmed = {15925412}, + pmid = {15925412}, Pst = {ppublish}, Title = {The functional significance of mu rhythms: translating "seeing" and "hearing" into "doing"}, Volume = {50}, @@ -6408,7 +6407,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Month = {Jul}, Number = {2}, Pages = {190-8}, - pubmed = {15993757}, + pmid = {15993757}, Pst = {ppublish}, Title = {EEG evidence for mirror neuron dysfunction in autism spectrum disorders}, Volume = {24}, @@ -6428,7 +6427,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Number = {5}, Pages = {20130037}, Pmc = {PMC3915827}, - pubmed = {24511388}, + pmid = {24511388}, Pst = {ppublish}, Title = {Magnetic field effects in flavoproteins and related systems}, Volume = {3}, @@ -6449,7 +6448,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Number = {7263}, Pages = {524-8}, Pmc = {PMC2874978}, - pubmed = {19759535}, + pmid = {19759535}, Pst = {ppublish}, Title = {Integration of neuronal clones in the radial cortical columns by EphA and ephrin-A signalling}, Volume = {461}, @@ -6469,7 +6468,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Month = {Apr}, Number = {4}, Pages = {240-56}, - pubmed = {26790531}, + pmid = {26790531}, Pst = {ppublish}, Title = {Mechanisms of ephrin-Eph signalling in development, physiology and disease}, Volume = {17}, @@ -6489,7 +6488,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Number = {Pt 3}, Pages = {919-27}, Pmc = {PMC2342977}, - pubmed = {12730344}, + pmid = {12730344}, Pst = {ppublish}, Title = {Dynamic imaging of somatosensory cortical activity in the rat visualized by flavoprotein autofluorescence}, Volume = {549}, @@ -6508,7 +6507,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Month = {Aug}, Number = {32}, Pages = {8665-75}, - pubmed = {17687044}, + pmid = {17687044}, Pst = {ppublish}, Title = {Functional imaging of primary visual cortex using flavoprotein autofluorescence}, Volume = {27}, @@ -6527,7 +6526,7 @@ CONCLUSIONS: We suggest that AEDs that increase the extracellular concentration Number = {1}, Pages = {e85225}, Pmc = {PMC3882276}, - pubmed = {24400130}, + pmid = {24400130}, Pst = {epublish}, Title = {Flavoprotein autofluorescence imaging of visual system activity in zebra finches and mice}, Volume = {9}, @@ -6551,7 +6550,7 @@ CONCLUSIONS: These results show that the dysfunction of astrocytic A2AR, by cont Number = {11}, Pages = {763-74}, Pmc = {PMC4714966}, - pubmed = {25869810}, + pmid = {25869810}, Pst = {ppublish}, Title = {Deletion of adenosine A2A receptors from astrocytes disrupts glutamate homeostasis leading to psychomotor and cognitive impairment: relevance to schizophrenia}, Volume = {78}, @@ -6571,7 +6570,7 @@ CONCLUSIONS: These results show that the dysfunction of astrocytic A2AR, by cont Month = {Aug}, Number = {197}, Pages = {197ra104}, - pubmed = {23926202}, + pmid = {23926202}, Pst = {ppublish}, Title = {Adenosine receptor antagonists including caffeine alter fetal brain development in mice}, Volume = {5}, @@ -6591,7 +6590,7 @@ CONCLUSIONS: These results show that the dysfunction of astrocytic A2AR, by cont Month = {Aug}, Number = {2}, Pages = {177-83}, - pubmed = {10926292}, + pmid = {10926292}, Pst = {ppublish}, Title = {Maternal caffeine intake has minor effects on adenosine receptor ontogeny in the rat brain}, Volume = {48}, @@ -6609,7 +6608,7 @@ CONCLUSIONS: These results show that the dysfunction of astrocytic A2AR, by cont Journal-Full = {Journal of toxicology}, Pages = {370460}, Pmc = {PMC3821942}, - pubmed = {24260033}, + pmid = {24260033}, Pst = {ppublish}, Title = {The benefits and risks of consuming brewed tea: beware of toxic element contamination}, Volume = {2013}, @@ -6632,7 +6631,7 @@ CONCLUSIONS: These results suggest that, in contrast to the situation in adult a Month = {Mar}, Number = {3}, Pages = {739-44}, - pubmed = {12624301}, + pmid = {12624301}, Pst = {ppublish}, Title = {Aggravated brain damage after hypoxic ischemia in immature adenosine A2A knockout mice}, Volume = {34}, @@ -6657,7 +6656,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Number = {12}, Pages = {1611-20}, Pmc = {PMC2786045}, - pubmed = {20041597}, + pmid = {20041597}, Pst = {ppublish}, Title = {Neonatal maternal separation disrupts regulation of sleep and breathing in adult male rats}, Volume = {32}, @@ -6676,7 +6675,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Number = {Pt 22}, Pages = {5493-507}, Pmc = {PMC2793879}, - pubmed = {19770189}, + pmid = {19770189}, Pst = {ppublish}, Title = {Caffeine in the neonatal period induces long-lasting changes in sleep and breathing in adult rats}, Volume = {587}, @@ -6696,7 +6695,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Month = {Oct}, Number = {1705}, Pmc = {PMC5003860}, - pubmed = {27574312}, + pmid = {27574312}, Pst = {ppublish}, Title = {Wide-field optical mapping of neural activity and brain haemodynamics: considerations and novel approaches}, Volume = {371}, @@ -6716,7 +6715,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Month = {May}, Number = {5}, Pages = {365-76}, - pubmed = {23571845}, + pmid = {23571845}, Pst = {ppublish}, Title = {Power failure: why small sample size undermines the reliability of neuroscience}, Volume = {14}, @@ -6734,7 +6733,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Month = {Sep}, Number = {9}, Pages = {5879-91}, - pubmed = {7666173}, + pmid = {7666173}, Pst = {ppublish}, Title = {Fear and the human amygdala}, Volume = {15}, @@ -6752,7 +6751,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Month = {Oct}, Number = {19}, Pages = {2609-2616}, - pubmed = {27641766}, + pmid = {27641766}, Pst = {ppublish}, Title = {Mitochondrial Dynamics in Visual Cortex Are Limited In Vivo and Not Affected by Axonal Structural Plasticity}, Volume = {26}, @@ -6772,7 +6771,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Month = {Jul}, Number = {2}, Pages = {399-410}, - pubmed = {26182421}, + pmid = {26182421}, Pst = {ppublish}, Title = {Spontaneous Activity Drives Local Synaptic Plasticity In Vivo}, Volume = {87}, @@ -6794,7 +6793,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Number = {12}, Pages = {3097-106}, Pmc = {PMC4224240}, - pubmed = {23843439}, + pmid = {23843439}, Pst = {ppublish}, Title = {Gap junctions in developing thalamic and neocortical neuronal networks}, Volume = {24}, @@ -6814,7 +6813,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Number = {1}, Pages = {13-31}, Pmc = {PMC3903349}, - pubmed = {24144877}, + pmid = {24144877}, Pst = {ppublish}, Title = {The developmental stages of synaptic plasticity}, Volume = {592}, @@ -6833,7 +6832,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Keywords = {auditory system development; developmental biology; plasticity mechanisms; spontaneous activity; synaptic plasticity; visual system development}, Pages = {71}, Pmc = {PMC5011135}, - pubmed = {27656131}, + pmid = {27656131}, Pst = {epublish}, Title = {The Wiring of Developing Sensory Circuits-From Patterned Spontaneous Activity to Synaptic Plasticity Mechanisms}, Volume = {10}, @@ -6849,7 +6848,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Journal-Full = {Acta neurochirurgica. Supplementum}, Mesh = {Adolescent; Aggression; Amygdala; Attention Deficit Disorder with Hyperactivity; Child; Child Behavior Disorders; Epilepsy; Follow-Up Studies; Humans; Hypothalamus; Neurocognitive Disorders; Neuropsychological Tests; Postoperative Complications; Psychomotor Agitation; Stereotaxic Techniques; Violence}, Pages = {152-7}, - pubmed = {3066131}, + pmid = {3066131}, Pst = {ppublish}, Title = {Stereotactic operation in behaviour disorders. Amygdalotomy and hypothalamotomy}, Volume = {44}, @@ -6867,7 +6866,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Month = {Jan}, Number = {1}, Pages = {309-80}, - pubmed = {19126760}, + pmid = {19126760}, Pst = {ppublish}, Title = {Endocannabinoid-mediated control of synaptic transmission}, Volume = {89}, @@ -6886,7 +6885,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Month = {Jul}, Number = {3}, Pages = {1215-65}, - pubmed = {10893434}, + pmid = {10893434}, Pst = {ppublish}, Title = {Calcium ion in skeletal muscle: its crucial role for muscle function, plasticity, and disease}, Volume = {80}, @@ -6906,7 +6905,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Number = {7481}, Pages = {56-61}, Pmc = {PMC3877713}, - pubmed = {24270805}, + pmid = {24270805}, Pst = {ppublish}, Title = {Structural basis for Ca2+ selectivity of a voltage-gated calcium channel}, Volume = {505}, @@ -6925,7 +6924,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Number = {4}, Pages = {263-74}, Pmc = {PMC165791}, - pubmed = {12921221}, + pmid = {12921221}, Pst = {ppublish}, Title = {The role of GABAA receptors in mediating the effects of alcohol in the central nervous system}, Volume = {28}, @@ -6944,7 +6943,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Month = {Sep}, Number = {6649}, Pages = {385-9}, - pubmed = {9311780}, + pmid = {9311780}, Pst = {ppublish}, Title = {Sites of alcohol and volatile anaesthetic action on GABA(A) and glycine receptors}, Volume = {389}, @@ -6964,7 +6963,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Month = {May}, Number = {5}, Pages = {451-65}, - pubmed = {10731620}, + pmid = {10731620}, Pst = {ppublish}, Title = {Nicotinic receptors in the brain. Links between molecular biology and behavior}, Volume = {22}, @@ -6982,7 +6981,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Month = {Mar}, Number = {6}, Pages = {2019-31}, - pubmed = {12657660}, + pmid = {12657660}, Pst = {ppublish}, Title = {Coexistence of excitatory and inhibitory GABA synapses in the cerebellar interneuron network}, Volume = {23}, @@ -7000,7 +6999,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Month = {Nov}, Pages = {52-67}, Pmc = {PMC1359785}, - pubmed = {13774972}, + pmid = {13774972}, Pst = {ppublish}, Title = {On the permeability of end-plate membrane during the action of transmitter}, Volume = {154}, @@ -7017,7 +7016,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Month = {Aug}, Number = {4}, Pages = {423-9}, - pubmed = {11447587}, + pmid = {11447587}, Pst = {ppublish}, Title = {Cannabinoid receptors are absent in insects}, Volume = {436}, @@ -7037,7 +7036,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Number = {9}, Pages = {1596-602}, Pmc = {PMC4023565}, - pubmed = {24650760}, + pmid = {24650760}, Pst = {ppublish}, Title = {Drosophila melanogaster as a model system to study long-chain fatty acid amide metabolism}, Volume = {588}, @@ -7055,7 +7054,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Month = {Aug}, Number = {6593}, Pages = {677-8}, - pubmed = {8751435}, + pmid = {8751435}, Pst = {ppublish}, Title = {Brain cannabinoids in chocolate}, Volume = {382}, @@ -7076,7 +7075,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Number = {3}, Pages = {389-462}, Pmc = {PMC2241751}, - pubmed = {16968947}, + pmid = {16968947}, Pst = {ppublish}, Title = {The endocannabinoid system as an emerging target of pharmacotherapy}, Volume = {58}, @@ -7096,7 +7095,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Number = {3}, Pages = {523-9}, Pmc = {PMC2931553}, - pubmed = {20590562}, + pmid = {20590562}, Pst = {ppublish}, Title = {Phytocannabinoids beyond the Cannabis plant - do they exist?}, Volume = {160}, @@ -7117,7 +7116,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Number = {283}, Pages = {re4}, Pmc = {PMC4000534}, - pubmed = {23838185}, + pmid = {23838185}, Pst = {epublish}, Title = {Neuroligins provide molecular links between syndromic and nonsyndromic autism}, Volume = {6}, @@ -7135,7 +7134,7 @@ CONCLUSION: Neonatal maternal separation results in persistent disruption of res Month = {Apr}, Number = {4}, Pages = {345-61}, - pubmed = {27050589}, + pmid = {27050589}, Pst = {ppublish}, Title = {Advancing the understanding of autism disease mechanisms through genetics}, Volume = {22}, @@ -7161,7 +7160,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Number = {17}, Pages = {1770-7}, Pmc = {PMC4381277}, - pubmed = {24794370}, + pmid = {24794370}, Pst = {ppublish}, Title = {The familial risk of autism}, Volume = {311}, @@ -7182,7 +7181,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Number = {3}, Pages = {1030-42}, Pmc = {PMC2941042}, - pubmed = {20176116}, + pmid = {20176116}, Pst = {ppublish}, Title = {Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2}, Volume = {53}, @@ -7202,7 +7201,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Number = {45}, Pages = {17849-54}, Pmc = {PMC2077018}, - pubmed = {17978184}, + pmid = {17978184}, Pst = {ppublish}, Title = {Genome-wide analyses of human perisylvian cerebral cortical patterning}, Volume = {104}, @@ -7222,7 +7221,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Number = {56}, Pages = {56ra80}, Pmc = {PMC3065863}, - pubmed = {21048216}, + pmid = {21048216}, Pst = {ppublish}, Title = {Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2}, Volume = {2}, @@ -7241,7 +7240,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Month = {Sep}, Number = {7569}, Pages = {324-5}, - pubmed = {26352474}, + pmid = {26352474}, Pst = {ppublish}, Title = {Neuroscience: Forgetfulness illuminated}, Volume = {525}, @@ -7261,7 +7260,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Number = {7275}, Pages = {915-9}, Pmc = {PMC2844762}, - pubmed = {19946267}, + pmid = {19946267}, Pst = {ppublish}, Title = {Rapid formation and selective stabilization of synapses for enduring motor memories}, Volume = {462}, @@ -7284,7 +7283,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Number = {7387}, Pages = {92-5}, Pmc = {PMC3292711}, - pubmed = {22343892}, + pmid = {22343892}, Pst = {epublish}, Title = {Repetitive motor learning induces coordinated formation of clustered dendritic spines in vivo}, Volume = {483}, @@ -7304,7 +7303,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Month = {May}, Number = {3}, Pages = {423-34}, - pubmed = {21481200}, + pmid = {21481200}, Pst = {ppublish}, Title = {Skyline-plot methods for estimating demographic history from nucleotide sequences}, Volume = {11}, @@ -7323,7 +7322,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Month = {May}, Number = {5979}, Pages = {710-22}, - pubmed = {20448178}, + pmid = {20448178}, Pst = {ppublish}, Title = {A draft sequence of the Neandertal genome}, Volume = {328}, @@ -7342,7 +7341,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Month = {Sep}, Number = {5740}, Pages = {1559-63}, - pubmed = {16141072}, + pmid = {16141072}, Pst = {ppublish}, Title = {The transcriptional landscape of the mammalian genome}, Volume = {309}, @@ -7360,7 +7359,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Month = {Mar}, Number = {5560}, Pages = {1683}, - pubmed = {11872833}, + pmid = {11872833}, Pst = {ppublish}, Title = {Flight of the dodo}, Volume = {295}, @@ -7377,7 +7376,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Journal-Full = {Proceedings of the National Academy of Sciences of the United States of America}, Keywords = {cluster inference; fMRI; false positives; permutation test; statistics}, Month = {Jun}, - pubmed = {27357684}, + pmid = {27357684}, Pst = {aheadofprint}, Title = {Cluster failure: Why fMRI inferences for spatial extent have inflated false-positive rates}, Year = {2016}, @@ -7395,7 +7394,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Month = {May}, Number = {5}, Pages = {1185-92}, - pubmed = {15703244}, + pmid = {15703244}, Pst = {ppublish}, Title = {Bayesian coalescent inference of past population dynamics from molecular sequences}, Volume = {22}, @@ -7416,7 +7415,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Number = {29}, Pages = {12090-5}, Pmc = {PMC3718101}, - pubmed = {23821744}, + pmid = {23821744}, Pst = {ppublish}, Title = {Intrinsically photosensitive ganglion cells contribute to plasticity in retinal wave circuits}, Volume = {110}, @@ -7436,7 +7435,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Number = {2}, Pages = {252-61}, Pmc = {PMC4334116}, - pubmed = {25599224}, + pmid = {25599224}, Pst = {ppublish}, Title = {The development of cortical circuits for motion discrimination}, Volume = {18}, @@ -7456,7 +7455,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Month = {Apr}, Pages = {133-40}, Pmc = {PMC4375098}, - pubmed = {25460069}, + pmid = {25460069}, Pst = {ppublish}, Title = {Brain state dependent activity in the cortex and thalamus}, Volume = {31}, @@ -7475,7 +7474,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Month = {Dec}, Pages = {iv-vii}, Pmc = {PMC4450677}, - pubmed = {25457725}, + pmid = {25457725}, Pst = {ppublish}, Title = {Editorial overview: neuromodulation: tuning the properties of neurons, networks and behavior}, Volume = {29}, @@ -7494,7 +7493,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Month = {Dec}, Pages = {178-86}, Pmc = {PMC4254046}, - pubmed = {25310628}, + pmid = {25310628}, Pst = {ppublish}, Title = {Neural control of brain state}, Volume = {29}, @@ -7514,7 +7513,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Number = {6}, Pages = {1143-61}, Pmc = {PMC4718218}, - pubmed = {26402600}, + pmid = {26402600}, Pst = {ppublish}, Title = {Waking State: Rapid Variations Modulate Neural and Behavioral Responses}, Volume = {87}, @@ -7535,7 +7534,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Number = {1}, Pages = {179-92}, Pmc = {PMC4631312}, - pubmed = {26074005}, + pmid = {26074005}, Pst = {ppublish}, Title = {Cortical Membrane Potential Signature of Optimal States for Sensory Signal Detection}, Volume = {87}, @@ -7554,7 +7553,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Month = {Jul}, Number = {2}, Pages = {332-47}, - pubmed = {21791291}, + pmid = {21791291}, Pst = {ppublish}, Title = {Coupled oscillations mediate directed interactions between prefrontal cortex and hippocampus of the neonatal rat}, Volume = {71}, @@ -7574,7 +7573,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Mesh = {Action Potentials; Algorithms; Animals; Animals, Newborn; Neocortex; Nerve Net; Neurons; Rats; Rats, Wistar}, Pages = {50}, Pmc = {PMC4034041}, - pubmed = {24904296}, + pmid = {24904296}, Pst = {epublish}, Title = {Unsupervised classification of neocortical activity patterns in neonatal and pre-juvenile rodents}, Volume = {8}, @@ -7596,7 +7595,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Number = {8}, Pages = {3370-83}, Pmc = {PMC4339350}, - pubmed = {25716837}, + pmid = {25716837}, Pst = {ppublish}, Title = {Layer-specific refinement of visual cortex function after eye opening in the awake mouse}, Volume = {35}, @@ -7617,7 +7616,7 @@ CONCLUSIONS AND RELEVANCE: Among children born in Sweden, the individual risk of Number = {3}, Pages = {1850-66}, Pmc = {PMC3665747}, - pubmed = {23514423}, + pmid = {23514423}, Pst = {ppublish}, Title = {Nanotools for neuroscience and brain activity mapping}, Volume = {7}, @@ -7639,7 +7638,7 @@ CONCLUSIONS: We demonstrate that interhemispheric connectivity and cortical area Mesh = {Agenesis of Corpus Callosum; Aging; Animals; Anterior Cerebellar Commissure; Autism Spectrum Disorder; Cerebral Cortex; Diffusion Tensor Imaging; Disease Models, Animal; Fornix, Brain; Mice; Mice, Inbred C57BL; Mice, Inbred Strains; Mice, Neurologic Mutants; Phenotype; Somatosensory Cortex; Visual Cortex}, Pages = {10}, Pmc = {PMC4412039}, - pubmed = {25879444}, + pmid = {25879444}, Pst = {epublish}, Title = {Formation of functional areas in the cerebral cortex is disrupted in a mouse model of autism spectrum disorder}, Volume = {10}, @@ -7660,7 +7659,7 @@ CONCLUSIONS: We demonstrate that interhemispheric connectivity and cortical area Month = {May}, Number = {5}, Pages = {264-72}, - pubmed = {25841797}, + pmid = {25841797}, Pst = {ppublish}, Title = {Contralateral targeting of the corpus callosum in normal and pathological brain function}, Volume = {38}, @@ -7681,7 +7680,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Jun}, Number = {25}, Pages = {6704-17}, - pubmed = {27335402}, + pmid = {27335402}, Pst = {ppublish}, Title = {Rapid Postnatal Expansion of Neural Networks Occurs in an Environment of Altered Neurovascular and Neurometabolic Coupling}, Volume = {36}, @@ -7699,7 +7698,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Mar}, Number = {2}, Pages = {187-208}, - pubmed = {627623}, + pmid = {627623}, Pst = {ppublish}, Title = {Developmental studies of thalamocortical and commissural connections in the rat somatic sensory cortex}, Volume = {178}, @@ -7719,7 +7718,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Sep}, Number = {2}, Pages = {129-57}, - pubmed = {408380}, + pmid = {408380}, Pst = {ppublish}, Title = {Cells of origin and terminal distribution of descending projections of the rat somatic sensory cortex}, Volume = {175}, @@ -7738,7 +7737,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Aug}, Number = {3}, Pages = {313-43}, - pubmed = {950383}, + pmid = {950383}, Pst = {ppublish}, Title = {The organization and postnatal development of the commissural projection of the rat somatic sensory cortex}, Volume = {168}, @@ -7759,7 +7758,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {10}, Pages = {1426-35}, Pmc = {PMC3928052}, - pubmed = {23974708}, + pmid = {23974708}, Pst = {ppublish}, Title = {Spontaneous cortical activity alternates between motifs defined by regional axonal projections}, Volume = {16}, @@ -7779,7 +7778,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Mar}, Number = {7542}, Pages = {229-32}, - pubmed = {25517100}, + pmid = {25517100}, Pst = {ppublish}, Title = {Orientation columns in the mouse superior colliculus}, Volume = {519}, @@ -7807,7 +7806,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Feb}, Number = {6}, Pages = {2626-38}, - pubmed = {23392690}, + pmid = {23392690}, Pst = {ppublish}, Title = {Arborization of dendrites by developing neocortical neurons is dependent on primary cilia and type 3 adenylyl cyclase}, Volume = {33}, @@ -7825,7 +7824,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Jul}, Number = {2}, Pages = {258-71}, - pubmed = {26146073}, + pmid = {26146073}, Pst = {ppublish}, Title = {Ets Factors Regulate Neural Stem Cell Depletion and Gliogenesis in Ras Pathway Glioma}, Volume = {12}, @@ -7846,7 +7845,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Mar}, Number = {6226}, Pages = {1138-42}, - pubmed = {25700174}, + pmid = {25700174}, Pst = {ppublish}, Title = {Cell types in the mouse cortex and hippocampus revealed by single-cell RNA-seq}, Volume = {347}, @@ -7867,7 +7866,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Feb}, Number = {1}, Pages = {61-73}, - pubmed = {21326363}, + pmid = {21326363}, Pst = {ppublish}, Title = {Activation and function of immediate-early genes in the nervous system}, Volume = {89}, @@ -7885,7 +7884,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Keywords = {BTBR; autism; c-Fos; empathy; mouse model}, Pages = {199}, Pmc = {PMC4526814}, - pubmed = {26300749}, + pmid = {26300749}, Pst = {epublish}, Title = {Neuronal correlates of asocial behavior in a BTBR T (+) Itpr3(tf)/J mouse model of autism}, Volume = {9}, @@ -7906,7 +7905,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {23}, Pages = {7285-90}, Pmc = {PMC4466750}, - pubmed = {26060301}, + pmid = {26060301}, Pst = {ppublish}, Title = {A survey of human brain transcriptome diversity at the single cell level}, Volume = {112}, @@ -7927,7 +7926,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {36}, Pages = {11929-47}, Pmc = {PMC4152602}, - pubmed = {25186741}, + pmid = {25186741}, Pst = {ppublish}, Title = {An RNA-sequencing transcriptome and splicing database of glia, neurons, and vascular cells of the cerebral cortex}, Volume = {34}, @@ -7946,7 +7945,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Jun}, Number = {6}, Pages = {3272-8}, - pubmed = {9636126}, + pmid = {9636126}, Pst = {ppublish}, Title = {Signal timing across the macaque visual system}, Volume = {79}, @@ -7966,7 +7965,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {2}, Pages = {e1501733}, Pmc = {PMC4771444}, - pubmed = {26933693}, + pmid = {26933693}, Pst = {epublish}, Title = {Bidirectional radial Ca(2+) activity regulates neurogenesis and migration during early cortical column formation}, Volume = {2}, @@ -7988,7 +7987,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {6047}, Pages = {1262-6}, Pmc = {PMC3523322}, - pubmed = {21885776}, + pmid = {21885776}, Pst = {ppublish}, Title = {A gustotopic map of taste qualities in the mammalian brain}, Volume = {333}, @@ -8010,7 +8009,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {7579}, Pages = {512-5}, Pmc = {PMC4712381}, - pubmed = {26580015}, + pmid = {26580015}, Pst = {ppublish}, Title = {Sweet and bitter taste in the brain of awake behaving animals}, Volume = {527}, @@ -8029,7 +8028,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Feb}, Number = {3}, Pages = {293-301}, - pubmed = {12581520}, + pmid = {12581520}, Pst = {ppublish}, Title = {Coding of sweet, bitter, and umami tastes: different receptor cells sharing similar signaling pathways}, Volume = {112}, @@ -8045,7 +8044,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Journal = {Nature}, Journal-Full = {Nature}, Month = {Jan}, - pubmed = {26814963}, + pmid = {26814963}, Pst = {aheadofprint}, Title = {Schizophrenia risk from complex variation of complement component 4}, Year = {2016}, @@ -8063,7 +8062,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Apr}, Number = {5}, Pages = {532-41}, - pubmed = {19226510}, + pmid = {19226510}, Pst = {ppublish}, Title = {Equal numbers of neuronal and nonneuronal cells make the human brain an isometrically scaled-up primate brain}, Volume = {513}, @@ -8080,7 +8079,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Sep}, Number = {3}, Pages = {612-28}, - pubmed = {23035258}, + pmid = {23035258}, Pst = {ppublish}, Title = {Probing the functional properties of mammalian dendrites. 1980}, Volume = {11}, @@ -8097,7 +8096,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Aug}, Pages = {197-213}, Pmc = {PMC1282967}, - pubmed = {7441553}, + pmid = {7441553}, Pst = {ppublish}, Title = {Electrophysiological properties of in vitro Purkinje cell dendrites in mammalian cerebellar slices}, Volume = {305}, @@ -8114,7 +8113,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Aug}, Pages = {171-95}, Pmc = {PMC1282966}, - pubmed = {7441552}, + pmid = {7441552}, Pst = {ppublish}, Title = {Electrophysiological properties of in vitro Purkinje cell somata in mammalian cerebellar slices}, Volume = {305}, @@ -8132,7 +8131,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {1}, Pages = {189-214}, Pmc = {PMC1307637}, - pubmed = {11339}, + pmid = {11339}, Pst = {ppublish}, Title = {Properties of the larval neuromuscular junction in Drosophila melanogaster}, Volume = {262}, @@ -8150,7 +8149,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {2}, Pages = {407-36}, Pmc = {PMC1365564}, - pubmed = {4383089}, + pmid = {4383089}, Pst = {ppublish}, Title = {A study of synaptic transmission in the absence of nerve impulses}, Volume = {192}, @@ -8168,7 +8167,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {2}, Pages = {326-74}, Pmc = {PMC1363415}, - pubmed = {13278905}, + pmid = {13278905}, Pst = {ppublish}, Title = {The specific ionic conductances and the ionic movements across the motoneuronal membrane that produce the inhibitory post-synaptic potential}, Volume = {130}, @@ -8187,7 +8186,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {1-2}, Pages = {171-204}, Pmc = {PMC1366030}, - pubmed = {13062231}, + pmid = {13062231}, Pst = {ppublish}, Title = {The electrical properties of crustacean muscle fibres}, Volume = {120}, @@ -8205,7 +8204,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Oct}, Number = {899}, Pages = {177-83}, - pubmed = {13003922}, + pmid = {13003922}, Pst = {ppublish}, Title = {Propagation of electrical signals along giant nerve fibers}, Volume = {140}, @@ -8223,7 +8222,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {4}, Pages = {500-44}, Pmc = {PMC1392413}, - pubmed = {12991237}, + pmid = {12991237}, Pst = {ppublish}, Title = {A quantitative description of membrane current and its application to conduction and excitation in nerve}, Volume = {117}, @@ -8242,7 +8241,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {4}, Pages = {497-506}, Pmc = {PMC1392212}, - pubmed = {14946715}, + pmid = {14946715}, Pst = {ppublish}, Title = {The dual effect of membrane potential on sodium conductance in the giant axon of Loligo}, Volume = {116}, @@ -8261,7 +8260,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {4}, Pages = {473-96}, Pmc = {PMC1392209}, - pubmed = {14946714}, + pmid = {14946714}, Pst = {ppublish}, Title = {The components of membrane conductance in the giant axon of Loligo}, Volume = {116}, @@ -8280,7 +8279,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {4}, Pages = {449-72}, Pmc = {PMC1392213}, - pubmed = {14946713}, + pmid = {14946713}, Pst = {ppublish}, Title = {Currents carried by sodium and potassium ions through the membrane of the giant axon of Loligo}, Volume = {116}, @@ -8299,7 +8298,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {4}, Pages = {424-48}, Pmc = {PMC1392219}, - pubmed = {14946712}, + pmid = {14946712}, Pst = {ppublish}, Title = {Measurement of current-voltage relations in the membrane of the giant axon of Loligo}, Volume = {116}, @@ -8330,7 +8329,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Oct}, Number = {3}, Pages = {292-4, pl}, - pubmed = {15395900}, + pmid = {15395900}, Pst = {ppublish}, Title = {The effect of calcium on the axoplasm of giant nerve fibers}, Volume = {26}, @@ -8348,7 +8347,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {1-2}, Pages = {240-9}, Pmc = {PMC1392577}, - pubmed = {15394322}, + pmid = {15394322}, Pst = {ppublish}, Title = {The effect of temperature on the electrical activity of the giant axon of the squid}, Volume = {109}, @@ -8366,7 +8365,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {1}, Pages = {37-77}, Pmc = {PMC1392331}, - pubmed = {18128147}, + pmid = {18128147}, Pst = {ppublish}, Title = {The effect of sodium ions on the electrical activity of giant axon of the squid}, Volume = {108}, @@ -8385,7 +8384,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Nov}, Number = {11}, Pages = {1543-51}, - pubmed = {25242304}, + pmid = {25242304}, Pst = {ppublish}, Title = {Single rodent mesohabenular axons release glutamate and GABA}, Volume = {17}, @@ -8406,7 +8405,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {38}, Pages = {13219-32}, Pmc = {PMC4579379}, - pubmed = {26400950}, + pmid = {26400950}, Pst = {ppublish}, Title = {Conditional Knock-Out of Vesicular GABA Transporter Gene from Starburst Amacrine Cells Reveals the Contributions of Multiple Synaptic Mechanisms Underlying Direction Selectivity in the Retina}, Volume = {35}, @@ -8426,7 +8425,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {8}, Pages = {5692-7}, Pmc = {PMC122833}, - pubmed = {11943853}, + pmid = {11943853}, Pst = {ppublish}, Title = {Somatosensory cortex dominated by the representation of teeth in the naked mole-rat brain}, Volume = {99}, @@ -8446,7 +8445,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Feb}, Number = {2}, Pages = {205-12}, - pubmed = {16419086}, + pmid = {16419086}, Pst = {ppublish}, Title = {Central visual system of the naked mole-rat (Heterocephalus glaber)}, Volume = {288}, @@ -8466,7 +8465,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Dec}, Number = {1}, Pages = {45-56}, - pubmed = {19720083}, + pmid = {19720083}, Pst = {ppublish}, Title = {The mammalian central pattern generator for locomotion}, Volume = {62}, @@ -8486,7 +8485,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Nov}, Number = {5}, Pages = {661-9}, - pubmed = {11165801}, + pmid = {11165801}, Pst = {ppublish}, Title = {Formation of the central pattern generator for locomotion in the rat and mouse}, Volume = {53}, @@ -8505,7 +8504,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Dec}, Number = {6}, Pages = {764-9}, - pubmed = {1335811}, + pmid = {1335811}, Pst = {ppublish}, Title = {Presynaptic control as a mechanism of sensory-motor integration}, Volume = {2}, @@ -8523,7 +8522,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Sep}, Pages = {187-204}, Pmc = {PMC1175639}, - pubmed = {1362441}, + pmid = {1362441}, Pst = {ppublish}, Title = {Activation of the central pattern generators for locomotion by serotonin and excitatory amino acids in neonatal rat}, Volume = {455}, @@ -8542,7 +8541,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Nov}, Number = {3}, Pages = {215-25}, - pubmed = {2285479}, + pmid = {2285479}, Pst = {ppublish}, Title = {Variability as a characteristic of immature motor systems: an electromyographic study of swimming in the newborn rat}, Volume = {40}, @@ -8561,7 +8560,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Mar}, Number = {3}, Pages = {825-40}, - pubmed = {3973698}, + pmid = {3973698}, Pst = {ppublish}, Title = {Deficits in visual motion processing following ibotenic acid lesions of the middle temporal visual area of the macaque monkey}, Volume = {5}, @@ -8580,7 +8579,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Jan}, Number = {1}, Pmc = {PMC4368861}, - pubmed = {25522378}, + pmid = {25522378}, Pst = {epublish}, Title = {DREADD: a chemogenetic GPCR signaling platform}, Volume = {18}, @@ -8601,7 +8600,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {12}, Pages = {5163-8}, Pmc = {PMC1829280}, - pubmed = {17360345}, + pmid = {17360345}, Pst = {ppublish}, Title = {Evolving the lock to fit the key to create a family of G protein-coupled receptors potently activated by an inert ligand}, Volume = {104}, @@ -8623,7 +8622,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {2}, Pages = {291-315}, Pmc = {PMC3082452}, - pubmed = {21415127}, + pmid = {21415127}, Pst = {ppublish}, Title = {Remote control of neuronal signaling}, Volume = {63}, @@ -8643,7 +8642,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Aug}, Number = {8}, Pages = {1376-80}, - pubmed = {20532295}, + pmid = {20532295}, Pst = {ppublish}, Title = {A chemical-genetic approach for precise spatio-temporal control of cellular signaling}, Volume = {6}, @@ -8664,7 +8663,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {4}, Pages = {936-46}, Pmc = {PMC4441592}, - pubmed = {25937170}, + pmid = {25937170}, Pst = {ppublish}, Title = {A New DREADD Facilitates the Multiplexed Chemogenetic Interrogation of Behavior}, Volume = {86}, @@ -8686,7 +8685,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {33}, Pages = {10982-8}, Pmc = {PMC4131013}, - pubmed = {25122898}, + pmid = {25122898}, Pst = {ppublish}, Title = {Chemogenetic silencing of neurons in retrosplenial cortex disrupts sensory preconditioning}, Volume = {34}, @@ -8707,7 +8706,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {2}, Pages = {875-85}, Pmc = {PMC3817277}, - pubmed = {19474177}, + pmid = {19474177}, Pst = {ppublish}, Title = {A novel neuronal pathway for visually guided escape in Drosophila melanogaster}, Volume = {102}, @@ -8727,7 +8726,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Feb}, Number = {3973}, Pages = {818-20}, - pubmed = {5541165}, + pmid = {5541165}, Pst = {ppublish}, Title = {Infant responses to impending collision: optical and real}, Volume = {171}, @@ -8746,7 +8745,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {9}, Pages = {e1002260}, Pmc = {PMC4587790}, - pubmed = {26418729}, + pmid = {26418729}, Pst = {epublish}, Title = {BOLD Response Selective to Flow-Motion in Very Young Infants}, Volume = {13}, @@ -8766,7 +8765,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Apr}, Number = {7495}, Pages = {207-14}, - pubmed = {24695228}, + pmid = {24695228}, Pst = {ppublish}, Title = {A mesoscale connectome of the mouse brain}, Volume = {508}, @@ -8786,7 +8785,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {6}, Pages = {e1002158}, Pmc = {PMC4454690}, - pubmed = {26039895}, + pmid = {26039895}, Pst = {epublish}, Title = {Mesoscopic patterns of neural activity support songbird cortical sequences}, Volume = {13}, @@ -8803,7 +8802,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Journal-Full = {Nature neuroscience}, Keywords = {visual system; Visual Cortex; activity manipulation; activity-dependent; activity-development; topographic map; Orientation; direction; mouse; mice; spontaneous activity}, Month = {Nov}, - pubmed = {26523644}, + pmid = {26523644}, Pst = {aheadofprint}, Title = {Neuronal activity is not required for the initial formation and maturation of visual selectivity}, Year = {2015}, @@ -8823,7 +8822,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {May}, Pages = {1-5}, Pmc = {PMC3663045}, - pubmed = {23422677}, + pmid = {23422677}, Pst = {ppublish}, Title = {Recent advances in optogenetics and pharmacogenetics}, Volume = {1511}, @@ -8844,7 +8843,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {4}, Pages = {1486-97}, Pmc = {PMC3727439}, - pubmed = {23345223}, + pmid = {23345223}, Pst = {ppublish}, Title = {Glutamatergic neurotransmission between the C1 neurons and the parasympathetic preganglionic neurons of the dorsal motor nucleus of the vagus}, Volume = {33}, @@ -8863,7 +8862,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {6125}, Pages = {1284-5}, Pmc = {PMC3722427}, - pubmed = {23470729}, + pmid = {23470729}, Pst = {ppublish}, Title = {Neuroscience. The brain activity map}, Volume = {339}, @@ -8883,7 +8882,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Aug}, Number = {8}, Pages = {653-9}, - pubmed = {16062172}, + pmid = {16062172}, Pst = {ppublish}, Title = {Forty-five years of split-brain research and still going strong}, Volume = {6}, @@ -8903,7 +8902,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {5}, Pages = {1049-64}, Pmc = {PMC4258148}, - pubmed = {25466916}, + pmid = {25466916}, Pst = {ppublish}, Title = {Visual circuit development requires patterned activity mediated by retinal acetylcholine receptors}, Volume = {84}, @@ -8923,7 +8922,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Nov}, Number = {3}, Pages = {362-9}, - pubmed = {11054699}, + pmid = {11054699}, Pst = {ppublish}, Title = {Binocular competition does not regulate retinogeniculate arbor size in fetal monkey}, Volume = {427}, @@ -8940,7 +8939,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Dec}, Number = {23}, Pages = {9910-23}, - pubmed = {9822747}, + pmid = {9822747}, Pst = {ppublish}, Title = {Neurogenesis and commitment of corticospinal neurons in reeler}, Volume = {18}, @@ -8957,7 +8956,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Jan}, Number = {1}, Pages = {220-8}, - pubmed = {9870952}, + pmid = {9870952}, Pst = {ppublish}, Title = {Prenatal development of retinogeniculate axons in the macaque monkey during segregation of binocular inputs}, Volume = {19}, @@ -8974,7 +8973,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Mesh = {Animals; Body Patterning; Cell Differentiation; Cell Proliferation; Haplorhini; Neocortex; Nerve Net; Neurons; Organogenesis}, Month = {Jul}, Pages = {i26-34}, - pubmed = {16766704}, + pmid = {16766704}, Pst = {ppublish}, Title = {The concerted modulation of proliferation and migration contributes to the specification of the cytoarchitecture and dimensions of cortical areas}, Volume = {16 Suppl 1}, @@ -8995,7 +8994,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {1}, Pages = {17-36}, Pmc = {PMC3862262}, - pubmed = {23010748}, + pmid = {23010748}, Pst = {ppublish}, Title = {A weighted and directed interareal connectivity matrix for macaque cerebral cortex}, Volume = {24}, @@ -9012,7 +9011,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Journal-Full = {Progress in brain research}, Mesh = {Animals; Biological Evolution; Cell Cycle; Cerebral Cortex; Humans; Nerve Net; Neurons; Primates}, Pages = {341-60}, - pubmed = {22230635}, + pmid = {22230635}, Pst = {ppublish}, Title = {Self-organization and interareal networks in the primate cortex}, Volume = {195}, @@ -9028,7 +9027,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Journal-Full = {Novartis Foundation symposium}, Mesh = {Animals; Body Patterning; Cerebral Cortex; Embryo, Mammalian; Models, Biological; Models, Neurological; Nerve Net; Neural Pathways; Neurons; Primates}, Pages = {178-94 discussion 195-8, 276-81}, - pubmed = {18494259}, + pmid = {18494259}, Pst = {ppublish}, Title = {Self-organization and pattern formation in primate cortical networks}, Volume = {288}, @@ -9046,7 +9045,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Jun}, Number = {6}, Pages = {438-50}, - pubmed = {17514197}, + pmid = {17514197}, Pst = {ppublish}, Title = {Cell-cycle control and cortical development}, Volume = {8}, @@ -9066,7 +9065,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {4}, Pages = {921-34}, Pmc = {PMC1931431}, - pubmed = {16519657}, + pmid = {16519657}, Pst = {ppublish}, Title = {Comparative aspects of cerebral cortical development}, Volume = {23}, @@ -9085,7 +9084,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Dec}, Number = {3}, Pages = {386-402}, - pubmed = {8956106}, + pmid = {8956106}, Pst = {ppublish}, Title = {Phenotypic characterisation of respecified visual cortex subsequent to prenatal enucleation in the monkey: development of acetylcholinesterase and cytochrome oxidase patterns}, Volume = {376}, @@ -9104,7 +9103,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Oct}, Number = {1}, Pages = {1-20}, - pubmed = {8891943}, + pmid = {8891943}, Pst = {ppublish}, Title = {Role of directed growth and target selection in the formation of cortical pathways: prenatal development of the projection of area V2 to area V4 in the monkey}, Volume = {374}, @@ -9123,7 +9122,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Mar}, Number = {1}, Pages = {70-89}, - pubmed = {8867284}, + pmid = {8867284}, Pst = {ppublish}, Title = {Contribution of thalamic input to the specification of cytoarchitectonic cortical fields in the primate: effects of bilateral enucleation in the fetal monkey on the boundaries, dimensions, and gyrification of striate and extrastriate cortex}, Volume = {367}, @@ -9141,7 +9140,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Mesh = {Amidines; Animals; Animals, Newborn; Axons; Female; Fluorescent Dyes; Histocytochemistry; Macaca fascicularis; Neural Pathways; Neurons, Afferent; Pregnancy; Visual Cortex; Visual Pathways}, Number = {1}, Pages = {22-38}, - pubmed = {7719128}, + pmid = {7719128}, Pst = {ppublish}, Title = {Developmental remodeling of primate visual cortical pathways}, Volume = {5}, @@ -9159,7 +9158,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Dec}, Number = {2}, Pages = {193-213}, - pubmed = {8308167}, + pmid = {8308167}, Pst = {ppublish}, Title = {Transient cortical pathways in the pyramidal tract of the neonatal ferret}, Volume = {338}, @@ -9178,7 +9177,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Dec}, Number = {6454}, Pages = {464-6}, - pubmed = {8247154}, + pmid = {8247154}, Pst = {ppublish}, Title = {Modulation of the cell cycle contributes to the parcellation of the primate visual cortex}, Volume = {366}, @@ -9196,7 +9195,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Dec}, Number = {6301}, Pages = {494}, - pubmed = {2174128}, + pmid = {2174128}, Pst = {ppublish}, Title = {Striate cortex periodicity}, Volume = {348}, @@ -9213,7 +9212,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Mesh = {Afferent Pathways; Animals; Anophthalmos; Cell Differentiation; Cerebral Cortex; Embryonic and Fetal Development; Eye Enucleation; Gene Expression Regulation; Humans; Morphogenesis; Primates; Rodentia; Species Specificity; Thalamus; Time Factors; Visual Cortex}, Number = {2}, Pages = {93-9}, - pubmed = {8087537}, + pmid = {8087537}, Pst = {ppublish}, Title = {The importance of developmental timing in cortical specification}, Volume = {1}, @@ -9230,7 +9229,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Mesh = {Animals; Cerebral Cortex; Humans; Mice; Primates; Rodentia; Species Specificity}, Number = {3}, Pages = {171-86}, - pubmed = {8324368}, + pmid = {8324368}, Pst = {ppublish}, Title = {Cortical specification of mice and men}, Volume = {3}, @@ -9247,7 +9246,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Aug}, Number = {3}, Pages = {237-44}, - pubmed = {3166701}, + pmid = {3166701}, Pst = {ppublish}, Title = {The maturational status of thalamocortical and callosal connections of visual areas V1 and V2 in the newborn monkey}, Volume = {29}, @@ -9264,7 +9263,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Aug}, Number = {3}, Pages = {225-36}, - pubmed = {3166700}, + pmid = {3166700}, Pst = {ppublish}, Title = {Functional implications of the anatomical organization of the callosal projections of visual areas V1 and V2 in the macaque monkey}, Volume = {29}, @@ -9282,7 +9281,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Jun}, Number = {1}, Pages = {68-89}, - pubmed = {2454978}, + pmid = {2454978}, Pst = {ppublish}, Title = {Characterization of transient cortical projections from auditory, somatosensory, and motor cortices to visual areas 17, 18, and 19 in the kitten}, Volume = {272}, @@ -9301,7 +9300,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {20}, Pages = {8093-7}, Pmc = {PMC298221}, - pubmed = {2479015}, + pmid = {2479015}, Pst = {ppublish}, Title = {Transient projection from the superior temporal sulcus to area 17 in the newborn macaque monkey}, Volume = {86}, @@ -9319,7 +9318,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Jan}, Number = {6204}, Pages = {265-7}, - pubmed = {2536139}, + pmid = {2536139}, Pst = {ppublish}, Title = {Maturation and connectivity of the visual cortex in monkey is altered by prenatal removal of retinal input}, Volume = {337}, @@ -9339,7 +9338,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {24}, Pages = {10085-97}, Pmc = {PMC3682386}, - pubmed = {23761904}, + pmid = {23761904}, Pst = {ppublish}, Title = {Retinal input regulates the timing of corticogeniculate innervation}, Volume = {33}, @@ -9359,7 +9358,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {20}, Pages = {2011-5}, Pmc = {PMC3809337}, - pubmed = {24120636}, + pmid = {24120636}, Pst = {ppublish}, Title = {Rapid innate defensive responses of mice to looming visual stimuli}, Volume = {23}, @@ -9382,7 +9381,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {1}, Pages = {202-13}, Pmc = {PMC4184914}, - pubmed = {25220812}, + pmid = {25220812}, Pst = {ppublish}, Title = {Visual cortex modulates the magnitude but not the selectivity of looming-evoked responses in the superior colliculus of awake mice}, Volume = {84}, @@ -9403,7 +9402,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Jun}, Number = {Pt 6}, Pages = {1679-95}, - pubmed = {25869851}, + pmid = {25869851}, Pst = {ppublish}, Title = {Functional connectivity of visual cortex in the blind follows retinotopic organization principles}, Volume = {138}, @@ -9422,7 +9421,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Nov}, Number = {11}, Pages = {1320-9}, - pubmed = {7310489}, + pmid = {7310489}, Pst = {ppublish}, Title = {Characterization of abnormalities in the visual system of the mutant mouse pearl}, Volume = {1}, @@ -9439,7 +9438,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Feb}, Number = {3870}, Pages = {895-902}, - pubmed = {5763873}, + pmid = {5763873}, Pst = {ppublish}, Title = {Two visual systems}, Volume = {163}, @@ -9457,7 +9456,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Mesh = {Adaptation, Physiological; Animals; Behavior, Animal; Mice; Mice, Inbred C57BL; Psychophysics; Rats; Rats, Long-Evans; Visual Acuity}, Number = {16}, Pages = {2201-9}, - pubmed = {10878281}, + pmid = {10878281}, Pst = {ppublish}, Title = {Behavioral assessment of visual acuity in mice and rats}, Volume = {40}, @@ -9477,7 +9476,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Month = {Nov}, Number = {6}, Pages = {2051-70}, - pubmed = {23942645}, + pmid = {23942645}, Pst = {ppublish}, Title = {Primary visual cortex projections to extrastriate cortices in enucleated and anophthalmic mice}, Volume = {219}, @@ -9497,7 +9496,7 @@ SIGNIFICANCE STATEMENT: This work demonstrates that the postnatal development of Number = {6}, Pages = {524-39}, Pmc = {PMC4096321}, - pubmed = {23722212}, + pmid = {23722212}, Pst = {ppublish}, Title = {Imaging human connectomes at the macroscale}, Volume = {10}, @@ -9518,7 +9517,7 @@ VIDEO ABSTRACT: }, Number = {5}, Pages = {942-58}, Pmc = {PMC4365051}, - pubmed = {25741722}, + pmid = {25741722}, Pst = {ppublish}, Title = {Transgenic mice for intersectional targeting of neural sensors and effectors with high specificity and performance}, Volume = {85}, @@ -9539,7 +9538,7 @@ VIDEO ABSTRACT: }, Month = {Apr}, Number = {4}, Pages = {453-61}, - pubmed = {17351636}, + pmid = {17351636}, Pst = {ppublish}, Title = {Coordinated developmental recruitment of latent fast spiking interneurons in layer IV barrel cortex}, Volume = {10}, @@ -9561,7 +9560,7 @@ VIDEO ABSTRACT: }, Number = {23}, Pages = {7793-803}, Pmc = {PMC2903441}, - pubmed = {20534828}, + pmid = {20534828}, Pst = {ppublish}, Title = {Delayed stabilization of dendritic spines in fragile X mice}, Volume = {30}, @@ -9582,7 +9581,7 @@ VIDEO ABSTRACT: }, Month = {Apr}, Number = {2}, Pages = {181-9}, - pubmed = {15848798}, + pmid = {15848798}, Pst = {ppublish}, Title = {Development of long-term dendritic spine stability in diverse regions of cerebral cortex}, Volume = {46}, @@ -9602,7 +9601,7 @@ VIDEO ABSTRACT: }, Month = {Apr}, Number = {8}, Pages = {2750-7}, - pubmed = {8786450}, + pmid = {8786450}, Pst = {ppublish}, Title = {Abnormal tactile experience early in life disrupts active touch}, Volume = {16}, @@ -9622,7 +9621,7 @@ VIDEO ABSTRACT: }, Month = {Jan}, Number = {7227}, Pages = {313-7}, - pubmed = {19005470}, + pmid = {19005470}, Pst = {ppublish}, Title = {Experience leaves a lasting structural trace in cortical circuits}, Volume = {457}, @@ -9642,7 +9641,7 @@ VIDEO ABSTRACT: }, Month = {Aug}, Number = {6}, Pages = {728-32}, - pubmed = {20488662}, + pmid = {20488662}, Pst = {ppublish}, Title = {Optimization of population decoding with distance metrics}, Volume = {23}, @@ -9660,7 +9659,7 @@ VIDEO ABSTRACT: }, Month = {Jun}, Number = {7401}, Pages = {41-2}, - pubmed = {22678277}, + pmid = {22678277}, Pst = {epublish}, Title = {Neuroscience: Sibling neurons bond to share sensations}, Volume = {486}, @@ -9678,7 +9677,7 @@ VIDEO ABSTRACT: }, Month = {Sep}, Number = {9}, Pages = {1166-8}, - pubmed = {23982448}, + pmid = {23982448}, Pst = {ppublish}, Title = {A finely tuned cortical amplifier}, Volume = {16}, @@ -9699,7 +9698,7 @@ VIDEO ABSTRACT: }, Number = {2}, Pages = {457-69}, Pmc = {PMC4210638}, - pubmed = {25263755}, + pmid = {25263755}, Pst = {ppublish}, Title = {Experience-dependent specialization of receptive field surround for selective coding of natural scenes}, Volume = {84}, @@ -9719,7 +9718,7 @@ VIDEO ABSTRACT: }, Month = {Feb}, Number = {7539}, Pages = {399-403}, - pubmed = {25652823}, + pmid = {25652823}, Pst = {ppublish}, Title = {Functional organization of excitatory synaptic strength in primary visual cortex}, Volume = {518}, @@ -9739,7 +9738,7 @@ VIDEO ABSTRACT: }, Month = {Nov}, Number = {7474}, Pages = {51-8}, - pubmed = {24201278}, + pmid = {24201278}, Pst = {ppublish}, Title = {Cortical connectivity and sensory coding}, Volume = {503}, @@ -9760,7 +9759,7 @@ VIDEO ABSTRACT: }, Number = {2}, Pages = {691-708}, Pmc = {PMC1300074}, - pubmed = {9929474}, + pmid = {9929474}, Pst = {ppublish}, Title = {Analysis of dynamic brain imaging data}, Volume = {76}, @@ -9778,7 +9777,7 @@ VIDEO ABSTRACT: }, Month = {Sep}, Number = {3}, Pages = {3389-92}, - pubmed = {11970154}, + pmid = {11970154}, Pst = {ppublish}, Title = {Distributions of singular values for some random matrices}, Volume = {60}, @@ -9794,7 +9793,7 @@ VIDEO ABSTRACT: }, Journal-Full = {Frontiers in cellular neuroscience}, Pages = {45}, Pmc = {PMC3494101}, - pubmed = {23162428}, + pmid = {23162428}, Pst = {epublish}, Title = {The Yin and Yen of GABA in Brain Development and Operation in Health and Disease}, Volume = {6}, @@ -9812,7 +9811,7 @@ VIDEO ABSTRACT: }, Keywords = {GABA; brain slices; chloride homeostasis; development; energy substrates; giant depolarizing potentials}, Pages = {35}, Pmc = {PMC3428604}, - pubmed = {22973192}, + pmid = {22973192}, Pst = {epublish}, Title = {Refuting the challenges of the developmental shift of polarity of GABA actions: GABA more exciting than ever!}, Volume = {6}, @@ -9831,7 +9830,7 @@ VIDEO ABSTRACT: }, Month = {Jan}, Number = {1}, Pages = {87-96}, - pubmed = {25485756}, + pmid = {25485756}, Pst = {ppublish}, Title = {Early depolarizing GABA controls critical-period plasticity in the rat visual cortex}, Volume = {18}, @@ -9851,7 +9850,7 @@ VIDEO ABSTRACT: }, Month = {Aug}, Number = {2}, Pages = {126-34}, - pubmed = {20096448}, + pmid = {20096448}, Pst = {ppublish}, Title = {Speech and oral motor profile after childhood hemispherectomy}, Volume = {114}, @@ -9868,7 +9867,7 @@ VIDEO ABSTRACT: }, Mesh = {Hemiplegia; Neurosurgery; Speech}, Month = {Sep}, Pages = {427-60}, - pubmed = {13969875}, + pmid = {13969875}, Pst = {ppublish}, Title = {Hemiplegia of early onset and the faculty of speech with special reference to the effects of hemispherectomy}, Volume = {85}, @@ -9924,7 +9923,7 @@ VIDEO ABSTRACT: }, Month = {Jan}, Number = {1}, Pages = {62-8}, - pubmed = {8989663}, + pmid = {8989663}, Pst = {ppublish}, Title = {Capacitative Ca2+ influx in the neural retina of chick embryo}, Volume = {32}, @@ -9942,7 +9941,7 @@ VIDEO ABSTRACT: }, Month = {May}, Number = {2}, Pages = {147-57}, - pubmed = {11331522}, + pmid = {11331522}, Pst = {ppublish}, Title = {A role for cingulate pioneering axons in the development of the corpus callosum}, Volume = {434}, @@ -9961,7 +9960,7 @@ VIDEO ABSTRACT: }, Number = {2}, Pages = {455-66}, Pmc = {PMC4151326}, - pubmed = {25033185}, + pmid = {25033185}, Pst = {ppublish}, Title = {Identification of a brainstem circuit regulating visual cortical state in parallel with locomotion}, Volume = {83}, @@ -9982,7 +9981,7 @@ VIDEO ABSTRACT: }, Month = {Apr}, Number = {14}, Pages = {4877-82}, - pubmed = {20371807}, + pmid = {20371807}, Pst = {ppublish}, Title = {Development of global cortical networks in early infancy}, Volume = {30}, @@ -10003,7 +10002,7 @@ VIDEO ABSTRACT: }, Number = {12}, Pages = {2852-62}, Pmc = {PMC2978240}, - pubmed = {20237243}, + pmid = {20237243}, Pst = {ppublish}, Title = {Longitudinal analysis of neural network development in preterm infants}, Volume = {20}, @@ -10023,7 +10022,7 @@ VIDEO ABSTRACT: }, Number = {16}, Pages = {5477-85}, Pmc = {PMC3988407}, - pubmed = {24741038}, + pmid = {24741038}, Pst = {ppublish}, Title = {Rapid developmental emergence of stable depolarization during wakefulness by inhibitory balancing of cortical network excitability}, Volume = {34}, @@ -10043,7 +10042,7 @@ VIDEO ABSTRACT: }, Month = {Oct}, Number = {4}, Pages = {2212-21}, - pubmed = {22387472}, + pmid = {22387472}, Pst = {ppublish}, Title = {Spontaneous activity in developing sensory circuits: Implications for resting state fMRI}, Volume = {62}, @@ -10063,7 +10062,7 @@ VIDEO ABSTRACT: }, Number = {23}, Pages = {8577-82}, Pmc = {PMC1482622}, - pubmed = {16723398}, + pmid = {16723398}, Pst = {ppublish}, Title = {Modularity and community structure in networks}, Volume = {103}, @@ -10120,7 +10119,7 @@ VIDEO ABSTRACT: }, Number = {4}, Pages = {e10232}, Pmc = {PMC2860504}, - pubmed = {20436911}, + pmid = {20436911}, Pst = {epublish}, Title = {Eigenvector centrality mapping for analyzing connectivity patterns in fMRI data of the human brain}, Volume = {5}, @@ -10165,7 +10164,7 @@ VIDEO ABSTRACT: }, Month = {Aug}, Number = {8}, Pages = {2356-66}, - pubmed = {19172655}, + pmid = {19172655}, Pst = {ppublish}, Title = {Changes in the interaction of resting-state neural networks from adolescence to adulthood}, Volume = {30}, @@ -10185,7 +10184,7 @@ VIDEO ABSTRACT: }, Mesh = {Adolescent; Adult; Age Factors; Aged; Aged, 80 and over; Aging; Brain; Brain Mapping; Child; Cognition; Connectome; Female; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Nerve Net; Sex Factors}, Month = {Jan}, Pages = {76-93}, - pubmed = {24333927}, + pmid = {24333927}, Pst = {ppublish}, Title = {Topological organization of the human brain functional connectome across the lifespan}, Volume = {7}, @@ -10206,7 +10205,7 @@ VIDEO ABSTRACT: }, Number = {4}, Pages = {e5226}, Pmc = {PMC2668183}, - pubmed = {19381298}, + pmid = {19381298}, Pst = {ppublish}, Title = {Uncovering intrinsic modular organization of spontaneous brain activity in humans}, Volume = {4}, @@ -10228,7 +10227,7 @@ VIDEO ABSTRACT: }, Number = {4}, Pages = {550-62}, Pmc = {PMC2848443}, - pubmed = {20188659}, + pmid = {20188659}, Pst = {ppublish}, Title = {Functional-anatomic fractionation of the brain's default network}, Volume = {65}, @@ -10247,7 +10246,7 @@ VIDEO ABSTRACT: }, Number = {5}, Pages = {e94423}, Pmc = {PMC4006774}, - pubmed = {24788455}, + pmid = {24788455}, Pst = {epublish}, Title = {Intrinsic functional brain architecture derived from graph theoretical analysis in the human fetus}, Volume = {9}, @@ -10269,7 +10268,7 @@ VIDEO ABSTRACT: }, Number = {173}, Pages = {173ra24}, Pmc = {PMC3618956}, - pubmed = {23427244}, + pmid = {23427244}, Pst = {ppublish}, Title = {Cross-hemispheric functional connectivity in the human fetal brain}, Volume = {5}, @@ -10290,7 +10289,7 @@ VIDEO ABSTRACT: }, Month = {Aug}, Number = {8}, Pages = {1862-75}, - pubmed = {21968567}, + pmid = {21968567}, Pst = {ppublish}, Title = {Network centrality in the human functional connectome}, Volume = {22}, @@ -10311,7 +10310,7 @@ VIDEO ABSTRACT: }, Month = {Oct}, Number = {10}, Pages = {3127-41}, - pubmed = {19235882}, + pmid = {19235882}, Pst = {ppublish}, Title = {Functionally linked resting-state networks reflect the underlying structural connectivity architecture of the human brain}, Volume = {30}, @@ -10333,7 +10332,7 @@ VIDEO ABSTRACT: }, Number = {37}, Pages = {13848-53}, Pmc = {PMC1564249}, - pubmed = {16945915}, + pmid = {16945915}, Pst = {ppublish}, Title = {Consistent resting-state networks across healthy subjects}, Volume = {103}, @@ -10354,7 +10353,7 @@ VIDEO ABSTRACT: }, Month = {Sep}, Number = {9}, Pages = {1332-42}, - pubmed = {15635061}, + pmid = {15635061}, Pst = {ppublish}, Title = {Neurophysiological architecture of functional magnetic resonance images of human brain}, Volume = {15}, @@ -10376,7 +10375,7 @@ VIDEO ABSTRACT: }, Number = {5}, Pages = {e1000381}, Pmc = {PMC2671306}, - pubmed = {19412534}, + pmid = {19412534}, Pst = {ppublish}, Title = {Functional brain networks develop from a "local to distributed" organization}, Volume = {5}, @@ -10397,7 +10396,7 @@ VIDEO ABSTRACT: }, Number = {16}, Pages = {6790-5}, Pmc = {PMC2672537}, - pubmed = {19351894}, + pmid = {19351894}, Pst = {ppublish}, Title = {Evidence on the emergence of the brain's default network from 2-week-old to 2-year-old healthy pediatric subjects}, Volume = {106}, @@ -10414,7 +10413,7 @@ VIDEO ABSTRACT: }, Journal-Full = {Annual review of neuroscience}, Mesh = {Animals; Association; Cerebral Cortex; Cognition; Humans; Neural Pathways; Primates; Psychomotor Performance}, Pages = {137-56}, - pubmed = {3284439}, + pmid = {3284439}, Pst = {ppublish}, Title = {Topography of cognition: parallel distributed networks in primate association cortex}, Volume = {11}, @@ -10436,7 +10435,7 @@ VIDEO ABSTRACT: }, Number = {3}, Pages = {1622-33}, Pmc = {PMC3408572}, - pubmed = {22613620}, + pmid = {22613620}, Pst = {ppublish}, Title = {Altered structural connectivity in neonates at genetic risk for schizophrenia: a combined study using morphological and white matter networks}, Volume = {62}, @@ -10458,7 +10457,7 @@ VIDEO ABSTRACT: }, Number = {44}, Pages = {19067-72}, Pmc = {PMC2973853}, - pubmed = {20956328}, + pmid = {20956328}, Pst = {ppublish}, Title = {White matter maturation reshapes structural connectivity in the late developing human brain}, Volume = {107}, @@ -10480,7 +10479,7 @@ VIDEO ABSTRACT: }, Number = {7}, Pages = {e1000157}, Pmc = {PMC2705656}, - pubmed = {19621066}, + pmid = {19621066}, Pst = {ppublish}, Title = {Development of large-scale functional brain networks in children}, Volume = {7}, @@ -10502,7 +10501,7 @@ VIDEO ABSTRACT: }, Number = {50}, Pages = {18578-89}, Pmc = {PMC3641286}, - pubmed = {22171056}, + pmid = {22171056}, Pst = {ppublish}, Title = {Dynamic reconfiguration of structural and functional connectivity across core neurocognitive brain networks with development}, Volume = {31}, @@ -10524,7 +10523,7 @@ VIDEO ABSTRACT: }, Number = {10}, Pages = {2380-93}, Pmc = {PMC3767958}, - pubmed = {22875861}, + pmid = {22875861}, Pst = {ppublish}, Title = {The development of hub architecture in the human functional brain network}, Volume = {23}, @@ -10545,7 +10544,7 @@ VIDEO ABSTRACT: }, Month = {Jan}, Number = {1}, Pages = {145-54}, - pubmed = {20421249}, + pmid = {20421249}, Pst = {ppublish}, Title = {The functional architecture of the infant brain as revealed by resting-state fMRI}, Volume = {21}, @@ -10566,7 +10565,7 @@ VIDEO ABSTRACT: }, Number = {6}, Pages = {1860-73}, Pmc = {PMC2750039}, - pubmed = {19211893}, + pmid = {19211893}, Pst = {ppublish}, Title = {Cortical hubs revealed by intrinsic functional connectivity: mapping, assessment of stability, and relation to Alzheimer's disease}, Volume = {29}, @@ -10588,7 +10587,7 @@ VIDEO ABSTRACT: }, Month = {Sep}, Number = {9}, Pages = {700-11}, - pubmed = {17704812}, + pmid = {17704812}, Pst = {ppublish}, Title = {Spontaneous fluctuations in brain activity observed with functional magnetic resonance imaging}, Volume = {8}, @@ -10609,7 +10608,7 @@ VIDEO ABSTRACT: }, Number = {12}, Pages = {603-5}, Pmc = {PMC3858486}, - pubmed = {24080424}, + pmid = {24080424}, Pst = {ppublish}, Title = {Brain network interactions in health and disease}, Volume = {17}, @@ -10630,7 +10629,7 @@ VIDEO ABSTRACT: }, Number = {12}, Pages = {600-2}, Pmc = {PMC3858496}, - pubmed = {24094797}, + pmid = {24094797}, Pst = {ppublish}, Title = {Complex relationships between structural and functional brain connectivity}, Volume = {17}, @@ -10651,7 +10650,7 @@ VIDEO ABSTRACT: }, Number = {12}, Pages = {602-3}, Pmc = {PMC3873155}, - pubmed = {24129332}, + pmid = {24129332}, Pst = {ppublish}, Title = {Fronto-parietal network: flexible hub of cognitive control}, Volume = {17}, @@ -10671,7 +10670,7 @@ VIDEO ABSTRACT: }, Month = {Dec}, Number = {12}, Pages = {616-26}, - pubmed = {24139950}, + pmid = {24139950}, Pst = {ppublish}, Title = {Cortical dynamics revisited}, Volume = {17}, @@ -10692,7 +10691,7 @@ VIDEO ABSTRACT: }, Month = {Dec}, Number = {12}, Pages = {606-15}, - pubmed = {24182697}, + pmid = {24182697}, Pst = {ppublish}, Title = {Neurocognitive biases and the patterns of spontaneous correlations in the human cortex}, Volume = {17}, @@ -10711,7 +10710,7 @@ VIDEO ABSTRACT: }, Month = {Dec}, Number = {12}, Pages = {627-40}, - pubmed = {24183779}, + pmid = {24183779}, Pst = {ppublish}, Title = {Developmental pathways to functional brain networks: emerging principles}, Volume = {17}, @@ -10732,7 +10731,7 @@ VIDEO ABSTRACT: }, Month = {Dec}, Number = {12}, Pages = {648-65}, - pubmed = {24210963}, + pmid = {24210963}, Pst = {ppublish}, Title = {The evolution of distributed association networks in the human brain}, Volume = {17}, @@ -10752,7 +10751,7 @@ VIDEO ABSTRACT: }, Month = {Dec}, Number = {12}, Pages = {596-9}, - pubmed = {24210964}, + pmid = {24210964}, Pst = {ppublish}, Title = {Light microscopy mapping of connections in the intact brain}, Volume = {17}, @@ -10773,7 +10772,7 @@ VIDEO ABSTRACT: }, Month = {Dec}, Number = {12}, Pages = {641-7}, - pubmed = {24238779}, + pmid = {24238779}, Pst = {ppublish}, Title = {Fledgling pathoconnectomics of psychiatric disorders}, Volume = {17}, @@ -10794,7 +10793,7 @@ VIDEO ABSTRACT: }, Month = {Dec}, Number = {12}, Pages = {683-96}, - pubmed = {24231140}, + pmid = {24231140}, Pst = {ppublish}, Title = {Network hubs in the human brain}, Volume = {17}, @@ -10814,7 +10813,7 @@ VIDEO ABSTRACT: }, Month = {Jan}, Number = {1}, Pages = {54-63}, - pubmed = {11163888}, + pmid = {11163888}, Pst = {ppublish}, Title = {Independent component analysis at the neural cocktail party}, Volume = {24}, @@ -10835,7 +10834,7 @@ VIDEO ABSTRACT: }, Number = {10}, Pages = {3776-83}, Pmc = {PMC3073070}, - pubmed = {21389232}, + pmid = {21389232}, Pst = {ppublish}, Title = {Uncovering intrinsic connectional architecture of functional networks in awake rat brain}, Volume = {31}, @@ -10856,7 +10855,7 @@ VIDEO ABSTRACT: }, Month = {Jun}, Number = {6}, Pages = {3398-406}, - pubmed = {20410359}, + pmid = {20410359}, Pst = {ppublish}, Title = {Functional networks in the anesthetized rat brain revealed by independent component analysis of resting-state FMRI}, Volume = {103}, @@ -10878,7 +10877,7 @@ VIDEO ABSTRACT: }, Number = {46}, Pages = {18265-9}, Pmc = {PMC2084331}, - pubmed = {17991778}, + pmid = {17991778}, Pst = {ppublish}, Title = {Synchronized delta oscillations correlate with the resting-state functional MRI signal}, Volume = {104}, @@ -10899,7 +10898,7 @@ VIDEO ABSTRACT: }, Month = {Feb}, Number = {2}, Pages = {179-85}, - pubmed = {18804545}, + pmid = {18804545}, Pst = {ppublish}, Title = {Parietal cortex, navigation, and the construction of arbitrary reference frames for spatial information}, Volume = {91}, @@ -10920,7 +10919,7 @@ VIDEO ABSTRACT: }, Number = {2}, Pages = {186-96}, Pmc = {PMC2666283}, - pubmed = {18929674}, + pmid = {18929674}, Pst = {ppublish}, Title = {Where am I and how will I get there from here? A role for posterior parietal cortex in the integration of spatial information and route planning}, Volume = {91}, @@ -10942,7 +10941,7 @@ VIDEO ABSTRACT: }, Number = {39}, Pages = {14755-62}, Pmc = {PMC2567440}, - pubmed = {18812502}, + pmid = {18812502}, Pst = {ppublish}, Title = {Navigating from hippocampus to parietal cortex}, Volume = {105}, @@ -10963,7 +10962,7 @@ VIDEO ABSTRACT: }, Month = {Mar}, Number = {5}, Pages = {747-56}, - pubmed = {16504949}, + pmid = {16504949}, Pst = {ppublish}, Title = {Tracking route progression in the posterior parietal cortex}, Volume = {49}, @@ -10983,7 +10982,7 @@ VIDEO ABSTRACT: }, Mesh = {Animals; Cerebral Cortex; Electrodes, Implanted; Electrophysiology; Male; Motor Cortex; Movement; Orientation; Rats; Rats, Inbred F344; Somatosensory Cortex; Space Perception}, Number = {1}, Pages = {27-39}, - pubmed = {8180489}, + pmid = {8180489}, Pst = {ppublish}, Title = {Cortical representation of motion during unrestrained spatial navigation in the rat}, Volume = {4}, @@ -11001,7 +11000,7 @@ VIDEO ABSTRACT: }, Mesh = {Animals; Cognition; Memory; Parietal Lobe; Rats; Space Perception; Spatial Behavior}, Number = {4}, Pages = {369-77}, - pubmed = {19621117}, + pmid = {19621117}, Pst = {ppublish}, Title = {The parietal association cortex of the rat}, Volume = {41}, @@ -11022,7 +11021,7 @@ VIDEO ABSTRACT: }, Month = {Aug}, Number = {31}, Pages = {6862-70}, - pubmed = {15295020}, + pmid = {15295020}, Pst = {ppublish}, Title = {The sleep slow oscillation as a traveling wave}, Volume = {24}, @@ -11039,7 +11038,7 @@ VIDEO ABSTRACT: }, Month = {Dec}, Number = {3597}, Pages = {1367}, - pubmed = {17752414}, + pmid = {17752414}, Pst = {ppublish}, Title = {Embryology}, Volume = {142}, @@ -11056,7 +11055,7 @@ VIDEO ABSTRACT: }, Mesh = {Embryo, Nonmammalian; Periodicity; Spinal Cord}, Month = {Mar}, Pages = {533-45}, - pubmed = {13952299}, + pmid = {13952299}, Pst = {ppublish}, Title = {Observations and experiments on spontaneous rhythmical behavior in the chick embryo}, Volume = {6}, @@ -11073,7 +11072,7 @@ VIDEO ABSTRACT: }, Mesh = {Animals; Behavior, Animal; Brain; Chick Embryo; Electrophysiology; Embryo, Nonmammalian; Fishes; Movement; Neurons; Periodicity; Physiology, Comparative; Reflex; Research; Spinal Cord; Urodela}, Month = {Dec}, Pages = {342-65}, - pubmed = {14111168}, + pmid = {14111168}, Pst = {ppublish}, Title = {SOME ASPECTS OF THE EMBRYOLOGY OF BEHAVIOR}, Volume = {38}, @@ -11090,7 +11089,7 @@ VIDEO ABSTRACT: }, Mesh = {Age Factors; Animals; Animals, Newborn; Anura; Brachyura; Chickens; Cockroaches; Fetus; Fishes; Lizards; Mollusca; Motor Activity; Muscle Contraction; Muscles; Phylogeny; Rats; Sheep; Sleep; Swimming; Wasps}, Number = {4}, Pages = {279-95}, - pubmed = {335440}, + pmid = {335440}, Pst = {ppublish}, Title = {Sleep and the beginnings of behavior in the animal kingdom--studies of ultradian motility cycles in early life}, Volume = {8}, @@ -11110,7 +11109,7 @@ VIDEO ABSTRACT: }, Month = {Nov}, Number = {6}, Pages = {501-15}, - pubmed = {1001836}, + pmid = {1001836}, Pst = {ppublish}, Title = {The development of the EEG in the rat}, Volume = {9}, @@ -11130,7 +11129,7 @@ VIDEO ABSTRACT: }, Mesh = {Animals; Bicuculline; Cerebral Cortex; Electric Conductivity; Evoked Potentials; Glutamates; Glutamic Acid; Guinea Pigs; Kinetics; Neurons}, Number = {5979}, Pages = {685-7}, - pubmed = {6147755}, + pmid = {6147755}, Pst = {ppublish}, Title = {Initiation of synchronized neuronal bursting in neocortex}, Volume = {310}, @@ -11147,7 +11146,7 @@ VIDEO ABSTRACT: }, Mesh = {Acetylcholine; Afferent Pathways; Animals; Arousal; Behavior; Brain; Brain Mapping; Choline O-Acetyltransferase; Cholinergic Fibers; Cognition; Efferent Pathways; Mammals; Motor Activity; Neurons; Rats; Sensation; Sleep; Spinal Cord}, Number = {6}, Pages = {475-524}, - pubmed = {1763188}, + pmid = {1763188}, Pst = {ppublish}, Title = {Cholinergic systems in mammalian brain and spinal cord}, Volume = {37}, @@ -11166,7 +11165,7 @@ VIDEO ABSTRACT: }, Month = {Jun}, Number = {11}, Pages = {4267-85}, - pubmed = {10818163}, + pmid = {10818163}, Pst = {ppublish}, Title = {Membrane mechanisms underlying contrast adaptation in cat area 17 in vivo}, Volume = {20}, @@ -11184,7 +11183,7 @@ VIDEO ABSTRACT: }, Month = {Jul}, Number = {5119}, Pages = {361-4}, - pubmed = {8392750}, + pmid = {8392750}, Pst = {ppublish}, Title = {Cellular mechanisms of a synchronized oscillation in the thalamus}, Volume = {261}, @@ -11201,7 +11200,7 @@ VIDEO ABSTRACT: }, Month = {Oct}, Number = {5134}, Pages = {679-85}, - pubmed = {8235588}, + pmid = {8235588}, Pst = {ppublish}, Title = {Thalamocortical oscillations in the sleeping and aroused brain}, Volume = {262}, @@ -11219,7 +11218,7 @@ VIDEO ABSTRACT: }, Month = {Jul}, Number = {13}, Pages = {5153-62}, - pubmed = {10864972}, + pmid = {10864972}, Pst = {ppublish}, Title = {Corticothalamic inputs control the pattern of activity generated in thalamocortical networks}, Volume = {20}, @@ -11235,7 +11234,7 @@ VIDEO ABSTRACT: }, Journal-Full = {Annual review of physiology}, Mesh = {Animals; Brain; Electroencephalography; Epilepsy; Humans; Neural Pathways; Neurons}, Pages = {815-46}, - pubmed = {11181977}, + pmid = {11181977}, Pst = {ppublish}, Title = {On the cellular and network bases of epileptic seizures}, Volume = {63}, @@ -11251,7 +11250,7 @@ VIDEO ABSTRACT: }, Journal-Full = {International review of neurobiology}, Mesh = {Cerebral Cortex; Electroencephalography; Epilepsy, Absence; Humans; Oscillometry; Periodicity; Reference Values; Thalamus}, Pages = {99-114}, - pubmed = {12040908}, + pmid = {12040908}, Pst = {ppublish}, Title = {Cortical and subcortical generators of normal and abnormal rhythmicity}, Volume = {49}, @@ -11269,7 +11268,7 @@ VIDEO ABSTRACT: }, Month = {Jul}, Number = {7}, Pages = {350-6}, - pubmed = {17544519}, + pmid = {17544519}, Pst = {ppublish}, Title = {Thalamic synchrony and dynamic regulation of global forebrain oscillations}, Volume = {30}, @@ -11289,7 +11288,7 @@ VIDEO ABSTRACT: }, Number = {1}, Pages = {129-43}, Pmc = {PMC3139922}, - pubmed = {20624597}, + pmid = {20624597}, Pst = {ppublish}, Title = {Endogenous electric fields may guide neocortical network activity}, Volume = {67}, @@ -11309,7 +11308,7 @@ VIDEO ABSTRACT: }, Number = {20}, Pages = {6891-902}, Pmc = {PMC2990270}, - pubmed = {20484631}, + pmid = {20484631}, Pst = {ppublish}, Title = {Action potentials initiate in the axon initial segment and propagate through axon collaterals reliably in cerebellar Purkinje neurons}, Volume = {30}, @@ -11329,7 +11328,7 @@ VIDEO ABSTRACT: }, Number = {35}, Pages = {12165-79}, Pmc = {PMC3466092}, - pubmed = {22933799}, + pmid = {22933799}, Pst = {ppublish}, Title = {Selective functional interactions between excitatory and inhibitory cortical neurons and differential contribution to persistent activity of the slow oscillation}, Volume = {32}, @@ -11348,7 +11347,7 @@ VIDEO ABSTRACT: }, Month = {Sep}, Number = {9}, Pages = {402-7}, - pubmed = {7482806}, + pmid = {7482806}, Pst = {ppublish}, Title = {The formation of a cortical somatotopic map}, Volume = {18}, @@ -11365,7 +11364,7 @@ VIDEO ABSTRACT: }, Mesh = {Animals; Brain Mapping; Brain Stem; Cardiovascular Physiological Phenomena; Cats; Cortical Synchronization; Eye Movements; Geniculate Bodies; Hippocampus; Humans; Locus Coeruleus; Muscle Contraction; Muscle Tonus; Occipital Lobe; Pons; Rats; Respiration; Reticular Formation; Sleep, REM}, Number = {3}, Pages = {241-88}, - pubmed = {6382442}, + pmid = {6382442}, Pst = {ppublish}, Title = {Brainstem control of the events of REM sleep}, Volume = {22}, @@ -11383,7 +11382,7 @@ VIDEO ABSTRACT: }, Mesh = {Age Factors; Animals; Animals, Newborn; Attention; Behavior, Animal; Cats; Circadian Rhythm; Electroencephalography; Guinea Pigs; Rats; Sleep; Sleep Stages; Wakefulness; Weaning}, Number = {4}, Pages = {216-39}, - pubmed = {5527153}, + pmid = {5527153}, Pst = {ppublish}, Title = {Ontogenesis of the states of sleep in rat, cat, and guinea pig during the first postnatal month}, Volume = {2}, @@ -11402,7 +11401,7 @@ VIDEO ABSTRACT: }, Month = {Jan}, Number = {1}, Pages = {156-77}, - pubmed = {1109335}, + pmid = {1109335}, Pst = {ppublish}, Title = {Effects of spinal transection in neonatal and weanling rats: survival of function}, Volume = {46}, @@ -11421,7 +11420,7 @@ VIDEO ABSTRACT: }, Month = {Nov}, Number = {4}, Pages = {896-920}, - pubmed = {1200422}, + pmid = {1200422}, Pst = {ppublish}, Title = {Postnatal development of locomotion in the laboratory rat}, Volume = {23}, @@ -11438,7 +11437,7 @@ VIDEO ABSTRACT: }, Mesh = {Animals; Embryonic and Fetal Development; Female; Fetus; Motor Activity; Pregnancy; Pregnancy, Animal; Rats; Rats, Inbred Strains}, Number = {1}, Pages = {100-34}, - pubmed = {5157515}, + pmid = {5157515}, Pst = {ppublish}, Title = {Prenatal development of spontaneous and evoked activity in the rat (Rattus norvegicus albinus)}, Volume = {40}, @@ -11457,7 +11456,7 @@ VIDEO ABSTRACT: }, Month = {Dec}, Number = {6}, Pages = {1196-202}, - pubmed = {7893412}, + pmid = {7893412}, Pst = {ppublish}, Title = {Dual mechanisms of twitching during sleep in neonatal rats}, Volume = {108}, @@ -11476,7 +11475,7 @@ VIDEO ABSTRACT: }, Month = {Apr}, Number = {2}, Pages = {328-36}, - pubmed = {10832794}, + pmid = {10832794}, Pst = {ppublish}, Title = {Spontaneous motor activity in fetal and infant rats is organized into discrete multilimb bouts}, Volume = {114}, @@ -11495,7 +11494,7 @@ VIDEO ABSTRACT: }, Month = {Jun}, Number = {3}, Pages = {585-93}, - pubmed = {10883808}, + pmid = {10883808}, Pst = {ppublish}, Title = {A comparative analysis of huddling in infant Norway rats and Syrian golden hamsters: does endothermy modulate behavior?}, Volume = {114}, @@ -11514,7 +11513,7 @@ VIDEO ABSTRACT: }, Month = {Dec}, Number = {6}, Pages = {693-7}, - pubmed = {15582370}, + pmid = {15582370}, Pst = {ppublish}, Title = {Learning in sensorimotor circuits}, Volume = {14}, @@ -11534,7 +11533,7 @@ VIDEO ABSTRACT: }, Month = {Apr}, Number = {4}, Pages = {229-39}, - pubmed = {11283746}, + pmid = {11283746}, Pst = {ppublish}, Title = {The brainweb: phase synchronization and large-scale integration}, Volume = {2}, @@ -11554,7 +11553,7 @@ VIDEO ABSTRACT: }, Month = {Jul}, Number = {1}, Pages = {41-8}, - pubmed = {11396986}, + pmid = {11396986}, Pst = {ppublish}, Title = {The effect of calcium pump inhibitors on the response of intracellular calcium to caffeine in snail neurones}, Volume = {30}, @@ -11573,7 +11572,7 @@ VIDEO ABSTRACT: }, Keywords = {data acquisition system; hippocampus; local field potential; microstimulation; multi-electrode array; population spike; recording; stimulation artifact}, Pages = {12}, Pmc = {PMC2722905}, - pubmed = {19668698}, + pmid = {19668698}, Pst = {epublish}, Title = {A low-cost multielectrode system for data acquisition enabling real-time closed-loop processing with rapid recovery from stimulation artifacts}, Volume = {2}, @@ -11593,7 +11592,7 @@ VIDEO ABSTRACT: }, Month = {Feb}, Number = {4}, Pages = {1491-504}, - pubmed = {9454857}, + pmid = {9454857}, Pst = {ppublish}, Title = {Synchronizing retinal activity in both eyes disrupts binocular map development in the optic tectum}, Volume = {18}, @@ -11612,7 +11611,7 @@ VIDEO ABSTRACT: }, Month = {Feb}, Number = {2}, Pages = {243-55}, - pubmed = {9052795}, + pmid = {9052795}, Pst = {ppublish}, Title = {Ca2+ oscillations mediated by the synergistic excitatory actions of GABA(A) and NMDA receptors in the neonatal hippocampus}, Volume = {18}, @@ -11632,7 +11631,7 @@ VIDEO ABSTRACT: }, Month = {May}, Number = {19}, Pages = {5117-30}, - pubmed = {16687503}, + pmid = {16687503}, Pst = {ppublish}, Title = {Depolarizing GABAergic conductances regulate the balance of excitation to inhibition in the developing retinotectal circuit in vivo}, Volume = {26}, @@ -11652,7 +11651,7 @@ VIDEO ABSTRACT: }, Month = {May}, Number = {6186}, Pages = {904-9}, - pubmed = {24855269}, + pmid = {24855269}, Pst = {ppublish}, Title = {Rapid Hebbian axonal remodeling mediated by visual stimulation}, Volume = {344}, @@ -11672,7 +11671,7 @@ VIDEO ABSTRACT: }, Month = {Sep}, Number = {9}, Pages = {1063-7}, - pubmed = {11533712}, + pmid = {11533712}, Pst = {ppublish}, Title = {In vivo optical mapping of epileptic foci and surround inhibition in ferret cerebral cortex}, Volume = {7}, @@ -11693,7 +11692,7 @@ VIDEO ABSTRACT: }, Month = {Jun}, Number = {6}, Pages = {1289-98}, - pubmed = {24945772}, + pmid = {24945772}, Pst = {ppublish}, Title = {Balanced interhemispheric cortical activity is required for correct targeting of the corpus callosum}, Volume = {82}, @@ -11727,7 +11726,7 @@ VIDEO ABSTRACT: }, Number = {4}, Pages = {e42}, Pmc = {PMC1239902}, - pubmed = {16201007}, + pmid = {16201007}, Pst = {ppublish}, Title = {The human connectome: A structural description of the human brain}, Volume = {1}, @@ -11749,7 +11748,7 @@ VIDEO ABSTRACT: }, Number = {12}, Pages = {666-82}, Pmc = {PMC4004765}, - pubmed = {24238796}, + pmid = {24238796}, Pst = {ppublish}, Title = {Functional connectomics from resting-state fMRI}, Volume = {17}, @@ -11766,7 +11765,7 @@ VIDEO ABSTRACT: }, Keywords = {goal directed behavior; rat; rodent; learning; memory; development; behavior; Locomotion; Motor Activity}, Mesh = {Animals; Cognition; Cues; Exploratory Behavior; Female; Hippocampus; Humans; Male; Models, Neurological; Neuronal Plasticity; Orientation; Rats; Spatial Behavior}, Pages = {613-26; discussion 626-36}, - pubmed = {2075964}, + pmid = {2075964}, Pst = {ppublish}, Title = {Varieties of spatial cognition. Psychobiological considerations}, Volume = {608}, @@ -11785,7 +11784,7 @@ VIDEO ABSTRACT: }, Month = {Aug}, Number = {6197}, Pages = {660-5}, - pubmed = {25104383}, + pmid = {25104383}, Pst = {ppublish}, Title = {Selective attention. Long-range and local circuits for top-down modulation of visual cortex processing}, Volume = {345}, @@ -11804,7 +11803,7 @@ VIDEO ABSTRACT: }, Month = {Aug}, Number = {33}, Pages = {10870-83}, - pubmed = {25122889}, + pmid = {25122889}, Pst = {ppublish}, Title = {Sensory-evoked and spontaneous gamma and spindle bursts in neonatal rat motor cortex}, Volume = {34}, @@ -11824,7 +11823,7 @@ VIDEO ABSTRACT: }, Month = {Feb}, Number = {2}, Pages = {94-106}, - pubmed = {22251956}, + pmid = {22251956}, Pst = {epublish}, Title = {Activity-dependent neurotransmitter respecification}, Volume = {13}, @@ -11850,7 +11849,7 @@ CONCLUSIONS AND RELEVANCE: Maternal use of valproate during pregnancy was associ Month = {Apr}, Number = {16}, Pages = {1696-703}, - pubmed = {23613074}, + pmid = {23613074}, Pst = {ppublish}, Title = {Prenatal valproate exposure and risk of autism spectrum disorders and childhood autism}, Volume = {309}, @@ -11874,7 +11873,7 @@ INTERPRETATION: Fetal valproate exposure has dose-dependent associations with re Number = {3}, Pages = {244-52}, Pmc = {PMC3684942}, - pubmed = {23352199}, + pmid = {23352199}, Pst = {ppublish}, Title = {Fetal antiepileptic drug exposure and cognitive outcomes at age 6 years (NEAD study): a prospective observational study}, Volume = {12}, @@ -11895,7 +11894,7 @@ INTERPRETATION: Fetal valproate exposure has dose-dependent associations with re Number = {37}, Pages = {9239-48}, Pmc = {PMC2878961}, - pubmed = {18784304}, + pmid = {18784304}, Pst = {ppublish}, Title = {Hierarchical organization of human cortical networks in health and schizophrenia}, Volume = {28}, @@ -11981,7 +11980,7 @@ INTERPRETATION: Fetal valproate exposure has dose-dependent associations with re Month = {Dec}, Number = {12}, Pages = {1002-12}, - pubmed = {14618156}, + pmid = {14618156}, Pst = {ppublish}, Title = {The developmental role of serotonin: news from mouse molecular genetics}, Volume = {4}, @@ -11999,7 +11998,7 @@ INTERPRETATION: Fetal valproate exposure has dose-dependent associations with re Month = {Nov}, Number = {4}, Pages = {506-24}, - pubmed = {9826275}, + pmid = {9826275}, Pst = {ppublish}, Title = {Transient developmental expression of monoamine transporters in the rodent forebrain}, Volume = {401}, @@ -12017,7 +12016,7 @@ INTERPRETATION: Fetal valproate exposure has dose-dependent associations with re Month = {Nov}, Number = {5}, Pages = {823-35}, - pubmed = {8938116}, + pmid = {8938116}, Pst = {ppublish}, Title = {Transient uptake and storage of serotonin in developing thalamic neurons}, Volume = {17}, @@ -12035,7 +12034,7 @@ INTERPRETATION: Fetal valproate exposure has dose-dependent associations with re Month = {Apr}, Number = {14}, Pages = {3201-4}, - pubmed = {11019047}, + pmid = {11019047}, Pst = {ppublish}, Title = {Mean-field solution of the small-world network model}, Volume = {84}, @@ -12056,7 +12055,7 @@ CONCLUSIONS/SIGNIFICANCE: We have shown how the notion of a small-world network Number = {4}, Pages = {e0002051}, Pmc = {PMC2323569}, - pubmed = {18446219}, + pmid = {18446219}, Pst = {epublish}, Title = {Network 'small-world-ness': a quantitative method for determining canonical network equivalence}, Volume = {3}, @@ -12076,7 +12075,7 @@ CONCLUSIONS/SIGNIFICANCE: We have shown how the notion of a small-world network Month = {Sep}, Number = {9}, Pages = {418-25}, - pubmed = {15350243}, + pmid = {15350243}, Pst = {ppublish}, Title = {Organization, development and function of complex brain networks}, Volume = {8}, @@ -12094,7 +12093,7 @@ CONCLUSIONS/SIGNIFICANCE: We have shown how the notion of a small-world network Journal-Full = {Cerebral cortex (New York, N.Y. : 1991)}, Keywords = {brain connectivity; connectome; maturation; network analysis; tractography; resting state; default mode network; technique; Methods; computation biology; Theoretical; graph theory; human; fmri; Software; neonate; Cerebral Cortex; Neocortex; wholeBrain}, Month = {Dec}, - pubmed = {24343892}, + pmid = {24343892}, Pst = {aheadofprint}, Title = {Preferential Detachment During Human Brain Development: Age- and Sex-Specific Structural Connectivity in Diffusion Tensor Imaging (DTI) Data}, Year = {2013}, @@ -12111,7 +12110,7 @@ CONCLUSIONS/SIGNIFICANCE: We have shown how the notion of a small-world network Journal-Full = {Cerebral cortex (New York, N.Y. : 1991)}, Keywords = {connectome; development; functional connectivity; neonatal; structural connectivity; resting state; default mode network; technique; Methods; computation biology; Theoretical; graph theory; human; fmri; Software; neonate; Cerebral Cortex; Neocortex; wholeBrain}, Month = {May}, - pubmed = {24833018}, + pmid = {24833018}, Pst = {aheadofprint}, Title = {The Neonatal Connectome During Preterm Brain Development}, Year = {2014}, @@ -12131,7 +12130,7 @@ CONCLUSIONS/SIGNIFICANCE: We have shown how the notion of a small-world network Number = {46}, Pages = {20015-20}, Pmc = {PMC2993415}, - pubmed = {21041625}, + pmid = {21041625}, Pst = {ppublish}, Title = {Emergence of resting state networks in the preterm human brain}, Volume = {107}, @@ -12150,7 +12149,7 @@ CONCLUSIONS/SIGNIFICANCE: We have shown how the notion of a small-world network Month = {Jul}, Number = {29}, Pages = {9812-6}, - pubmed = {25031418}, + pmid = {25031418}, Pst = {ppublish}, Title = {Emergence of feature-specific connectivity in cortical microcircuits in the absence of visual experience}, Volume = {34}, @@ -12172,7 +12171,7 @@ CONCLUSIONS/SIGNIFICANCE: We have shown how the notion of a small-world network Number = {1}, Pages = {21-6}, Pmc = {PMC3890828}, - pubmed = {24367107}, + pmid = {24367107}, Pst = {ppublish}, Title = {High-resolution photoacoustic tomography of resting-state functional connectivity in the mouse brain}, Volume = {111}, @@ -12193,7 +12192,7 @@ CONCLUSIONS/SIGNIFICANCE: We have shown how the notion of a small-world network Number = {40}, Pages = {10134-44}, Pmc = {PMC2678192}, - pubmed = {18829971}, + pmid = {18829971}, Pst = {ppublish}, Title = {Synchronous bursts of neuronal activity in the developing hippocampus: modulation by active sleep and association with emerging gamma and theta rhythms}, Volume = {28}, @@ -12213,7 +12212,7 @@ CONCLUSIONS/SIGNIFICANCE: We have shown how the notion of a small-world network Number = {5}, Pages = {e143}, Pmc = {PMC1079781}, - pubmed = {15826218}, + pmid = {15826218}, Pst = {ppublish}, Title = {The neural substrates of infant sleep in rats}, Volume = {3}, @@ -12233,7 +12232,7 @@ CONCLUSIONS/SIGNIFICANCE: We have shown how the notion of a small-world network Number = {5}, Pages = {1301-10}, Pmc = {PMC2645537}, - pubmed = {16553791}, + pmid = {16553791}, Pst = {ppublish}, Title = {The preoptic hypothalamus and basal forebrain play opposing roles in the descending modulation of sleep and wakefulness in infant rats}, Volume = {23}, @@ -12249,7 +12248,7 @@ CONCLUSIONS/SIGNIFICANCE: We have shown how the notion of a small-world network Mesh = {Bibliography as Topic; History, 20th Century; Psychophysiology; United States}, Number = {4}, Pages = {307-24}, - pubmed = {359102}, + pmid = {359102}, Pst = {ppublish}, Title = {C. N. Woolsey--scientist and artist: a complete bibliography (1933--1974)}, Volume = {15}, @@ -12286,7 +12285,7 @@ From http://braininfo.rprc.washington.edu/Source.aspx?ID=90&questID=1350: Number = {4}, Pages = {2333-7}, Pmc = {PMC348709}, - pubmed = {6246540}, + pmid = {6246540}, Pst = {ppublish}, Title = {Histochemical changes in cytochrome oxidase of cortical barrels after vibrissal removal in neonatal and adult mice}, Volume = {77}, @@ -12303,7 +12302,7 @@ From http://braininfo.rprc.washington.edu/Source.aspx?ID=90&questID=1350: Month = {Aug}, Number = {2}, Pages = {91-112}, - pubmed = {6032827}, + pmid = {6032827}, Pst = {ppublish}, Title = {Somatosensory, auditory and visual cortical areas of the mouse}, Volume = {121}, @@ -12321,7 +12320,7 @@ From http://braininfo.rprc.washington.edu/Source.aspx?ID=90&questID=1350: Month = {Jan}, Number = {2}, Pages = {205-42}, - pubmed = {4904874}, + pmid = {4904874}, Pst = {ppublish}, Title = {The structural organization of layer IV in the somatosensory region (SI) of mouse cerebral cortex. The description of a cortical field composed of discrete cytoarchitectonic units}, Volume = {17}, @@ -12341,7 +12340,7 @@ From http://braininfo.rprc.washington.edu/Source.aspx?ID=90&questID=1350: Month = {Nov}, Number = {6}, Pages = {994-1005}, - pubmed = {18789954}, + pmid = {18789954}, Pst = {ppublish}, Title = {Serotonin transporter transgenic (SERTcre) mouse line reveals developmental targets of serotonin specific reuptake inhibitors (SSRIs)}, Volume = {55}, @@ -12361,7 +12360,7 @@ From http://braininfo.rprc.washington.edu/Source.aspx?ID=90&questID=1350: Month = {Apr}, Number = {1}, Pages = {27-32}, - pubmed = {15763133}, + pmid = {15763133}, Pst = {ppublish}, Title = {Targeted gene expression in dopamine and serotonin neurons of the mouse brain}, Volume = {143}, @@ -12382,7 +12381,7 @@ From http://braininfo.rprc.washington.edu/Source.aspx?ID=90&questID=1350: Number = {5}, Pages = {970-86}, Pmc = {PMC3768017}, - pubmed = {24012009}, + pmid = {24012009}, Pst = {ppublish}, Title = {Laminar and columnar development of barrel cortex relies on thalamocortical neurotransmission}, Volume = {79}, @@ -12400,7 +12399,7 @@ From http://braininfo.rprc.washington.edu/Source.aspx?ID=90&questID=1350: Mesh = {Body Weight; Brain; Growth}, Month = {Feb}, Pages = {343-6}, - pubmed = {14033949}, + pmid = {14033949}, Pst = {ppublish}, Title = {Brain-to-body ratios and time of maturation of the mouse brain}, Volume = {204}, @@ -12418,7 +12417,7 @@ From http://braininfo.rprc.washington.edu/Source.aspx?ID=90&questID=1350: Mesh = {Amygdala; Animals; Cell Differentiation; Cell Movement; Electroporation; Female; Gene Expression Regulation, Developmental; Microtubule-Associated Proteins; Nerve Tissue Proteins; Neural Pathways; Neuropeptides; Olfactory Pathways; Prosencephalon; Pyramidal Cells; RNA Interference; Rats; Rats, Wistar; Stem Cells}, Number = {1-3}, Pages = {144-56}, - pubmed = {18075262}, + pmid = {18075262}, Pst = {ppublish}, Title = {The role of DCX and LIS1 in migration through the lateral cortical stream of developing forebrain}, Volume = {30}, @@ -12437,7 +12436,7 @@ From http://braininfo.rprc.washington.edu/Source.aspx?ID=90&questID=1350: Month = {Mar}, Number = {5}, Pages = {1057-69}, - pubmed = {24607228}, + pmid = {24607228}, Pst = {ppublish}, Title = {Retinal input directs the recruitment of inhibitory interneurons into thalamic visual circuits}, Volume = {81}, @@ -12459,7 +12458,7 @@ From http://braininfo.rprc.washington.edu/Source.aspx?ID=90&questID=1350: Number = {7458}, Pages = {295-300}, Pmc = {PMC3777791}, - pubmed = {23868258}, + pmid = {23868258}, Pst = {ppublish}, Title = {Ultrasensitive fluorescent proteins for imaging neuronal activity}, Volume = {499}, @@ -12477,7 +12476,7 @@ From http://braininfo.rprc.washington.edu/Source.aspx?ID=90&questID=1350: Month = {Feb}, Number = {5}, Pages = {1096-111}, - pubmed = {24581503}, + pmid = {24581503}, Pst = {ppublish}, Title = {Neural networks of the mouse neocortex}, Volume = {156}, @@ -12501,7 +12500,7 @@ From http://braininfo.rprc.washington.edu/Source.aspx?ID=90&questID=1350: Number = {43}, Pages = {15604-17}, Pmc = {PMC3235689}, - pubmed = {22031906}, + pmid = {22031906}, Pst = {ppublish}, Title = {FGF signaling expands embryonic cortical surface area by regulating Notch-dependent neurogenesis}, Volume = {31}, @@ -12523,7 +12522,7 @@ From http://braininfo.rprc.washington.edu/Source.aspx?ID=90&questID=1350: Number = {26}, Pages = {10802-14}, Pmc = {PMC3693057}, - pubmed = {23804101}, + pmid = {23804101}, Pst = {ppublish}, Title = {Cortical gyrification induced by fibroblast growth factor 2 in the mouse brain}, Volume = {33}, @@ -12544,7 +12543,7 @@ From http://braininfo.rprc.washington.edu/Source.aspx?ID=90&questID=1350: Month = {Mar}, Number = {10}, Pages = {3683-95}, - pubmed = {21389223}, + pmid = {21389223}, Pst = {ppublish}, Title = {Oblique radial glial divisions in the developing mouse neocortex induce self-renewing progenitors outside the germinal zone that resemble primate outer subventricular zone progenitors}, Volume = {31}, @@ -12567,7 +12566,7 @@ CONCLUSIONS: These findings indicate that twitches are not produced randomly but Number = {21}, Pages = {2100-9}, Pmc = {PMC3823644}, - pubmed = {24139739}, + pmid = {24139739}, Pst = {ppublish}, Title = {Spatiotemporal structure of REM sleep twitching reveals developmental origins of motor synergies}, Volume = {23}, @@ -12588,7 +12587,7 @@ CONCLUSIONS: These findings indicate that twitches are not produced randomly but Number = {12}, Pages = {R532-7}, Pmc = {PMC3709969}, - pubmed = {23787051}, + pmid = {23787051}, Pst = {ppublish}, Title = {Twitching in sensorimotor development from sleeping rats to robots}, Volume = {23}, @@ -12607,7 +12606,7 @@ CONCLUSIONS: These findings indicate that twitches are not produced randomly but Month = {Feb}, Pages = {166-175}, Pmc = {PMC3957181}, - pubmed = {24492092}, + pmid = {24492092}, Pst = {ppublish}, Title = {Role of emergent neural activity in visual map development}, Volume = {24C}, @@ -12628,7 +12627,7 @@ CONCLUSIONS: These findings indicate that twitches are not produced randomly but Month = {Apr}, Number = {5722}, Pages = {662-7}, - pubmed = {15860620}, + pmid = {15860620}, Pst = {ppublish}, Title = {Parietal lobe: from action organization to intention understanding}, Volume = {308}, @@ -12649,7 +12648,7 @@ CONCLUSIONS: These findings indicate that twitches are not produced randomly but Number = {1}, Pages = {167-79}, Pmc = {PMC3757094}, - pubmed = {23849202}, + pmid = {23849202}, Pst = {ppublish}, Title = {Sensory population decoding for visually guided movements}, Volume = {79}, @@ -12672,7 +12671,7 @@ CONCLUSIONS: These findings indicate that twitches are not produced randomly but Number = {22}, Pages = {9420-30}, Pmc = {PMC3705569}, - pubmed = {23719810}, + pmid = {23719810}, Pst = {ppublish}, Title = {Control of the gain of visual-motor transmission occurs in visual coordinates for smooth pursuit eye movements}, Volume = {33}, @@ -12693,7 +12692,7 @@ CONCLUSIONS: These findings indicate that twitches are not produced randomly but Number = {4}, Pages = {477-91}, Pmc = {PMC2887486}, - pubmed = {20510853}, + pmid = {20510853}, Pst = {ppublish}, Title = {Visual guidance of smooth-pursuit eye movements: sensation, action, and what happens in between}, Volume = {66}, @@ -12713,7 +12712,7 @@ CONCLUSIONS: These findings indicate that twitches are not produced randomly but Month = {Oct}, Number = {5}, Pages = {456-67}, - pubmed = {21518811}, + pmid = {21518811}, Pst = {ppublish}, Title = {Cerebral asymmetry in schizophrenia}, Volume = {17}, @@ -12736,7 +12735,7 @@ CONCLUSION: An increase of exclusive left-handedness is at variance with the pre Month = {Jun}, Number = {6}, Pages = {410-9}, - pubmed = {15877707}, + pmid = {15877707}, Pst = {ppublish}, Title = {Handedness in schizophrenia: a quantitative review of evidence}, Volume = {111}, @@ -12758,7 +12757,7 @@ CONCLUSION: Strong evidence is provided for decreased cerebral lateralisation in Mesh = {Brain; Dichotic Listening Tests; Functional Laterality; Humans; Schizophrenia; Schizophrenic Psychology; Speech Perception}, Month = {Apr}, Pages = {344-51}, - pubmed = {11282814}, + pmid = {11282814}, Pst = {ppublish}, Title = {Handedness, language lateralisation and anatomical asymmetry in schizophrenia: meta-analysis}, Volume = {178}, @@ -12778,7 +12777,7 @@ CONCLUSION: Strong evidence is provided for decreased cerebral lateralisation in Month = {Mar}, Number = {6}, Pages = {809-18}, - pubmed = {18367082}, + pmid = {18367082}, Pst = {ppublish}, Title = {Behavioral phenotyping strategies for mutant mice}, Volume = {57}, @@ -12797,7 +12796,7 @@ CONCLUSION: Strong evidence is provided for decreased cerebral lateralisation in Month = {Jul}, Number = {1}, Pages = {18-26}, - pubmed = {10448192}, + pmid = {10448192}, Pst = {ppublish}, Title = {Behavioral phenotyping of transgenic and knockout mice: experimental design and evaluation of general health, sensory functions, motor abilities, and specific behavioral tests}, Volume = {835}, @@ -12817,7 +12816,7 @@ CONCLUSION: Strong evidence is provided for decreased cerebral lateralisation in Month = {Feb}, Number = {2}, Pages = {173-86, 115}, - pubmed = {17848917}, + pmid = {17848917}, Pst = {ppublish}, Title = {Inducible expression of mutant human DISC1 in mice is associated with brain and behavioral abnormalities reminiscent of schizophrenia}, Volume = {13}, @@ -12837,7 +12836,7 @@ CONCLUSION: Strong evidence is provided for decreased cerebral lateralisation in Month = {Jul}, Number = {7}, Pages = {824-31}, - pubmed = {23799475}, + pmid = {23799475}, Pst = {ppublish}, Title = {Probing perceptual decisions in rodents}, Volume = {16}, @@ -12854,7 +12853,7 @@ CONCLUSION: Strong evidence is provided for decreased cerebral lateralisation in Journal-Full = {Nature communications}, Keywords = {graph theory; Mathematics; models; self organization; network; Game Theory; Methods}, Pages = {2002}, - pubmed = {23774965}, + pmid = {23774965}, Pst = {ppublish}, Title = {Emergence of bimodality in controlling complex networks}, Volume = {4}, @@ -12875,7 +12874,7 @@ CONCLUSION: Strong evidence is provided for decreased cerebral lateralisation in Number = {2}, Pages = {216-26}, Pmc = {PMC3118044}, - pubmed = {18957198}, + pmid = {18957198}, Pst = {ppublish}, Title = {Nature, nurture, or chance: stochastic gene expression and its consequences}, Volume = {135}, @@ -12894,7 +12893,7 @@ CONCLUSION: Strong evidence is provided for decreased cerebral lateralisation in Number = {6}, Pages = {540-7}, Pmc = {PMC3713494}, - pubmed = {23817127}, + pmid = {23817127}, Pst = {ppublish}, Title = {Improved tools for the Brainbow toolbox}, Volume = {10}, @@ -12914,7 +12913,7 @@ CONCLUSION: Strong evidence is provided for decreased cerebral lateralisation in Month = {Aug}, Number = {3}, Pages = {389-94}, - pubmed = {15307007}, + pmid = {15307007}, Pst = {ppublish}, Title = {Fever after immunization: current concepts and improved future scientific understanding}, Volume = {39}, @@ -12935,7 +12934,7 @@ CONCLUSION: Strong evidence is provided for decreased cerebral lateralisation in Month = {Oct}, Number = {17}, Pages = {906-11}, - pubmed = {39253}, + pmid = {39253}, Pst = {ppublish}, Title = {Pertussis vaccine--an analysis of benefits, risks and costs}, Volume = {301}, @@ -12956,7 +12955,7 @@ CONCLUSION: Strong evidence is provided for decreased cerebral lateralisation in Month = {Nov}, Number = {19}, Pages = {1029-33}, - pubmed = {972656}, + pmid = {972656}, Pst = {ppublish}, Title = {Predictors of epilepsy in children who have experienced febrile seizures}, Volume = {295}, @@ -12980,7 +12979,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Month = {Jul}, Number = {1}, Pages = {e1-8}, - pubmed = {20587679}, + pmid = {20587679}, Pst = {ppublish}, Title = {Measles-mumps-rubella-varicella combination vaccine and the risk of febrile seizures}, Volume = {126}, @@ -13001,7 +13000,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Month = {Jul}, Number = {7458}, Pages = {336-40}, - pubmed = {23792559}, + pmid = {23792559}, Pst = {ppublish}, Title = {Behaviour-dependent recruitment of long-range projection neurons in somatosensory cortex}, Volume = {499}, @@ -13021,7 +13020,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Month = {Jul}, Number = {7}, Pages = {511-22}, - pubmed = {16791141}, + pmid = {16791141}, Pst = {ppublish}, Title = {The primate cortico-cerebellar system: anatomy and function}, Volume = {7}, @@ -13039,7 +13038,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Month = {Jul}, Number = {3}, Pages = {269-93}, - pubmed = {5788129}, + pmid = {5788129}, Pst = {ppublish}, Title = {Autoradiographic and histological studies of postnatal neurogenesis. 3. Dating the time of production and onset of differentiation of cerebellar microneurons in rats}, Volume = {136}, @@ -13060,7 +13059,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Month = {May}, Number = {5}, Pages = {413-20}, - pubmed = {23524393}, + pmid = {23524393}, Pst = {ppublish}, Title = {Whole-brain functional imaging at cellular resolution using light-sheet microscopy}, Volume = {10}, @@ -13082,7 +13081,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Month = {Jan}, Number = {1}, Pages = {274-80}, - pubmed = {17056278}, + pmid = {17056278}, Pst = {ppublish}, Title = {The effect of handedness on cortical motor activation during simple bilateral movements}, Volume = {34}, @@ -13099,7 +13098,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Journal-Full = {Cerebral cortex (New York, N.Y. : 1991)}, Keywords = {cerebral cortex; lateralization; asymmetry; hemisphere; Grants; behavior; Hand Strength; handedness; Laterality; human; gene; forelimb; language; MRI}, Month = {Jan}, - pubmed = {23307634}, + pmid = {23307634}, Pst = {aheadofprint}, Title = {Mapping Longitudinal Hemispheric Structural Asymmetries of the Human Cerebral Cortex From Birth to 2 Years of Age}, Year = {2013}, @@ -13119,7 +13118,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Number = {6}, Pages = {2268-76}, Pmc = {PMC2836191}, - pubmed = {20147553}, + pmid = {20147553}, Pst = {ppublish}, Title = {A surface-based analysis of hemispheric asymmetries and folding of cerebral cortex in term-born human infants}, Volume = {30}, @@ -13139,7 +13138,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Month = {Jun}, Number = {6138}, Pages = {1230531}, - pubmed = {23766329}, + pmid = {23766329}, Pst = {ppublish}, Title = {Cerebral asymmetry and language development: cause, correlate, or consequence?}, Volume = {340}, @@ -13159,7 +13158,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Month = {Feb}, Number = {3}, Pages = {565-74}, - pubmed = {20105238}, + pmid = {20105238}, Pst = {ppublish}, Title = {Functional hemispheric asymmetries in humans: electrophysiological evidence from preterm infants}, Volume = {31}, @@ -13178,7 +13177,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Month = {Oct}, Number = {1}, Pages = {84-8}, - pubmed = {3690305}, + pmid = {3690305}, Pst = {ppublish}, Title = {The relationship between callosal variation and lateralization in mice is genotype-dependent}, Volume = {424}, @@ -13197,7 +13196,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Month = {Jun}, Number = {2}, Pages = {129-38}, - pubmed = {2144194}, + pmid = {2144194}, Pst = {ppublish}, Title = {Immune function in lines of mice selected for high or low degrees of behavioral asymmetry}, Volume = {4}, @@ -13215,7 +13214,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Month = {Jun}, Number = {2}, Pages = {162-9}, - pubmed = {1893219}, + pmid = {1893219}, Pst = {ppublish}, Title = {Natural killer cell activity is associated with brain asymmetry in male mice}, Volume = {5}, @@ -13234,7 +13233,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Month = {Sep}, Number = {2}, Pages = {69-72}, - pubmed = {12902020}, + pmid = {12902020}, Pst = {ppublish}, Title = {Neonatal transection of the corpus callosum affects paw preference lateralization of adult Swiss mice}, Volume = {348}, @@ -13253,7 +13252,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Month = {Dec}, Number = {1}, Pages = {9-16}, - pubmed = {1786116}, + pmid = {1786116}, Pst = {ppublish}, Title = {Weak or missing paw lateralization in a mouse strain (I/LnJ) with congenital absence of the corpus callosum}, Volume = {46}, @@ -13274,7 +13273,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Number = {1519}, Pages = {943-54}, Pmc = {PMC2666076}, - pubmed = {19064357}, + pmid = {19064357}, Pst = {ppublish}, Title = {Hand and paw preferences in relation to the lateralized brain}, Volume = {364}, @@ -13294,7 +13293,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Month = {Oct}, Number = {10}, Pages = {1213-7}, - pubmed = {17001339}, + pmid = {17001339}, Pst = {ppublish}, Title = {From genes to behavior in developmental dyslexia}, Volume = {9}, @@ -13312,7 +13311,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Month = {Jan-Feb}, Number = {1}, Pages = {9-12}, - pubmed = {5656926}, + pmid = {5656926}, Pst = {ppublish}, Title = {On the inheritance of handedness. I. Laterality in inbred mice}, Volume = {59}, @@ -13332,7 +13331,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Month = {Aug}, Number = {8}, Pages = {655-62}, - pubmed = {16858393}, + pmid = {16858393}, Pst = {ppublish}, Title = {Molecular approaches to brain asymmetry and handedness}, Volume = {7}, @@ -13352,7 +13351,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Month = {Oct}, Number = {5}, Pages = {935-43}, - pubmed = {8270204}, + pmid = {8270204}, Pst = {ppublish}, Title = {Genetic variation in paw preference (handedness) in the mouse}, Volume = {36}, @@ -13371,7 +13370,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Month = {Apr}, Number = {4}, Pages = {701-4}, - pubmed = {1881972}, + pmid = {1881972}, Pst = {ppublish}, Title = {An assessment of handedness in mice}, Volume = {49}, @@ -13390,7 +13389,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Number = {9}, Pages = {1147-9}, Pmc = {PMC3760628}, - pubmed = {23917527}, + pmid = {23917527}, Pst = {ppublish}, Title = {Establishing brain functional laterality in adult mice through unilateral gene manipulation in the embryonic cortex}, Volume = {23}, @@ -13408,7 +13407,7 @@ CONCLUSIONS: Among 12- to 23-month-olds who received their first dose of measles Mesh = {Animals; Brain Mapping; Cell Division; Cell Movement; Cerebral Cortex; Humans; Models, Neurological; Neurons}, Month = {Apr}, Pages = {701-22}, - pubmed = {9153131}, + pmid = {9153131}, Pst = {ppublish}, Title = {The columnar organization of the neocortex}, Volume = {120 ( Pt 4)}, @@ -13429,7 +13428,7 @@ In the present investigation we wished to study the functional organiza- tion of Month = {Jul}, Number = {4}, Pages = {374-407}, - pubmed = {13439409}, + pmid = {13439409}, Pst = {ppublish}, Title = {Response properties of neurons of cat's somatic sensory cortex to peripheral stimuli}, Volume = {20}, @@ -13448,7 +13447,7 @@ In the present investigation we wished to study the functional organiza- tion of Month = {Jul}, Number = {4}, Pages = {408-34}, - pubmed = {13439410}, + pmid = {13439410}, Pst = {ppublish}, Title = {Modality and topographic properties of single neurons of cat's somatic sensory cortex}, Volume = {20}, @@ -13466,7 +13465,7 @@ In the present investigation we wished to study the functional organiza- tion of Keywords = {technique; Methods; in vivo; Microscopy; Dyes}, Month = {Aug}, Pages = {2326}, - pubmed = {23933660}, + pmid = {23933660}, Pst = {ppublish}, Title = {In vivo time-gated fluorescence imaging with biodegradable luminescent porous silicon nanoparticles}, Volume = {4}, @@ -13486,7 +13485,7 @@ In the present investigation we wished to study the functional organiza- tion of Number = {2}, Pages = {375-90}, Pmc = {PMC3732581}, - pubmed = {23889937}, + pmid = {23889937}, Pst = {ppublish}, Title = {A biophysically detailed model of neocortical local field potentials predicts the critical role of active membrane currents}, Volume = {79}, @@ -13507,7 +13506,7 @@ In the present investigation we wished to study the functional organiza- tion of Number = {8}, Pages = {1060-7}, Pmc = {PMC3769112}, - pubmed = {23831966}, + pmid = {23831966}, Pst = {ppublish}, Title = {Sensory cortex limits cortical maps and drives top-down plasticity in thalamocortical circuits}, Volume = {16}, @@ -13526,7 +13525,7 @@ In the present investigation we wished to study the functional organiza- tion of Month = {Aug}, Number = {8}, Pages = {1154-61}, - pubmed = {23792946}, + pmid = {23792946}, Pst = {ppublish}, Title = {SeeDB: a simple and morphology-preserving optical clearing agent for neuronal circuit reconstruction}, Volume = {16}, @@ -13546,7 +13545,7 @@ In the present investigation we wished to study the functional organiza- tion of Number = {3}, Pages = {408-10}, Pmc = {PMC3739006}, - pubmed = {23931991}, + pmid = {23931991}, Pst = {ppublish}, Title = {Top-down control of cortical state}, Volume = {79}, @@ -13567,7 +13566,7 @@ In the present investigation we wished to study the functional organiza- tion of Number = {3}, Pages = {567-78}, Pmc = {PMC3742632}, - pubmed = {23850595}, + pmid = {23850595}, Pst = {ppublish}, Title = {Motor cortex feedback influences sensory processing by modulating network state}, Volume = {79}, @@ -13587,7 +13586,7 @@ In the present investigation we wished to study the functional organiza- tion of Month = {Aug}, Number = {3}, Pages = {579-93}, - pubmed = {23850594}, + pmid = {23850594}, Pst = {ppublish}, Title = {Cellular and synaptic architecture of multisensory integration in the mouse neocortex}, Volume = {79}, @@ -13607,7 +13606,7 @@ In the present investigation we wished to study the functional organiza- tion of Month = {Sep}, Number = {37}, Pages = {15145-50}, - pubmed = {23980148}, + pmid = {23980148}, Pst = {ppublish}, Title = {Learning-induced neural plasticity of speech processing before birth}, Volume = {110}, @@ -13627,7 +13626,7 @@ In the present investigation we wished to study the functional organiza- tion of Number = {35}, Pages = {14432-7}, Pmc = {PMC3761619}, - pubmed = {23940340}, + pmid = {23940340}, Pst = {ppublish}, Title = {Surge of neurophysiological coherence and connectivity in the dying brain}, Volume = {110}, @@ -13647,7 +13646,7 @@ In the present investigation we wished to study the functional organiza- tion of Month = {May}, Number = {5}, Pages = {3751-62}, - pubmed = {17360827}, + pmid = {17360827}, Pst = {ppublish}, Title = {Combined voltage and calcium epifluorescence imaging in vitro and in vivo reveals subthreshold and suprathreshold dynamics of mouse barrel cortex}, Volume = {97}, @@ -13669,7 +13668,7 @@ In the present investigation we wished to study the functional organiza- tion of Number = {6}, Pages = {3691-704}, Pmc = {PMC3007657}, - pubmed = {20554834}, + pmid = {20554834}, Pst = {ppublish}, Title = {Fast nonnegative deconvolution for spike train inference from population calcium imaging}, Volume = {104}, @@ -13690,7 +13689,7 @@ In the present investigation we wished to study the functional organiza- tion of Month = {Apr}, Number = {7443}, Pages = {96-100}, - pubmed = {23552948}, + pmid = {23552948}, Pst = {ppublish}, Title = {The emergence of functional microcircuits in visual cortex}, Volume = {496}, @@ -13712,7 +13711,7 @@ In the present investigation we wished to study the functional organiza- tion of Number = {21}, Pages = {7258-66}, Pmc = {PMC3368384}, - pubmed = {22623671}, + pmid = {22623671}, Pst = {ppublish}, Title = {Initial neighborhood biases and the quality of motion stimulation jointly influence the rapid emergence of direction preference in visual cortex}, Volume = {32}, @@ -13734,7 +13733,7 @@ In the present investigation we wished to study the functional organiza- tion of Number = {16}, Pages = {5426-39}, Pmc = {PMC3353326}, - pubmed = {22514306}, + pmid = {22514306}, Pst = {ppublish}, Title = {Spontaneous activity promotes synapse formation in a cell-type-dependent manner in the developing retina}, Volume = {32}, @@ -13756,7 +13755,7 @@ In the present investigation we wished to study the functional organiza- tion of Number = {5}, Pages = {713-27}, Pmc = {PMC2947444}, - pubmed = {20826304}, + pmid = {20826304}, Pst = {ppublish}, Title = {Brain mechanisms in early language acquisition}, Volume = {67}, @@ -13774,7 +13773,7 @@ In the present investigation we wished to study the functional organiza- tion of Month = {Jun}, Number = {5115}, Pages = {1819-21}, - pubmed = {8511592}, + pmid = {8511592}, Pst = {ppublish}, Title = {Rapid remodeling of axonal arbors in the visual cortex}, Volume = {260}, @@ -13792,7 +13791,7 @@ In the present investigation we wished to study the functional organiza- tion of Month = {Aug}, Number = {8}, Pages = {3549-73}, - pubmed = {8340819}, + pmid = {8340819}, Pst = {ppublish}, Title = {Development of individual geniculocortical arbors in cat striate cortex and effects of binocular impulse blockade}, Volume = {13}, @@ -13808,7 +13807,7 @@ In the present investigation we wished to study the functional organiza- tion of Journal-Full = {Journal of neurophysiology}, Keywords = {retinal waves; spontaneous activity; synapses; Patch-Clamp Techniques; in vitro; mice; mouse; Neurophysiology; activity-dependent; development; retinal waves; superior colliculus; vision; currOpinRvw}, Month = {Jun}, - pubmed = {23741047}, + pmid = {23741047}, Pst = {aheadofprint}, Title = {Competition driven by retinal waves promotes the morphological and functional synaptic development of neurons in the superior colliculus}, Year = {2013}, @@ -13827,7 +13826,7 @@ In the present investigation we wished to study the functional organiza- tion of Month = {Jun}, Number = {11}, Pages = {3200-16}, - pubmed = {22402661}, + pmid = {22402661}, Pst = {ppublish}, Title = {Synapse maturation is enhanced in the binocular region of the retinocollicular map prior to eye opening}, Volume = {107}, @@ -13845,7 +13844,7 @@ In the present investigation we wished to study the functional organiza- tion of Keywords = {Visual Cortex; plasticity; homeostatic plasticity; neurophysiology; currOpinRvw}, Mesh = {Animals; Cerebral Cortex; Homeostasis; Models, Neurological; Nerve Net; Neurons; Synapses}, Pages = {89-103}, - pubmed = {21438687}, + pmid = {21438687}, Pst = {ppublish}, Title = {Too many cooks? Intrinsic and synaptic homeostatic mechanisms in cortical circuit refinement}, Volume = {34}, @@ -13864,7 +13863,7 @@ In the present investigation we wished to study the functional organiza- tion of Keywords = {activity-development; visual system; Visual Cortex; plasticity; Critical Period; currOpinRvw}, Mesh = {Aging; Animals; Critical Period (Psychology); Dominance, Ocular; Humans; Models, Neurological; Neural Inhibition; Neuronal Plasticity; Signal Transduction; Synaptic Transmission; Visual Cortex}, Pages = {309-30}, - pubmed = {22462544}, + pmid = {22462544}, Pst = {ppublish}, Title = {Critical-period plasticity in the visual cortex}, Volume = {35}, @@ -13885,7 +13884,7 @@ In the present investigation we wished to study the functional organiza- tion of Month = {May}, Number = {5}, Pages = {1999-2009}, - pubmed = {14681336}, + pmid = {14681336}, Pst = {ppublish}, Title = {Spontaneous waves in the ventricular zone of developing mammalian retina}, Volume = {91}, @@ -13904,7 +13903,7 @@ In the present investigation we wished to study the functional organiza- tion of Month = {Nov}, Number = {11}, Pages = {1368-70}, - pubmed = {8939594}, + pmid = {8939594}, Pst = {ppublish}, Title = {Retinal development: on the crest of an exciting wave}, Volume = {6}, @@ -13923,7 +13922,7 @@ In the present investigation we wished to study the functional organiza- tion of Month = {Jun}, Number = {11}, Pages = {4155-65}, - pubmed = {9592095}, + pmid = {9592095}, Pst = {ppublish}, Title = {Direct participation of starburst amacrine cells in spontaneous rhythmic activities in the developing mammalian retina}, Volume = {18}, @@ -13940,7 +13939,7 @@ In the present investigation we wished to study the functional organiza- tion of Month = {Jun}, Number = {2}, Pages = {481-93}, - pubmed = {5034730}, + pmid = {5034730}, Pst = {ppublish}, Title = {Visual habituation in the human infant}, Volume = {43}, @@ -13961,7 +13960,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Mesh = {Animals; Brain; Computer Graphics; Computer Simulation; Gene Expression; Gene Expression Profiling; Mice; Mice, Inbred C57BL; Models, Anatomic; Models, Biological; Nerve Tissue Proteins; Oligonucleotide Array Sequence Analysis; Software; Tissue Distribution; User-Computer Interface}, Pages = {153}, Pmc = {PMC2375125}, - pubmed = {18366675}, + pmid = {18366675}, Pst = {epublish}, Title = {Exploration and visualization of gene expression with neuroanatomy in the adult mouse brain}, Volume = {9}, @@ -13980,7 +13979,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Mesh = {Animals; Basic Helix-Loop-Helix Transcription Factors; Cell Differentiation; Cell Lineage; Cell Movement; Female; GABAergic Neurons; Gene Expression Regulation, Developmental; Geniculate Bodies; Immunohistochemistry; In Situ Hybridization; Mice; Mice, Transgenic; Models, Animal; Nerve Tissue Proteins; Stem Cells; Subthalamus; Tamoxifen; Ventral Thalamic Nuclei}, Number = {2}, Pages = {118-29}, - pubmed = {21865661}, + pmid = {21865661}, Pst = {ppublish}, Title = {Olig2 lineage cells generate GABAergic neurons in the prethalamic nuclei, including the zona incerta, ventral lateral geniculate nucleus and reticular thalamic nucleus}, Volume = {33}, @@ -13999,7 +13998,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Mesh = {Animals; Cats; Guinea Pigs; Mammals; Rabbits; Rats; Synapses; Thalamic Nuclei; Thalamus; gamma-Aminobutyric Acid}, Number = {1}, Pages = {27-37}, - pubmed = {8978932}, + pmid = {8978932}, Pst = {ppublish}, Title = {GABAergic neurons in mammalian thalamus: a marker of thalamic complexity?}, Volume = {42}, @@ -14020,7 +14019,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Number = {5}, Pages = {291-301}, Pmc = {PMC3601545}, - pubmed = {19380167}, + pmid = {19380167}, Pst = {ppublish}, Title = {Decision by division: making cortical maps}, Volume = {32}, @@ -14037,7 +14036,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Journal-Full = {Neuron}, Keywords = {retinal waves; spontaneous activity; development; retina; Retinal Ganglion Cells; bipolar cells; currOpinRvw}, Month = {Jul}, - pubmed = {23830830}, + pmid = {23830830}, Pst = {aheadofprint}, Title = {Intersecting Circuits Generate Precisely Patterned Retinal Waves}, Year = {2013}, @@ -14058,7 +14057,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Number = {3}, Pages = {518-25}, Pmc = {PMC3496185}, - pubmed = {23141064}, + pmid = {23141064}, Pst = {ppublish}, Title = {Visual stimulation reverses the directional preference of direction-selective retinal ganglion cells}, Volume = {76}, @@ -14078,7 +14077,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Sep}, Number = {6}, Pages = {611-20}, - pubmed = {10498279}, + pmid = {10498279}, Pst = {ppublish}, Title = {Role of thalamic axons in the expression of H-2Z1, a mouse somatosensory cortex specific marker}, Volume = {9}, @@ -14098,7 +14097,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Feb}, Number = {1}, Pages = {1-17}, - pubmed = {15733063}, + pmid = {15733063}, Pst = {ppublish}, Title = {How to make an egg: transcriptional regulation in oocytes}, Volume = {73}, @@ -14119,7 +14118,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Aug}, Number = {5893}, Pages = {1218-21}, - pubmed = {18669821}, + pmid = {18669821}, Pst = {ppublish}, Title = {Induced pluripotent stem cells generated from patients with ALS can be differentiated into motor neurons}, Volume = {321}, @@ -14138,7 +14137,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Aug}, Number = {4}, Pages = {153-61}, - pubmed = {10944576}, + pmid = {10944576}, Pst = {ppublish}, Title = {New ideas about binocular coordination of eye movements: is there a chameleon in the primate family tree?}, Volume = {261}, @@ -14157,7 +14156,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Jan}, Number = {1}, Pages = {1-12}, - pubmed = {10631781}, + pmid = {10631781}, Pst = {ppublish}, Title = {Do birds possess homologues of mammalian primary visual, somatosensory and motor cortices?}, Volume = {23}, @@ -14177,7 +14176,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Jun}, Number = {4}, Pages = {531-47}, - pubmed = {2358551}, + pmid = {2358551}, Pst = {ppublish}, Title = {Organization of geniculocortical projections in turtles: isoazimuth lamellae in the visual cortex}, Volume = {296}, @@ -14198,7 +14197,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Jun}, Number = {4}, Pages = {548-58}, - pubmed = {2358552}, + pmid = {2358552}, Pst = {ppublish}, Title = {Spatial organization of axons in turtle visual cortex: intralamellar and interlamellar projections}, Volume = {296}, @@ -14218,7 +14217,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Mesh = {5,7-Dihydroxytryptamine; Animals; Immunologic Techniques; Male; Nerve Fibers; Neurons; Optic Nerve; Preoptic Area; Rats; Rats, Inbred Strains; Retina; Serotonin; Suprachiasmatic Nucleus; Visual Pathways}, Number = {6}, Pages = {1083-92}, - pubmed = {8962828}, + pmid = {8962828}, Pst = {ppublish}, Title = {Centrifugal innervation of the rat retina}, Volume = {12}, @@ -14238,7 +14237,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Oct}, Number = {1}, Pages = {92-112}, - pubmed = {3192765}, + pmid = {3192765}, Pst = {ppublish}, Title = {Organization of retinogeniculate projections in turtles of the genera Pseudemys and Chrysemys}, Volume = {276}, @@ -14259,7 +14258,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Number = {7192}, Pages = {175-83}, Pmc = {PMC2803040}, - pubmed = {18464734}, + pmid = {18464734}, Pst = {ppublish}, Title = {Genome analysis of the platypus reveals unique signatures of evolution}, Volume = {453}, @@ -14280,7 +14279,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Sep}, Number = {1}, Pages = {101-22}, - pubmed = {5459208}, + pmid = {5459208}, Pst = {ppublish}, Title = {Thalamotelencephalic projections in the turtle (Pseudemys scripta)}, Volume = {140}, @@ -14301,7 +14300,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Number = {14}, Pages = {7621-6}, Pmc = {PMC23872}, - pubmed = {9207142}, + pmid = {9207142}, Pst = {ppublish}, Title = {Visual stimuli induce waves of electrical activity in turtle cortex}, Volume = {94}, @@ -14320,7 +14319,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Apr}, Number = {1}, Pages = {139-55}, - pubmed = {23473800}, + pmid = {23473800}, Pst = {ppublish}, Title = {A method for closed-loop presentation of sensory stimuli conditional on the internal brain-state of awake animals}, Volume = {215}, @@ -14340,7 +14339,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Jan}, Number = {1}, Pages = {178-91}, - pubmed = {2868076}, + pmid = {2868076}, Pst = {ppublish}, Title = {Cellular physiology of the turtle visual cortex: synaptic properties and intrinsic circuitry}, Volume = {6}, @@ -14361,7 +14360,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Number = {5}, Pages = {487-502}, Pmc = {PMC2679998}, - pubmed = {18997124}, + pmid = {18997124}, Pst = {ppublish}, Title = {Propagating waves of activity in the neocortex: what they are, what they do}, Volume = {14}, @@ -14381,7 +14380,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {May}, Number = {10}, Pages = {RC3}, - pubmed = {10234049}, + pmid = {10234049}, Pst = {ppublish}, Title = {Modal behavior of cortical neural networks during visual processing}, Volume = {19}, @@ -14400,7 +14399,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Mar}, Number = {3}, Pages = {1499-514}, - pubmed = {11877522}, + pmid = {11877522}, Pst = {ppublish}, Title = {High-speed VSD imaging of visually evoked cortical waves: decomposition into intra- and intercortical wave motions}, Volume = {87}, @@ -14420,7 +14419,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Mesh = {Animals; Computer Simulation; Dose-Response Relationship, Radiation; Evoked Potentials, Visual; Geniculate Bodies; Membrane Potentials; Models, Neurological; Neurons; Photic Stimulation; Principal Component Analysis; Reaction Time; Receptors, AMPA; Receptors, GABA; Receptors, N-Methyl-D-Aspartate; Space Perception; Time Factors; Turtles; Visual Cortex; Visual Pathways}, Number = {3}, Pages = {267-98}, - pubmed = {15114050}, + pmid = {15114050}, Pst = {ppublish}, Title = {Extracting wave structure from biological data with application to responses in turtle visual cortex}, Volume = {16}, @@ -14440,7 +14439,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Mesh = {Algorithms; Animals; Axons; Computer Simulation; Demography; Dendrites; Excitatory Postsynaptic Potentials; Geniculate Bodies; Membrane Potentials; Models, Neurological; Neurons; Photic Stimulation; Pyramidal Cells; Reaction Time; Receptors, AMPA; Receptors, GABA-A; Receptors, GABA-B; Receptors, N-Methyl-D-Aspartate; Synapses; Time Factors; Turtles; Visual Cortex; Visual Pathways}, Number = {2}, Pages = {161-84}, - pubmed = {12567015}, + pmid = {12567015}, Pst = {ppublish}, Title = {Propagating waves in visual cortex: a large-scale model of turtle visual cortex}, Volume = {14}, @@ -14461,7 +14460,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Jan}, Number = {6562}, Pages = {251-4}, - pubmed = {8538789}, + pmid = {8538789}, Pst = {ppublish}, Title = {Development of identical orientation maps for two eyes without common visual experience}, Volume = {379}, @@ -14481,7 +14480,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Sep}, Number = {1-2}, Pages = {43-7}, - pubmed = {2510094}, + pmid = {2510094}, Pst = {ppublish}, Title = {Retino-retinal projections in three anuran species}, Volume = {104}, @@ -14498,7 +14497,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Journal-Full = {Cerebral cortex (New York, N.Y. : 1991)}, Keywords = {spontaneous activity; topographic map; mouse; neurophysiology; activity-development; currOpinRvw; Orientation; Visual Cortex; visual system; currOpinRvw}, Month = {Feb}, - pubmed = {23389996}, + pmid = {23389996}, Pst = {aheadofprint}, Title = {Experience-Dependent and Independent Binocular Correspondence of Receptive Field Subregions in Mouse Visual Cortex}, Year = {2013}, @@ -14519,7 +14518,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Number = {8}, Pages = {1013-21}, Pmc = {PMC2652399}, - pubmed = {16025110}, + pmid = {16025110}, Pst = {ppublish}, Title = {Ephrin-As mediate targeting of eye-specific projections to the lateral geniculate nucleus}, Volume = {8}, @@ -14537,7 +14536,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Journal-Full = {Annual review of neuroscience}, Keywords = {currOpinRvw; spontaneous activity; visual system; retina; superior colliculus; review literature; Visual Cortex; topographic map; activity-development; activity manipulation; Genes; trophic signal; currOpinRvw}, Month = {Apr}, - pubmed = {23642132}, + pmid = {23642132}, Pst = {aheadofprint}, Title = {Developmental Mechanisms of Topographic Map Formation and Alignment}, Year = {2013}, @@ -14556,7 +14555,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Dec}, Number = {6}, Pages = {2059-71}, - pubmed = {1812236}, + pmid = {1812236}, Pst = {ppublish}, Title = {Changing patterns of synaptic input to subplate and cortical plate during development of visual cortex}, Volume = {66}, @@ -14575,7 +14574,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Sep}, Number = {4921}, Pages = {978-82}, - pubmed = {2475909}, + pmid = {2475909}, Pst = {ppublish}, Title = {Subplate neurons pioneer the first axon pathway from the cerebral cortex}, Volume = {245}, @@ -14594,7 +14593,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Jan}, Number = {1}, Pages = {39-55}, - pubmed = {1729444}, + pmid = {1729444}, Pst = {ppublish}, Title = {Pathfinding and target selection by developing geniculocortical axons}, Volume = {12}, @@ -14612,7 +14611,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Jun}, Number = {6}, Pages = {3862-80}, - pubmed = {8207493}, + pmid = {8207493}, Pst = {ppublish}, Title = {Segregation of geniculocortical afferents during the critical period: a role for subplate neurons}, Volume = {14}, @@ -14630,7 +14629,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Apr}, Number = {4}, Pages = {1892-907}, - pubmed = {7512631}, + pmid = {7512631}, Pst = {ppublish}, Title = {Subplate pioneers and the formation of descending connections from cerebral cortex}, Volume = {14}, @@ -14648,7 +14647,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Mar}, Number = {5050}, Pages = {1441-3}, - pubmed = {1542795}, + pmid = {1542795}, Pst = {ppublish}, Title = {Involvement of subplate neurons in the formation of ocular dominance columns}, Volume = {255}, @@ -14668,7 +14667,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {Sep}, Number = {6289}, Pages = {179-81}, - pubmed = {2395469}, + pmid = {2395469}, Pst = {ppublish}, Title = {Requirement for subplate neurons in the formation of thalamocortical connections}, Volume = {347}, @@ -14690,7 +14689,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Number = {4}, Pages = {537-46}, Pmc = {PMC3157589}, - pubmed = {21312343}, + pmid = {21312343}, Pst = {ppublish}, Title = {Vision drives correlated activity without patterned spontaneous activity in developing Xenopus retina}, Volume = {72}, @@ -14710,7 +14709,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Mesh = {Animals; Cluster Analysis; Electrophysiology; Microelectrodes; Retinal Ganglion Cells; Turtles}, Number = {2}, Pages = {229-41}, - pubmed = {10824677}, + pmid = {10824677}, Pst = {ppublish}, Title = {Spontaneous activity in developing turtle retinal ganglion cells: statistical analysis}, Volume = {17}, @@ -14728,7 +14727,7 @@ CONCLUSION: These tools offer convenient access to detailed expression informati Month = {May}, Number = {10}, Pages = {3874-87}, - pubmed = {10234019}, + pmid = {10234019}, Pst = {ppublish}, Title = {Spontaneous activity in developing turtle retinal ganglion cells: pharmacological studies}, Volume = {19}, @@ -14749,7 +14748,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Nov}, Number = {11}, Pages = {1503-8}, - pubmed = {8939611}, + pmid = {8939611}, Pst = {ppublish}, Title = {Influence of spontaneous activity and visual experience on developing retinal receptive fields}, Volume = {6}, @@ -14768,7 +14767,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Apr}, Number = {4}, Pages = {1355-64}, - pubmed = {7643153}, + pmid = {7643153}, Pst = {ppublish}, Title = {Emergence of complex receptive field properties of ganglion cells in the developing turtle retina}, Volume = {73}, @@ -14787,7 +14786,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Nov}, Number = {21}, Pages = {8839-52}, - pubmed = {9786990}, + pmid = {9786990}, Pst = {ppublish}, Title = {Developmentally regulated spontaneous activity in the embryonic chick retina}, Volume = {18}, @@ -14806,7 +14805,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Feb}, Number = {5}, Pages = {283-6}, - pubmed = {9501073}, + pmid = {9501073}, Pst = {ppublish}, Title = {Spontaneous Ca2+ transients and their transmission in the developing chick retina}, Volume = {8}, @@ -14826,7 +14825,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {3}, Pages = {442-55}, Pmc = {PMC3005332}, - pubmed = {21040846}, + pmid = {21040846}, Pst = {ppublish}, Title = {Visual activity regulates neural progenitor cells in developing xenopus CNS through musashi1}, Volume = {68}, @@ -14845,7 +14844,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Apr}, Number = {1}, Pages = {134-46}, - pubmed = {15007832}, + pmid = {15007832}, Pst = {ppublish}, Title = {Insights into activity-dependent map formation from the retinotectal system: a middle-of-the-brain perspective}, Volume = {59}, @@ -14864,7 +14863,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Sep}, Number = {1-2}, Pages = {168-78}, - pubmed = {7834339}, + pmid = {7834339}, Pst = {ppublish}, Title = {An N-methyl-D-aspartate receptor antagonist does not prevent eye-specific segregation in the ferret retinogeniculate pathway}, Volume = {658}, @@ -14883,7 +14882,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Mar}, Number = {5}, Pages = {622-35}, - pubmed = {20034053}, + pmid = {20034053}, Pst = {ppublish}, Title = {Synaptic development of the mouse dorsal lateral geniculate nucleus}, Volume = {518}, @@ -14904,7 +14903,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {Pt 18}, Pages = {4357-62}, Pmc = {PMC2614014}, - pubmed = {18556365}, + pmid = {18556365}, Pst = {ppublish}, Title = {Refinement of the retinogeniculate pathway}, Volume = {586}, @@ -14925,7 +14924,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {6}, Pages = {3082-90}, Pmc = {PMC2804430}, - pubmed = {19776360}, + pmid = {19776360}, Pst = {ppublish}, Title = {LTD and LTP at the developing retinogeniculate synapse}, Volume = {102}, @@ -14944,7 +14943,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Mar}, Number = {3}, Pages = {1175-85}, - pubmed = {11877491}, + pmid = {11877491}, Pst = {ppublish}, Title = {Synaptic mechanisms regulating the activation of a Ca(2+)-mediated plateau potential in developing relay cells of the LGN}, Volume = {87}, @@ -14965,7 +14964,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {18}, Pages = {6842-9}, Pmc = {PMC3319043}, - pubmed = {21543614}, + pmid = {21543614}, Pst = {ppublish}, Title = {Homeostatic plasticity in the visual thalamus by monocular deprivation}, Volume = {31}, @@ -14986,7 +14985,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {Pt 4}, Pages = {919-37}, Pmc = {PMC3060370}, - pubmed = {21173075}, + pmid = {21173075}, Pst = {ppublish}, Title = {Requirements for synaptically evoked plateau potentials in relay cells of the dorsal lateral geniculate nucleus of the mouse}, Volume = {589}, @@ -15006,7 +15005,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {25}, Pages = {8759-70}, Pmc = {PMC3066032}, - pubmed = {14507976}, + pmid = {14507976}, Pst = {ppublish}, Title = {Development of columnar topography in the excitatory layer 4 to layer 2/3 projection in rat barrel cortex}, Volume = {23}, @@ -15027,7 +15026,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {11}, Pages = {4700-5}, Pmc = {PMC1838663}, - pubmed = {17360587}, + pmid = {17360587}, Pst = {ppublish}, Title = {TORC1 is a calcium- and cAMP-sensitive coincidence detector involved in hippocampal long-term synaptic plasticity}, Volume = {104}, @@ -15049,7 +15048,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {Pt 16}, Pages = {3045-62}, Pmc = {PMC2956944}, - pubmed = {20603333}, + pmid = {20603333}, Pst = {ppublish}, Title = {Distinct coincidence detectors govern the corticostriatal spike timing-dependent plasticity}, Volume = {588}, @@ -15070,7 +15069,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {16}, Pages = {4166-77}, Pmc = {PMC3071735}, - pubmed = {16624937}, + pmid = {16624937}, Pst = {ppublish}, Title = {Two coincidence detectors for spike timing-dependent plasticity in somatosensory cortex}, Volume = {26}, @@ -15090,7 +15089,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Jun}, Number = {3}, Pages = {312-22}, - pubmed = {16713246}, + pmid = {16713246}, Pst = {ppublish}, Title = {Novel presynaptic mechanisms for coincidence detection in synaptic plasticity}, Volume = {16}, @@ -15108,7 +15107,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Mesh = {Animals; Brain Mapping; Cerebral Cortex; Computers; Male; Mice; Temporal Lobe; Visual Cortex}, Number = {3}, Pages = {333-53}, - pubmed = {6869850}, + pmid = {6869850}, Pst = {ppublish}, Title = {A quantitative approach to cytoarchitectonics. VIII. The areal pattern of the cortex of the albino mouse}, Volume = {166}, @@ -15129,7 +15128,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {22}, Pages = {4491-512}, Pmc = {PMC3432265}, - pubmed = {20886618}, + pmid = {20886618}, Pst = {ppublish}, Title = {Comparative studies of diurnal and nocturnal rodents: differences in lifestyle result in alterations in cortical field size and number}, Volume = {518}, @@ -15149,7 +15148,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {2}, Pages = {116-30}, Pmc = {PMC3094678}, - pubmed = {21525748}, + pmid = {21525748}, Pst = {ppublish}, Title = {Comparison of area 17 cellular composition in laboratory and wild-caught rats including diurnal and nocturnal species}, Volume = {77}, @@ -15170,7 +15169,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Nov}, Number = {2}, Pages = {247-63}, - pubmed = {1184785}, + pmid = {1184785}, Pst = {ppublish}, Title = {Architectonic map of neocortex of the normal mouse}, Volume = {164}, @@ -15191,7 +15190,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Feb}, Number = {2}, Pages = {104-13}, - pubmed = {18824116}, + pmid = {18824116}, Pst = {ppublish}, Title = {Posterior parietal cortex as part of a neural network for directed attention in rats}, Volume = {91}, @@ -15209,7 +15208,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Keywords = {neocortex; cerebral cortex; areas; parcellation; patterning; topographic map; cytoarchitectonics}, Pages = {34}, Pmc = {PMC3116136}, - pubmed = {21716641}, + pmid = {21716641}, Pst = {ppublish}, Title = {The organization and evolution of dorsal stream multisensory motor pathways in primates}, Volume = {5}, @@ -15355,7 +15354,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Keywords = {downloads}, Pages = {11}, Pmc = {PMC3304170}, - pubmed = {22435052}, + pmid = {22435052}, Pst = {ppublish}, Title = {In vivo Large-Scale Cortical Mapping Using Channelrhodopsin-2 Stimulation in Transgenic Mice Reveals Asymmetric and Reciprocal Relationships between Cortical Areas}, Volume = {6}, @@ -15376,7 +15375,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {7393}, Pages = {201-7}, Pmc = {PMC3345284}, - pubmed = {22425994}, + pmid = {22425994}, Pst = {epublish}, Title = {Teneurins instruct synaptic partner matching in an olfactory map}, Volume = {484}, @@ -15397,7 +15396,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {7392}, Pages = {105-9}, Pmc = {PMC3321067}, - pubmed = {22425995}, + pmid = {22425995}, Pst = {epublish}, Title = {Wild-type microglia arrest pathology in a mouse model of Rett syndrome}, Volume = {484}, @@ -15418,7 +15417,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {7393}, Pages = {237-41}, Pmc = {PMC3326183}, - pubmed = {22426000}, + pmid = {22426000}, Pst = {epublish}, Title = {Trans-synaptic Teneurin signalling in neuromuscular synapse organization and target choice}, Volume = {484}, @@ -15438,7 +15437,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Mar}, Number = {5}, Pages = {862-85}, - pubmed = {22405199}, + pmid = {22405199}, Pst = {ppublish}, Title = {Imaging calcium in neurons}, Volume = {73}, @@ -15459,7 +15458,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {27}, Pages = {9301-11}, Pmc = {PMC3417346}, - pubmed = {22764237}, + pmid = {22764237}, Pst = {ppublish}, Title = {Generating synchrony from the asynchronous: compensation for cochlear traveling wave delays by the dendrites of individual brainstem neurons}, Volume = {32}, @@ -15480,7 +15479,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {49}, Pages = {17932-40}, Pmc = {PMC3272675}, - pubmed = {22159108}, + pmid = {22159108}, Pst = {ppublish}, Title = {Regional and temporal specificity of intrinsic plasticity mechanisms in rodent primary visual cortex}, Volume = {31}, @@ -15498,7 +15497,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Keywords = {downloads}, Pages = {53}, Pmc = {PMC3343305}, - pubmed = {22586359}, + pmid = {22586359}, Pst = {ppublish}, Title = {Development of the corticothalamic projections}, Volume = {6}, @@ -15516,7 +15515,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Keywords = {downloads}, Pages = {33}, Pmc = {PMC3343474}, - pubmed = {22586376}, + pmid = {22586376}, Pst = {ppublish}, Title = {Histamine neurons in the tuberomamillary nucleus: a whole center or distinct subpopulations?}, Volume = {6}, @@ -15536,7 +15535,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {May}, Number = {6081}, Pages = {604-8}, - pubmed = {22556257}, + pmid = {22556257}, Pst = {ppublish}, Title = {Radio-wave heating of iron oxide nanoparticles can regulate plasma glucose in mice}, Volume = {336}, @@ -15556,7 +15555,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Aug}, Number = {8}, Pages = {361-3}, - pubmed = {16850473}, + pmid = {16850473}, Pst = {ppublish}, Title = {Rx-Cre, a tool for inactivation of gene expression in the developing retina}, Volume = {44}, @@ -15577,7 +15576,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {7401}, Pages = {118-21}, Pmc = {PMC3375857}, - pubmed = {22678292}, + pmid = {22678292}, Pst = {epublish}, Title = {Clonally related visual cortical neurons show similar stimulus feature selectivity}, Volume = {486}, @@ -15598,7 +15597,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {7401}, Pages = {113-7}, Pmc = {PMC3599787}, - pubmed = {22678291}, + pmid = {22678291}, Pst = {epublish}, Title = {Preferential electrical coupling regulates neocortical lineage-dependent microcircuit assembly}, Volume = {486}, @@ -15618,7 +15617,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Jul}, Number = {Pt 7}, Pages = {1803-21}, - pubmed = {16731540}, + pmid = {16731540}, Pst = {ppublish}, Title = {Functional circuitry underlying visual neglect}, Volume = {129}, @@ -15638,7 +15637,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {May}, Number = {18}, Pages = {6053-60}, - pubmed = {22553012}, + pmid = {22553012}, Pst = {ppublish}, Title = {Methods for simultaneous EEG-fMRI: an introductory review}, Volume = {32}, @@ -15658,7 +15657,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {May}, Number = {5}, Pages = {746-53}, - pubmed = {22446881}, + pmid = {22446881}, Pst = {epublish}, Title = {Astrocyte signaling controls spike timing-dependent depression at neocortical synapses}, Volume = {15}, @@ -15678,7 +15677,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Apr}, Number = {7395}, Pages = {473-8}, - pubmed = {22538608}, + pmid = {22538608}, Pst = {epublish}, Title = {Multiple dynamic representations in the motor cortex during sensorimotor learning}, Volume = {484}, @@ -15699,7 +15698,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {5}, Pages = {793-802}, Pmc = {PMC3337962}, - pubmed = {22446880}, + pmid = {22446880}, Pst = {epublish}, Title = {A toolbox of Cre-dependent optogenetic transgenic mice for light-induced activation and silencing}, Volume = {15}, @@ -15720,7 +15719,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {16}, Pages = {5454-71}, Pmc = {PMC3415278}, - pubmed = {22514308}, + pmid = {22514308}, Pst = {ppublish}, Title = {Columnar interactions determine horizontal propagation of recurrent network activity in neocortex}, Volume = {32}, @@ -15741,7 +15740,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {7392}, Pages = {105-9}, Pmc = {PMC3321067}, - pubmed = {22425995}, + pmid = {22425995}, Pst = {epublish}, Title = {Wild-type microglia arrest pathology in a mouse model of Rett syndrome}, Volume = {484}, @@ -15761,7 +15760,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Apr}, Number = {7392}, Pages = {96-100}, - pubmed = {22367540}, + pmid = {22367540}, Pst = {epublish}, Title = {A universal model for mobility and migration patterns}, Volume = {484}, @@ -15782,7 +15781,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {7392}, Pages = {62-8}, Pmc = {PMC3321074}, - pubmed = {22419153}, + pmid = {22419153}, Pst = {epublish}, Title = {Choice-specific sequences in parietal cortex during a virtual-navigation decision task}, Volume = {484}, @@ -15803,7 +15802,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Apr}, Number = {5671}, Pages = {739-42}, - pubmed = {15118164}, + pmid = {15118164}, Pst = {ppublish}, Title = {Synaptic changes in layer 2/3 underlying map plasticity of developing barrel cortex}, Volume = {304}, @@ -15824,7 +15823,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {7411}, Pages = {379-83}, Pmc = {PMC3422431}, - pubmed = {22878719}, + pmid = {22878719}, Pst = {ppublish}, Title = {Activation of specific interneurons improves V1 feature selectivity and visual perception}, Volume = {488}, @@ -15844,7 +15843,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Aug}, Number = {7411}, Pages = {343-8}, - pubmed = {22878717}, + pmid = {22878717}, Pst = {ppublish}, Title = {Division and subtraction by distinct cortical inhibitory networks in vivo}, Volume = {488}, @@ -15864,7 +15863,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Jun}, Number = {6}, Pmc = {PMC3098681}, - pubmed = {21555405}, + pmid = {21555405}, Pst = {epublish}, Title = {Neuronal activity-regulated gene transcription in synapse development and cognitive function}, Volume = {3}, @@ -15885,7 +15884,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {8}, Pages = {1678-86}, Pmc = {PMC3561675}, - pubmed = {22120996}, + pmid = {22120996}, Pst = {ppublish}, Title = {Two populations of corticothalamic and interareal corticocortical cells in the subgranular layers of the mouse primary sensory cortices}, Volume = {520}, @@ -15906,7 +15905,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {5}, Pages = {360-72}, Pmc = {PMC2771435}, - pubmed = {19352403}, + pmid = {19352403}, Pst = {ppublish}, Title = {Parallel processing strategies of the primate visual system}, Volume = {10}, @@ -15926,7 +15925,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Jul}, Number = {14}, Pages = {1351-7}, - pubmed = {22704993}, + pmid = {22704993}, Pst = {ppublish}, Title = {A specialized area in limbic cortex for fast analysis of peripheral vision}, Volume = {22}, @@ -15944,7 +15943,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Keywords = {downloads}, Pages = {37}, Pmc = {PMC3385560}, - pubmed = {22754500}, + pmid = {22754500}, Pst = {ppublish}, Title = {Developmental Coordination of Gene Expression between Synaptic Partners During GABAergic Circuit Assembly in Cerebellar Cortex}, Volume = {6}, @@ -15962,7 +15961,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Keywords = {downloads}, Pages = {13}, Pmc = {PMC2885865}, - pubmed = {20556241}, + pmid = {20556241}, Pst = {epublish}, Title = {Neocortical layer 6, a review}, Volume = {4}, @@ -15982,7 +15981,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Aug}, Number = {8}, Pages = {815-8}, - pubmed = {22772730}, + pmid = {22772730}, Pst = {epublish}, Title = {Multicolor two-photon tissue imaging by wavelength mixing}, Volume = {9}, @@ -16003,7 +16002,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {50}, Pages = {18177-85}, Pmc = {PMC3532899}, - pubmed = {23238731}, + pmid = {23238731}, Pst = {ppublish}, Title = {The laminar development of direction selectivity in ferret visual cortex}, Volume = {32}, @@ -16023,7 +16022,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Dec}, Number = {7427}, Pages = {72-8}, - pubmed = {23222610}, + pmid = {23222610}, Pst = {ppublish}, Title = {The entorhinal grid map is discretized}, Volume = {492}, @@ -16044,7 +16043,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {7427}, Pages = {66-71}, Pmc = {PMC3518700}, - pubmed = {23172146}, + pmid = {23172146}, Pst = {ppublish}, Title = {Non-synaptic inhibition between grouped neurons in an olfactory circuit}, Volume = {492}, @@ -16064,7 +16063,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Feb}, Number = {2}, Pages = {201-8}, - pubmed = {20134419}, + pmid = {20134419}, Pst = {ppublish}, Title = {Thinned-skull cranial window technique for long-term imaging of the cortex in live mice}, Volume = {5}, @@ -16084,7 +16083,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Nov}, Number = {48}, Pages = {17073-85}, - pubmed = {23197701}, + pmid = {23197701}, Pst = {ppublish}, Title = {The early maturation of visual cortical area MT is dependent on input from the retinorecipient medial portion of the inferior pulvinar}, Volume = {32}, @@ -16105,7 +16104,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {48}, Pages = {17108-19}, Pmc = {PMC3520056}, - pubmed = {23197704}, + pmid = {23197704}, Pst = {ppublish}, Title = {Population rate dynamics and multineuron firing patterns in sensory cortex}, Volume = {32}, @@ -16126,7 +16125,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {48}, Pages = {17155-62}, Pmc = {PMC3529201}, - pubmed = {23197708}, + pmid = {23197708}, Pst = {ppublish}, Title = {Fine-grained nociceptive maps in primary somatosensory cortex}, Volume = {32}, @@ -16146,7 +16145,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Nov}, Number = {48}, Pages = {17230-40}, - pubmed = {23197715}, + pmid = {23197715}, Pst = {ppublish}, Title = {Anxiety-related mechanisms of respiratory dysfunction in a mouse model of Rett syndrome}, Volume = {32}, @@ -16165,7 +16164,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {11}, Pages = {e1002775}, Pmc = {PMC3499254}, - pubmed = {23166484}, + pmid = {23166484}, Pst = {ppublish}, Title = {Functional connectivity and tuning curves in populations of simultaneously recorded neurons}, Volume = {8}, @@ -16184,7 +16183,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {11}, Pages = {e1002756}, Pmc = {PMC3493502}, - pubmed = {23144602}, + pmid = {23144602}, Pst = {ppublish}, Title = {Coordinated optimization of visual cortical maps (II) numerical studies}, Volume = {8}, @@ -16205,7 +16204,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {8}, Pages = {750-6}, Pmc = {PMC2904852}, - pubmed = {20381353}, + pmid = {20381353}, Pst = {ppublish}, Title = {Single-neuron responses in humans during execution and observation of actions}, Volume = {20}, @@ -16225,7 +16224,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Oct}, Number = {44}, Pages = {15388-402}, - pubmed = {23115177}, + pmid = {23115177}, Pst = {ppublish}, Title = {Thalamus-derived molecules promote survival and dendritic growth of developing cortical neurons}, Volume = {32}, @@ -16244,7 +16243,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Sep}, Number = {6100}, Pages = {1301-3}, - pubmed = {22984058}, + pmid = {22984058}, Pst = {ppublish}, Title = {Neuroscience. The emerging biology of autism spectrum disorders}, Volume = {337}, @@ -16264,7 +16263,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Sep}, Number = {38}, Pages = {13326-32}, - pubmed = {22993447}, + pmid = {22993447}, Pst = {ppublish}, Title = {Superior colliculus mediates cervical dystonia evoked by inhibition of the substantia nigra pars reticulata}, Volume = {32}, @@ -16284,7 +16283,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Sep}, Number = {38}, Pages = {13085-99}, - pubmed = {22993426}, + pmid = {22993426}, Pst = {ppublish}, Title = {A role for silent synapses in the development of the pathway from layer 2/3 to 5 pyramidal cells in the neocortex}, Volume = {32}, @@ -16303,7 +16302,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Sep}, Number = {6100}, Pages = {1300-1}, - pubmed = {22984057}, + pmid = {22984057}, Pst = {ppublish}, Title = {Cell biology. Staging membrane fusion}, Volume = {337}, @@ -16322,7 +16321,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Sep}, Number = {6100}, Pages = {1304-5}, - pubmed = {22984060}, + pmid = {22984060}, Pst = {ppublish}, Title = {Ecology. When paths to cooperation converge}, Volume = {337}, @@ -16343,7 +16342,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {37}, Pages = {15018-23}, Pmc = {PMC3443128}, - pubmed = {22923692}, + pmid = {22923692}, Pst = {ppublish}, Title = {Brain conditioning is instrumental for successful microglia reconstitution following hematopoietic stem cell transplantation}, Volume = {109}, @@ -16362,7 +16361,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {10}, Pages = {e47419}, Pmc = {PMC3482231}, - pubmed = {23110071}, + pmid = {23110071}, Pst = {ppublish}, Title = {Quantitative linking hypotheses for infant eye movements}, Volume = {7}, @@ -16382,7 +16381,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Nov}, Number = {11}, Pages = {1539-46}, - pubmed = {23086335}, + pmid = {23086335}, Pst = {ppublish}, Title = {Reorganization of cortical population activity imaged throughout long-term sensory deprivation}, Volume = {15}, @@ -16401,7 +16400,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {10}, Pages = {e46338}, Pmc = {PMC3468571}, - pubmed = {23071557}, + pmid = {23071557}, Pst = {ppublish}, Title = {Odor memory stability after reinnervation of the olfactory bulb}, Volume = {7}, @@ -16420,7 +16419,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {10}, Pages = {e46157}, Pmc = {PMC3465318}, - pubmed = {23071541}, + pmid = {23071541}, Pst = {ppublish}, Title = {Visualization of cortical projection neurons with retrograde TET-off lentiviral vector}, Volume = {7}, @@ -16439,7 +16438,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {10}, Pages = {e40483}, Pmc = {PMC3465333}, - pubmed = {23071485}, + pmid = {23071485}, Pst = {ppublish}, Title = {Analyzing self-similar and fractal properties of the C. elegans neural network}, Volume = {7}, @@ -16457,7 +16456,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Keywords = {downloads}, Pages = {7}, Pmc = {PMC3147162}, - pubmed = {21847380}, + pmid = {21847380}, Pst = {ppublish}, Title = {The retrosplenial cortex: intrinsic connectivity and connections with the (para)hippocampal region in the rat. An interactive connectome}, Volume = {5}, @@ -16477,7 +16476,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Aug}, Number = {8}, Pages = {663-78}, - pubmed = {16858394}, + pmid = {16858394}, Pst = {ppublish}, Title = {Path integration and the neural basis of the 'cognitive map'}, Volume = {7}, @@ -16497,7 +16496,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Jul}, Number = {2}, Pages = {329-40}, - pubmed = {16836633}, + pmid = {16836633}, Pst = {ppublish}, Title = {Retinoic acid delineates the topography of neuronal plasticity in postnatal cerebral cortex}, Volume = {24}, @@ -16517,7 +16516,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {3}, Pages = {e17460}, Pmc = {PMC3052362}, - pubmed = {21408007}, + pmid = {21408007}, Pst = {epublish}, Title = {Development of social vocalizations in mice}, Volume = {6}, @@ -16537,7 +16536,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Jan}, Number = {6115}, Pages = {70-4}, - pubmed = {23180771}, + pmid = {23180771}, Pst = {ppublish}, Title = {The spatial and temporal origin of chandelier cells in mouse neocortex}, Volume = {339}, @@ -16558,7 +16557,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {7430}, Pages = {97-100}, Pmc = {PMC3537822}, - pubmed = {23172139}, + pmid = {23172139}, Pst = {ppublish}, Title = {Inhibition dominates sensory responses in the awake cortex}, Volume = {493}, @@ -16579,7 +16578,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {27}, Pages = {9324-34}, Pmc = {PMC2910363}, - pubmed = {20610767}, + pmid = {20610767}, Pst = {ppublish}, Title = {Anesthetic activation of central respiratory chemoreceptor neurons involves inhibition of a THIK-1-like background K(+) current}, Volume = {30}, @@ -16599,7 +16598,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {May}, Number = {5}, Pages = {663-8}, - pubmed = {22504349}, + pmid = {22504349}, Pst = {epublish}, Title = {Neural mechanisms of social risk for psychiatric disorders}, Volume = {15}, @@ -16619,7 +16618,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Nov}, Number = {47}, Pages = {16541-51}, - pubmed = {23175810}, + pmid = {23175810}, Pst = {ppublish}, Title = {Levodopa-induced dyskinesia is strongly associated with resonant cortical oscillations}, Volume = {32}, @@ -16639,7 +16638,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Feb}, Number = {2}, Pages = {119-24}, - pubmed = {21118215}, + pmid = {21118215}, Pst = {ppublish}, Title = {Enhancing collection efficiency in large field of view multiphoton microscopy}, Volume = {241}, @@ -16659,7 +16658,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {1}, Pages = {1-5}, Pmc = {PMC2880024}, - pubmed = {20676302}, + pmid = {20676302}, Pst = {ppublish}, Title = {Toward reconstructing spike trains from large-scale calcium imaging data}, Volume = {4}, @@ -16679,7 +16678,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Jul}, Number = {7}, Pages = {1047-53}, - pubmed = {22634730}, + pmid = {22634730}, Pst = {epublish}, Title = {pHTomato, a red, genetically encoded indicator that enables multiplex interrogation of synaptic activity}, Volume = {15}, @@ -16700,7 +16699,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {7389}, Pages = {331-5}, Pmc = {PMC3477868}, - pubmed = {22388818}, + pmid = {22388818}, Pst = {epublish}, Title = {Corticostriatal plasticity is necessary for learning intentional neuroprosthetic skills}, Volume = {483}, @@ -16720,7 +16719,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Jul}, Number = {7406}, Pages = {235-8}, - pubmed = {22722837}, + pmid = {22722837}, Pst = {ppublish}, Title = {Genetic dissection of the circuit for hand dexterity in primates}, Volume = {487}, @@ -16741,7 +16740,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {4}, Pages = {1747-56}, Pmc = {PMC2753672}, - pubmed = {19398014}, + pmid = {19398014}, Pst = {ppublish}, Title = {Different roles of the parahippocampal place area (PPA) and retrosplenial cortex (RSC) in panoramic scene perception}, Volume = {47}, @@ -16761,7 +16760,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Nov}, Number = {46}, Pages = {14553-70}, - pubmed = {19923289}, + pmid = {19923289}, Pst = {ppublish}, Title = {Correlations of neuronal and microvascular densities in murine cortex revealed by direct counting and colocalization of nuclei and vessels}, Volume = {29}, @@ -16782,7 +16781,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {10}, Pages = {1540-53}, Pmc = {PMC3359866}, - pubmed = {22607000}, + pmid = {22607000}, Pst = {ppublish}, Title = {Development and critical period plasticity of the barrel cortex}, Volume = {35}, @@ -16802,7 +16801,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {May}, Number = {7398}, Pages = {372-5}, - pubmed = {22596161}, + pmid = {22596161}, Pst = {epublish}, Title = {Reach and grasp by people with tetraplegia using a neurally controlled robotic arm}, Volume = {485}, @@ -16822,7 +16821,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {May}, Number = {7399}, Pages = {471-7}, - pubmed = {22622571}, + pmid = {22622571}, Pst = {epublish}, Title = {Brain-wide neuronal dynamics during motor adaptation in zebrafish}, Volume = {485}, @@ -16843,7 +16842,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {19}, Pages = {6688-98}, Pmc = {PMC3371585}, - pubmed = {22573691}, + pmid = {22573691}, Pst = {ppublish}, Title = {Dynamic changes in interneuron morphophysiological properties mark the maturation of hippocampal network activity}, Volume = {32}, @@ -16864,7 +16863,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {27}, Pages = {9429-37}, Pmc = {PMC3419577}, - pubmed = {22764251}, + pmid = {22764251}, Pst = {ppublish}, Title = {Otx2 binding to perineuronal nets persistently regulates plasticity in the mature visual cortex}, Volume = {32}, @@ -16885,7 +16884,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {27}, Pages = {9159-72}, Pmc = {PMC3402176}, - pubmed = {22764225}, + pmid = {22764225}, Pst = {ppublish}, Title = {Robustness of cortical topography across fields, laminae, anesthetic states, and neurophysiological signal types}, Volume = {32}, @@ -16906,7 +16905,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {2}, Pages = {a002519}, Pmc = {PMC2742095}, - pubmed = {20066088}, + pmid = {20066088}, Pst = {ppublish}, Title = {Gradients in the brain: the control of the development of form and function in the cerebral cortex}, Volume = {1}, @@ -16926,7 +16925,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Mar}, Number = {6}, Pages = {1055-8}, - pubmed = {22445332}, + pmid = {22445332}, Pst = {ppublish}, Title = {Sonic hedgehog, BOC, and synaptic development: new players for an old game}, Volume = {73}, @@ -16947,7 +16946,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {6}, Pages = {1058-60}, Pmc = {PMC3353540}, - pubmed = {22445333}, + pmid = {22445333}, Pst = {ppublish}, Title = {Human structural plasticity at record speed}, Volume = {73}, @@ -16966,7 +16965,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Dec}, Number = {6}, Pages = {1053-5}, - pubmed = {14687538}, + pmid = {14687538}, Pst = {ppublish}, Title = {Mapping by waves. Patterned spontaneous activity regulates retinotopic map refinement}, Volume = {40}, @@ -16987,7 +16986,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {6}, Pages = {1116-26}, Pmc = {PMC3551478}, - pubmed = {22445340}, + pmid = {22445340}, Pst = {ppublish}, Title = {Sonic hedgehog expression in corticofugal projection neurons directs cortical microcircuit formation}, Volume = {73}, @@ -17006,7 +17005,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Aug}, Number = {8}, Pages = {349-55}, - pubmed = {17629544}, + pmid = {17629544}, Pst = {ppublish}, Title = {Perceptual resonance: action-induced modulation of perception}, Volume = {11}, @@ -17027,7 +17026,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {4}, Pages = {750-62}, Pmc = {PMC2990987}, - pubmed = {21092863}, + pmid = {21092863}, Pst = {ppublish}, Title = {Visual deprivation suppresses L5 pyramidal neuron excitability by preventing the induction of intrinsic plasticity}, Volume = {68}, @@ -17047,7 +17046,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Dec}, Number = {5}, Pages = {851-64}, - pubmed = {15572115}, + pmid = {15572115}, Pst = {ppublish}, Title = {A developmental switch in the excitability and function of the starburst network in the mammalian retina}, Volume = {44}, @@ -17067,7 +17066,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Jul}, Number = {7}, Pages = {384-91}, - pubmed = {15219737}, + pmid = {15219737}, Pst = {ppublish}, Title = {Developmental mechanisms patterning thalamocortical projections: intrinsic, extrinsic and in between}, Volume = {27}, @@ -17087,7 +17086,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Dec}, Number = {28}, Pages = {3401-10}, - pubmed = {15536008}, + pmid = {15536008}, Pst = {ppublish}, Title = {Using eye movements to assess brain function in mice}, Volume = {44}, @@ -17108,7 +17107,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {4}, Pages = {923-35}, Pmc = {PMC3357949}, - pubmed = {22559944}, + pmid = {22559944}, Pst = {ppublish}, Title = {Inhibition of SRGAP2 function by its human-specific paralogs induces neoteny during spine maturation}, Volume = {149}, @@ -17128,7 +17127,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Aug}, Number = {15}, Pages = {1449-55}, - pubmed = {22748315}, + pmid = {22748315}, Pst = {ppublish}, Title = {Subcortical connections to human amygdala and changes following destruction of the visual cortex}, Volume = {22}, @@ -17149,7 +17148,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Oct}, Number = {43}, Pages = {15106-11}, - pubmed = {23100431}, + pmid = {23100431}, Pst = {ppublish}, Title = {Deficiency of the microglial receptor CX3CR1 impairs postnatal functional development of thalamocortical synapses in the barrel cortex}, Volume = {32}, @@ -17169,7 +17168,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Oct}, Number = {44}, Pages = {15388-402}, - pubmed = {23115177}, + pmid = {23115177}, Pst = {ppublish}, Title = {Thalamus-derived molecules promote survival and dendritic growth of developing cortical neurons}, Volume = {32}, @@ -17191,7 +17190,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {5}, Pages = {1094-104}, Pmc = {PMC3077430}, - pubmed = {20855494}, + pmid = {20855494}, Pst = {ppublish}, Title = {Reorganization of inhibitory synaptic circuits in rodent chronically injured epileptogenic neocortex}, Volume = {21}, @@ -17211,7 +17210,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {21}, Pages = {2075-80}, Pmc = {PMC3494768}, - pubmed = {23084988}, + pmid = {23084988}, Pst = {ppublish}, Title = {Rapid whisker movements in sleeping newborn rats}, Volume = {22}, @@ -17232,7 +17231,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Oct}, Number = {2}, Pages = {297-308}, - pubmed = {23083733}, + pmid = {23083733}, Pst = {ppublish}, Title = {Imaging neural activity using Thy1-GCaMP transgenic mice}, Volume = {76}, @@ -17254,7 +17253,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Dec}, Number = {4}, Pages = {362-75}, - pubmed = {20976563}, + pmid = {20976563}, Pst = {ppublish}, Title = {Development of the brain's functional network architecture}, Volume = {20}, @@ -17272,7 +17271,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Jul}, Number = {14}, Pages = {5967-79}, - pubmed = {10407035}, + pmid = {10407035}, Pst = {ppublish}, Title = {Molecular evidence for the early specification of presumptive functional domains in the embryonic primate cerebral cortex}, Volume = {19}, @@ -17293,7 +17292,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {10}, Pages = {3979-84}, Pmc = {PMC3309754}, - pubmed = {22355129}, + pmid = {22355129}, Pst = {ppublish}, Title = {Rat brains also have a default mode network}, Volume = {109}, @@ -17315,7 +17314,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {40}, Pages = {13860-72}, Pmc = {PMC3500840}, - pubmed = {23035095}, + pmid = {23035095}, Pst = {ppublish}, Title = {Brain activity mapping in Mecp2 mutant mice reveals functional deficits in forebrain circuits, including key nodes in the default mode network, that are reversed with ketamine treatment}, Volume = {32}, @@ -17335,7 +17334,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Feb}, Number = {3}, Pages = {2529-38}, - pubmed = {21925609}, + pmid = {21925609}, Pst = {ppublish}, Title = {Bedside optical imaging of occipital resting-state functional connectivity in neonates}, Volume = {59}, @@ -17355,7 +17354,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Number = {1}, Pages = {e16322}, Pmc = {PMC3024435}, - pubmed = {21283729}, + pmid = {21283729}, Pst = {epublish}, Title = {Imaging of functional connectivity in the mouse brain}, Volume = {6}, @@ -17380,7 +17379,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {May}, Number = {1-2}, Pages = {126-32}, - pubmed = {1907877}, + pmid = {1907877}, Pst = {ppublish}, Title = {A factor analysis of the human's corpus callosum}, Volume = {548}, @@ -17397,7 +17396,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Oct}, Number = {4}, Pages = {857-61}, - pubmed = {1775564}, + pmid = {1775564}, Pst = {ppublish}, Title = {A computer-aided procedure for measuring Lashley III maze performance}, Volume = {50}, @@ -17415,7 +17414,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Aug}, Number = {4}, Pages = {562-6}, - pubmed = {1930724}, + pmid = {1930724}, Pst = {ppublish}, Title = {Corpus callosum: interactive effects of infantile handling and testosterone in the rat}, Volume = {105}, @@ -17433,7 +17432,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Oct}, Number = {1}, Pages = {98-104}, - pubmed = {1799876}, + pmid = {1799876}, Pst = {ppublish}, Title = {Spatial learning, discrimination learning, paw preference and neocortical ectopias in two autoimmune strains of mice}, Volume = {562}, @@ -17452,7 +17451,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Oct}, Number = {4}, Pages = {853-6}, - pubmed = {1775563}, + pmid = {1775563}, Pst = {ppublish}, Title = {A measure of lateral paw preference in the mouse}, Volume = {50}, @@ -17472,7 +17471,7 @@ CONCLUSIONS: These results strongly suggest that early, acetylcholine-dependent Month = {Feb}, Number = {2}, Pages = {969-75}, - pubmed = {18077659}, + pmid = {18077659}, Pst = {ppublish}, Title = {Handedness leads to interhemispheric EEG asymmetry during sleep in the rat}, Volume = {99}, @@ -17493,7 +17492,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {9}, Pages = {e43083}, Pmc = {PMC3446960}, - pubmed = {23028443}, + pmid = {23028443}, Pst = {ppublish}, Title = {Ten-m3 is required for the development of topography in the ipsilateral retinocollicular pathway}, Volume = {7}, @@ -17514,7 +17513,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {7}, Pages = {949-51}, Pmc = {PMC3386353}, - pubmed = {22706266}, + pmid = {22706266}, Pst = {epublish}, Title = {Pattern and not magnitude of neural activity determines dendritic spine stability in awake mice}, Volume = {15}, @@ -17533,7 +17532,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Dec}, Number = {6}, Pages = {1303-13}, - pubmed = {9883724}, + pmid = {9883724}, Pst = {ppublish}, Title = {Topographic guidance labels in a sensory projection to the forebrain}, Volume = {21}, @@ -17552,7 +17551,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Dec}, Number = {2}, Pages = {243-50}, - pubmed = {23263442}, + pmid = {23263442}, Pst = {ppublish}, Title = {Neuronal reference frames for social decisions in primate frontal cortex}, Volume = {16}, @@ -17571,7 +17570,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Mesh = {Animals; Brain; Brain Diseases; Brain Mapping; Humans; Models, Neurological; Nerve Net}, Month = {Mar}, Pages = {1-38}, - pubmed = {18400922}, + pmid = {18400922}, Pst = {ppublish}, Title = {The brain's default network: anatomy, function, and relevance to disease}, Volume = {1124}, @@ -17591,7 +17590,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Mar}, Number = {3}, Pages = {1381-402}, - pubmed = {14573558}, + pmid = {14573558}, Pst = {ppublish}, Title = {What the brain stem tells the frontal cortex. I. Oculomotor signals sent from superior colliculus to frontal eye field via mediodorsal thalamus}, Volume = {91}, @@ -17610,7 +17609,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Jan}, Number = {3}, Pages = {987-1001}, - pubmed = {23325237}, + pmid = {23325237}, Pst = {ppublish}, Title = {Layer III Neurons Control Synchronized Waves in the Immature Cerebral Cortex}, Volume = {33}, @@ -17629,7 +17628,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Jan}, Number = {2}, Pages = {193-200}, - pubmed = {23292682}, + pmid = {23292682}, Pst = {ppublish}, Title = {In vivo reprogramming of circuit connectivity in postmitotic neocortical neurons}, Volume = {16}, @@ -17648,7 +17647,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Jan}, Number = {2}, Pages = {201-9}, - pubmed = {23313911}, + pmid = {23313911}, Pst = {ppublish}, Title = {Timothy syndrome is associated with activity-dependent dendritic retraction in rodent and human neurons}, Volume = {16}, @@ -17667,7 +17666,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Jan}, Number = {2}, Pages = {219-26}, - pubmed = {23292681}, + pmid = {23292681}, Pst = {ppublish}, Title = {Cortico-cortical projections in mouse visual cortex are functionally target specific}, Volume = {16}, @@ -17686,7 +17685,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Jan}, Number = {2}, Pages = {227-34}, - pubmed = {23313909}, + pmid = {23313909}, Pst = {ppublish}, Title = {Layer-specific excitatory circuits differentially control recurrent network dynamics in the neocortex}, Volume = {16}, @@ -17706,7 +17705,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Oct}, Number = {2}, Pages = {193-6}, - pubmed = {22017982}, + pmid = {22017982}, Pst = {ppublish}, Title = {Movement, confusion, and orienting in frontal cortices}, Volume = {72}, @@ -17727,7 +17726,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {4}, Pages = {416-29}, Pmc = {PMC2731651}, - pubmed = {18281458}, + pmid = {18281458}, Pst = {ppublish}, Title = {Eph/ephrin signaling: networks}, Volume = {22}, @@ -17748,7 +17747,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {38}, Pages = {31804-12}, Pmc = {PMC3442514}, - pubmed = {22843694}, + pmid = {22843694}, Pst = {ppublish}, Title = {Color-tuned channelrhodopsins for multiwavelength optogenetics}, Volume = {287}, @@ -17769,7 +17768,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {29}, Pages = {7607-18}, Pmc = {PMC2548311}, - pubmed = {16855088}, + pmid = {16855088}, Pst = {ppublish}, Title = {Saccades exert spatial control of motion processing for smooth pursuit eye movements}, Volume = {26}, @@ -17790,7 +17789,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {2}, Pages = {248-60}, Pmc = {PMC2426736}, - pubmed = {18439409}, + pmid = {18439409}, Pst = {ppublish}, Title = {Cortical mechanisms of smooth eye movements revealed by dynamic covariations of neural and behavioral responses}, Volume = {58}, @@ -17809,7 +17808,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Mar}, Number = {3}, Pages = {945-74}, - pubmed = {3346731}, + pmid = {3346731}, Pst = {ppublish}, Title = {Fates of visual cortical neurons in the ferret after isochronic and heterochronic transplantation}, Volume = {8}, @@ -17826,7 +17825,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Sep}, Number = {4719}, Pages = {1268-71}, - pubmed = {4035355}, + pmid = {4035355}, Pst = {ppublish}, Title = {Migration and differentiation of cerebral cortical neurons after transplantation into the brains of ferrets}, Volume = {229}, @@ -17844,7 +17843,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Jul}, Number = {7}, Pages = {2230-46}, - pubmed = {2545833}, + pmid = {2545833}, Pst = {ppublish}, Title = {Selective elimination of axons extended by developing cortical neurons is dependent on regional locale: experiments utilizing fetal cortical transplants}, Volume = {9}, @@ -17862,7 +17861,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Oct}, Number = {10}, Pages = {400-6}, - pubmed = {2479138}, + pmid = {2479138}, Pst = {ppublish}, Title = {Do cortical areas emerge from a protocortex?}, Volume = {12}, @@ -17879,7 +17878,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Mesh = {2-Amino-5-phosphonovalerate; Animals; Autoradiography; Behavior, Animal; Chromatography, High Pressure Liquid; Excitatory Amino Acid Antagonists; Hippocampus; Long-Term Potentiation; Male; Maze Learning; Memory, Short-Term; Microinjections; Psychomotor Performance; Rats; Rats, Inbred Strains; Reaction Time; Receptors, N-Methyl-D-Aspartate; Space Perception; Tritium}, Number = {2}, Pages = {118-36}, - pubmed = {10226773}, + pmid = {10226773}, Pst = {ppublish}, Title = {Delay-dependent impairment of a matching-to-place task with chronic and intrahippocampal infusion of the NMDA-antagonist D-AP5}, Volume = {9}, @@ -17898,7 +17897,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Feb}, Number = {1270}, Pages = {77-98}, - pubmed = {2895934}, + pmid = {2895934}, Pst = {ppublish}, Title = {The organization of corticocortical projections from area 17 to area 18 of the cat's visual cortex}, Volume = {233}, @@ -17917,7 +17916,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Mar}, Number = {6159}, Pages = {73-6}, - pubmed = {3347247}, + pmid = {3347247}, Pst = {ppublish}, Title = {Developmental plasticity in the visual and auditory representations in the mammalian superior colliculus}, Volume = {332}, @@ -17937,7 +17936,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Apr}, Number = {4}, Pages = {255-66}, - pubmed = {18354398}, + pmid = {18354398}, Pst = {ppublish}, Title = {Multisensory integration: current issues from the perspective of the single neuron}, Volume = {9}, @@ -17958,7 +17957,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Aug}, Number = {4}, Pages = {688-99}, - pubmed = {22920259}, + pmid = {22920259}, Pst = {ppublish}, Title = {Visual input modulates audiomotor function via hypothalamic dopaminergic neurons through a cooperative mechanism}, Volume = {75}, @@ -17979,7 +17978,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {May}, Number = {4}, Pages = {486-512}, - pubmed = {2745751}, + pmid = {2745751}, Pst = {ppublish}, Title = {Convergence and divergence in the afferent projections to cat area 17}, Volume = {283}, @@ -17997,7 +17996,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Journal-Full = {Neural plasticity}, Keywords = {visual system, connectivity, visual cortex, neocortex, histology, spontaneous activity, retina, brain mapping, mirror symmetry, corpus callosum}, Pages = {250196}, - pubmed = {23213572}, + pmid = {23213572}, Pst = {ppublish}, Title = {Deafferentation-induced plasticity of visual callosal connections: predicting critical periods and analyzing cortical abnormalities using diffusion tensor imaging}, Volume = {2012}, @@ -18017,7 +18016,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Oct}, Number = {14}, Pages = {3256-76}, - pubmed = {22430936}, + pmid = {22430936}, Pst = {ppublish}, Title = {Role of retinal input on the development of striate-extrastriate patterns of connections in the rat}, Volume = {520}, @@ -18038,7 +18037,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Apr}, Number = {5}, Pages = {914-32}, - pubmed = {21830218}, + pmid = {21830218}, Pst = {ppublish}, Title = {Retinal input influences the size and corticocortical connectivity of visual cortex during postnatal development in the ferret}, Volume = {520}, @@ -18060,7 +18059,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {3}, Pages = {152-6}, Pmc = {PMC3155624}, - pubmed = {21782890}, + pmid = {21782890}, Pst = {ppublish}, Title = {Neonatal enucleation during a critical period reduces the precision of cortico-cortical projections in visual cortex}, Volume = {501}, @@ -18079,7 +18078,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Keywords = {visual system, connectivity, visual cortex, neocortex, histology, spontaneous activity, retina, brain mapping, mirror symmetry, corpus callosum}, Pages = {149}, Pmc = {PMC2971465}, - pubmed = {21048904}, + pmid = {21048904}, Pst = {epublish}, Title = {Diffusion tensor imaging detects early cerebral cortex abnormalities in neuronal architecture induced by bilateral neonatal enucleation: an experimental model in the ferret}, Volume = {4}, @@ -18100,7 +18099,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Dec}, Number = {24}, Pages = {4963-79}, - pubmed = {21031561}, + pmid = {21031561}, Pst = {ppublish}, Title = {Role of interstitial branching in the development of visual corticocortical connections: a time-lapse and fixed-tissue analysis}, Volume = {518}, @@ -18120,7 +18119,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Mesh = {Animals; Animals, Newborn; Axons; Brain Mapping; Corpus Callosum; Dizocilpine Maleate; Excitatory Amino Acid Antagonists; Eye Enucleation; Rats; Rats, Long-Evans; Receptors, N-Methyl-D-Aspartate; Visual Pathways}, Number = {4}, Pages = {413-24}, - pubmed = {19621122}, + pmid = {19621122}, Pst = {ppublish}, Title = {Topography and axon arbor architecture in the visual callosal pathway: effects of deafferentation and blockade of N-methyl-D-aspartate receptors}, Volume = {41}, @@ -18140,7 +18139,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Sep}, Number = {3}, Pages = {683-99}, - pubmed = {17706364}, + pmid = {17706364}, Pst = {ppublish}, Title = {Retinal influences induce bidirectional changes in the kinetics of N-methyl-D-aspartate receptor-mediated responses in striate cortex cells during postnatal development}, Volume = {148}, @@ -18158,7 +18157,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Jul}, Number = {5719}, Pages = {231-4}, - pubmed = {450139}, + pmid = {450139}, Pst = {ppublish}, Title = {Effects of visual experience on the maturation of the efferent system to the corpus callosum}, Volume = {280}, @@ -18175,7 +18174,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Journal-Full = {Cerebral cortex (New York, N.Y. : 1991)}, Keywords = {genes; self organization; Competitive Behavior; optical imaging; optical physiology; toread; wholeBrain; Somatosensory Cortex; thalamus; barrels; Mouse; development; synchrony; oscillations; microglia}, Month = {Jun}, - pubmed = {22700645}, + pmid = {22700645}, Pst = {aheadofprint}, Title = {LPS-Induced Microglial Secretion of TNFα Increases Activity-Dependent Neuronal Apoptosis in the Neonatal Cerebral Cortex}, Year = {2012}, @@ -18192,7 +18191,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Journal-Full = {Cerebral cortex (New York, N.Y. : 1991)}, Keywords = {genes; self organization; Competitive Behavior; optical imaging; optical physiology; toread; wholeBrain; Somatosensory Cortex; thalamus; barrels; Mouse; development; synchrony; oscillations}, Month = {May}, - pubmed = {22593243}, + pmid = {22593243}, Pst = {aheadofprint}, Title = {Thalamic Network Oscillations Synchronize Ontogenetic Columns in the Newborn Rat Barrel Cortex}, Year = {2012}, @@ -18212,7 +18211,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {20}, Pages = {8027-30}, Pmc = {PMC54885}, - pubmed = {1978317}, + pmid = {1978317}, Pst = {ppublish}, Title = {Endogenous neurotransmitter activates N-methyl-D-aspartate receptors on differentiating neurons in embryonic cortex}, Volume = {87}, @@ -18231,7 +18230,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Dec}, Number = {6}, Pages = {512-23}, - pubmed = {17079517}, + pmid = {17079517}, Pst = {ppublish}, Title = {Small-world brain networks}, Volume = {12}, @@ -18251,7 +18250,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Mar}, Number = {3}, Pages = {186-98}, - pubmed = {19190637}, + pmid = {19190637}, Pst = {ppublish}, Title = {Complex brain networks: graph theoretical analysis of structural and functional systems}, Volume = {10}, @@ -18272,7 +18271,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {28}, Pages = {9477-87}, Pmc = {PMC2914251}, - pubmed = {20631176}, + pmid = {20631176}, Pst = {ppublish}, Title = {Functional connectivity and brain networks in schizophrenia}, Volume = {30}, @@ -18292,7 +18291,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Mesh = {Adolescent; Adult; Animals; Brain; Brain Mapping; Child; Child Development; Cognition Disorders; Disease Models, Animal; Environment; Genetic Predisposition to Disease; Genotype; Humans; Magnetic Resonance Imaging; Models, Neurological; Neural Conduction; Neurons; Risk Factors; Schizophrenia; Synapses; Young Adult}, Number = {4}, Pages = {1297-327}, - pubmed = {18838043}, + pmid = {18838043}, Pst = {ppublish}, Title = {Developmental disruptions in neural connectivity in the pathophysiology of schizophrenia}, Volume = {20}, @@ -18312,7 +18311,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Jun}, Number = {6}, Pages = {277-90}, - pubmed = {20493761}, + pmid = {20493761}, Pst = {ppublish}, Title = {Large-scale brain networks in cognition: emerging methods and principles}, Volume = {14}, @@ -18332,7 +18331,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Oct}, Number = {10}, Pages = {483-506}, - pubmed = {21908230}, + pmid = {21908230}, Pst = {ppublish}, Title = {Large-scale brain networks and psychopathology: a unifying triple network model}, Volume = {15}, @@ -18352,7 +18351,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Apr}, Number = {2}, Pages = {225-30}, - pubmed = {15831407}, + pmid = {15831407}, Pst = {ppublish}, Title = {Why the frontal cortex in autism might be talking only to itself: local over-connectivity but long-distance disconnection}, Volume = {15}, @@ -18371,7 +18370,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Keywords = {GABA; interneurons; development; Cerebral Cortex; Neocortex; visual cortex; visual system; multimodal; vision; Sensory Deprivation; plasticity; structural remodeling; Structure-Activity Relationship; Spontaneous activity}, Pages = {590725}, Pmc = {PMC3377178}, - pubmed = {22720175}, + pmid = {22720175}, Pst = {ppublish}, Title = {Cortical GABAergic interneurons in cross-modal plasticity following early blindness}, Volume = {2012}, @@ -18390,7 +18389,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Nov}, Number = {11}, Pages = {682-3}, - pubmed = {23034454}, + pmid = {23034454}, Pst = {ppublish}, Title = {Development: Knowing left from right}, Volume = {13}, @@ -18411,7 +18410,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Sep}, Number = {18}, Pages = {3257-62}, - pubmed = {22912409}, + pmid = {22912409}, Pst = {ppublish}, Title = {Left-right patterning: conserved and divergent mechanisms}, Volume = {139}, @@ -18431,7 +18430,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Dec}, Number = {12}, Pages = {3131-46}, - pubmed = {21031419}, + pmid = {21031419}, Pst = {ppublish}, Title = {Far from solved: a perspective on what we know about early mechanisms of left-right asymmetry}, Volume = {239}, @@ -18450,7 +18449,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Mesh = {Animals; Body Patterning; Brain; Functional Laterality; Humans; Mesoderm; Stereoisomerism}, Number = {3}, Pages = {159-63}, - pubmed = {9842710}, + pmid = {9842710}, Pst = {ppublish}, Title = {Left-right development from embryos to brains}, Volume = {23}, @@ -18471,7 +18470,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Jun}, Number = {6991}, Pages = {523-30}, - pubmed = {15175743}, + pmid = {15175743}, Pst = {ppublish}, Title = {Activity-dependent homeostatic specification of transmitter expression in embryonic neurons}, Volume = {429}, @@ -18493,7 +18492,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {8}, Pages = {944-50}, Pmc = {PMC2910808}, - pubmed = {20581840}, + pmid = {20581840}, Pst = {ppublish}, Title = {cJun integrates calcium activity and tlx3 expression to regulate neurotransmitter specification}, Volume = {13}, @@ -18514,7 +18513,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Aug}, Number = {8}, Pages = {1134-43}, - pubmed = {22772332}, + pmid = {22772332}, Pst = {epublish}, Title = {Spontaneous activity regulates Robo1 transcription to mediate a switch in thalamocortical axon growth}, Volume = {15}, @@ -18533,7 +18532,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Mesh = {Animals; Female; Immunohistochemistry; Mice; Mice, Mutant Strains; Microscopy, Electron; Munc18 Proteins; Neocortex; Nerve Tissue Proteins; Neurons; Pregnancy; Synapses; Synaptic Transmission; Synaptic Vesicles; Vesicular Transport Proteins}, Number = {1}, Pages = {115-26}, - pubmed = {15145078}, + pmid = {15145078}, Pst = {ppublish}, Title = {Quantification of synapse formation and maintenance in vivo in the absence of synaptic release}, Volume = {126}, @@ -18552,7 +18551,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Dec}, Number = {6}, Pages = {393-407}, - pubmed = {12576293}, + pmid = {12576293}, Pst = {ppublish}, Title = {Wiring of the brain by a range of guidance cues}, Volume = {68}, @@ -18571,7 +18570,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Oct}, Number = {41}, Pages = {12735-47}, - pubmed = {19828784}, + pmid = {19828784}, Pst = {ppublish}, Title = {The development of developmental neuroscience}, Volume = {29}, @@ -18592,7 +18591,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Jul}, Number = {2}, Pages = {218-29}, - pubmed = {22841308}, + pmid = {22841308}, Pst = {ppublish}, Title = {Traveling waves in visual cortex}, Volume = {75}, @@ -18613,7 +18612,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {2}, Pages = {194-208}, Pmc = {PMC3477598}, - pubmed = {22841306}, + pmid = {22841306}, Pst = {ppublish}, Title = {Mechanisms of neuronal computation in mammalian visual cortex}, Volume = {75}, @@ -18635,7 +18634,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {2}, Pages = {250-64}, Pmc = {PMC3408614}, - pubmed = {22841310}, + pmid = {22841310}, Pst = {ppublish}, Title = {Adult visual cortical plasticity}, Volume = {75}, @@ -18656,7 +18655,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Jul}, Number = {2}, Pages = {209-17}, - pubmed = {22841307}, + pmid = {22841307}, Pst = {ppublish}, Title = {From functional architecture to functional connectomics}, Volume = {75}, @@ -18686,7 +18685,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Apr}, Number = {3722}, Pages = {604-19}, - pubmed = {17779492}, + pmid = {17779492}, Pst = {ppublish}, Title = {Ontogenetic development of the human sleep-dream cycle}, Volume = {152}, @@ -18707,7 +18706,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Jul}, Number = {2}, Pages = {230-49}, - pubmed = {22841309}, + pmid = {22841309}, Pst = {ppublish}, Title = {Development and plasticity of the primary visual cortex}, Volume = {75}, @@ -18729,7 +18728,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {1}, Pages = {200-11}, Pmc = {PMC3025725}, - pubmed = {20494968}, + pmid = {20494968}, Pst = {ppublish}, Title = {Developing neocortex organization and connectivity in cats revealed by direct correlation of diffusion tractography and histology}, Volume = {21}, @@ -18747,7 +18746,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Keywords = {Non-programmatic; toread; review literature}, Mesh = {Animals; Auditory Pathways; Cell Communication; Cell Differentiation; Cell Movement; Cochlear Nucleus; Gene Expression Regulation, Developmental; Hair Cells, Auditory; Humans; Nerve Growth Factors; Neurons, Afferent; Spiral Ganglion}, Pages = {51-101}, - pubmed = {12052904}, + pmid = {12052904}, Pst = {ppublish}, Title = {Auditory system development: primary auditory neurons and their targets}, Volume = {25}, @@ -18768,7 +18767,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {30}, Pages = {10306-17}, Pmc = {PMC3435432}, - pubmed = {22836264}, + pmid = {22836264}, Pst = {ppublish}, Title = {Diverse strategies engaged in establishing stereotypic wiring patterns among neurons sharing a common input at the visual system's first synapse}, Volume = {32}, @@ -18789,7 +18788,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {30}, Pages = {10170-82}, Pmc = {PMC3485085}, - pubmed = {22836252}, + pmid = {22836252}, Pst = {ppublish}, Title = {Balanced increases in selectivity and tolerance produce constant sparseness along the ventral visual stream}, Volume = {32}, @@ -18809,7 +18808,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Oct}, Number = {5594}, Pages = {770-6}, - pubmed = {12399577}, + pmid = {12399577}, Pst = {ppublish}, Title = {The developing synapse: construction and modulation of synaptic structures and circuits}, Volume = {298}, @@ -18830,7 +18829,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {30}, Pages = {10286-95}, Pmc = {PMC3435149}, - pubmed = {22836262}, + pmid = {22836262}, Pst = {ppublish}, Title = {Perception via the deviated eye in strabismus}, Volume = {32}, @@ -18851,7 +18850,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {30}, Pages = {10183-91}, Pmc = {PMC3422560}, - pubmed = {22836253}, + pmid = {22836253}, Pst = {ppublish}, Title = {Intrinsic organization of the anesthetized brain}, Volume = {32}, @@ -18872,7 +18871,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {30}, Pages = {10338-51}, Pmc = {PMC3428959}, - pubmed = {22836267}, + pmid = {22836267}, Pst = {ppublish}, Title = {Compromise of auditory cortical tuning and topography after cross-modal invasion by visual inputs}, Volume = {32}, @@ -18893,7 +18892,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {4}, Pages = {452-71}, Pmc = {PMC534952}, - pubmed = {15717047}, + pmid = {15717047}, Pst = {ppublish}, Title = {The repair of complex neuronal circuitry by transplanted and endogenous precursors}, Volume = {1}, @@ -18913,7 +18912,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Jun}, Number = {6}, Pages = {655-64}, - pubmed = {15054062}, + pmid = {15054062}, Pst = {ppublish}, Title = {Experience-dependent changes in basal dendritic branching of layer 2/3 pyramidal neurons during a critical period for developmental plasticity in rat barrel cortex}, Volume = {14}, @@ -18932,7 +18931,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Oct}, Number = {43}, Pages = {14915-20}, - pubmed = {23100414}, + pmid = {23100414}, Pst = {ppublish}, Title = {Electrical stimulation of human fusiform face-selective regions distorts face perception}, Volume = {32}, @@ -18953,7 +18952,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {May}, Number = {18}, Pages = {6183-96}, - pubmed = {22553025}, + pmid = {22553025}, Pst = {ppublish}, Title = {Neurotransmitter release at the thalamocortical synapse instructs barrel formation but not axon patterning in the somatosensory cortex}, Volume = {32}, @@ -18972,7 +18971,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Jan}, Pages = {7}, Pmc = {PMC3294267}, - pubmed = {22408608}, + pmid = {22408608}, Pst = {ppublish}, Title = {Developmental disorders of the midbrain and hindbrain}, Volume = {6}, @@ -18993,7 +18992,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {13}, Pages = {4386-99}, Pmc = {PMC3328193}, - pubmed = {22457489}, + pmid = {22457489}, Pst = {ppublish}, Title = {Network analysis of corticocortical connections reveals ventral and dorsal processing streams in mouse visual cortex}, Volume = {32}, @@ -19013,7 +19012,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Mar}, Number = {3}, Pages = {340-7}, - pubmed = {17259982}, + pmid = {17259982}, Pst = {ppublish}, Title = {cAMP oscillations and retinal activity are permissive for ephrin signaling during the establishment of the retinotopic map}, Volume = {10}, @@ -19034,7 +19033,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {8}, Pages = {750-6}, Pmc = {PMC2904852}, - pubmed = {20381353}, + pmid = {20381353}, Pst = {ppublish}, Title = {Single-neuron responses in humans during execution and observation of actions}, Volume = {20}, @@ -19053,7 +19052,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {8}, Pages = {e43981}, Pmc = {PMC3430631}, - pubmed = {22952835}, + pmid = {22952835}, Pst = {ppublish}, Title = {Temporo-spectral imaging of intrinsic optical signals during hypoxia-induced spreading depression-like depolarization}, Volume = {7}, @@ -19072,7 +19071,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {8}, Pages = {e43373}, Pmc = {PMC3427333}, - pubmed = {22937041}, + pmid = {22937041}, Pst = {ppublish}, Title = {Altered spontaneous activity in anisometropic amblyopia subjects: revealed by resting-state FMRI}, Volume = {7}, @@ -19092,7 +19091,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Sep}, Number = {36}, Pages = {8250-8}, - pubmed = {16148232}, + pmid = {16148232}, Pst = {ppublish}, Title = {Monosynaptic pathway from rat vibrissa motor cortex to facial motor neurons revealed by lentivirus-based axonal tracing}, Volume = {25}, @@ -19112,7 +19111,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Sep}, Number = {9}, Pages = {1125-33}, - pubmed = {16921372}, + pmid = {16921372}, Pst = {ppublish}, Title = {Postsynaptic excitability is necessary for strengthening of cortical sensory responses during experience-dependent development}, Volume = {9}, @@ -19132,7 +19131,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Oct}, Number = {6103}, Pages = {128-32}, - pubmed = {22983708}, + pmid = {22983708}, Pst = {ppublish}, Title = {Shared synaptic pathophysiology in syndromic and nonsyndromic rodent models of autism}, Volume = {338}, @@ -19153,7 +19152,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {3}, Pages = {255-8}, Pmc = {PMC3297424}, - pubmed = {22245809}, + pmid = {22245809}, Pst = {epublish}, Title = {Serial two-photon tomography for automated ex vivo mouse brain imaging}, Volume = {9}, @@ -19172,7 +19171,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Oct}, Number = {43}, Pages = {15142-7}, - pubmed = {23100435}, + pmid = {23100435}, Pst = {ppublish}, Title = {Differences in Sensitivity to Neural Timing among Cortical Areas}, Volume = {32}, @@ -19191,7 +19190,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {9}, Pages = {e45592}, Pmc = {PMC3458919}, - pubmed = {23049819}, + pmid = {23049819}, Pst = {ppublish}, Title = {Male microchimerism in the human female brain}, Volume = {7}, @@ -19211,7 +19210,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {May}, Number = {5}, Pages = {575-83}, - pubmed = {18425116}, + pmid = {18425116}, Pst = {ppublish}, Title = {Extensive fusion of haematopoietic cells with Purkinje neurons in response to chronic inflammation}, Volume = {10}, @@ -19231,7 +19230,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Nov}, Number = {11}, Pages = {2694-701}, - pubmed = {20164125}, + pmid = {20164125}, Pst = {ppublish}, Title = {Spontaneous epileptic manifestations in a DCX knockdown model of human double cortex}, Volume = {20}, @@ -19251,7 +19250,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Oct}, Number = {1}, Pages = {25-36}, - pubmed = {19628007}, + pmid = {19628007}, Pst = {ppublish}, Title = {Fluorescent Arc/Arg3.1 indicator mice: a versatile tool to study brain activity changes in vitro and in vivo}, Volume = {184}, @@ -19271,7 +19270,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {10}, Pages = {1005-12}, Pmc = {PMC3461113}, - pubmed = {22961245}, + pmid = {22961245}, Pst = {ppublish}, Title = {Improving FRET dynamic range with bright green and red fluorescent proteins}, Volume = {9}, @@ -19295,7 +19294,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {4}, Pages = {1067-79}, Pmc = {PMC3289460}, - pubmed = {22114160}, + pmid = {22114160}, Pst = {ppublish}, Title = {Impact of neural noise on a sensory-motor pathway signaling impending collision}, Volume = {107}, @@ -19316,7 +19315,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Jul}, Number = {7407}, Pages = {320-4}, - pubmed = {22763444}, + pmid = {22763444}, Pst = {ppublish}, Title = {Non-invasive prenatal measurement of the fetal genome}, Volume = {487}, @@ -19337,7 +19336,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {7}, Pages = {e1001363}, Pmc = {PMC3398959}, - pubmed = {22815651}, + pmid = {22815651}, Pst = {ppublish}, Title = {Stimulation of host bone marrow stromal cells by sympathetic nerves promotes breast cancer bone metastasis in mice}, Volume = {10}, @@ -19357,7 +19356,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Jul}, Number = {29}, Pages = {9817-23}, - pubmed = {22815496}, + pmid = {22815496}, Pst = {ppublish}, Title = {Critical-state dynamics of avalanches and oscillations jointly emerge from balanced excitation/inhibition in neuronal networks}, Volume = {32}, @@ -19378,7 +19377,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {29}, Pages = {9859-69}, Pmc = {PMC3437549}, - pubmed = {22815501}, + pmid = {22815501}, Pst = {ppublish}, Title = {The influence of visual motion on motor learning}, Volume = {32}, @@ -19398,7 +19397,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Jul}, Number = {29}, Pages = {10075-85}, - pubmed = {22815521}, + pmid = {22815521}, Pst = {ppublish}, Title = {Robustness of a rhythmic circuit to short- and long-term temperature changes}, Volume = {32}, @@ -19419,7 +19418,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {29}, Pages = {10021-34}, Pmc = {PMC3461266}, - pubmed = {22815516}, + pmid = {22815516}, Pst = {ppublish}, Title = {MeCP2 is critical for maintaining mature neuronal networks and global brain anatomy during late stages of postnatal brain development and in the mature adult brain}, Volume = {32}, @@ -19438,7 +19437,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Sep}, Number = {11}, Pages = {1498-505}, - pubmed = {23001062}, + pmid = {23001062}, Pst = {ppublish}, Title = {Slow dynamics and high variability in balanced cortical networks with clustered connections}, Volume = {15}, @@ -19459,7 +19458,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {7}, Pages = {718-37}, Pmc = {PMC3030662}, - pubmed = {20692278}, + pmid = {20692278}, Pst = {ppublish}, Title = {Imaging retinotopic maps in the human brain}, Volume = {51}, @@ -19478,7 +19477,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {May}, Number = {9}, Pages = {R318-21}, - pubmed = {10419335}, + pmid = {10419335}, Pst = {ppublish}, Title = {Visual attention: spotlight on the primary visual cortex}, Volume = {9}, @@ -19498,7 +19497,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {3}, Pages = {393-401}, Pmc = {PMC3427398}, - pubmed = {22884323}, + pmid = {22884323}, Pst = {ppublish}, Title = {Plasticity and stability of the visual system in human achiasma}, Volume = {75}, @@ -19521,7 +19520,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {3}, Pages = {567-80}, Pmc = {PMC3291715}, - pubmed = {22325207}, + pmid = {22325207}, Pst = {ppublish}, Title = {Gamma oscillations are generated locally in an attention-related midbrain network}, Volume = {73}, @@ -19540,7 +19539,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Oct}, Number = {5796}, Pages = {64-5}, - pubmed = {17023638}, + pmid = {17023638}, Pst = {ppublish}, Title = {Cell signaling. The double life of a transcription factor takes it outside the nucleus}, Volume = {314}, @@ -19561,7 +19560,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {3}, Pages = {591-606}, Pmc = {PMC1750862}, - pubmed = {17081980}, + pmid = {17081980}, Pst = {ppublish}, Title = {The C terminus of the L-type voltage-gated calcium channel Ca(V)1.2 encodes a transcription factor}, Volume = {127}, @@ -19583,7 +19582,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Apr}, Number = {6679}, Pages = {933-6}, - pubmed = {9582075}, + pmid = {9582075}, Pst = {ppublish}, Title = {Calcium oscillations increase the efficiency and specificity of gene expression}, Volume = {392}, @@ -19603,7 +19602,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Mesh = {Calcium; Calcium Signaling; Cerebral Cortex; Fluorescent Dyes; Fura-2; Microscopy, Fluorescence; Neurons}, Number = {23}, Pmc = {PMC2763293}, - pubmed = {19229178}, + pmid = {19229178}, Pst = {epublish}, Title = {Calcium imaging of cortical neurons using Fura-2 AM}, Year = {2009}, @@ -19623,7 +19622,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {5}, Pages = {617-22}, Pmc = {PMC2993759}, - pubmed = {20850295}, + pmid = {20850295}, Pst = {ppublish}, Title = {Using light to control signaling cascades in live neurons}, Volume = {20}, @@ -19643,7 +19642,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Number = {7419}, Pages = {219-25}, Pmc = {PMC3962269}, - pubmed = {23060192}, + pmid = {23060192}, Pst = {ppublish}, Title = {Retinal waves coordinate patterned activity throughout the developing visual system}, Volume = {490}, @@ -19664,7 +19663,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {Apr}, Number = {4}, Pages = {951-61}, - pubmed = {16772313}, + pmid = {16772313}, Pst = {ppublish}, Title = {Functional and anatomical cortical underconnectivity in autism: evidence from an FMRI study of an executive function task and corpus callosum morphometry}, Volume = {17}, @@ -19685,7 +19684,7 @@ CONCLUSIONS: We conclude that important aspects of adult visuotopy are establish Month = {May}, Number = {9419}, Pages = {1451-60}, - pubmed = {15121410}, + pmid = {15121410}, Pst = {ppublish}, Title = {Developmental dyslexia}, Volume = {363}, @@ -19711,7 +19710,7 @@ CONCLUSIONS: Evidence is found of a reduced size of the corpus callosum in autis Month = {Aug}, Number = {8}, Pages = {794-801}, - pubmed = {7639631}, + pmid = {7639631}, Pst = {ppublish}, Title = {Reduced size of corpus callosum in autism}, Volume = {52}, @@ -19730,7 +19729,7 @@ CONCLUSIONS: Evidence is found of a reduced size of the corpus callosum in autis Month = {Aug}, Number = {Pt 8}, Pages = {1839-49}, - pubmed = {12135974}, + pmid = {12135974}, Pst = {ppublish}, Title = {Autism, Asperger syndrome and brain mechanisms for the attribution of mental states to animated shapes}, Volume = {125}, @@ -19748,7 +19747,7 @@ CONCLUSIONS: Evidence is found of a reduced size of the corpus callosum in autis Month = {Feb}, Number = {4}, Pages = {899-915}, - pubmed = {19011893}, + pmid = {19011893}, Pst = {ppublish}, Title = {A potential reservoir of immature dopaminergic replacement neurons in the adult mammalian olfactory bulb}, Volume = {457}, @@ -19767,7 +19766,7 @@ CONCLUSIONS: Evidence is found of a reduced size of the corpus callosum in autis Month = {Aug}, Number = {3}, Pages = {479-89}, - pubmed = {22884331}, + pmid = {22884331}, Pst = {ppublish}, Title = {Activity-induced long-term potentiation of excitatory synapses in developing zebrafish retina in vivo}, Volume = {75}, @@ -19788,7 +19787,7 @@ CONCLUSIONS: Evidence is found of a reduced size of the corpus callosum in autis Month = {Mar}, Number = {12}, Pages = {4049-64}, - pubmed = {22442071}, + pmid = {22442071}, Pst = {ppublish}, Title = {The mechanism of orientation selectivity in primary visual cortex without a functional map}, Volume = {32}, @@ -19809,7 +19808,7 @@ CONCLUSIONS: Evidence is found of a reduced size of the corpus callosum in autis Number = {15}, Pages = {5264-71}, Pmc = {PMC3342701}, - pubmed = {22496572}, + pmid = {22496572}, Pst = {ppublish}, Title = {Alignment of multimodal sensory input in the superior colliculus through a gradient-matching mechanism}, Volume = {32}, @@ -19828,7 +19827,7 @@ CONCLUSIONS: Evidence is found of a reduced size of the corpus callosum in autis Number = {8}, Pages = {e43157}, Pmc = {PMC3422228}, - pubmed = {22912815}, + pmid = {22912815}, Pst = {ppublish}, Title = {Impacts of Brain Serotonin Deficiency following Tph2 Inactivation on Development and Raphe Neuron Serotonergic Specification}, Volume = {7}, @@ -19847,7 +19846,7 @@ CONCLUSIONS: Evidence is found of a reduced size of the corpus callosum in autis Number = {8}, Pages = {e43030}, Pmc = {PMC3420863}, - pubmed = {22916201}, + pmid = {22916201}, Pst = {ppublish}, Title = {Altered serotonin, dopamine and norepinepherine levels in 15q duplication and angelman syndrome mouse models}, Volume = {7}, @@ -19868,7 +19867,7 @@ CONCLUSION/SIGNIFICANCE: An upregulation of pyramidal neurons and a downregulati Number = {8}, Pages = {e41986}, Pmc = {PMC3424151}, - pubmed = {22927919}, + pmid = {22927919}, Pst = {ppublish}, Title = {The functional upregulation of piriform cortex is associated with cross-modal plasticity in loss of whisker tactile inputs}, Volume = {7}, @@ -19888,7 +19887,7 @@ CONCLUSION/SIGNIFICANCE: An upregulation of pyramidal neurons and a downregulati Number = {8}, Pages = {e1002653}, Pmc = {PMC3426566}, - pubmed = {22927808}, + pmid = {22927808}, Pst = {ppublish}, Title = {Model-free reconstruction of excitatory neuronal connectivity from calcium imaging signals}, Volume = {8}, @@ -19907,7 +19906,7 @@ CONCLUSION/SIGNIFICANCE: An upregulation of pyramidal neurons and a downregulati Number = {8}, Pages = {e42618}, Pmc = {PMC3422225}, - pubmed = {22912714}, + pmid = {22912714}, Pst = {ppublish}, Title = {The neuromagnetic dynamics of time perception}, Volume = {7}, @@ -19928,7 +19927,7 @@ CONCLUSION/SIGNIFICANCE: An upregulation of pyramidal neurons and a downregulati Number = {7400}, Pages = {646-50}, Pmc = {PMC3367801}, - pubmed = {22660328}, + pmid = {22660328}, Pst = {epublish}, Title = {Recurrent network activity drives striatal synaptogenesis}, Volume = {485}, @@ -19947,7 +19946,7 @@ CONCLUSION/SIGNIFICANCE: An upregulation of pyramidal neurons and a downregulati Month = {Jun}, Number = {2}, Pages = {237-94}, - pubmed = {5318481}, + pmid = {5318481}, Pst = {ppublish}, Title = {Disconnexion syndromes in animals and man. I}, Volume = {88}, @@ -19966,7 +19965,7 @@ CONCLUSION/SIGNIFICANCE: An upregulation of pyramidal neurons and a downregulati Month = {Sep}, Number = {6}, Pages = {889-901}, - pubmed = {11580891}, + pmid = {11580891}, Pst = {ppublish}, Title = {The cortical motor system}, Volume = {31}, @@ -19984,7 +19983,7 @@ CONCLUSION/SIGNIFICANCE: An upregulation of pyramidal neurons and a downregulati Keywords = {mirror neuron; mirror symmetry; Social Behavior; monkey; connectivity; Cognitive neuroscience; autism; Autistic Disorder; Attention; sensory-motor; multimodal; review; Neurophysiology; extracellular}, Mesh = {Animals; Dogs; Haplorhini; Humans; Imitative Behavior; Learning; Motor Cortex; Nerve Net; Neurons; Psychomotor Performance; Social Behavior; Verbal Behavior}, Pages = {169-92}, - pubmed = {15217330}, + pmid = {15217330}, Pst = {ppublish}, Title = {The mirror-neuron system}, Volume = {27}, @@ -20003,7 +20002,7 @@ CONCLUSION/SIGNIFICANCE: An upregulation of pyramidal neurons and a downregulati Month = {Dec}, Number = {2-3}, Pages = {143-56}, - pubmed = {9468349}, + pmid = {9468349}, Pst = {ppublish}, Title = {The dysplastic net hypothesis: an integration of developmental and dysconnectivity theories of schizophrenia}, Volume = {28}, @@ -20023,7 +20022,7 @@ CONCLUSION/SIGNIFICANCE: An upregulation of pyramidal neurons and a downregulati Month = {Dec}, Number = {12}, Pages = {942-51}, - pubmed = {17115076}, + pmid = {17115076}, Pst = {ppublish}, Title = {The mirror neuron system and the consequences of its dysfunction}, Volume = {7}, @@ -20043,7 +20042,7 @@ CONCLUSION/SIGNIFICANCE: An upregulation of pyramidal neurons and a downregulati Month = {Apr}, Number = {2}, Pages = {73-90}, - pubmed = {19360654}, + pmid = {19360654}, Pst = {ppublish}, Title = {Self-other relations in social development and autism: multiple roles for mirror neurons and other brain bases}, Volume = {1}, @@ -20067,7 +20066,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {3}, Pages = {270-3}, Pmc = {PMC2001237}, - pubmed = {17336944}, + pmid = {17336944}, Pst = {ppublish}, Title = {Resting state cortical connectivity reflected in EEG coherence in individuals with autism}, Volume = {62}, @@ -20085,7 +20084,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Oct}, Number = {1}, Pages = {19-24}, - pubmed = {11086979}, + pmid = {11086979}, Pst = {ppublish}, Title = {Identifying autism susceptibility genes}, Volume = {28}, @@ -20104,7 +20103,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Oct}, Number = {10}, Pages = {1325-6}, - pubmed = {15489156}, + pmid = {15489156}, Pst = {ppublish}, Title = {The genetics of autism}, Volume = {11}, @@ -20122,7 +20121,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Nov}, Number = {1165}, Pages = {1-340}, - pubmed = {22462104}, + pmid = {22462104}, Pst = {ppublish}, Title = {The structure of the nervous system of the nematode Caenorhabditis elegans}, Volume = {314}, @@ -20141,7 +20140,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Dec}, Number = {6}, Pages = {969-79}, - pubmed = {11754830}, + pmid = {11754830}, Pst = {ppublish}, Title = {Mind blindness and the brain in autism}, Volume = {32}, @@ -20160,7 +20159,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Jun}, Number = {6}, Pages = {970-4}, - pubmed = {22726828}, + pmid = {22726828}, Pst = {ppublish}, Title = {The brain activity map project and the challenge of functional connectomics}, Volume = {74}, @@ -20180,7 +20179,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Apr}, Number = {2}, Pages = {100-12}, - pubmed = {22505666}, + pmid = {22505666}, Pst = {ppublish}, Title = {Neural circuit development in the mammalian cochlea}, Volume = {27}, @@ -20201,7 +20200,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {10}, Pages = {4028-32}, Pmc = {PMC2268790}, - pubmed = {18322013}, + pmid = {18322013}, Pst = {ppublish}, Title = {The maturing architecture of the brain's default network}, Volume = {105}, @@ -20222,7 +20221,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Dec}, Number = {49}, Pages = {13028-37}, - pubmed = {19052194}, + pmid = {19052194}, Pst = {ppublish}, Title = {mGluR5 regulates glutamate-dependent development of the mouse somatosensory cortex}, Volume = {28}, @@ -20242,7 +20241,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {16}, Pages = {6965-78}, Pmc = {PMC2413141}, - pubmed = {10436053}, + pmid = {10436053}, Pst = {ppublish}, Title = {The critical period for ocular dominance plasticity in the Ferret's visual cortex}, Volume = {19}, @@ -20261,7 +20260,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Aug}, Number = {3}, Pages = {327-42}, - pubmed = {8873864}, + pmid = {8873864}, Pst = {ppublish}, Title = {Development of connections within and between areas V1 and V2 of macaque monkeys}, Volume = {372}, @@ -20282,7 +20281,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {7}, Pages = {3088-93}, Pmc = {PMC20326}, - pubmed = {9096350}, + pmid = {9096350}, Pst = {ppublish}, Title = {rax, a novel paired-type homeobox gene, shows expression in the anterior neural fold and developing retina}, Volume = {94}, @@ -20302,7 +20301,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Aug}, Number = {8}, Pages = {361-3}, - pubmed = {16850473}, + pmid = {16850473}, Pst = {ppublish}, Title = {Rx-Cre, a tool for inactivation of gene expression in the developing retina}, Volume = {44}, @@ -20320,7 +20319,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Jun}, Number = {3}, Pages = {250-68}, - pubmed = {5655873}, + pmid = {5655873}, Pst = {ppublish}, Title = {An electron microscopic study of synapse formation, receptor outer segment development, and other aspects of developing mouse retina}, Volume = {7}, @@ -20338,7 +20337,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Apr}, Number = {5138}, Pages = {281-2}, - pubmed = {4869714}, + pmid = {4869714}, Pst = {ppublish}, Title = {Centripetal sequence of appearance of receptor-bipolar synaptic structures in developing mouse retina}, Volume = {218}, @@ -20357,7 +20356,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Mar}, Number = {2}, Pages = {147-66}, - pubmed = {1112924}, + pmid = {1112924}, Pst = {ppublish}, Title = {The development of synapses in the visual system of the cat}, Volume = {160}, @@ -20377,7 +20376,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Nov}, Number = {3-4}, Pages = {353-69}, - pubmed = {729659}, + pmid = {729659}, Pst = {ppublish}, Title = {Synaptic development in the rabbit superior colliculus and visual cortex}, Volume = {33}, @@ -20396,7 +20395,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Aug}, Number = {4}, Pages = {697-712}, - pubmed = {6619907}, + pmid = {6619907}, Pst = {ppublish}, Title = {The formation and maturation of synapses in the visual cortex of the rat. II. Quantitative analysis}, Volume = {12}, @@ -20415,7 +20414,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Dec}, Number = {12}, Pages = {5251-62}, - pubmed = {8254372}, + pmid = {8254372}, Pst = {ppublish}, Title = {Development of orientation selectivity in ferret visual cortex and effects of deprivation}, Volume = {13}, @@ -20433,7 +20432,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Nov}, Number = {22}, Pages = {7253-69}, - pubmed = {8929433}, + pmid = {8929433}, Pst = {ppublish}, Title = {The role of activity in the development of long-range horizontal connections in area 17 of the ferret}, Volume = {16}, @@ -20452,7 +20451,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Dec}, Number = {6198}, Pages = {468-71}, - pubmed = {2461517}, + pmid = {2461517}, Pst = {ppublish}, Title = {Modification of retinal ganglion cell axon morphology by prenatal infusion of tetrodotoxin}, Volume = {336}, @@ -20471,7 +20470,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Oct}, Number = {4875}, Pages = {87-9}, - pubmed = {3175636}, + pmid = {3175636}, Pst = {ppublish}, Title = {Prenatal tetrodotoxin infusion blocks segregation of retinogeniculate afferents}, Volume = {242}, @@ -20489,7 +20488,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Apr}, Number = {7}, Pages = {2851-60}, - pubmed = {12684472}, + pmid = {12684472}, Pst = {ppublish}, Title = {Developmental loss of synchronous spontaneous activity in the mouse retina is independent of visual experience}, Volume = {23}, @@ -20509,7 +20508,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Sep}, Number = {7}, Pages = {901-12}, - pubmed = {19196491}, + pmid = {19196491}, Pst = {ppublish}, Title = {How does non-random spontaneous activity contribute to brain development?}, Volume = {22}, @@ -20530,7 +20529,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {6}, Pages = {851-8}, Pmc = {PMC2553397}, - pubmed = {18579076}, + pmid = {18579076}, Pst = {ppublish}, Title = {A precisely timed asynchronous pattern of ON and OFF retinal ganglion cell activity during propagation of retinal waves}, Volume = {58}, @@ -20550,7 +20549,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Apr}, Number = {2}, Pages = {247-59}, - pubmed = {16630836}, + pmid = {16630836}, Pst = {ppublish}, Title = {Failure to maintain eye-specific segregation in nob, a mutant with abnormally patterned retinal activity}, Volume = {50}, @@ -20570,7 +20569,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Mesh = {Age Factors; Aging; Animals; Animals, Newborn; Autoradiography; Bicyclo Compounds, Heterocyclic; Binding Sites; Brain; Brain Chemistry; Bungarotoxins; Embryo, Mammalian; Female; Iodine Isotopes; Male; Nicotinic Agonists; Pyridines; Rats; Rats, Sprague-Dawley; Rats, Wistar; Receptors, Nicotinic; Tissue Distribution; Tritium}, Number = {2}, Pages = {405-20}, - pubmed = {14980390}, + pmid = {14980390}, Pst = {ppublish}, Title = {Comparative distribution of nicotinic receptor subtypes during development, adulthood and aging: an autoradiographic study in the rat brain}, Volume = {124}, @@ -20589,7 +20588,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Aug}, Number = {2}, Pages = {163-74}, - pubmed = {1394965}, + pmid = {1394965}, Pst = {ppublish}, Title = {Pre- and postnatal development of high-affinity [3H]nicotine binding sites in rat brain regions: an autoradiographic study}, Volume = {68}, @@ -20608,7 +20607,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Dec}, Number = {4}, Pages = {524-34}, - pubmed = {12436417}, + pmid = {12436417}, Pst = {ppublish}, Title = {Nicotinic receptor signaling in nonexcitable cells}, Volume = {53}, @@ -20628,7 +20627,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {22}, Pages = {10593-7}, Pmc = {PMC50387}, - pubmed = {1359542}, + pmid = {1359542}, Pst = {ppublish}, Title = {N-methyl-D-aspartate receptor antagonists disrupt the formation of a mammalian neural map}, Volume = {89}, @@ -20648,7 +20647,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {21}, Pages = {9419-29}, Pmc = {PMC2662346}, - pubmed = {12417667}, + pmid = {12417667}, Pst = {ppublish}, Title = {Decoupling eye-specific segregation from lamination in the lateral geniculate nucleus}, Volume = {22}, @@ -20667,7 +20666,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Jun}, Number = {5}, Pages = {1102-15}, - pubmed = {12065623}, + pmid = {12065623}, Pst = {ppublish}, Title = {Characterization of [(125) I]epibatidine binding and nicotinic agonist-mediated (86) Rb(+) efflux in interpeduncular nucleus and inferior colliculus of beta2 null mutant mice}, Volume = {81}, @@ -20686,7 +20685,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Jun}, Number = {3}, Pages = {1383-96}, - pubmed = {8667201}, + pmid = {8667201}, Pst = {ppublish}, Title = {Nicotinic agonists differ in activation and desensitization of 86Rb+ efflux from mouse thalamic synaptosomes}, Volume = {277}, @@ -20706,7 +20705,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Jul}, Number = {13}, Pages = {5259-64}, - pubmed = {12097474}, + pmid = {12097474}, Pst = {ppublish}, Title = {Retinogeniculate axons undergo eye-specific segregation in the absence of eye-specific layers}, Volume = {22}, @@ -20728,7 +20727,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {8}, Pages = {1022-7}, Pmc = {PMC1352169}, - pubmed = {16025107}, + pmid = {16025107}, Pst = {ppublish}, Title = {Ephrin-As and neural activity are required for eye-specific patterning during retinogeniculate mapping}, Volume = {8}, @@ -20748,7 +20747,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {12}, Pages = {e15211}, Pmc = {PMC2999540}, - pubmed = {21170332}, + pmid = {21170332}, Pst = {epublish}, Title = {Mouse embryonic retina delivers information controlling cortical neurogenesis}, Volume = {5}, @@ -20767,7 +20766,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {May}, Number = {4}, Pages = {691-705}, - pubmed = {22632727}, + pmid = {22632727}, Pst = {ppublish}, Title = {Microglia sculpt postnatal neural circuits in an activity and complement-dependent manner}, Volume = {74}, @@ -20787,7 +20786,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Oct}, Number = {6053}, Pages = {226-9}, - pubmed = {21998388}, + pmid = {21998388}, Pst = {ppublish}, Title = {Early γ oscillations synchronize developing thalamus and cortex}, Volume = {334}, @@ -20809,7 +20808,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {15}, Pages = {8057-62}, Pmc = {PMC38874}, - pubmed = {8755602}, + pmid = {8755602}, Pst = {ppublish}, Title = {Starburst amacrine cells change from spiking to nonspiking neurons during retinal development}, Volume = {93}, @@ -20829,7 +20828,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Sep}, Number = {6}, Pages = {787-99}, - pubmed = {16982423}, + pmid = {16982423}, Pst = {ppublish}, Title = {The synaptic mechanism of direction selectivity in distal processes of starburst amacrine cells}, Volume = {51}, @@ -20850,7 +20849,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {Pt 2}, Pages = {533-49}, Pmc = {PMC1665265}, - pubmed = {15308679}, + pmid = {15308679}, Pst = {ppublish}, Title = {Stage-dependent dynamics and modulation of spontaneous waves in the developing rabbit retina}, Volume = {560}, @@ -20872,7 +20871,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Keywords = {review; optical imaging; optical physiology; Stimulation; Gene Expression}, Pages = {43}, Pmc = {PMC3219918}, - pubmed = {22121343}, + pmid = {22121343}, Pst = {ppublish}, Title = {Visualization and manipulation of neural activity in the developing vertebrate nervous system}, Volume = {4}, @@ -20893,7 +20892,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {9}, Pages = {1050-2}, Pmc = {PMC2928883}, - pubmed = {20676105}, + pmid = {20676105}, Pst = {ppublish}, Title = {Calcium action potentials in hair cells pattern auditory neuron activity before hearing onset}, Volume = {13}, @@ -20913,7 +20912,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Jul}, Number = {1}, Pages = {23-34}, - pubmed = {7619527}, + pmid = {7619527}, Pst = {ppublish}, Title = {Emergence of functional circuits in ferret visual cortex visualized by optical imaging}, Volume = {15}, @@ -20932,7 +20931,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Jul}, Number = {5169}, Pages = {255-8}, - pubmed = {7912852}, + pmid = {7912852}, Pst = {ppublish}, Title = {Rearrangements of synaptic connections in visual cortex revealed by laser photostimulation}, Volume = {265}, @@ -20952,7 +20951,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {3}, Pages = {745-9}, Pmc = {PMC50890}, - pubmed = {1704130}, + pmid = {1704130}, Pst = {ppublish}, Title = {Effects of binocular deprivation on the development of clustered horizontal connections in cat striate cortex}, Volume = {88}, @@ -20971,7 +20970,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Feb}, Number = {1}, Pages = {93-99}, - pubmed = {8453297}, + pmid = {8453297}, Pst = {ppublish}, Title = {Coordinate activity in retinal and cortical development}, Volume = {3}, @@ -20990,7 +20989,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Sep}, Number = {3}, Pages = {541-52}, - pubmed = {7546734}, + pmid = {7546734}, Pst = {ppublish}, Title = {Patterns of excitation and inhibition evoked by horizontal connections in visual cortex share a common relationship to orientation columns}, Volume = {15}, @@ -21009,7 +21008,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Feb}, Number = {4}, Pages = {1419-27}, - pubmed = {9454851}, + pmid = {9454851}, Pst = {ppublish}, Title = {Coordination of neuronal activity in developing visual cortex by gap junction-mediated biochemical communication}, Volume = {18}, @@ -21027,7 +21026,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Mesh = {Animals; Biotin; Calcium; Cell Communication; Coloring Agents; Ferrets; Gap Junctions; Patch-Clamp Techniques; Second Messenger Systems; Synapses; Synaptic Transmission; Visual Cortex}, Number = {1}, Pages = {59-64}, - pubmed = {9600391}, + pmid = {9600391}, Pst = {ppublish}, Title = {Relationship between dye coupling and spontaneous activity in developing ferret visual cortex}, Volume = {20}, @@ -21047,7 +21046,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Mar}, Number = {3}, Pages = {363-71}, - pubmed = {16462736}, + pmid = {16462736}, Pst = {ppublish}, Title = {A transient network of intrinsically bursting starburst cells underlies the generation of retinal waves}, Volume = {9}, @@ -21067,7 +21066,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {9}, Pages = {3131-41}, Pmc = {PMC3315707}, - pubmed = {22378886}, + pmid = {22378886}, Pst = {ppublish}, Title = {A Cre-dependent GCaMP3 reporter mouse for neuronal imaging in vivo}, Volume = {32}, @@ -21086,7 +21085,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Aug}, Number = {4}, Pages = {405-10}, - pubmed = {12139988}, + pmid = {12139988}, Pst = {ppublish}, Title = {Direction selectivity in the retina}, Volume = {12}, @@ -21106,7 +21105,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Jan}, Number = {7330}, Pages = {402-6}, - pubmed = {21131947}, + pmid = {21131947}, Pst = {ppublish}, Title = {Development of asymmetric inhibition underlying direction selectivity in the retina}, Volume = {469}, @@ -21124,7 +21123,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Dec}, Number = {2}, Pages = {85-100}, - pubmed = {4786750}, + pmid = {4786750}, Pst = {ppublish}, Title = {Self-organization of orientation sensitive cells in the striate cortex}, Volume = {14}, @@ -21143,7 +21142,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Feb}, Number = {1}, Pages = {50-8}, - pubmed = {11179872}, + pmid = {11179872}, Pst = {ppublish}, Title = {Patterning the mammalian cerebral cortex}, Volume = {11}, @@ -21163,7 +21162,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Jul}, Number = {28}, Pages = {6550-60}, - pubmed = {16014716}, + pmid = {16014716}, Pst = {ppublish}, Title = {Fibroblast growth factor 8 regulates neocortical guidance of area-specific thalamic innervation}, Volume = {25}, @@ -21183,7 +21182,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Jul}, Number = {13}, Pages = {2203-6}, - pubmed = {18539920}, + pmid = {18539920}, Pst = {ppublish}, Title = {Turning neurons into a nervous system}, Volume = {135}, @@ -21204,7 +21203,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {20}, Pages = {3439-48}, Pmc = {PMC2947756}, - pubmed = {20843859}, + pmid = {20843859}, Pst = {ppublish}, Title = {FGF8 acts as a classic diffusible morphogen to pattern the neocortex}, Volume = {137}, @@ -21224,7 +21223,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Oct}, Number = {43}, Pages = {11595-603}, - pubmed = {17959802}, + pmid = {17959802}, Pst = {ppublish}, Title = {Patterning the dorsal telencephalon: a role for sonic hedgehog?}, Volume = {27}, @@ -21244,7 +21243,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Feb}, Number = {1}, Pages = {25-34}, - pubmed = {16426837}, + pmid = {16426837}, Pst = {ppublish}, Title = {Area and layer patterning in the developing cerebral cortex}, Volume = {16}, @@ -21262,7 +21261,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Keywords = {neocortex; review literature; patterning; topographic map; Somatosensory Cortex; Visual Cortex; genes; development}, Mesh = {Animals; Body Patterning; Cerebral Cortex; DNA-Binding Proteins; Fibroblast Growth Factor 8; Fibroblast Growth Factors; Gene Expression Regulation, Developmental; Mice; Mice, Transgenic; Models, Neurological; Proto-Oncogene Proteins; Signal Transduction; Species Specificity; Thalamus; Transcription Factors; Wnt Proteins; Zebrafish Proteins}, Pages = {355-80}, - pubmed = {14527269}, + pmid = {14527269}, Pst = {ppublish}, Title = {Generating the cerebral cortical area map}, Volume = {26}, @@ -21281,7 +21280,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Jan}, Number = {3}, Pages = {850-63}, - pubmed = {22262883}, + pmid = {22262883}, Pst = {ppublish}, Title = {Cellular mechanisms underlying spatiotemporal features of cholinergic retinal waves}, Volume = {32}, @@ -21302,7 +21301,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {52}, Pages = {20994-9}, Pmc = {PMC2605417}, - pubmed = {19095802}, + pmid = {19095802}, Pst = {ppublish}, Title = {Neurogenesis and widespread forebrain migration of distinct GABAergic neurons from the postnatal subventricular zone}, Volume = {105}, @@ -21324,7 +21323,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {46}, Pages = {14484-95}, Pmc = {PMC2830901}, - pubmed = {19923282}, + pmid = {19923282}, Pst = {ppublish}, Title = {Adult-born hippocampal neurons are more numerous, faster maturing, and more involved in behavior in rats than in mice}, Volume = {29}, @@ -21344,7 +21343,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Feb}, Number = {3}, Pages = {253-8}, - pubmed = {22264606}, + pmid = {22264606}, Pst = {ppublish}, Title = {Peripheral and central inputs shape network dynamics in the developing visual cortex in vivo}, Volume = {22}, @@ -21367,7 +21366,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Dec}, Number = {6}, Pages = {612-27}, - pubmed = {18371403}, + pmid = {18371403}, Pst = {ppublish}, Title = {Everything that glitters isn't gold: a critical review of postnatal neural precursor analyses}, Volume = {1}, @@ -21386,7 +21385,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Jan}, Number = {1}, Pages = {55-64}, - pubmed = {9974159}, + pmid = {9974159}, Pst = {ppublish}, Title = {Maturation of visual receptive field properties in the rat superior colliculus}, Volume = {112}, @@ -21405,7 +21404,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Nov}, Number = {11}, Pages = {2989-3009}, - pubmed = {4056863}, + pmid = {4056863}, Pst = {ppublish}, Title = {Correlations between the structural and functional characteristics of neurons in the superficial laminae and the hamster's superior colliculus}, Volume = {5}, @@ -21423,7 +21422,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Dec}, Number = {6}, Pages = {938-50}, - pubmed = {22196330}, + pmid = {22196330}, Pst = {ppublish}, Title = {A cre-dependent, anterograde transsynaptic viral tracer for mapping output pathways of genetically marked neurons}, Volume = {72}, @@ -21442,7 +21441,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Dec}, Number = {6}, Pages = {1012-24}, - pubmed = {22196336}, + pmid = {22196336}, Pst = {ppublish}, Title = {Activity-dependent clustering of functional synaptic inputs on developing hippocampal dendrites}, Volume = {72}, @@ -21462,7 +21461,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {6}, Pages = {1040-54}, Pmc = {PMC3248795}, - pubmed = {22196338}, + pmid = {22196338}, Pst = {ppublish}, Title = {Functional specialization of seven mouse visual cortical areas}, Volume = {72}, @@ -21481,7 +21480,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Dec}, Number = {6}, Pages = {1025-39}, - pubmed = {22196337}, + pmid = {22196337}, Pst = {ppublish}, Title = {Functional specialization of mouse higher visual cortical areas}, Volume = {72}, @@ -21501,7 +21500,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Keywords = {synapses; microscopy; gene; technique; ideas; mouse; hippocampus; connectivity; connectome}, Number = {1}, Pages = {96-102}, - pubmed = {22138823}, + pmid = {22138823}, Pst = {epublish}, Title = {mGRASP enables mapping mammalian synaptic connectivity with light microscopy}, Volume = {9}, @@ -21520,7 +21519,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {1}, Pages = {90-5}, Pmc = {PMC3248630}, - pubmed = {22120467}, + pmid = {22120467}, Pst = {epublish}, Title = {Optical recording of action potentials in mammalian neurons using a microbial rhodopsin}, Volume = {9}, @@ -21542,7 +21541,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {1}, Pages = {22-7}, Pmc = {PMC3252919}, - pubmed = {22190489}, + pmid = {22190489}, Pst = {ppublish}, Title = {Characterization and adaptive optical correction of aberrations during in vivo imaging in the mouse cortex}, Volume = {109}, @@ -21561,7 +21560,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Jan}, Number = {2}, Pages = {692-702}, - pubmed = {22238105}, + pmid = {22238105}, Pst = {ppublish}, Title = {Subplate neurons promote spindle bursts and thalamocortical patterning in the neonatal rat somatosensory cortex}, Volume = {32}, @@ -21581,7 +21580,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {1}, Pages = {e1001236}, Pmc = {PMC3254648}, - pubmed = {22253571}, + pmid = {22253571}, Pst = {ppublish}, Title = {Functional Clustering Drives Encoding Improvement in a Developing Brain Network during Awake Visual Learning}, Volume = {10}, @@ -21600,7 +21599,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Jan}, Number = {1}, Pages = {331-43}, - pubmed = {22219294}, + pmid = {22219294}, Pst = {ppublish}, Title = {GABA Signaling Promotes Synapse Elimination and Axon Pruning in Developing Cortical Inhibitory Interneurons}, Volume = {32}, @@ -21620,7 +21619,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Feb}, Number = {1}, Pages = {160-8}, - pubmed = {21074988}, + pmid = {21074988}, Pst = {ppublish}, Title = {The maturation of cortical interneuron diversity: how multiple developmental journeys shape the emergence of proper network function}, Volume = {21}, @@ -21641,7 +21640,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {May}, Number = {5}, Pages = {225-36}, - pubmed = {21459463}, + pmid = {21459463}, Pst = {ppublish}, Title = {Dissecting functional connectivity of neuronal microcircuits: experimental and theoretical insights}, Volume = {34}, @@ -21663,7 +21662,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {4}, Pages = {695-709}, Pmc = {PMC3163067}, - pubmed = {21867885}, + pmid = {21867885}, Pst = {ppublish}, Title = {Pioneer GABA cells comprise a subpopulation of hub neurons in the developing hippocampus}, Volume = {71}, @@ -21685,7 +21684,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Mesh = {Animals; Cats; Electrophysiology; Geniculate Bodies; Neuronal Plasticity; Retina; Tetrodotoxin; Vision, Ocular; Visual Cortex; Visual Pathways}, Number = {6093}, Pages = {154-6}, - pubmed = {3785380}, + pmid = {3785380}, Pst = {ppublish}, Title = {Ocular dominance shift in kitten visual cortex caused by imbalance in retinal electrical activity}, Volume = {324}, @@ -21706,7 +21705,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Sep}, Number = {4}, Pages = {426-37}, - pubmed = {12900914}, + pmid = {12900914}, Pst = {ppublish}, Title = {Rearrangement of synaptic connections with inhibitory neurons in developing mouse visual cortex}, Volume = {464}, @@ -21728,7 +21727,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {5}, Pages = {1905-18}, Pmc = {PMC3040111}, - pubmed = {21289200}, + pmid = {21289200}, Pst = {ppublish}, Title = {Gateways of ventral and dorsal streams in mouse visual cortex}, Volume = {31}, @@ -21749,7 +21748,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {May}, Number = {3}, Pages = {339-57}, - pubmed = {17366604}, + pmid = {17366604}, Pst = {ppublish}, Title = {Area map of mouse visual cortex}, Volume = {502}, @@ -21770,7 +21769,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Jan}, Number = {2}, Pages = {268-76}, - pubmed = {16945423}, + pmid = {16945423}, Pst = {ppublish}, Title = {In vivo transcranial imaging of connections in mouse visual cortex}, Volume = {159}, @@ -21789,7 +21788,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Keywords = {retina; Retinal Ganglion Cells; Electroporation; Technique;}, Mesh = {Animals; Electroporation; Mice; Retinal Ganglion Cells; Transfection}, Number = {50}, - pubmed = {21525846}, + pmid = {21525846}, Pst = {epublish}, Title = {Transfection of mouse retinal ganglion cells by in vivo electroporation}, Year = {2011}, @@ -21808,7 +21807,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {2}, Pages = {298-307}, Pmc = {PMC3267873}, - pubmed = {22179110}, + pmid = {22179110}, Pst = {aheadofprint}, Title = {Visual map development depends on the temporal pattern of binocular activity in mice}, Volume = {15}, @@ -21867,7 +21866,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {7345}, Pages = {87-91}, Pmc = {PMC3089591}, - pubmed = {21478872}, + pmid = {21478872}, Pst = {ppublish}, Title = {Functional specificity of local synaptic connections in neocortical networks}, Volume = {473}, @@ -21887,7 +21886,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Oct}, Number = {7370}, Pages = {483-9}, - pubmed = {22031440}, + pmid = {22031440}, Pst = {epublish}, Title = {Spatio-temporal transcriptome of the human brain}, Volume = {478}, @@ -21908,7 +21907,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {1}, Pages = {72-8}, Pmc = {PMC1463890}, - pubmed = {15608630}, + pmid = {15608630}, Pst = {ppublish}, Title = {High frequency, synchronized bursting drives eye-specific segregation of retinogeniculate projections}, Volume = {8}, @@ -21929,7 +21928,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {May}, Number = {1-2}, Pages = {17-26}, - pubmed = {15020085}, + pmid = {15020085}, Pst = {ppublish}, Title = {Unbiased analysis of bulk axonal segregation patterns}, Volume = {135}, @@ -21950,7 +21949,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {4}, Pages = {420-2}, Pmc = {PMC3077927}, - pubmed = {21336273}, + pmid = {21336273}, Pst = {ppublish}, Title = {Ventral medial prefrontal cortex neuronal ensembles mediate context-induced relapse to heroin}, Volume = {14}, @@ -21972,7 +21971,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {8}, Pages = {1069-73}, Pmc = {PMC2752202}, - pubmed = {19620976}, + pmid = {19620976}, Pst = {ppublish}, Title = {Targeted disruption of cocaine-activated nucleus accumbens neurons prevents context-specific sensitization}, Volume = {12}, @@ -21993,7 +21992,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Apr}, Number = {15}, Pages = {5764-76}, - pubmed = {21490218}, + pmid = {21490218}, Pst = {ppublish}, Title = {The Down syndrome critical region regulates retinogeniculate refinement}, Volume = {31}, @@ -22011,7 +22010,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Keywords = {memory; Learning; epigenetic; Methylation; neuron; activity manipulation; plasticity; Adult Neurogenesis; mouse; Dentate Gyrus; hippocampus; Genomics}, Number = {10}, Pages = {1345-51}, - pubmed = {21874013}, + pmid = {21874013}, Pst = {epublish}, Title = {Neuronal activity modifies the DNA methylation landscape in the adult brain}, Volume = {14}, @@ -22030,7 +22029,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Aug}, Number = {2}, Pages = {293-306}, - pubmed = {9292720}, + pmid = {9292720}, Pst = {ppublish}, Title = {Dynamic processes shape spatiotemporal properties of retinal waves}, Volume = {19}, @@ -22050,7 +22049,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Sep}, Number = {18}, Pages = {2842-7}, - pubmed = {16647739}, + pmid = {16647739}, Pst = {ppublish}, Title = {Perception of visual motion coherence by rats and mice}, Volume = {46}, @@ -22071,7 +22070,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Nov}, Number = {45}, Pages = {11554-61}, - pubmed = {17093076}, + pmid = {17093076}, Pst = {ppublish}, Title = {Enhancement of vision by monocular deprivation in adult mice}, Volume = {26}, @@ -22092,7 +22091,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Dec}, Number = {28}, Pages = {3411-8}, - pubmed = {15536009}, + pmid = {15536009}, Pst = {ppublish}, Title = {Characterization of mouse cortical spatial vision}, Volume = {44}, @@ -22113,7 +22112,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Sep}, Number = {39}, Pages = {9817-27}, - pubmed = {18815266}, + pmid = {18815266}, Pst = {ppublish}, Title = {Experience-dependent plasticity from eye opening enables lasting, visual cortex-dependent enhancement of motion vision}, Volume = {28}, @@ -22132,7 +22131,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Keywords = {mouse; function; Behavior; visual system; Retina; visual cortex; plasticity; acuity; Sensory Deprivation; 21 Activity-development; Binocular; Monocular; bilateral; sensory map; topographic map}, Pages = {44}, Pmc = {PMC3118448}, - pubmed = {21720522}, + pmid = {21720522}, Pst = {ppublish}, Title = {Experience-induced interocular plasticity of vision in infancy}, Volume = {5}, @@ -22154,7 +22153,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {3}, Pages = {327-34}, Pmc = {PMC3140054}, - pubmed = {19447089}, + pmid = {19447089}, Pst = {ppublish}, Title = {Genetic identification of an On-Off direction-selective retinal ganglion cell subtype reveals a layer-specific subcortical map of posterior motion}, Volume = {62}, @@ -22175,7 +22174,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Feb}, Number = {1}, Pages = {73-80}, - pubmed = {17254766}, + pmid = {17254766}, Pst = {ppublish}, Title = {Mechanisms of eye-specific visual circuit development}, Volume = {17}, @@ -22195,7 +22194,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Sep}, Number = {9}, Pages = {464-73}, - pubmed = {21840069}, + pmid = {21840069}, Pst = {ppublish}, Title = {What can mice tell us about how vision works?}, Volume = {34}, @@ -22215,7 +22214,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Jul}, Number = {7}, Pages = {1674-94}, - pubmed = {21127018}, + pmid = {21127018}, Pst = {ppublish}, Title = {A role for intermediate radial glia in the tangential expansion of the mammalian cerebral cortex}, Volume = {21}, @@ -22235,7 +22234,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Dec}, Number = {2}, Pages = {249-68}, - pubmed = {6512020}, + pmid = {6512020}, Pst = {ppublish}, Title = {Callosal connections of the posterior neocortex in normal-eyed, congenitally anophthalmic, and neonatally enucleated mice}, Volume = {230}, @@ -22256,7 +22255,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {6}, Pages = {2083-7}, Pmc = {PMC51173}, - pubmed = {2006147}, + pmid = {2006147}, Pst = {ppublish}, Title = {A novel cytoarchitectonic area induced experimentally within the primate visual cortex}, Volume = {88}, @@ -22276,7 +22275,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Number = {14}, Pages = {5303-6}, Pmc = {PMC54311}, - pubmed = {2164675}, + pmid = {2164675}, Pst = {ppublish}, Title = {Hypercolumns in primate visual cortex can develop in the absence of cues from photoreceptors}, Volume = {87}, @@ -22295,7 +22294,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Sep}, Number = {1}, Pages = {137-41}, - pubmed = {1760867}, + pmid = {1760867}, Pst = {ppublish}, Title = {The effects of bilateral enucleation in the primate fetus on the parcellation of visual cortex}, Volume = {62}, @@ -22314,7 +22313,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Aug}, Number = {4}, Pages = {1039-46}, - pubmed = {6483189}, + pmid = {6483189}, Pst = {ppublish}, Title = {Binocular interaction in the fetal cat regulates the size of the ganglion cell population}, Volume = {12}, @@ -22332,7 +22331,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Nov}, Number = {4523}, Pages = {928-31}, - pubmed = {7302569}, + pmid = {7302569}, Pst = {ppublish}, Title = {Development of visual centers in the primate brain depends on binocular competition before birth}, Volume = {214}, @@ -22350,7 +22349,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Apr}, Number = {961}, Pages = {245-60}, - pubmed = {19781}, + pmid = {19781}, Pst = {ppublish}, Title = {Prenatal development of the visual system in rhesus monkey}, Volume = {278}, @@ -22369,7 +22368,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Nov}, Number = {1}, Pages = {23-52}, - pubmed = {409739}, + pmid = {409739}, Pst = {ppublish}, Title = {Genesis of the dorsal lateral geniculate nucleus in the rhesus monkey: site and time of origin, kinetics of proliferation, routes of migration and pattern of distribution of neurons}, Volume = {176}, @@ -22388,7 +22387,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Aug}, Number = {4407}, Pages = {698-700}, - pubmed = {462177}, + pmid = {462177}, Pst = {ppublish}, Title = {Development of the rat's uncrossed retinotectal pathway and its relation to plasticity studies}, Volume = {205}, @@ -22407,7 +22406,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Feb}, Number = {123}, Pages = {425-7}, - pubmed = {4203022}, + pmid = {4203022}, Pst = {ppublish}, Title = {Neurons in rhesus monkey visual cortex: systematic relation between time of origin and eventual disposition}, Volume = {183}, @@ -22427,7 +22426,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Mar}, Number = {3}, Pages = {997-1006}, - pubmed = {17307296}, + pmid = {17307296}, Pst = {ppublish}, Title = {Development of the spontaneous activity transients and ongoing cortical activity in human preterm babies}, Volume = {145}, @@ -22448,7 +22447,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Dec}, Number = {11}, Pages = {2799-804}, - pubmed = {16324114}, + pmid = {16324114}, Pst = {ppublish}, Title = {Slow endogenous activity transients and developmental expression of K+-Cl- cotransporter 2 in the immature human cortex}, Volume = {22}, @@ -22467,7 +22466,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Keywords = {retinal wave paper; retina; visual system; Spontaneous activity; 21 Activity-development; Structure-Activity Relationship; structural remodeling; sensory map; topographic map; development; review; currOpinRvw}, Mesh = {Animals; Electrophysiology; Embryo, Mammalian; Embryo, Nonmammalian; Embryonic and Fetal Development; Retina; Visual Pathways}, Pages = {29-47}, - pubmed = {10202531}, + pmid = {10202531}, Pst = {ppublish}, Title = {Retinal waves and visual system development}, Volume = {22}, @@ -22487,7 +22486,7 @@ CONCLUSIONS: Robust patterns of over- and under-connectivity are apparent at dis Month = {Sep}, Number = {3}, Pages = {183-206}, - pubmed = {2487102}, + pmid = {2487102}, Pst = {ppublish}, Title = {Centrifugal pathways to the retina: influence of the optic tectum}, Volume = {3}, @@ -22509,7 +22508,7 @@ CONCLUSIONS: Immunoreactive serotonin is present in a distinct population of ret Month = {Dec}, Number = {12}, Pages = {1089-95}, - pubmed = {16354622}, + pmid = {16354622}, Pst = {ppublish}, Title = {Serotonergic retinopetal axons in the monkey retina}, Volume = {30}, @@ -22532,7 +22531,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {2}, Pages = {487-95}, - pubmed = {9950609}, + pmid = {9950609}, Pst = {ppublish}, Title = {Histamine immunoreactive axons in the macaque retina}, Volume = {40}, @@ -22551,7 +22550,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {3}, Pages = {1707-26}, - pubmed = {16105954}, + pmid = {16105954}, Pst = {ppublish}, Title = {Commissural excitation and inhibition by the superior colliculus in tectoreticular neurons projecting to omnipause neuron and inhibitory burst neuron regions}, Volume = {94}, @@ -22572,7 +22571,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {1}, Pages = {119-37}, - pubmed = {8550874}, + pmid = {8550874}, Pst = {ppublish}, Title = {Two rules for callosal connectivity in striate cortex of the rat}, Volume = {361}, @@ -22593,7 +22592,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {2}, Pages = {161-76}, - pubmed = {8642068}, + pmid = {8642068}, Pst = {ppublish}, Title = {Overall pattern of callosal connections in visual cortex of normal and enucleated cats}, Volume = {363}, @@ -22614,7 +22613,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {1}, Pages = {138-51}, - pubmed = {8550875}, + pmid = {8550875}, Pst = {ppublish}, Title = {Effects of neonatal enucleation on the organization of callosal linkages in striate cortex of the rat}, Volume = {361}, @@ -22635,7 +22634,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {1}, Pages = {1-26}, - pubmed = {4044927}, + pmid = {4044927}, Pst = {ppublish}, Title = {Organization and postnatal development of callosal connections in the visual cortex of the rat}, Volume = {239}, @@ -22657,7 +22656,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {9}, Pages = {e241}, Pmc = {PMC1964777}, - pubmed = {17803360}, + pmid = {17803360}, Pst = {ppublish}, Title = {Ten_m3 regulates eye-specific patterning in the mammalian visual pathway and is required for binocular vision}, Volume = {5}, @@ -22677,7 +22676,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {1}, Pages = {53-66}, - pubmed = {17478416}, + pmid = {17478416}, Pst = {ppublish}, Title = {Differential gene expression between sensory neocortical areas: potential roles for Ten_m3 and Bcl6 in patterning visual and somatosensory pathways}, Volume = {18}, @@ -22698,7 +22697,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1528}, Pages = {2369-80}, Pmc = {PMC2865072}, - pubmed = {19620108}, + pmid = {19620108}, Pst = {ppublish}, Title = {Associative sequence learning: the role of experience in the development of imitation and the mirror system}, Volume = {364}, @@ -22717,7 +22716,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {13}, Pages = {5602-18}, - pubmed = {10377367}, + pmid = {10377367}, Pst = {ppublish}, Title = {Binocular neurons in V1 of awake monkeys are selective for absolute, not relative, disparity}, Volume = {19}, @@ -22737,7 +22736,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {2}, Pages = {e251}, Pmc = {PMC1804100}, - pubmed = {17330140}, + pmid = {17330140}, Pst = {epublish}, Title = {On the origin of the functional architecture of the cortex}, Volume = {2}, @@ -22756,7 +22755,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {3}, Pages = {419-24}, - pubmed = {456450}, + pmid = {456450}, Pst = {ppublish}, Title = {Collicular function in human vision}, Volume = {35}, @@ -22774,7 +22773,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {2}, Pages = {173-90}, - pubmed = {913514}, + pmid = {913514}, Pst = {ppublish}, Title = {Subcortical control of visual thresholds in humans: evidence for modality specific and retinotopically organized mechanisms of selective attention}, Volume = {29}, @@ -22791,7 +22790,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {Superior Colliculus; optic tectum; Retina; visual cortex; visual system; sensory map; topographic map; synapse formation; Structure-Activity Relationship; 21 Activity-development; structural remodeling; mirror symmetry; bilateral; human; monkey; blindsight; Sensory Deprivation}, Mesh = {Animals; Brain; Models, Neurological; Postoperative Period; Retina; Synaptic Transmission; Visual Cortex; Visual Pathways}, Pages = {379-97}, - pubmed = {11702556}, + pmid = {11702556}, Pst = {ppublish}, Title = {Visual pathways following cerebral hemispherectomy}, Volume = {134}, @@ -22807,7 +22806,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {Superior Colliculus; optic tectum; Retina; visual cortex; visual system; sensory map; topographic map; synapse formation; Structure-Activity Relationship; 21 Activity-development; structural remodeling; mirror symmetry; bilateral; human; monkey; blindsight; Sensory Deprivation}, Mesh = {Awareness; Brain; Hemianopsia; Humans; Magnetic Resonance Imaging; Postoperative Period; Psychophysics}, Pages = {367-78}, - pubmed = {11702555}, + pmid = {11702555}, Pst = {ppublish}, Title = {'Seeing' in the blind hemifield following hemispherectomy}, Volume = {134}, @@ -22825,7 +22824,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Animals; Depth Perception; Male; Mice; Psychology, Experimental}, Number = {2}, Pages = {232-3}, - pubmed = {5835839}, + pmid = {5835839}, Pst = {ppublish}, Title = {The visual cliff test for the study of visual depth perception in the mouse}, Volume = {13}, @@ -22845,7 +22844,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {8}, Pages = {1840-52}, - pubmed = {16262624}, + pmid = {16262624}, Pst = {ppublish}, Title = {Eph/ephrin expression in the adult rat visual system following localized retinal lesions: localized and transneuronal up-regulation in the retina and superior colliculus}, Volume = {22}, @@ -22864,7 +22863,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {1}, Pages = {296-307}, - pubmed = {8987756}, + pmid = {8987756}, Pst = {ppublish}, Title = {Postnatal development of binocular disparity sensitivity in neurons of the primate visual cortex}, Volume = {17}, @@ -22882,7 +22881,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Animals; Neurons; Opossums; Photic Stimulation; Superior Colliculi; Vision, Binocular; Vision, Monocular; Visual Cortex; Visual Perception}, Number = {3}, Pages = {546-52}, - pubmed = {1783025}, + pmid = {1783025}, Pst = {ppublish}, Title = {Disparity selective units in the superior colliculus of the opossum}, Volume = {87}, @@ -22903,7 +22902,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {2}, Pages = {561-71}, Pmc = {PMC2735235}, - pubmed = {19327388}, + pmid = {19327388}, Pst = {ppublish}, Title = {Anatomical origins of ocular dominance in mouse primary visual cortex}, Volume = {161}, @@ -22923,7 +22922,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {3}, Pages = {595-615}, Pmc = {PMC1309437}, - pubmed = {1133788}, + pmid = {1133788}, Pst = {ppublish}, Title = {Binocular interaction in the cat's superior colliculus}, Volume = {246}, @@ -22943,7 +22942,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {2}, Pages = {1495-502}, - pubmed = {17135475}, + pmid = {17135475}, Pst = {ppublish}, Title = {Visual FMRI responses in human superior colliculus show a temporal-nasal asymmetry that is absent in lateral geniculate and visual cortex}, Volume = {97}, @@ -22963,7 +22962,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {9}, Pages = {5572-4}, Pmc = {PMC350104}, - pubmed = {6933571}, + pmid = {6933571}, Pst = {ppublish}, Title = {Stereoacuity of human infants}, Volume = {77}, @@ -22984,7 +22983,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {2}, Pages = {246-56}, Pmc = {PMC2822731}, - pubmed = {20152130}, + pmid = {20152130}, Pst = {ppublish}, Title = {Critical period plasticity matches binocular orientation preference in the visual cortex}, Volume = {65}, @@ -23003,7 +23002,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {2}, Pages = {399-404}, - pubmed = {6165434}, + pmid = {6165434}, Pst = {ppublish}, Title = {Development of a transient retino-retinal pathway in hooded and albino rats}, Volume = {211}, @@ -23023,7 +23022,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {9}, Pages = {e302}, Pmc = {PMC1560174}, - pubmed = {16953662}, + pmid = {16953662}, Pst = {ppublish}, Title = {Neonatal imitation in rhesus macaques}, Volume = {4}, @@ -23040,7 +23039,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {Learning; Memory; multisensory integration; function; Behavior; human; Infant; Newborn; neonatal; visual system; 21 Activity-development}, Mesh = {Aging; Auditory Perception; Child Development; Child, Preschool; Cognition; Conditioning (Psychology); Facial Expression; Humans; Imitative Behavior; Infant; Infant, Newborn; Language Development; Memory; Models, Neurological; Mouth; Neurosciences; Phonetics; Speech Perception; Touch; Visual Perception}, Pages = {1-31; discussion 31-7}, - pubmed = {2075949}, + pmid = {2075949}, Pst = {ppublish}, Title = {Towards a developmental cognitive science. The implications of cross-modal matching and imitation for the development of representation and memory in infancy}, Volume = {608}, @@ -23057,7 +23056,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Proceedings of the National Academy of Sciences of the United States of America}, Keywords = {Vesicular stomatitis-Indiana virus; tracer; anterograde tracing; connectivity; connectome; Technique; ideas; Grants; Glycoproteins; Trans-synaptic; retrograde tracing; Genetic Engineering}, Month = {Aug}, - pubmed = {21825165}, + pmid = {21825165}, Pst = {aheadofprint}, Title = {Anterograde or retrograde transsynaptic labeling of CNS neurons with vesicular stomatitis virus vectors}, Year = {2011}, @@ -23073,7 +23072,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Proceedings of the National Academy of Sciences of the United States of America}, Keywords = {visual system; neurological disorder; Stroke; Hypoxia-Ischemia; Somatosensory Cortex; visual cortex; sensory map; topographic map; Sensory Deprivation; Binocular; Monocular; plasticity; Inflammation; Immune System}, Month = {Aug}, - pubmed = {21873250}, + pmid = {21873250}, Pst = {aheadofprint}, Title = {Global impairment and therapeutic restoration of visual plasticity mechanisms after a localized cortical stroke}, Year = {2011}, @@ -23089,7 +23088,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Proceedings of the National Academy of Sciences of the United States of America}, Keywords = {Sleep; oscillations; synchrony; neocortex; visual cortex; Stimulation; Auditory Cortex; Electroencephalography; function; human; fmri; Spontaneous activity}, Month = {Sep}, - pubmed = {21896732}, + pmid = {21896732}, Pst = {aheadofprint}, Title = {Interplay between spontaneous and induced brain activity during human non-rapid eye movement sleep}, Year = {2011}, @@ -23108,7 +23107,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jun}, Number = {3}, Pages = {383-412}, - pubmed = {7410600}, + pmid = {7410600}, Pst = {ppublish}, Title = {Origins of crossed and uncrossed retinal projections in pigmented and albino mice}, Volume = {191}, @@ -23129,7 +23128,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {17}, Pages = {9406-11}, Pmc = {PMC23203}, - pubmed = {9256495}, + pmid = {9256495}, Pst = {ppublish}, Title = {Pattern of neuronal activity associated with conscious and unconscious processing of visual signals}, Volume = {94}, @@ -23150,7 +23149,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {36}, Pages = {11149-52}, Pmc = {PMC2785715}, - pubmed = {19741121}, + pmid = {19741121}, Pst = {ppublish}, Title = {Does retinotopy influence cortical folding in primate visual cortex?}, Volume = {29}, @@ -23169,7 +23168,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {10}, Pages = {3900-17}, - pubmed = {10234021}, + pmid = {10234021}, Pst = {ppublish}, Title = {Genesis, neurotrophin responsiveness, and apoptosis of a pronounced direct connection between the two eyes of the chick embryo: a natural error or a meaningful developmental event?}, Volume = {19}, @@ -23189,7 +23188,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Nov}, Number = {5}, Pages = {2664-82}, - pubmed = {17728384}, + pmid = {17728384}, Pst = {ppublish}, Title = {Commissural mirror-symmetric excitation and reciprocal inhibition between the two superior colliculi and their roles in vertical and horizontal eye movements}, Volume = {98}, @@ -23209,7 +23208,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {6}, Pages = {3146-67}, - pubmed = {20926614}, + pmid = {20926614}, Pst = {ppublish}, Title = {Topographic organization of excitatory and inhibitory commissural connections in the superior colliculi and their functional roles in saccade generation}, Volume = {104}, @@ -23226,7 +23225,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Nature neuroscience}, Keywords = {Sensory Deprivation; Structure-Activity Relationship; structural remodeling; microRNAs; 21 Activity-development; visual cortex; visual system; topographic map; sensory map; Binocular; Monocular}, Month = {Sep}, - pubmed = {21892154}, + pmid = {21892154}, Pst = {aheadofprint}, Title = {Experience-dependent expression of miR-132 regulates ocular dominance plasticity}, Year = {2011}, @@ -23243,7 +23242,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Nature neuroscience}, Keywords = {Sensory Deprivation; Structure-Activity Relationship; structural remodeling; microRNAs; 21 Activity-development; visual cortex; visual system; topographic map; sensory map; Binocular; Monocular}, Month = {Sep}, - pubmed = {21892155}, + pmid = {21892155}, Pst = {aheadofprint}, Title = {miR-132, an experience-dependent microRNA, is essential for visual cortex plasticity}, Year = {2011}, @@ -23263,7 +23262,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {4}, Pages = {643-55}, - pubmed = {8833114}, + pmid = {8833114}, Pst = {ppublish}, Title = {Non-mirror-symmetric patterns of callosal linkages in areas 17 and 18 in cat visual cortex}, Volume = {366}, @@ -23284,7 +23283,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {2}, Pages = {156-72}, - pubmed = {12640667}, + pmid = {12640667}, Pst = {ppublish}, Title = {Retinal influences specify cortico-cortical maps by postnatal day six in rats and mice}, Volume = {459}, @@ -23304,7 +23303,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {23}, Pages = {R818-26}, - pubmed = {12477410}, + pmid = {12477410}, Pst = {ppublish}, Title = {The role of activity in development of the visual system}, Volume = {12}, @@ -23324,7 +23323,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {17}, Pages = {8277-81}, Pmc = {PMC47332}, - pubmed = {8367493}, + pmid = {8367493}, Pst = {ppublish}, Title = {A correlational model for the development of disparity selectivity in visual cortex that depends on prenatal and postnatal phases}, Volume = {90}, @@ -23342,7 +23341,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {33}, Pages = {11745-7}, - pubmed = {21849534}, + pmid = {21849534}, Pst = {ppublish}, Title = {Superior tactile abilities in the blind: is blindness required?}, Volume = {31}, @@ -23361,7 +23360,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {6}, Pages = {709-20}, - pubmed = {8160387}, + pmid = {8160387}, Pst = {ppublish}, Title = {Functional postnatal development of the rat primary visual cortex and the role of visual experience: dark rearing and monocular deprivation}, Volume = {34}, @@ -23381,7 +23380,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {4}, Pages = {495-512}, Pmc = {PMC2577613}, - pubmed = {16572463}, + pmid = {16572463}, Pst = {ppublish}, Title = {Development of callosal topography in visual cortex of normal and enucleated rats}, Volume = {496}, @@ -23400,7 +23399,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {2}, Pages = {113-4}, - pubmed = {12536211}, + pmid = {12536211}, Pst = {ppublish}, Title = {Capricious expression of cortical columns in the primate brain}, Volume = {6}, @@ -23420,7 +23419,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {19}, Pages = {5190-7}, - pubmed = {16687510}, + pmid = {16687510}, Pst = {ppublish}, Title = {Dynamics of spontaneous activity in the fetal macaque retina during development of retinogeniculate pathways}, Volume = {26}, @@ -23439,7 +23438,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {4}, Pages = {710-24}, - pubmed = {21867886}, + pmid = {21867886}, Pst = {ppublish}, Title = {A synaptic strategy for consolidation of convergent visuotopic maps}, Volume = {71}, @@ -23461,7 +23460,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {22}, Pages = {8025-36}, Pmc = {PMC3169172}, - pubmed = {21632924}, + pmid = {21632924}, Pst = {ppublish}, Title = {Visual experience-dependent maturation of correlated neuronal activity patterns in a developing visual system}, Volume = {31}, @@ -23481,7 +23480,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {1}, Pages = {187-202}, - pubmed = {6776164}, + pmid = {6776164}, Pst = {ppublish}, Title = {Retinotopic organization of striate and extrastriate visual cortex in the mouse}, Volume = {193}, @@ -23501,7 +23500,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {4}, Pages = {465-74}, - pubmed = {3988995}, + pmid = {3988995}, Pst = {ppublish}, Title = {Depth segregation of retinal ganglion cells projecting to mouse superior colliculus}, Volume = {234}, @@ -23521,7 +23520,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {8}, Pages = {2855-67}, - pubmed = {21414907}, + pmid = {21414907}, Pst = {ppublish}, Title = {Imaging light responses of targeted neuron populations in the rodent retina}, Volume = {31}, @@ -23542,7 +23541,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {16}, Pages = {7562-7}, Pmc = {PMC2867758}, - pubmed = {20368417}, + pmid = {20368417}, Pst = {ppublish}, Title = {Role of pre- and postsynaptic activity in thalamocortical axon branching}, Volume = {107}, @@ -23561,7 +23560,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {2}, Pages = {235-42}, - pubmed = {21791283}, + pmid = {21791283}, Pst = {ppublish}, Title = {Pathway-specific genetic attenuation of glutamate release alters select features of competition-based visual circuit refinement}, Volume = {71}, @@ -23582,7 +23581,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {14}, Pages = {14280-6}, - pubmed = {14742421}, + pmid = {14742421}, Pst = {ppublish}, Title = {Genetically encoded indicators of cellular calcium dynamics based on troponin C and green fluorescent protein}, Volume = {279}, @@ -23603,7 +23602,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {13}, Pages = {5425-30}, Pmc = {PMC3069178}, - pubmed = {21383146}, + pmid = {21383146}, Pst = {ppublish}, Title = {Genetic visualization with an improved GCaMP calcium indicator reveals spatiotemporal activation of the spinal motor neurons in zebrafish}, Volume = {108}, @@ -23623,7 +23622,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {6}, Pages = {3986-97}, - pubmed = {12930818}, + pmid = {12930818}, Pst = {ppublish}, Title = {Imaging neuronal activity during zebrafish behavior with a genetically encoded calcium indicator}, Volume = {90}, @@ -23643,7 +23642,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jun}, Number = {3}, Pages = {583-94}, - pubmed = {10896155}, + pmid = {10896155}, Pst = {ppublish}, Title = {Optical imaging of calcium transients in neurons and pharyngeal muscle of C. elegans}, Volume = {26}, @@ -23660,7 +23659,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {calcium sensor; calcium imaging; optical physiology; optical imaging; Drosophila; Behavior; microscopy; 21 Neurophysiology; sensory map; Olfactory Bulb; frontiers review}, Pages = {3}, Pmc = {PMC2526281}, - pubmed = {18946545}, + pmid = {18946545}, Pst = {ppublish}, Title = {Evaluating a genetically encoded optical sensor of neural activity using electrophysiology in intact adult fruit flies}, Volume = {1}, @@ -23680,7 +23679,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Nov}, Number = {7166}, Pages = {63-70}, - pubmed = {17972877}, + pmid = {17972877}, Pst = {ppublish}, Title = {Dissecting a circuit for olfactory behaviour in Caenorhabditis elegans}, Volume = {450}, @@ -23701,7 +23700,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {6}, Pages = {1128-42}, Pmc = {PMC3124368}, - pubmed = {21689599}, + pmid = {21689599}, Pst = {ppublish}, Title = {Multiple forms of activity-dependent competition refine hippocampal circuits in vivo}, Volume = {70}, @@ -23721,7 +23720,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {6}, Pages = {711-7}, Pmc = {PMC3103712}, - pubmed = {21572434}, + pmid = {21572434}, Pst = {ppublish}, Title = {Position-dependent patterning of spontaneous action potentials in immature cochlear inner hair cells}, Volume = {14}, @@ -23740,7 +23739,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {3}, Pages = {425-32}, - pubmed = {21835340}, + pmid = {21835340}, Pst = {ppublish}, Title = {Development of direction selectivity in mouse cortical neurons}, Volume = {71}, @@ -23759,7 +23758,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {31}, Pages = {11208-19}, - pubmed = {21813682}, + pmid = {21813682}, Pst = {ppublish}, Title = {Lack of evidence for direct corticospinal contributions to control of the ipsilateral forelimb in monkey}, Volume = {31}, @@ -23778,7 +23777,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {31}, Pages = {11313-27}, - pubmed = {21813691}, + pmid = {21813691}, Pst = {ppublish}, Title = {Temporal Precision in the Visual Pathway through the Interplay of Excitation and Stimulus-Driven Suppression}, Volume = {31}, @@ -23798,7 +23797,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {6042}, Pages = {642-6}, - pubmed = {21798953}, + pmid = {21798953}, Pst = {ppublish}, Title = {RNA mimics of green fluorescent protein}, Volume = {333}, @@ -23818,7 +23817,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {6040}, Pages = {345-8}, - pubmed = {21764748}, + pmid = {21764748}, Pst = {ppublish}, Title = {Electrical spiking in Escherichia coli probed with a fluorescent voltage-indicating protein}, Volume = {333}, @@ -23838,7 +23837,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {6042}, Pages = {637-42}, - pubmed = {21798952}, + pmid = {21798952}, Pst = {ppublish}, Title = {Impaired respiratory and body temperature control upon acute serotonergic neuron inhibition}, Volume = {333}, @@ -23857,7 +23856,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {30}, Pages = {10767-75}, - pubmed = {21795529}, + pmid = {21795529}, Pst = {ppublish}, Title = {Synaptogenesis of electrical and GABAergic synapses of fast-spiking inhibitory neurons in the neocortex}, Volume = {31}, @@ -23874,7 +23873,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Nature}, Keywords = {optogenetics; mice; in vivo; inhibition; GABA; interneurons; neurological disorder; Behavior; Systems Biology; Neocortex; optical physiology}, Month = {Jul}, - pubmed = {21796121}, + pmid = {21796121}, Pst = {aheadofprint}, Title = {Neocortical excitation/inhibition balance in information processing and social dysfunction}, Year = {2011}, @@ -23892,7 +23891,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {29}, Pages = {10689-700}, - pubmed = {21775612}, + pmid = {21775612}, Pst = {ppublish}, Title = {Late emergence of the vibrissa direction selectivity map in the rat barrel cortex}, Volume = {31}, @@ -23911,7 +23910,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {29}, Pages = {10445-50}, - pubmed = {21775590}, + pmid = {21775590}, Pst = {ppublish}, Title = {Endogenous patterns of activity are required for the maturation of a motor network}, Volume = {31}, @@ -23931,7 +23930,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {7358}, Pages = {92-5}, Pmc = {PMC3150726}, - pubmed = {21765429}, + pmid = {21765429}, Pst = {epublish}, Title = {Photoentrainment and pupillary light reflex are mediated by distinct populations of ipRGCs}, Volume = {476}, @@ -23948,7 +23947,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Archives of general psychiatry}, Keywords = {Autistic Disorder; neurological disorder; human; Genetic; Environment}, Month = {Jul}, - pubmed = {21727247}, + pmid = {21727247}, Pst = {aheadofprint}, Title = {Antidepressant Use During Pregnancy and Childhood Autism Spectrum Disorders}, Year = {2011}, @@ -23964,7 +23963,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Archives of general psychiatry}, Keywords = {Autistic Disorder; neurological disorder; human; twin study; Genetic; Environment}, Month = {Jul}, - pubmed = {21727249}, + pmid = {21727249}, Pst = {aheadofprint}, Title = {Genetic Heritability and Shared Environmental Factors Among Twin Pairs With Autism}, Year = {2011}, @@ -23985,7 +23984,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {40}, Pages = {17374-8}, Pmc = {PMC2951438}, - pubmed = {20855606}, + pmid = {20855606}, Pst = {ppublish}, Title = {Melanopsin-dependent light avoidance in neonatal mice}, Volume = {107}, @@ -24004,7 +24003,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {7}, Pages = {919-25}, - pubmed = {21623365}, + pmid = {21623365}, Pst = {epublish}, Title = {Retinal origin of orientation maps in visual cortex}, Volume = {14}, @@ -24026,7 +24025,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {5}, Pages = {555-61}, Pmc = {PMC3083489}, - pubmed = {21478886}, + pmid = {21478886}, Pst = {ppublish}, Title = {A new subtype of progenitor cell in the mouse embryonic neocortex}, Volume = {14}, @@ -24046,7 +24045,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {6}, Pages = {1115-27}, Pmc = {PMC3119851}, - pubmed = {21689598}, + pmid = {21689598}, Pst = {ppublish}, Title = {An instructive role for patterned spontaneous retinal activity in mouse visual map development}, Volume = {70}, @@ -24069,7 +24068,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {25}, Pages = {9353-8}, Pmc = {PMC3142876}, - pubmed = {21697385}, + pmid = {21697385}, Pst = {ppublish}, Title = {Bulk loading of calcium indicator dyes to study astrocyte physiology: key limitations and improvements using morphological maps}, Volume = {31}, @@ -24089,7 +24088,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {25}, Pages = {9205-21}, Pmc = {PMC3142780}, - pubmed = {21697371}, + pmid = {21697371}, Pst = {ppublish}, Title = {Cortical glial fibrillary acidic protein-positive cells generate neurons after perinatal hypoxic injury}, Volume = {31}, @@ -24107,7 +24106,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jun}, Number = {25}, Pages = {9147-58}, - pubmed = {21697366}, + pmid = {21697366}, Pst = {ppublish}, Title = {The locus ceruleus responds to signaling molecules obtained from the CSF by transfer through tanycytes}, Volume = {31}, @@ -24127,7 +24126,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {25}, Pages = {10326-31}, Pmc = {PMC3121825}, - pubmed = {21646517}, + pmid = {21646517}, Pst = {ppublish}, Title = {Maturation time of new granule cells in the dentate gyrus of adult macaque monkeys exceeds six months}, Volume = {108}, @@ -24147,7 +24146,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {5}, Pages = {e1001064}, Pmc = {PMC3096604}, - pubmed = {21610856}, + pmid = {21610856}, Pst = {ppublish}, Title = {Cracking the code of oscillatory activity}, Volume = {9}, @@ -24168,7 +24167,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {7343}, Pages = {351-5}, - pubmed = {21460837}, + pmid = {21460837}, Pst = {ppublish}, Title = {Neuronal activity is required for the development of specific cortical interneuron subtypes}, Volume = {472}, @@ -24186,7 +24185,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {optogenetics; frontiers review; activity manipulation; Primates; Genetic Engineering; Gene Transfer Techniques}, Pages = {18}, Pmc = {PMC3082132}, - pubmed = {21811444}, + pmid = {21811444}, Pst = {ppublish}, Title = {A high-light sensitivity optical neural silencer: development and application to optogenetic control of non-human primate cortex}, Volume = {5}, @@ -24204,7 +24203,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {development; GABA; Neocortex; neonatal; Newborn; Oxytocin/antagonists &inhibitors/pharmacology; neurophysiology; Anesthesia; rat}, Pages = {3}, Pmc = {PMC3080614}, - pubmed = {21519396}, + pmid = {21519396}, Pst = {epublish}, Title = {Newborn Analgesia Mediated by Oxytocin during Delivery}, Volume = {5}, @@ -24221,7 +24220,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Proceedings of the National Academy of Sciences of the United States of America}, Keywords = {development; Cell Adhesion Molecules; 21 Neurophysiology; circuit formation; Neocortex; Hippocampus; structural remodeling; neuroligin; Autistic Disorder; neurological disorder; mice}, Month = {Aug}, - pubmed = {21808020}, + pmid = {21808020}, Pst = {aheadofprint}, Title = {Autism-linked neuroligin-3 R451C mutation differentially alters hippocampal and cortical synaptic function}, Year = {2011}, @@ -24237,7 +24236,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Nature neuroscience}, Keywords = {optical physiology; optical imaging; calcium imaging; microscopy; in vivo; Technique; multiphoton; Zebrafish; retina; bipolar cells; visual system; 21 Neurophysiology; development}, Month = {Jun}, - pubmed = {21706020}, + pmid = {21706020}, Pst = {aheadofprint}, Title = {In vivo evidence that retinal bipolar cells generate spikes modulated by light}, Year = {2011}, @@ -24253,7 +24252,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Nature neuroscience}, Keywords = {optical physiology; frontiers review; 21 Cortical oscillations; 21 Neurophysiology; calcium imaging; multiphoton; Visual Cortex; visual system; mouse; microscopy; read; Technique}, Month = {Jul}, - pubmed = {21765421}, + pmid = {21765421}, Pst = {aheadofprint}, Title = {Differential connectivity and response dynamics of excitatory and inhibitory neurons in visual cortex}, Year = {2011}, @@ -24271,7 +24270,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {14}, Pages = {1220-4}, - pubmed = {21723130}, + pmid = {21723130}, Pst = {ppublish}, Title = {Early specialization for voice and emotion processing in the infant brain}, Volume = {21}, @@ -24290,7 +24289,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {14}, Pages = {1176-85}, - pubmed = {21723129}, + pmid = {21723129}, Pst = {ppublish}, Title = {Rhythmic TMS causes local entrainment of natural oscillatory signatures}, Volume = {21}, @@ -24307,7 +24306,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Nature neuroscience}, Keywords = {21 Cortical oscillations; 21 Neurophysiology; Neocortex; Technique; calcium imaging; microscopy; multiphoton; Pyramidal Cells; Reporter/genetics; layer 5; optical physiology; frontiers review; adult; mouse; read}, Month = {Jul}, - pubmed = {21743473}, + pmid = {21743473}, Pst = {aheadofprint}, Title = {Two-photon calcium imaging of evoked activity from L5 somatosensory neurons in vivo}, Year = {2011}, @@ -24327,7 +24326,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {12}, Pages = {4753-8}, Pmc = {PMC1450242}, - pubmed = {16537386}, + pmid = {16537386}, Pst = {ppublish}, Title = {Imaging cellular signals in the heart in vivo: Cardiac expression of the high-signal Ca2+ indicator GCaMP2}, Volume = {103}, @@ -24346,7 +24345,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {5958}, Pages = {1419-24}, - pubmed = {19965761}, + pmid = {19965761}, Pst = {ppublish}, Title = {GABAergic hub neurons orchestrate synchrony in developing hippocampal networks}, Volume = {326}, @@ -24368,7 +24367,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {3}, Pages = {1627-32}, Pmc = {PMC122241}, - pubmed = {11830673}, + pmid = {11830673}, Pst = {ppublish}, Title = {The SNARE protein SNAP-25 is linked to fast calcium triggering of exocytosis}, Volume = {99}, @@ -24387,7 +24386,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {8}, Pages = {3130-5}, - pubmed = {12716920}, + pmid = {12716920}, Pst = {ppublish}, Title = {Presynaptic modulation of the retinogeniculate synapse}, Volume = {23}, @@ -24404,7 +24403,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {4}, Pages = {e19294}, Pmc = {PMC3082564}, - pubmed = {21541289}, + pmid = {21541289}, Pst = {epublish}, Title = {Spreading depression sends microglia on l{\'e}vy flights}, Volume = {6}, @@ -24423,7 +24422,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Animals; Animals, Newborn; Fluorescent Dyes; Functional Laterality; Horseradish Peroxidase; Rabbits; Rats; Rats, Inbred Strains; Retina; Retinal Ganglion Cells; Species Specificity}, Number = {3}, Pages = {611-7}, - pubmed = {3416972}, + pmid = {3416972}, Pst = {ppublish}, Title = {A small population of retinal ganglion cells projecting to the retina of the other eye. An experimental study in the rat and the rabbit}, Volume = {71}, @@ -24441,7 +24440,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Cell Communication; Signal Transduction; Systems Biology; Terminology as Topic}, Number = {50}, Pages = {mr2}, - pubmed = {19091693}, + pmid = {19091693}, Pst = {epublish}, Title = {Ontologies of cellular networks}, Volume = {1}, @@ -24462,7 +24461,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {7}, Pages = {557-68}, Pmc = {PMC2868386}, - pubmed = {18568015}, + pmid = {18568015}, Pst = {ppublish}, Title = {Petilla terminology: nomenclature of features of GABAergic interneurons of the cerebral cortex}, Volume = {9}, @@ -24504,7 +24503,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {1130}, Pages = {1-59}, - pubmed = {20635}, + pmid = {20635}, Pst = {ppublish}, Title = {Ferrier lecture. Functional architecture of macaque monkey visual cortex}, Volume = {198}, @@ -24523,7 +24522,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {6}, Pages = {2112-27}, - pubmed = {9045738}, + pmid = {9045738}, Pst = {ppublish}, Title = {Orientation selectivity and the arrangement of horizontal connections in tree shrew striate cortex}, Volume = {17}, @@ -24542,7 +24541,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {4}, Pages = {514-22}, - pubmed = {9287203}, + pmid = {9287203}, Pst = {ppublish}, Title = {New perspectives on the mechanisms for orientation selectivity}, Volume = {7}, @@ -24561,7 +24560,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {1}, Pages = {73-82}, - pubmed = {12466218}, + pmid = {12466218}, Pst = {ppublish}, Title = {Understanding layer 4 of the cortical circuit: a model based on cat V1}, Volume = {13}, @@ -24580,7 +24579,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {3}, Pages = {445-76}, - pubmed = {15006089}, + pmid = {15006089}, Pst = {ppublish}, Title = {Geometrical computations explain projection patterns of long-range horizontal connections in visual cortex}, Volume = {16}, @@ -24600,7 +24599,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jun}, Number = {3}, Pages = {416-21}, - pubmed = {10851181}, + pmid = {10851181}, Pst = {ppublish}, Title = {Recent advances in technology for measuring and manipulating cell signals}, Volume = {10}, @@ -24619,7 +24618,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {11}, Pages = {2396-404}, - pubmed = {6770893}, + pmid = {6770893}, Pst = {ppublish}, Title = {New calcium indicators and buffers with high selectivity against magnesium and protons: design, synthesis, and properties of prototype structures}, Volume = {19}, @@ -24638,7 +24637,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {5806}, Pages = {527-8}, - pubmed = {7219539}, + pmid = {7219539}, Pst = {ppublish}, Title = {A non-disruptive technique for loading calcium buffers and indicators into cells}, Volume = {290}, @@ -24656,7 +24655,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {6}, Pages = {3440-50}, - pubmed = {3838314}, + pmid = {3838314}, Pst = {ppublish}, Title = {A new generation of Ca2+ indicators with greatly improved fluorescence properties}, Volume = {260}, @@ -24672,7 +24671,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {calcium sensor; calcium imaging; optical physiology; optical imaging; Fluorescence; Indicators and Reagents}, Mesh = {Calcium; Chlorine; Fluorescent Dyes; Hydrogen-Ion Concentration; Indicators and Reagents; Protons; Sodium}, Pages = {127-56}, - pubmed = {2538708}, + pmid = {2538708}, Pst = {ppublish}, Title = {Fluorescent indicators of ion concentrations}, Volume = {30}, @@ -24687,7 +24686,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {calcium sensor; calcium imaging; optical physiology; optical imaging; Fluorescence; Indicators and Reagents}, Mesh = {Animals; Fluorescent Dyes; Ions; Neurons}, Pages = {227-53}, - pubmed = {2648950}, + pmid = {2648950}, Pst = {ppublish}, Title = {Fluorescent probes of cell signaling}, Volume = {12}, @@ -24704,7 +24703,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {calcium sensor; calcium imaging; optical physiology; optical imaging; Fluorescence; Indicators and Reagents}, Mesh = {Animals; Calcium; Calcium Channels; Humans; Signal Transduction}, Pages = {715-60}, - pubmed = {2177344}, + pmid = {2177344}, Pst = {ppublish}, Title = {Calcium channels, stores, and oscillations}, Volume = {6}, @@ -24724,7 +24723,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {6645}, Pages = {882-7}, - pubmed = {9278050}, + pmid = {9278050}, Pst = {ppublish}, Title = {Fluorescent indicators for Ca2+ based on green fluorescent proteins and calmodulin}, Volume = {388}, @@ -24744,7 +24743,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {12}, Pages = {905-9}, - pubmed = {16299475}, + pmid = {16299475}, Pst = {ppublish}, Title = {A guide to choosing fluorescent proteins}, Volume = {2}, @@ -24762,7 +24761,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Animals; Biological Markers; Calcium; Calmodulin; Calmodulin-Binding Proteins; Cells, Cultured; Fluorescence Resonance Energy Transfer; Fluorescent Dyes; Microscopy, Fluorescence}, Number = {3}, Pages = {1057-65}, - pubmed = {17406387}, + pmid = {17406387}, Pst = {ppublish}, Title = {Measuring calcium signaling using genetically targetable fluorescent indicators}, Volume = {1}, @@ -24783,7 +24782,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {7}, Pages = {423-31}, Pmc = {PMC2909385}, - pubmed = {17572670}, + pmid = {17572670}, Pst = {ppublish}, Title = {Calcium Green FlAsH as a genetically targeted small-molecule calcium indicator}, Volume = {3}, @@ -24801,7 +24800,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {10}, Pages = {419-24}, - pubmed = {2469158}, + pmid = {2469158}, Pst = {ppublish}, Title = {Fluorescence measurement and photochemical manipulation of cytosolic free calcium}, Volume = {11}, @@ -24820,7 +24819,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Animals; Cats; Cerebral Cortex; Models, Neurological; Rats; Somatosensory Cortex; Vision, Ocular; Visual Perception}, Number = {6095}, Pages = {361-4}, - pubmed = {3785405}, + pmid = {3785405}, Pst = {ppublish}, Title = {Functional architecture of cortex revealed by optical imaging of intrinsic signals}, Volume = {324}, @@ -24841,7 +24840,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1}, Pages = {119-29}, Pmc = {PMC1988694}, - pubmed = {17610821}, + pmid = {17610821}, Pst = {ppublish}, Title = {Compression and reflection of visually evoked cortical waves}, Volume = {55}, @@ -24862,7 +24861,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1}, Pages = {103-17}, Pmc = {PMC2171365}, - pubmed = {17610820}, + pmid = {17610820}, Pst = {ppublish}, Title = {Standing waves and traveling waves distinguish two circuits in visual cortex}, Volume = {55}, @@ -24883,7 +24882,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {4}, Pages = {617-29}, - pubmed = {16701211}, + pmid = {16701211}, Pst = {ppublish}, Title = {Visualizing the cortical representation of whisker touch: voltage-sensitive dye imaging in freely moving mice}, Volume = {50}, @@ -24905,7 +24904,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {23}, Pages = {13638-43}, Pmc = {PMC263866}, - pubmed = {14595013}, + pmid = {14595013}, Pst = {ppublish}, Title = {Interaction of sensory responses with spontaneous depolarization in layer 2/3 barrel cortex}, Volume = {100}, @@ -24925,7 +24924,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Nov}, Number = {11}, Pages = {2585-92}, - pubmed = {17259645}, + pmid = {17259645}, Pst = {ppublish}, Title = {Nestin-CreER mice reveal DNA synthesis by nonapoptotic neurons following cerebral ischemia hypoxia}, Volume = {17}, @@ -24946,7 +24945,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1}, Pages = {347-52}, Pmc = {PMC1765463}, - pubmed = {17185420}, + pmid = {17185420}, Pst = {ppublish}, Title = {Sequential structure of neocortical spontaneous activity in vivo}, Volume = {104}, @@ -24965,7 +24964,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {3}, Pages = {427-30}, - pubmed = {11055425}, + pmid = {11055425}, Pst = {ppublish}, Title = {Correlated neuronal activity and visual cortical development}, Volume = {27}, @@ -24983,7 +24982,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {30}, Pages = {6703-14}, - pubmed = {15282273}, + pmid = {15282273}, Pst = {ppublish}, Title = {Voltage imaging from dendrites of mitral cells: EPSP attenuation and spike trigger zones}, Volume = {24}, @@ -25003,7 +25002,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {4}, Pages = {1756-68}, - pubmed = {7823100}, + pmid = {7823100}, Pst = {ppublish}, Title = {Spread of epileptiform activity in the immature rat neocortex studied with voltage-sensitive dyes and laser scanning microscopy}, Volume = {72}, @@ -25022,7 +25021,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {4}, Pages = {791-802}, - pubmed = {10624943}, + pmid = {10624943}, Pst = {ppublish}, Title = {Imaging cortical dynamics at high spatial and temporal resolution with novel blue voltage-sensitive dyes}, Volume = {24}, @@ -25041,7 +25040,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {8}, Pages = {862-71}, - pubmed = {15273692}, + pmid = {15273692}, Pst = {ppublish}, Title = {Multiplexing using synchrony in the zebrafish olfactory bulb}, Volume = {7}, @@ -25061,7 +25060,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {23}, Pages = {9977-88}, - pubmed = {9822753}, + pmid = {9822753}, Pst = {ppublish}, Title = {Chemotopic, combinatorial, and noncombinatorial odorant representations in the olfactory bulb revealed using a voltage-sensitive axon tracer}, Volume = {18}, @@ -25080,7 +25079,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {7294}, Pages = {47-52}, - pubmed = {20393466}, + pmid = {20393466}, Pst = {ppublish}, Title = {Olfactory pattern classification by discrete neuronal network states}, Volume = {465}, @@ -25098,7 +25097,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {review; optical imaging; structural remodeling; 21 Activity-development; calcium imaging; optical physiology; microscopy;}, Mesh = {Animals; Axons; Brain Mapping; Cell Division; Cell Movement; Diagnostic Imaging; Humans; Nervous System; Nervous System Physiological Phenomena; Neural Pathways; Optics and Photonics; Synapses}, Pages = {771-98}, - pubmed = {14977421}, + pmid = {14977421}, Pst = {ppublish}, Title = {Live optical imaging of nervous system development}, Volume = {66}, @@ -25118,7 +25117,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {5}, Pages = {737-52}, - pubmed = {9182799}, + pmid = {9182799}, Pst = {ppublish}, Title = {Combinatorial and chemotopic odorant coding in the zebrafish olfactory bulb visualized by optical imaging}, Volume = {18}, @@ -25137,7 +25136,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {6152}, Pages = {166-8}, - pubmed = {3340163}, + pmid = {3340163}, Pst = {ppublish}, Title = {Real-time imaging of evoked activity in local circuits of the salamander olfactory bulb}, Volume = {331}, @@ -25157,7 +25156,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {3}, Pages = {499-511}, - pubmed = {10433262}, + pmid = {10433262}, Pst = {ppublish}, Title = {Optical imaging of odorant representations in the mammalian olfactory bulb}, Volume = {23}, @@ -25176,7 +25175,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {1}, Pages = {98-105}, - pubmed = {7773012}, + pmid = {7773012}, Pst = {ppublish}, Title = {Neuronal coupling and uncoupling in the developing nervous system}, Volume = {5}, @@ -25195,7 +25194,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Nov}, Number = {11}, Pages = {2251-62}, - pubmed = {6631479}, + pmid = {6631479}, Pst = {ppublish}, Title = {Optical monitoring of activity from many areas of the in vitro and in vivo salamander olfactory bulb: a new method for studying functional organization in the vertebrate central nervous system}, Volume = {3}, @@ -25214,7 +25213,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {4}, Pages = {1351-60}, - pubmed = {11160406}, + pmid = {11160406}, Pst = {ppublish}, Title = {Tuning and topography in an odor map on the rat olfactory bulb}, Volume = {21}, @@ -25233,7 +25232,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {4951}, Pages = {73-6}, - pubmed = {2321027}, + pmid = {2321027}, Pst = {ppublish}, Title = {Two-photon laser scanning fluorescence microscopy}, Volume = {248}, @@ -25252,7 +25251,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {2}, Pages = {339-48}, Pmc = {PMC1329750}, - pubmed = {3741986}, + pmid = {3741986}, Pst = {ppublish}, Title = {Optical imaging of cell membrane potential changes induced by applied electric fields}, Volume = {50}, @@ -25270,7 +25269,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {3-4}, Pages = {304-27}, Pmc = {PMC1392827}, - pubmed = {14795441}, + pmid = {14795441}, Pst = {ppublish}, Title = {The volume change resulting from stimulation of a giant nerve fibre}, Volume = {111}, @@ -25289,7 +25288,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {4952}, Pages = {229-31}, - pubmed = {2326637}, + pmid = {2326637}, Pst = {ppublish}, Title = {Reorganization of retinotopic cortical maps in adult mammals after lesions of the retina}, Volume = {248}, @@ -25304,7 +25303,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Nature neuroscience}, Keywords = {visual cortex; fmri; visual system; retina; function; topographic map; Sensory Deprivation; neurological disorder; human; 21 Activity-development; structural remodeling}, Month = {Mar}, - pubmed = {21441924}, + pmid = {21441924}, Pst = {aheadofprint}, Title = {Large-scale remapping of visual cortex is absent in adult humans with macular degeneration}, Year = {2011}, @@ -25322,7 +25321,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Action Potentials; Animals; Cadmium; Calcium; Hypothalamus; Nickel; Pituitary Gland, Posterior; Sodium; Tetrodotoxin; Xenopus laevis}, Number = {5938}, Pages = {36-40}, - pubmed = {6633657}, + pmid = {6633657}, Pst = {ppublish}, Title = {Optical recording of action potentials from vertebrate nerve terminals using potentiometric probes provides evidence for sodium and calcium components}, Volume = {306}, @@ -25341,7 +25340,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {5446}, Pages = {1943-6}, - pubmed = {10583955}, + pmid = {10583955}, Pst = {ppublish}, Title = {Linking spontaneous activity of single cortical neurons and the underlying functional architecture}, Volume = {286}, @@ -25360,7 +25359,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {5}, Pages = {2072-93}, - pubmed = {7623099}, + pmid = {7623099}, Pst = {ppublish}, Title = {Coherent spatiotemporal patterns of ongoing activity revealed by real-time optical imaging coupled with single-unit recording in the cat visual cortex}, Volume = {73}, @@ -25378,7 +25377,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {3}, Pages = {278-81}, Pmc = {PMC1392485}, - pubmed = {16991859}, + pmid = {16991859}, Pst = {ppublish}, Title = {Opacity changes in stimulated nerve}, Volume = {108}, @@ -25394,7 +25393,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {optical physiology; imaging; intrinsic signal; voltage sensor; optics; Technique; review; optical imaging}, Mesh = {Animals; Cell Communication; Cerebral Cortex; Coloring Agents; Diagnostic Imaging; Electrophysiology; Humans; Neurons; Optics and Photonics; Time Factors}, Pages = {543-59}, - pubmed = {2653196}, + pmid = {2653196}, Pst = {ppublish}, Title = {Optical imaging of cortical activity: real-time imaging using extrinsic dye-signals and high resolution imaging based on slow intrinsic-signals}, Volume = {51}, @@ -25414,7 +25413,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {6343}, Pages = {429-31}, - pubmed = {1896085}, + pmid = {1896085}, Pst = {ppublish}, Title = {Iso-orientation domains in cat visual cortex are arranged in pinwheel-like patterns}, Volume = {353}, @@ -25434,7 +25433,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {4967}, Pages = {417-20}, - pubmed = {2165630}, + pmid = {2165630}, Pst = {ppublish}, Title = {Functional organization of primate visual cortex revealed by high resolution optical imaging}, Volume = {249}, @@ -25453,7 +25452,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {7}, Pages = {1886-95}, - pubmed = {4020423}, + pmid = {4020423}, Pst = {ppublish}, Title = {Optical mapping of electrical activity in rat somatosensory and visual cortex}, Volume = {5}, @@ -25472,7 +25471,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Nov}, Number = {6}, Pages = {1281-91}, - pubmed = {925730}, + pmid = {925730}, Pst = {ppublish}, Title = {Optical recording of neuronal activity in an invertebrate central nervous system: simultaneous monitoring of several neurons}, Volume = {40}, @@ -25491,7 +25490,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Animals; Evoked Potentials; Fluorescent Dyes; Neurons; Photic Stimulation; Rana ridibunda; Retina; Superior Colliculi; Visual Pathways; Visual Perception}, Number = {5962}, Pages = {848-50}, - pubmed = {6717577}, + pmid = {6717577}, Pst = {ppublish}, Title = {Real-time optical imaging of naturally evoked electrical activity in intact frog brain}, Volume = {308}, @@ -25510,7 +25509,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {4627}, Pages = {1025-7}, - pubmed = {6648515}, + pmid = {6648515}, Pst = {ppublish}, Title = {Identification of presynaptic neurons by laser photostimulation}, Volume = {222}, @@ -25528,7 +25527,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {5140}, Pages = {438-41}, - pubmed = {5649693}, + pmid = {5649693}, Pst = {ppublish}, Title = {Light scattering and birefringence changes during nerve activity}, Volume = {218}, @@ -25547,7 +25546,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {3}, Pages = {883-8}, Pmc = {PMC305410}, - pubmed = {4301149}, + pmid = {4301149}, Pst = {ppublish}, Title = {Changes in fluorescence, turbidity, and birefringence associated with nerve excitation}, Volume = {61}, @@ -25565,7 +25564,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {109}, Pages = {159-60}, - pubmed = {4512623}, + pmid = {4512623}, Pst = {ppublish}, Title = {A large change in axon fluorescence that provides a promising method for measuring membrane potential}, Volume = {241}, @@ -25583,7 +25582,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jun}, Number = {908}, Pages = {411-23}, - pubmed = {238238}, + pmid = {238238}, Pst = {ppublish}, Title = {The optical spike}, Volume = {270}, @@ -25601,7 +25600,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {5616}, Pages = {140-2}, - pubmed = {593306}, + pmid = {593306}, Pst = {ppublish}, Title = {Simultaneous recording from several neurones in an invertebrate central nervous system}, Volume = {268}, @@ -25617,7 +25616,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {optical physiology; imaging; intrinsic signal; voltage sensor; optics}, Mesh = {Action Potentials; Animals; Axons; Central Nervous System; Decapodiformes; Membrane Potentials; Neurons; Spectrophotometry; Thoracica}, Pages = {171-82}, - pubmed = {386900}, + pmid = {386900}, Pst = {ppublish}, Title = {Optical methods for monitoring neuron activity}, Volume = {1}, @@ -25637,7 +25636,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {4467}, Pages = {338-9}, - pubmed = {7423196}, + pmid = {7423196}, Pst = {ppublish}, Title = {Swelling of nerve fibers associated with action potentials}, Volume = {210}, @@ -25655,7 +25654,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {9}, Pages = {1055-9}, - pubmed = {7346626}, + pmid = {7346626}, Pst = {ppublish}, Title = {Rapid mechanical changes in crab nerve and squid axon during action potentials}, Volume = {77}, @@ -25673,7 +25672,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Pages = {269-91}, Pmc = {PMC1197248}, - pubmed = {7182467}, + pmid = {7182467}, Pst = {ppublish}, Title = {Visualization of the spread of electrical activity in rat hippocampal slices by voltage-sensitive optical probes}, Volume = {333}, @@ -25691,7 +25690,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Nov}, Number = {4}, Pages = {469-84}, - pubmed = {10531540}, + pmid = {10531540}, Pst = {ppublish}, Title = {Retinal afferents to the dorsal raphe nucleus in rats and Mongolian gerbils}, Volume = {414}, @@ -25710,7 +25709,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {1-2}, Pages = {213-7}, - pubmed = {10996155}, + pmid = {10996155}, Pst = {ppublish}, Title = {Serotonergic retinopetal projections from the dorsal raphe nucleus in the mouse demonstrated by combined [(3)H] 5-HT retrograde tracing and immunolabeling of endogenous 5-HT}, Volume = {878}, @@ -25728,7 +25727,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Animals; Axons; Carrier Proteins; Fenclonine; Geniculate Bodies; Membrane Glycoproteins; Membrane Transport Proteins; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Knockout; Monoamine Oxidase; Nerve Tissue Proteins; Receptor, Serotonin, 5-HT1B; Receptors, Serotonin; Retinal Ganglion Cells; Serotonin Plasma Membrane Transport Proteins; Superior Colliculi; Visual Pathways}, Number = {3}, Pages = {597-610}, - pubmed = {12031347}, + pmid = {12031347}, Pst = {ppublish}, Title = {Lack of 5-HT(1B) receptor and of serotonin transporter have different effects on the segregation of retinal axons in the lateral geniculate nucleus compared to the superior colliculus}, Volume = {111}, @@ -25747,7 +25746,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {16}, Pages = {7007-24}, - pubmed = {10436056}, + pmid = {10436056}, Pst = {ppublish}, Title = {Excess of serotonin (5-HT) alters the segregation of ispilateral and contralateral retinal projections in monoamine oxidase A knock-out mice: possible role of 5-HT uptake in retinal ganglion cells during development}, Volume = {19}, @@ -25765,7 +25764,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {11}, Pages = {4233-41}, - pubmed = {21411664}, + pmid = {21411664}, Pst = {ppublish}, Title = {Neural substrate of spatial memory in the superior colliculus after damage to the primary visual cortex}, Volume = {31}, @@ -25785,7 +25784,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {2}, Pages = {932-44}, - pubmed = {19015005}, + pmid = {19015005}, Pst = {ppublish}, Title = {Characterization of histamine projections and their potential cellular targets in the mouse retina}, Volume = {158}, @@ -25805,7 +25804,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Animals; Axons; Histamine; Humans; Optic Nerve; Retina; Serotonin; Signal Transduction}, Number = {7-8}, Pages = {655-67}, - pubmed = {16877274}, + pmid = {16877274}, Pst = {ppublish}, Title = {Retinopetal axons in mammals: emphasis on histamine and serotonin}, Volume = {31}, @@ -25825,7 +25824,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Nov}, Number = {3}, Pages = {403-7}, - pubmed = {17088207}, + pmid = {17088207}, Pst = {ppublish}, Title = {Arc/Arg3.1: linking gene expression to synaptic plasticity and memory}, Volume = {52}, @@ -25846,7 +25845,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {4}, Pages = {1079-103}, Pmc = {PMC2828052}, - pubmed = {19789377}, + pmid = {19789377}, Pst = {ppublish}, Title = {The function of activity-regulated genes in the nervous system}, Volume = {89}, @@ -25867,7 +25866,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1}, Pages = {316-21}, Pmc = {PMC2629236}, - pubmed = {19116276}, + pmid = {19116276}, Pst = {ppublish}, Title = {Synaptic activity-responsive element in the Arc/Arg3.1 promoter essential for synapse-to-nucleus signaling in activated neurons}, Volume = {106}, @@ -25888,7 +25887,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {7266}, Pages = {941-6}, Pmc = {PMC2771429}, - pubmed = {19829374}, + pmid = {19829374}, Pst = {ppublish}, Title = {Intracellular dynamics of hippocampal place cells during virtual navigation}, Volume = {461}, @@ -25908,7 +25907,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {5}, Pages = {443-6}, Pmc = {PMC2974076}, - pubmed = {21057636}, + pmid = {21057636}, Pst = {ppublish}, Title = {Synaptic activity-responsive element (SARE): A unique genomic structure with an unusual sensitivity to neuronal activity}, Volume = {3}, @@ -25928,7 +25927,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {23}, Pages = {10067-71}, - pubmed = {12451105}, + pmid = {12451105}, Pst = {ppublish}, Title = {Experience-dependent coincident expression of the effector immediate-early genes arc and Homer 1a in hippocampal and neocortical neuronal networks}, Volume = {22}, @@ -25948,7 +25947,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {20}, Pages = {6580-92}, Pmc = {PMC2805025}, - pubmed = {19458228}, + pmid = {19458228}, Pst = {ppublish}, Title = {Multisensory integration in the superior colliculus requires synergy among corticocollicular inputs}, Volume = {29}, @@ -25968,7 +25967,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {10}, Pages = {831-6}, - pubmed = {19409786}, + pmid = {19409786}, Pst = {ppublish}, Title = {Spontaneous motor entrainment to music in multiple vocal mimicking species}, Volume = {19}, @@ -25989,7 +25988,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {21}, Pages = {8743-7}, Pmc = {PMC2689012}, - pubmed = {19420221}, + pmid = {19420221}, Pst = {ppublish}, Title = {Strengthening of lateral activation in adult rat visual cortex after retinal lesions captured with voltage-sensitive dye imaging in vivo}, Volume = {106}, @@ -26010,7 +26009,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {4}, Pages = {1539-50}, Pmc = {PMC2814371}, - pubmed = {20107081}, + pmid = {20107081}, Pst = {ppublish}, Title = {Developmental regulation of spontaneous activity in the Mammalian cochlea}, Volume = {30}, @@ -26030,7 +26029,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {4}, Pages = {1611-20}, - pubmed = {8989397}, + pmid = {8989397}, Pst = {ppublish}, Title = {Synaptically evoked prolonged depolarizations in the developing auditory system}, Volume = {74}, @@ -26050,7 +26049,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {6}, Pages = {711-7}, Pmc = {PMC2780022}, - pubmed = {19471270}, + pmid = {19471270}, Pst = {ppublish}, Title = {Tonotopic reorganization of developing auditory brainstem circuits}, Volume = {12}, @@ -26070,7 +26069,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {5}, Pages = {603-6}, - pubmed = {14630225}, + pmid = {14630225}, Pst = {ppublish}, Title = {Recent advances in the use of neurotropic viruses for circuit analysis}, Volume = {13}, @@ -26089,7 +26088,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {8}, Pages = {3377-82}, Pmc = {PMC3044368}, - pubmed = {21292985}, + pmid = {21292985}, Pst = {ppublish}, Title = {Microdissection of neural networks by conditional reporter expression from a Brainbow herpesvirus}, Volume = {108}, @@ -26108,7 +26107,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {7337}, Pages = {177-82}, - pubmed = {21390124}, + pmid = {21390124}, Pst = {ppublish}, Title = {Network anatomy and in vivo physiology of visual cortical neurons}, Volume = {471}, @@ -26130,7 +26129,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {16}, Pages = {1429-33}, Pmc = {PMC2766847}, - pubmed = {19794318}, + pmid = {19794318}, Pst = {ppublish}, Title = {NMDA receptor-independent control of transcription factors and gene expression}, Volume = {20}, @@ -26151,7 +26150,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {6}, Pages = {777-83}, Pmc = {PMC2741303}, - pubmed = {19430469}, + pmid = {19430469}, Pst = {ppublish}, Title = {Ube3a is required for experience-dependent maturation of the neocortex}, Volume = {12}, @@ -26170,7 +26169,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {3}, Pages = {279-84}, - pubmed = {21278731}, + pmid = {21278731}, Pst = {ppublish}, Title = {New views of Arc, a master regulator of synaptic plasticity}, Volume = {14}, @@ -26189,7 +26188,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {4}, Pages = {763-79}, - pubmed = {21338885}, + pmid = {21338885}, Pst = {ppublish}, Title = {Excitatory projection neuron subtypes control the distribution of local inhibitory interneurons in the cerebral cortex}, Volume = {69}, @@ -26208,7 +26207,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {10}, Pages = {3862-70}, - pubmed = {21389241}, + pmid = {21389241}, Pst = {ppublish}, Title = {Cell Diversity and Connection Specificity between Callosal Projection Neurons in the Frontal Cortex}, Volume = {31}, @@ -26227,7 +26226,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {7337}, Pages = {183-8}, - pubmed = {21390125}, + pmid = {21390125}, Pst = {ppublish}, Title = {Wiring specificity in the direction-selectivity circuit of the retina}, Volume = {471}, @@ -26247,7 +26246,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {17}, Pages = {5536-45}, - pubmed = {19403821}, + pmid = {19403821}, Pst = {ppublish}, Title = {Excitotoxic death of retinal neurons in vivo occurs via a non-cell-autonomous mechanism}, Volume = {29}, @@ -26268,7 +26267,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {16}, Pages = {6760-5}, Pmc = {PMC2672480}, - pubmed = {19346492}, + pmid = {19346492}, Pst = {ppublish}, Title = {Compensatory changes in cellular excitability, not synaptic scaling, contribute to homeostatic recovery of embryonic network activity}, Volume = {106}, @@ -26288,7 +26287,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {8}, Pages = {645-9}, - pubmed = {19285405}, + pmid = {19285405}, Pst = {ppublish}, Title = {Development of global motion perception requires early postnatal exposure to patterned light}, Volume = {19}, @@ -26309,7 +26308,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {16}, Pages = {5266-75}, - pubmed = {19386923}, + pmid = {19386923}, Pst = {ppublish}, Title = {Learning signals from the superior colliculus for adaptation of saccadic eye movements in the monkey}, Volume = {29}, @@ -26330,7 +26329,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {6}, Pages = {895-905}, Pmc = {PMC2892759}, - pubmed = {19323998}, + pmid = {19323998}, Pst = {ppublish}, Title = {Subcellular topography of visually driven dendritic activity in the vertebrate visual system}, Volume = {61}, @@ -26350,7 +26349,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {6}, Pages = {1719-34}, - pubmed = {19211879}, + pmid = {19211879}, Pst = {ppublish}, Title = {In vivo voltage-sensitive dye imaging in adult mice reveals that somatosensory maps lost to stroke are replaced over weeks by new structural and functional circuits with prolonged modes of activation within both the peri-infarct zone and distant sites}, Volume = {29}, @@ -26370,7 +26369,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {5}, Pages = {1030-3}, - pubmed = {18234881}, + pmid = {18234881}, Pst = {ppublish}, Title = {Immediate-early gene expression at rest recapitulates recent experience}, Volume = {28}, @@ -26390,7 +26389,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {12}, Pages = {1120-4}, - pubmed = {10570490}, + pmid = {10570490}, Pst = {ppublish}, Title = {Environment-specific expression of the immediate-early gene Arc in hippocampal neuronal ensembles}, Volume = {2}, @@ -26410,7 +26409,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {5}, Pages = {599-606}, - pubmed = {16150584}, + pmid = {16150584}, Pst = {ppublish}, Title = {Mapping behaviorally relevant neural circuits with immediate-early gene expression}, Volume = {15}, @@ -26431,7 +26430,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {46}, Pages = {11760-7}, Pmc = {PMC2615463}, - pubmed = {19005037}, + pmid = {19005037}, Pst = {ppublish}, Title = {The immediate early gene arc/arg3.1: regulation, mechanisms, and function}, Volume = {28}, @@ -26452,7 +26451,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {3}, Pages = {441-8}, Pmc = {PMC2661113}, - pubmed = {18995818}, + pmid = {18995818}, Pst = {ppublish}, Title = {Seeing circuits assemble}, Volume = {60}, @@ -26473,7 +26472,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {43}, Pages = {16797-802}, Pmc = {PMC2575499}, - pubmed = {18940923}, + pmid = {18940923}, Pst = {ppublish}, Title = {Delayed plasticity of inhibitory neurons in developing visual cortex}, Volume = {105}, @@ -26493,7 +26492,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {43}, Pages = {11071-8}, - pubmed = {18945914}, + pmid = {18945914}, Pst = {ppublish}, Title = {Nigral inhibition of GABAergic neurons in mouse superior colliculus}, Volume = {28}, @@ -26513,7 +26512,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {37}, Pages = {9309-18}, - pubmed = {18784311}, + pmid = {18784311}, Pst = {ppublish}, Title = {Spatiotemporal profiles of field potentials in mouse superior colliculus analyzed by multichannel recording}, Volume = {28}, @@ -26533,7 +26532,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {7266}, Pages = {930-9}, - pubmed = {19829373}, + pmid = {19829373}, Pst = {ppublish}, Title = {Electrophysiology in the age of light}, Volume = {461}, @@ -26554,7 +26553,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1}, Pages = {133-40}, Pmc = {PMC2840225}, - pubmed = {20023653}, + pmid = {20023653}, Pst = {ppublish}, Title = {A robust and high-throughput Cre reporting and characterization system for the whole mouse brain}, Volume = {13}, @@ -26573,7 +26572,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Animals; Axons; Cerebral Cortex; Dendrites; Equipment Design; Indicators and Reagents; Luminescent Proteins; Mice; Mice, Transgenic; Microscopy, Confocal; Neurons; Photons; Skull; Synapses}, Number = {2}, Pages = {201-8}, - pubmed = {20134419}, + pmid = {20134419}, Pst = {ppublish}, Title = {Thinned-skull cranial window technique for long-term imaging of the cortex in live mice}, Volume = {5}, @@ -26593,7 +26592,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {9}, Pages = {729-32}, - pubmed = {20693999}, + pmid = {20693999}, Pst = {ppublish}, Title = {Spontaneous network activity visualized by ultrasensitive Ca(2+) indicators, yellow Cameleon-Nano}, Volume = {7}, @@ -26613,7 +26612,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {2}, Pages = {139-42}, - pubmed = {21217749}, + pmid = {21217749}, Pst = {ppublish}, Title = {Simultaneous two-photon calcium imaging at different depths with spatiotemporal multiplexing}, Volume = {8}, @@ -26632,7 +26631,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {3}, Pages = {387-97}, - pubmed = {21278729}, + pmid = {21278729}, Pst = {ppublish}, Title = {An optogenetic toolbox designed for primates}, Volume = {14}, @@ -26652,7 +26651,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {27}, Pages = {7013-23}, - pubmed = {18596175}, + pmid = {18596175}, Pst = {ppublish}, Title = {Backpropagating action potentials trigger dendritic release of BDNF during spontaneous network activity}, Volume = {28}, @@ -26671,7 +26670,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {9}, Pages = {3384-99}, - pubmed = {21368050}, + pmid = {21368050}, Pst = {ppublish}, Title = {Development of Single Retinofugal Axon Arbors in Normal and {beta}2 Knock-Out Mice}, Volume = {31}, @@ -26692,7 +26691,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {4}, Pages = {503-15}, Pmc = {PMC3037728}, - pubmed = {20188655}, + pmid = {20188655}, Pst = {ppublish}, Title = {The immune protein CD3zeta is required for normal development of neural circuits in the retina}, Volume = {65}, @@ -26712,7 +26711,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {2}, Pages = {271-82}, - pubmed = {12553914}, + pmid = {12553914}, Pst = {ppublish}, Title = {Two-photon calcium imaging reveals an odor-evoked map of activity in the fly brain}, Volume = {112}, @@ -26731,7 +26730,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jun}, Number = {7247}, Pages = {663-7}, - pubmed = {19396156}, + pmid = {19396156}, Pst = {ppublish}, Title = {Driving fast-spiking cells induces gamma rhythm and controls sensory responses}, Volume = {459}, @@ -26752,7 +26751,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1}, Pages = {150-60}, Pmc = {PMC2504695}, - pubmed = {18614036}, + pmid = {18614036}, Pst = {ppublish}, Title = {Cellular mechanisms underlying stimulus-dependent gain modulation in primary visual cortex neurons in vivo}, Volume = {59}, @@ -26773,7 +26772,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {39}, Pages = {10333-44}, Pmc = {PMC3025280}, - pubmed = {17898205}, + pmid = {17898205}, Pst = {ppublish}, Title = {Stimulus feature selectivity in excitatory and inhibitory neurons in primary visual cortex}, Volume = {27}, @@ -26794,7 +26793,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {15}, Pages = {1133-7}, Pmc = {PMC2891506}, - pubmed = {18682213}, + pmid = {18682213}, Pst = {ppublish}, Title = {Escape behavior elicited by single, channelrhodopsin-2-evoked spikes in zebrafish somatosensory neurons}, Volume = {18}, @@ -26814,7 +26813,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Nov}, Number = {7168}, Pages = {420-4}, - pubmed = {17943086}, + pmid = {17943086}, Pst = {ppublish}, Title = {Neural substrates of awakening probed with optogenetic control of hypocretin neurons}, Volume = {450}, @@ -26834,7 +26833,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {7174}, Pages = {61-4}, - pubmed = {18094685}, + pmid = {18094685}, Pst = {ppublish}, Title = {Sparse optical microstimulation in barrel cortex drives learned behaviour in freely moving mice}, Volume = {451}, @@ -26854,7 +26853,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Nov}, Number = {11}, Pages = {874-85}, - pubmed = {15496865}, + pmid = {15496865}, Pst = {ppublish}, Title = {VSDI: a new era in functional imaging of cortical dynamics}, Volume = {5}, @@ -26872,7 +26871,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {optical physiology;optical imaging;voltage sensor;Technique;review;microscopy;calcium sensor;calcium imaging;frontiers review}, Mesh = {Animals; Brain; Calcium; Coloring Agents; Evoked Potentials; Humans; Photons}, Pages = {43-79}, - pubmed = {18839087}, + pmid = {18839087}, Pst = {ppublish}, Title = {Wide-field and two-photon imaging of brain activity with voltage- and calcium-sensitive dyes}, Volume = {489}, @@ -26893,7 +26892,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {7233}, Pages = {1142-5}, Pmc = {PMC2745650}, - pubmed = {19151697}, + pmid = {19151697}, Pst = {ppublish}, Title = {The subcellular organization of neocortical excitatory connections}, Volume = {457}, @@ -26913,7 +26912,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {5}, Pages = {663-8}, - pubmed = {17435752}, + pmid = {17435752}, Pst = {ppublish}, Title = {Channelrhodopsin-2-assisted circuit mapping of long-range callosal projections}, Volume = {10}, @@ -26933,7 +26932,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {2}, Pages = {171-89}, - pubmed = {19409263}, + pmid = {19409263}, Pst = {ppublish}, Title = {Rapid neocortical dynamics: cellular and network mechanisms}, Volume = {62}, @@ -26953,7 +26952,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {1-2}, Pages = {31-44}, - pubmed = {7859089}, + pmid = {7859089}, Pst = {ppublish}, Title = {Spontaneous activity of first- and second-order neurons in the frog olfactory system}, Volume = {662}, @@ -26973,7 +26972,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {5462}, Pages = {2479-82}, Pmc = {PMC2637940}, - pubmed = {10741966}, + pmid = {10741966}, Pst = {ppublish}, Title = {Necessity for afferent activity to maintain eye-specific segregation in ferret lateral geniculate nucleus}, Volume = {287}, @@ -26992,7 +26991,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {6}, Pages = {1161-72}, - pubmed = {14687550}, + pmid = {14687550}, Pst = {ppublish}, Title = {Abnormal functional organization in the dorsal lateral geniculate nucleus of mice lacking the beta 2 subunit of the nicotinic acetylcholine receptor}, Volume = {40}, @@ -27011,7 +27010,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {2}, Pages = {587-600}, - pubmed = {12533619}, + pmid = {12533619}, Pst = {ppublish}, Title = {Characterization of the circuits that generate spontaneous episodes of activity in the early embryonic mouse spinal cord}, Volume = {23}, @@ -27030,7 +27029,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {3 Pt 2}, Pages = {1486-95}, - pubmed = {8126550}, + pmid = {8126550}, Pst = {ppublish}, Title = {Rhythmic spontaneous activity in the developing avian auditory system}, Volume = {14}, @@ -27050,7 +27049,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {4}, Pages = {1898-908}, Pmc = {PMC2234389}, - pubmed = {17686914}, + pmid = {17686914}, Pst = {ppublish}, Title = {Spontaneous discharge patterns in cochlear spiral ganglion cells before the onset of hearing in cats}, Volume = {98}, @@ -27070,7 +27069,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {20}, Pages = {8129-35}, - pubmed = {11588185}, + pmid = {11588185}, Pst = {ppublish}, Title = {Primordial rhythmic bursting in embryonic cochlear ganglion cells}, Volume = {21}, @@ -27089,7 +27088,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {6}, Pages = {685-8}, - pubmed = {8199338}, + pmid = {8199338}, Pst = {ppublish}, Title = {Patterned neural activity in brain stem auditory areas of a prehearing mammal, the tammar wallaby (Macropus eugenii)}, Volume = {5}, @@ -27108,7 +27107,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Nov}, Number = {7166}, Pages = {50-5}, - pubmed = {17972875}, + pmid = {17972875}, Pst = {ppublish}, Title = {The origin of spontaneous activity in the developing auditory system}, Volume = {450}, @@ -27129,7 +27128,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {4}, Pages = {463-73}, Pmc = {PMC2912499}, - pubmed = {19287389}, + pmid = {19287389}, Pst = {ppublish}, Title = {Traveling waves in developing cerebellar cortex mediated by asymmetrical Purkinje cell connectivity}, Volume = {12}, @@ -27149,7 +27148,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {11}, Pages = {689-704}, - pubmed = {19449313}, + pmid = {19449313}, Pst = {ppublish}, Title = {Spontaneous activity in the developing mouse midbrain driven by an external pacemaker}, Volume = {69}, @@ -27170,7 +27169,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1}, Pages = {18-29}, Pmc = {PMC2902252}, - pubmed = {19953103}, + pmid = {19953103}, Pst = {ppublish}, Title = {Mechanisms underlying spontaneous patterned activity in developing neural circuits}, Volume = {11}, @@ -27191,7 +27190,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {18}, Pages = {4807-17}, Pmc = {PMC2793334}, - pubmed = {18448657}, + pmid = {18448657}, Pst = {ppublish}, Title = {Vision triggers an experience-dependent sensitive period at the retinogeniculate synapse}, Volume = {28}, @@ -27211,7 +27210,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {2}, Pages = {281-91}, - pubmed = {17046691}, + pmid = {17046691}, Pst = {ppublish}, Title = {Distinct roles for spontaneous and visual activity in remodeling of the retinogeniculate synapse}, Volume = {52}, @@ -27232,7 +27231,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {2}, Pages = {181-7}, - pubmed = {19502049}, + pmid = {19502049}, Pst = {ppublish}, Title = {Intrinsic patterning and experience-dependent mechanisms that generate eye-specific projections and binocular circuits in the visual pathway}, Volume = {19}, @@ -27251,7 +27250,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {1}, Pages = {1-51}, - pubmed = {6772696}, + pmid = {6772696}, Pst = {ppublish}, Title = {The development of ocular dominance columns in normal and visually deprived monkeys}, Volume = {191}, @@ -27269,7 +27268,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {961}, Pages = {377-409}, - pubmed = {19791}, + pmid = {19791}, Pst = {ppublish}, Title = {Plasticity of ocular dominance columns in monkey striate cortex}, Volume = {278}, @@ -27289,7 +27288,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {3}, Pages = {701-9}, Pmc = {PMC1395553}, - pubmed = {5499804}, + pmid = {5499804}, Pst = {ppublish}, Title = {Neuromuscular transmission in new-born rats}, Volume = {209}, @@ -27308,7 +27307,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {1}, Pages = {67-73}, - pubmed = {12526773}, + pmid = {12526773}, Pst = {ppublish}, Title = {In vivo time-lapse imaging of synaptic takeover associated with naturally occurring synapse elimination}, Volume = {37}, @@ -27325,7 +27324,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {21 Activity-development;Spontaneous activity;review;Spinal Cord;Neuromuscular Junction;Competitive Behavior;synapse formation;Synaptic Transmission;structural remodeling;connectivity;frontiers review}, Mesh = {Animals; Glycoproteins; Nerve Regeneration; Neuregulins; Neuromuscular Junction; Presynaptic Terminals; Signal Transduction; Synapses; Transcription, Genetic; Vertebrates}, Pages = {389-442}, - pubmed = {10202544}, + pmid = {10202544}, Pst = {ppublish}, Title = {Development of the vertebrate neuromuscular junction}, Volume = {22}, @@ -27345,7 +27344,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {5454}, Pages = {864-9}, - pubmed = {10657302}, + pmid = {10657302}, Pst = {ppublish}, Title = {Synaptic assembly of the brain in the absence of neurotransmitter secretion}, Volume = {287}, @@ -27365,7 +27364,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {13}, Pages = {9037-42}, Pmc = {PMC124419}, - pubmed = {12070347}, + pmid = {12070347}, Pst = {ppublish}, Title = {Total arrest of spontaneous and evoked synaptic transmission but normal synaptogenesis in the absence of Munc13-mediated vesicle priming}, Volume = {99}, @@ -27385,7 +27384,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {3}, Pages = {859-69}, - pubmed = {17161628}, + pmid = {17161628}, Pst = {ppublish}, Title = {In vivo calcium imaging from genetically specified target cells in mouse cerebellum}, Volume = {34}, @@ -27406,7 +27405,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {2}, Pages = {817-30}, Pmc = {PMC2724327}, - pubmed = {19474178}, + pmid = {19474178}, Pst = {ppublish}, Title = {Optical imaging of postsynaptic odor representation in the glomerular layer of the mouse olfactory bulb}, Volume = {102}, @@ -27426,7 +27425,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {6}, Pages = {1048-61}, - pubmed = {20869600}, + pmid = {20869600}, Pst = {ppublish}, Title = {Neural activity in barrel cortex underlying vibrissa-based object localization in mice}, Volume = {67}, @@ -27447,7 +27446,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {29}, Pages = {10554-9}, Pmc = {PMC490022}, - pubmed = {15247428}, + pmid = {15247428}, Pst = {ppublish}, Title = {Expanded dynamic range of fluorescent indicators for Ca(2+) by circularly permuted yellow fluorescent proteins}, Volume = {101}, @@ -27468,7 +27467,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {2}, Pages = {214-25}, Pmc = {PMC2578820}, - pubmed = {18667150}, + pmid = {18667150}, Pst = {ppublish}, Title = {Abeta plaques lead to aberrant regulation of calcium homeostasis in vivo resulting in structural and functional disruption of neuronal networks}, Volume = {59}, @@ -27488,7 +27487,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {29}, Pages = {6466-75}, - pubmed = {15269256}, + pmid = {15269256}, Pst = {ppublish}, Title = {Alteration of neuronal firing properties after in vivo experience in a FosGFP transgenic mouse}, Volume = {24}, @@ -27508,7 +27507,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {1}, Pages = {39-42}, - pubmed = {17128267}, + pmid = {17128267}, Pst = {ppublish}, Title = {Fast manipulation of cellular cAMP level by light in vivo}, Volume = {4}, @@ -27528,7 +27527,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {9}, Pages = {1263-8}, - pubmed = {16116447}, + pmid = {16116447}, Pst = {ppublish}, Title = {Millisecond-timescale, genetically targeted optical control of neural activity}, Volume = {8}, @@ -27549,7 +27548,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {49}, Pages = {17816-21}, Pmc = {PMC1292990}, - pubmed = {16306259}, + pmid = {16306259}, Pst = {ppublish}, Title = {Fast noninvasive activation and inhibition of neural and network activity by vertebrate rhodopsin and green algae channelrhodopsin}, Volume = {102}, @@ -27570,7 +27569,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {5}, Pages = {544-52}, Pmc = {PMC2788492}, - pubmed = {19828309}, + pmid = {19828309}, Pst = {ppublish}, Title = {New photochemical tools for controlling neuronal activity}, Volume = {19}, @@ -27591,7 +27590,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {24}, Pages = {13940-5}, Pmc = {PMC283525}, - pubmed = {14615590}, + pmid = {14615590}, Pst = {ppublish}, Title = {Channelrhodopsin-2, a directly light-gated cation-selective membrane channel}, Volume = {100}, @@ -27611,7 +27610,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {3}, Pages = {410-24}, - pubmed = {20105242}, + pmid = {20105242}, Pst = {ppublish}, Title = {Pre-synaptic and post-synaptic neuronal activity supports the axon development of callosal projection neurons during different post-natal periods in the mouse cerebral cortex}, Volume = {31}, @@ -27631,7 +27630,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {42}, Pages = {11334-42}, - pubmed = {17942728}, + pmid = {17942728}, Pst = {ppublish}, Title = {Activity-dependent development of callosal projections in the somatosensory cortex}, Volume = {27}, @@ -27652,7 +27651,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {11}, Pages = {911-21}, Pmc = {PMC2175069}, - pubmed = {17493809}, + pmid = {17493809}, Pst = {ppublish}, Title = {Genetic modulation of BDNF signaling affects the outcome of axonal competition in vivo}, Volume = {17}, @@ -27672,7 +27671,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {4}, Pages = {553-66}, - pubmed = {15157418}, + pmid = {15157418}, Pst = {ppublish}, Title = {Spontaneous neural activity is required for the establishment and maintenance of the olfactory sensory map}, Volume = {42}, @@ -27688,7 +27687,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Developmental neurobiology}, Keywords = {21 Activity-development;development;structural remodeling;activity manipulation;review;Zebrafish;frontiers review}, Month = {Jan}, - pubmed = {21309080}, + pmid = {21309080}, Pst = {aheadofprint}, Title = {Imaging circuit formation in zebrafish}, Year = {2011}, @@ -27707,7 +27706,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {32}, Pages = {10939-51}, - pubmed = {20702722}, + pmid = {20702722}, Pst = {ppublish}, Title = {Synaptic activity and activity-dependent competition regulates axon arbor maturation, growth arrest, and territory in the retinotectal projection}, Volume = {30}, @@ -27728,7 +27727,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {2}, Pages = {306-19}, Pmc = {PMC2267481}, - pubmed = {18160134}, + pmid = {18160134}, Pst = {ppublish}, Title = {Imaging of glutamate in brain slices using FRET sensors}, Volume = {168}, @@ -27748,7 +27747,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {1}, Pages = {9-21}, - pubmed = {21220095}, + pmid = {21220095}, Pst = {ppublish}, Title = {Imaging voltage in neurons}, Volume = {69}, @@ -27768,7 +27767,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {2}, Pages = {1636-44}, - pubmed = {16079125}, + pmid = {16079125}, Pst = {ppublish}, Title = {In vivo calcium imaging of circuit activity in cerebellar cortex}, Volume = {94}, @@ -27786,7 +27785,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {21 Activity-development;Neocortex;10 circuit formation;Spontaneous activity;Acetylcholine;review}, Mesh = {Animals; Cerebral Cortex; Humans; Neural Pathways; Neuronal Plasticity; Neurons; Stem Cells}, Pages = {23-48}, - pubmed = {20201645}, + pmid = {20201645}, Pst = {ppublish}, Title = {The subplate and early cortical circuits}, Volume = {33}, @@ -27807,7 +27806,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {45}, Pages = {14998-5004}, Pmc = {PMC2997431}, - pubmed = {21068304}, + pmid = {21068304}, Pst = {ppublish}, Title = {Toward the second generation of optogenetic tools}, Volume = {30}, @@ -27827,7 +27826,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1}, Pages = {35-8}, Pmc = {PMC3024327}, - pubmed = {21191370}, + pmid = {21191370}, Pst = {ppublish}, Title = {The promise of optogenetics in cell biology: interrogating molecular circuits in space and time}, Volume = {8}, @@ -27848,7 +27847,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {34}, Pages = {10463-73}, Pmc = {PMC2783593}, - pubmed = {19710300}, + pmid = {19710300}, Pst = {ppublish}, Title = {Reliable coding emerges from coactivation of climbing fibers in microbands of cerebellar Purkinje neurons}, Volume = {29}, @@ -27869,7 +27868,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1495}, Pages = {1393-9}, Pmc = {PMC2610128}, - pubmed = {18198155}, + pmid = {18198155}, Pst = {ppublish}, Title = {Implications of activity-dependent neurotransmitter-receptor matching}, Volume = {363}, @@ -27888,7 +27887,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {1}, Pages = {26-9}, - pubmed = {21191368}, + pmid = {21191368}, Pst = {ppublish}, Title = {Optogenetics}, Volume = {8}, @@ -27910,7 +27909,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {7266}, Pages = {900-7}, Pmc = {PMC2884271}, - pubmed = {19829369}, + pmid = {19829369}, Pst = {ppublish}, Title = {Molecular genetics and imaging technologies for circuit-based neuroanatomy}, Volume = {461}, @@ -27930,7 +27929,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {1}, Pages = {9-21}, - pubmed = {15066261}, + pmid = {15066261}, Pst = {ppublish}, Title = {In vivo imaging of neuronal activity by targeted expression of a genetically encoded probe in the mouse}, Volume = {42}, @@ -27948,7 +27947,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Animals; Behavior; Brain; Gene Targeting; Genes, Dominant; Genetic Research; Mice; Models, Animal; Nerve Net; Pharmacogenetics}, Pages = {1-38}, Pmc = {PMC2861997}, - pubmed = {19615530}, + pmid = {19615530}, Pst = {ppublish}, Title = {Genetic dissection of neural circuits and behavior in Mus musculus}, Volume = {65}, @@ -27967,7 +27966,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {1}, Pages = {61-72}, - pubmed = {21110347}, + pmid = {21110347}, Pst = {ppublish}, Title = {Identifying roles for neurotransmission in circuit assembly: insights gained from multiple model systems and experimental approaches}, Volume = {33}, @@ -27986,7 +27985,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Animals; Models, Neurological; Nerve Net; Neurons; Superior Colliculi; Visual Pathways; Visual Perception; Zebrafish}, Pages = {126}, Pmc = {PMC2949621}, - pubmed = {20920150}, + pmid = {20920150}, Pst = {epublish}, Title = {Focusing on optic tectum circuitry through the lens of genetics}, Volume = {8}, @@ -28006,7 +28005,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {7120}, Pages = {707-12}, - pubmed = {17151658}, + pmid = {17151658}, Pst = {ppublish}, Title = {Electrical activity in early neuronal development}, Volume = {444}, @@ -28024,7 +28023,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {frontiers review;activity manipulation;Synaptic Transmission;Genetic Engineering}, Pages = {16}, Pmc = {PMC2773177}, - pubmed = {19893765}, + pmid = {19893765}, Pst = {ppublish}, Title = {Engineered G-protein Coupled Receptors are Powerful Tools to Investigate Biological Processes and Behaviors}, Volume = {2}, @@ -28044,7 +28043,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {9}, Pages = {e6923}, Pmc = {PMC2735035}, - pubmed = {19742327}, + pmid = {19742327}, Pst = {epublish}, Title = {Fluorescence-based monitoring of in vivo neural activity using a circuit-tracing pseudorabies virus}, Volume = {4}, @@ -28063,7 +28062,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {1}, Pages = {30-4}, - pubmed = {21191369}, + pmid = {21191369}, Pst = {ppublish}, Title = {From cudgel to scalpel: toward precise neural control with optogenetics}, Volume = {8}, @@ -28081,7 +28080,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {frontiers review; example;optical physiology; technique}, Pages = {31}, Pmc = {PMC2814554}, - pubmed = {20126433}, + pmid = {20126433}, Pst = {epublish}, Title = {Optogenetic deconstruction of sleep-wake circuitry in the brain}, Volume = {2}, @@ -28099,7 +28098,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {frontiers review; example; optical physiology; technique}, Pages = {15}, Pmc = {PMC2802328}, - pubmed = {20057911}, + pmid = {20057911}, Pst = {ppublish}, Title = {Genetically encoded optical sensors for monitoring of intracellular chloride and chloride-selective channel activity}, Volume = {2}, @@ -28117,7 +28116,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {frontiers review; example; optical physiology; technique}, Pages = {13}, Pmc = {PMC2741205}, - pubmed = {19750193}, + pmid = {19750193}, Pst = {ppublish}, Title = {Ion channels to inactivate neurons in Drosophila}, Volume = {2}, @@ -28135,7 +28134,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {frontiers review; example; optical physiology; technique}, Pages = {21}, Pmc = {PMC2776481}, - pubmed = {19915728}, + pmid = {19915728}, Pst = {ppublish}, Title = {Manipulating neuronal circuits with endogenous and recombinant cell-surface tethered modulators}, Volume = {2}, @@ -28153,7 +28152,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {frontiers review; example; optical physiology;voltage sensor; technique}, Pages = {5}, Pmc = {PMC2706653}, - pubmed = {19623246}, + pmid = {19623246}, Pst = {ppublish}, Title = {Second and third generation voltage-sensitive fluorescent proteins for monitoring membrane potential}, Volume = {2}, @@ -28171,7 +28170,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {frontiers review; example; optical physiology; technique}, Pages = {27}, Pmc = {PMC2802553}, - pubmed = {20057936}, + pmid = {20057936}, Pst = {ppublish}, Title = {Genetic control of active neural circuits}, Volume = {2}, @@ -28189,7 +28188,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {frontiers review; example; optical physiology; technique}, Pages = {8}, Pmc = {PMC2724028}, - pubmed = {19668708}, + pmid = {19668708}, Pst = {ppublish}, Title = {Activity-dependent modulation of neural circuit synaptic connectivity}, Volume = {2}, @@ -28209,7 +28208,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {5567}, Pages = {503-7}, - pubmed = {11964472}, + pmid = {11964472}, Pst = {ppublish}, Title = {Multicolor and electron microscopic imaging of connexin trafficking}, Volume = {296}, @@ -28228,7 +28227,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1}, Pages = {e16493}, Pmc = {PMC3029380}, - pubmed = {21304595}, + pmid = {21304595}, Pst = {epublish}, Title = {A quantitative comparison of cell-type-specific microarray gene expression profiling methods in the mouse brain}, Volume = {6}, @@ -28248,7 +28247,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {3}, Pages = {1402-19}, - pubmed = {7807221}, + pmid = {7807221}, Pst = {ppublish}, Title = {Dynamics of propagating waves in the olfactory network of a terrestrial mollusk: an electrical and optical study}, Volume = {72}, @@ -28267,7 +28266,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {1}, Pages = {95-106}, - pubmed = {8189755}, + pmid = {8189755}, Pst = {ppublish}, Title = {Multi-neuronal signals from the retina: acquisition and analysis}, Volume = {51}, @@ -28287,7 +28286,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {24}, Pages = {9097-102}, Pmc = {PMC428479}, - pubmed = {15184670}, + pmid = {15184670}, Pst = {ppublish}, Title = {Functional organization of sensory input to the olfactory bulb glomerulus analyzed by two-photon calcium imaging}, Volume = {101}, @@ -28307,7 +28306,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {4}, Pages = {313-29}, - pubmed = {2271447}, + pmid = {2271447}, Pst = {ppublish}, Title = {Topographic organization of the retinocollicular projection in the neonatal rat}, Volume = {4}, @@ -28326,7 +28325,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {3}, Pages = {955-66}, - pubmed = {11163279}, + pmid = {11163279}, Pst = {ppublish}, Title = {Developmental remodeling of the retinogeniculate synapse}, Volume = {28}, @@ -28345,7 +28344,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {1}, Pages = {25-32}, - pubmed = {10939328}, + pmid = {10939328}, Pst = {ppublish}, Title = {Monitoring presynaptic calcium dynamics in projection fibers by in vivo loading of a novel calcium indicator}, Volume = {27}, @@ -28364,7 +28363,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {12}, Pages = {981-4}, - pubmed = {20966916}, + pmid = {20966916}, Pst = {ppublish}, Title = {Chronic optical access through a polished and reinforced thinned skull}, Volume = {7}, @@ -28384,7 +28383,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {11}, Pages = {1433-40}, Pmc = {PMC2967725}, - pubmed = {20890294}, + pmid = {20890294}, Pst = {ppublish}, Title = {Functional imaging of hippocampal place cells at cellular resolution during virtual navigation}, Volume = {13}, @@ -28403,7 +28402,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {6}, Pages = {747-60}, - pubmed = {19778505}, + pmid = {19778505}, Pst = {ppublish}, Title = {Automated analysis of cellular signals from large-scale calcium imaging data}, Volume = {63}, @@ -28423,7 +28422,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {6}, Pages = {803-14}, - pubmed = {17570502}, + pmid = {17570502}, Pst = {ppublish}, Title = {Morphological properties of mouse retinal ganglion cells during postnatal development}, Volume = {503}, @@ -28444,7 +28443,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {12}, Pages = {875-81}, Pmc = {PMC2858873}, - pubmed = {19898485}, + pmid = {19898485}, Pst = {ppublish}, Title = {Imaging neural activity in worms, flies and mice with improved GCaMP calcium indicators}, Volume = {6}, @@ -28464,7 +28463,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {1}, Pages = {22-4}, - pubmed = {20371341}, + pmid = {20371341}, Pst = {ppublish}, Title = {Optogenetics 3.0}, Volume = {141}, @@ -28485,7 +28484,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {35}, Pages = {15025-30}, Pmc = {PMC2736443}, - pubmed = {19706471}, + pmid = {19706471}, Pst = {ppublish}, Title = {Two-photon excitation of channelrhodopsin-2 at saturation}, Volume = {106}, @@ -28505,7 +28504,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {7292}, Pages = {1182-6}, - pubmed = {20376005}, + pmid = {20376005}, Pst = {ppublish}, Title = {Learning-related fine-scale specificity imaged in motor cortex circuits of behaving mice}, Volume = {464}, @@ -28526,7 +28525,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {4}, Pages = {508-22}, Pmc = {PMC2874753}, - pubmed = {19709632}, + pmid = {19709632}, Pst = {ppublish}, Title = {Direct activation of sparse, distributed populations of cortical neurons by electrical microstimulation}, Volume = {63}, @@ -28547,7 +28546,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1-4}, Pages = {53-67}, Pmc = {PMC2775812}, - pubmed = {18679801}, + pmid = {18679801}, Pst = {ppublish}, Title = {Genetically encoded fluorescent sensors of membrane potential}, Volume = {36}, @@ -28567,7 +28566,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {1}, Pages = {29-37}, - pubmed = {11574117}, + pmid = {11574117}, Pst = {ppublish}, Title = {Two-photon microscopy in brain tissue: parameters influencing the imaging depth}, Volume = {111}, @@ -28587,7 +28586,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {7}, Pages = {511-2}, Pmc = {PMC2849805}, - pubmed = {19525959}, + pmid = {19525959}, Pst = {ppublish}, Title = {In vivo fluorescence imaging with high-resolution microlenses}, Volume = {6}, @@ -28607,7 +28606,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jun}, Number = {7299}, Pages = {788-92}, - pubmed = {20473285}, + pmid = {20473285}, Pst = {ppublish}, Title = {Global and local fMRI signals driven by neurons defined optogenetically by type and wiring}, Volume = {465}, @@ -28629,7 +28628,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1-4}, Pages = {69-86}, Pmc = {PMC2755531}, - pubmed = {18941901}, + pmid = {18941901}, Pst = {ppublish}, Title = {Reporting neural activity with genetically encoded calcium indicators}, Volume = {36}, @@ -28648,7 +28647,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Action Potentials; Animals; Microscopy, Confocal; Models, Theoretical; Neurons; Optics and Photonics; Photons}, Month = {Feb}, Pages = {47-55}, - pubmed = {17289930}, + pmid = {17289930}, Pst = {ppublish}, Title = {Optical recording of action potentials and other discrete physiological events: a perspective from signal detection theory}, Volume = {22}, @@ -28669,7 +28668,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {35}, Pages = {15049-54}, Pmc = {PMC2736444}, - pubmed = {19706480}, + pmid = {19706480}, Pst = {ppublish}, Title = {Sparsification of neuronal activity in the visual cortex at eye-opening}, Volume = {106}, @@ -28691,7 +28690,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {12}, Pages = {1268-77}, Pmc = {PMC2818747}, - pubmed = {20064437}, + pmid = {20064437}, Pst = {ppublish}, Title = {Red-shifted voltage-sensitive fluorescent proteins}, Volume = {16}, @@ -28711,7 +28710,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {3}, Pages = {160-6}, - pubmed = {16443289}, + pmid = {16443289}, Pst = {ppublish}, Title = {Optical probing of neuronal circuit dynamics: genetically encoded versus classical fluorescent sensors}, Volume = {29}, @@ -28732,7 +28731,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {46}, Pages = {19557-62}, Pmc = {PMC2773198}, - pubmed = {19889973}, + pmid = {19889973}, Pst = {ppublish}, Title = {Visually evoked activity in cortical cells imaged in freely moving animals}, Volume = {106}, @@ -28754,7 +28753,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {Pt 3}, Pages = {339-52}, Pmc = {PMC2740625}, - pubmed = {18503659}, + pmid = {18503659}, Pst = {ppublish}, Title = {Automated identification of neurons and their locations}, Volume = {230}, @@ -28774,7 +28773,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {5}, Pages = {399-405}, - pubmed = {20400966}, + pmid = {20400966}, Pst = {ppublish}, Title = {High-speed in vivo calcium imaging reveals neuronal network activity with near-millisecond precision}, Volume = {7}, @@ -28793,7 +28792,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {optical physiology; frontiers review; calcium imaging; Technique;in vivo}, Pages = {9}, Pmc = {PMC2866455}, - pubmed = {20461230}, + pmid = {20461230}, Pst = {epublish}, Title = {Optical recording of neuronal activity with a genetically-encoded calcium indicator in anesthetized and freely moving mice}, Volume = {4}, @@ -28814,7 +28813,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {5918}, Pages = {1211-5}, Pmc = {PMC2884172}, - pubmed = {19251629}, + pmid = {19251629}, Pst = {ppublish}, Title = {Synchronous hyperactivity and intercellular calcium waves in astrocytes in Alzheimer mice}, Volume = {323}, @@ -28834,7 +28833,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {1}, Pages = {154-65}, - pubmed = {20303157}, + pmid = {20303157}, Pst = {ppublish}, Title = {Molecular and cellular approaches for diversifying and extending optogenetics}, Volume = {141}, @@ -28855,7 +28854,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {12}, Pages = {883-9}, Pmc = {PMC2859341}, - pubmed = {19898484}, + pmid = {19898484}, Pst = {ppublish}, Title = {A genetically encoded reporter of synaptic activity in vivo}, Volume = {6}, @@ -28876,7 +28875,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {35}, Pages = {10890-9}, Pmc = {PMC2771734}, - pubmed = {19726647}, + pmid = {19726647}, Pst = {ppublish}, Title = {Internally mediated developmental desynchronization of neocortical network activity}, Volume = {29}, @@ -28897,7 +28896,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {5}, Pages = {636-41}, - pubmed = {15464898}, + pmid = {15464898}, Pst = {ppublish}, Title = {Fluorescent proteins as sensors for cellular functions}, Volume = {14}, @@ -28917,7 +28916,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {9}, Pages = {797-804}, - pubmed = {19160514}, + pmid = {19160514}, Pst = {ppublish}, Title = {Single-spike detection in vitro and in vivo with a genetic Ca2+ sensor}, Volume = {5}, @@ -28937,7 +28936,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {5-6}, Pages = {458-64}, - pubmed = {20105103}, + pmid = {20105103}, Pst = {ppublish}, Title = {Advanced tracing tools: functional neuronal expression of virally encoded fluorescent calcium indicator proteins}, Volume = {15}, @@ -28957,7 +28956,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {14}, Pages = {2149-53}, - pubmed = {15371723}, + pmid = {15371723}, Pst = {ppublish}, Title = {Transient microcircuits formed by subplate neurons and their role in functional development of thalamocortical connections}, Volume = {15}, @@ -28977,7 +28976,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {5}, Pages = {749-62}, Pmc = {PMC2446609}, - pubmed = {18549786}, + pmid = {18549786}, Pst = {ppublish}, Title = {Activity-dependent regulation of synaptic AMPA receptor composition and abundance by beta3 integrins}, Volume = {58}, @@ -28998,7 +28997,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {17}, Pages = {4377-84}, Pmc = {PMC2655203}, - pubmed = {18434516}, + pmid = {18434516}, Pst = {ppublish}, Title = {Multiple modes of network homeostasis in visual cortical layer 2/3}, Volume = {28}, @@ -29017,7 +29016,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {2}, Pages = {97-107}, - pubmed = {14735113}, + pmid = {14735113}, Pst = {ppublish}, Title = {Homeostatic plasticity in the developing nervous system}, Volume = {5}, @@ -29037,7 +29036,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {3}, Pages = {473-85}, - pubmed = {12741993}, + pmid = {12741993}, Pst = {ppublish}, Title = {Robust spatial working memory through homeostatic synaptic scaling in heterogeneous cortical networks}, Volume = {38}, @@ -29054,7 +29053,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {optogenetics;imaging;in vivo;review;optical imaging;frontiers review;23 Technique}, Pages = {5}, Pmc = {PMC2718781}, - pubmed = {19649169}, + pmid = {19649169}, Pst = {ppublish}, Title = {Optical imaging as a link between cellular neurophysiology and circuit modeling}, Volume = {3}, @@ -29073,7 +29072,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {5439}, Pages = {509-12}, - pubmed = {10521342}, + pmid = {10521342}, Pst = {ppublish}, Title = {Emergence of scaling in random networks}, Volume = {286}, @@ -29093,7 +29092,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {6}, Pages = {1043-50}, Pmc = {PMC3022325}, - pubmed = {21172607}, + pmid = {21172607}, Pst = {ppublish}, Title = {An embedded subnetwork of highly active neurons in the neocortex}, Volume = {68}, @@ -29114,7 +29113,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {4}, Pages = {390-2}, Pmc = {PMC2669755}, - pubmed = {19252494}, + pmid = {19252494}, Pst = {ppublish}, Title = {Thalamic activity that drives visual cortical plasticity}, Volume = {12}, @@ -29134,7 +29133,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {49}, Pages = {16509-13}, - pubmed = {21147990}, + pmid = {21147990}, Pst = {ppublish}, Title = {Transgenic targeting of recombinant rabies virus reveals monosynaptic connectivity of specific neurons}, Volume = {30}, @@ -29154,7 +29153,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {49}, Pages = {16573-84}, - pubmed = {21147997}, + pmid = {21147997}, Pst = {ppublish}, Title = {Visual receptive field properties of neurons in the superficial superior colliculus of the mouse}, Volume = {30}, @@ -29174,7 +29173,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jun}, Number = {24}, Pages = {6452-60}, - pubmed = {17567806}, + pmid = {17567806}, Pst = {ppublish}, Title = {The relationship between blood flow and neuronal activity in the rodent olfactory bulb}, Volume = {27}, @@ -29194,7 +29193,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {10}, Pages = {3067-72}, - pubmed = {19279243}, + pmid = {19279243}, Pst = {ppublish}, Title = {Peripheral adaptation codes for high odor concentration in glomeruli}, Volume = {29}, @@ -29215,7 +29214,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {6}, Pages = {1509-17}, Pmc = {PMC2375708}, - pubmed = {18202093}, + pmid = {18202093}, Pst = {ppublish}, Title = {The regulation of dendritic arbor development and plasticity by glutamatergic synaptic input: a review of the synaptotrophic hypothesis}, Volume = {586}, @@ -29236,7 +29235,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {44}, Pages = {13751-60}, Pmc = {PMC2872549}, - pubmed = {19889987}, + pmid = {19889987}, Pst = {ppublish}, Title = {Functional clustering of neurons in motor cortex determined by cellular resolution imaging in awake behaving mice}, Volume = {29}, @@ -29257,7 +29256,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {3}, Pages = {305-15}, Pmc = {PMC2814245}, - pubmed = {19679071}, + pmid = {19679071}, Pst = {ppublish}, Title = {Linking genetically defined neurons to behavior through a broadly applicable silencing allele}, Volume = {63}, @@ -29278,7 +29277,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1}, Pages = {175-85}, Pmc = {PMC2814139}, - pubmed = {19804762}, + pmid = {19804762}, Pst = {ppublish}, Title = {Retinal input instructs alignment of visual topographic maps}, Volume = {139}, @@ -29300,7 +29299,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {8}, Pages = {e1000184}, Pmc = {PMC2724735}, - pubmed = {19707574}, + pmid = {19707574}, Pst = {ppublish}, Title = {Glia and muscle sculpt neuromuscular arbors by engulfing destabilized synaptic boutons and shed presynaptic debris}, Volume = {7}, @@ -29321,7 +29320,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {4}, Pages = {484-97}, Pmc = {PMC2850049}, - pubmed = {19945391}, + pmid = {19945391}, Pst = {ppublish}, Title = {DSCAM and DSCAML1 function in self-avoidance in multiple cell types in the developing mouse retina}, Volume = {64}, @@ -29341,7 +29340,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {2}, Pages = {240-50}, - pubmed = {19874791}, + pmid = {19874791}, Pst = {ppublish}, Title = {Metaplasticity governs natural experience-driven plasticity of nascent embryonic brain circuits}, Volume = {64}, @@ -29361,7 +29360,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {6}, Pages = {903-12}, - pubmed = {11580892}, + pmid = {11580892}, Pst = {ppublish}, Title = {A miniature head-mounted two-photon microscope. high-resolution brain imaging in freely moving animals}, Volume = {31}, @@ -29380,7 +29379,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {3}, Pages = {141-4}, - pubmed = {9406889}, + pmid = {9406889}, Pst = {ppublish}, Title = {Early detection of optic nerve-evoked response in the superior colliculus of the neonatal rat}, Volume = {235}, @@ -29399,7 +29398,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Nov}, Number = {10}, Pages = {1878-87}, - pubmed = {19895560}, + pmid = {19895560}, Pst = {ppublish}, Title = {Large-scale reorganization of corticofugal fibers after neonatal hemidecortication for functional restoration of forelimb movements}, Volume = {30}, @@ -29420,7 +29419,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {5}, Pages = {2581-93}, Pmc = {PMC2777828}, - pubmed = {19710376}, + pmid = {19710376}, Pst = {ppublish}, Title = {Exploring the superior colliculus in vitro}, Volume = {102}, @@ -29440,7 +29439,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {6345}, Pages = {655-6}, - pubmed = {1922382}, + pmid = {1922382}, Pst = {ppublish}, Title = {Retinal receptors in rodents maximally sensitive to ultraviolet light}, Volume = {353}, @@ -29461,7 +29460,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {8}, Pages = {e1000185}, Pmc = {PMC2722723}, - pubmed = {19707269}, + pmid = {19707269}, Pst = {ppublish}, Title = {Selective remodeling: refining neural connectivity at the neuromuscular junction}, Volume = {7}, @@ -29481,7 +29480,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {11}, Pages = {e1000527}, Pmc = {PMC2970556}, - pubmed = {21072242}, + pmid = {21072242}, Pst = {epublish}, Title = {Microglial interactions with synapses are modulated by visual experience}, Volume = {8}, @@ -29502,7 +29501,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {12}, Pages = {e1000600}, Pmc = {PMC2782179}, - pubmed = {20011124}, + pmid = {20011124}, Pst = {ppublish}, Title = {A multi-component model of the developing retinocollicular pathway incorporating axonal and synaptic growth}, Volume = {5}, @@ -29523,7 +29522,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {12}, Pages = {e1000618}, Pmc = {PMC2790088}, - pubmed = {20041207}, + pmid = {20041207}, Pst = {ppublish}, Title = {Burst-time-dependent plasticity robustly guides ON/OFF segregation in the lateral geniculate nucleus}, Volume = {5}, @@ -29544,7 +29543,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1}, Pages = {161-74}, Pmc = {PMC2812434}, - pubmed = {19804761}, + pmid = {19804761}, Pst = {ppublish}, Title = {Stringent specificity in the construction of a GABAergic presynaptic inhibitory circuit}, Volume = {139}, @@ -29565,7 +29564,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {7258}, Pages = {1016-20}, Pmc = {PMC2746695}, - pubmed = {19693082}, + pmid = {19693082}, Pst = {ppublish}, Title = {Neurotransmission selectively regulates synapse formation in parallel circuits in vivo}, Volume = {460}, @@ -29587,7 +29586,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1}, Pages = {32-9}, Pmc = {PMC2822732}, - pubmed = {20152111}, + pmid = {20152111}, Pst = {ppublish}, Title = {Genetically increased cell-intrinsic excitability enhances neuronal integration into adult brain circuits}, Volume = {65}, @@ -29606,7 +29605,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {12}, Pages = {e1000558}, Pmc = {PMC2998442}, - pubmed = {21151887}, + pmid = {21151887}, Pst = {epublish}, Title = {Melanopsin contributions to irradiance coding in the thalamo-cortical visual system}, Volume = {8}, @@ -29626,7 +29625,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {28}, Pages = {9011-25}, - pubmed = {19605639}, + pmid = {19605639}, Pst = {ppublish}, Title = {Three patterns of oscillatory activity differentially synchronize developing neocortical networks in vivo}, Volume = {29}, @@ -29644,7 +29643,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Nature}, Keywords = {23 Technique;Viral;Gene Therapy;imaging;cell interaction;Synapses;frontiers review}, Month = {Dec}, - pubmed = {21179085}, + pmid = {21179085}, Pst = {aheadofprint}, Title = {Cortical representations of olfactory input by trans-synaptic tracing}, Year = {2010}, @@ -29664,7 +29663,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {3}, Pages = {397-405}, Pmc = {PMC2743253}, - pubmed = {19679078}, + pmid = {19679078}, Pst = {ppublish}, Title = {Category-specific organization in the human brain does not require visual experience}, Volume = {63}, @@ -29685,7 +29684,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {10}, Pages = {e1000640}, Pmc = {PMC2763221}, - pubmed = {19876391}, + pmid = {19876391}, Pst = {ppublish}, Title = {Pseudorabies virus infection alters neuronal activity and connectivity in vitro}, Volume = {5}, @@ -29706,7 +29705,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {6}, Pages = {e1000125}, Pmc = {PMC2688840}, - pubmed = {19513122}, + pmid = {19513122}, Pst = {ppublish}, Title = {Melanopsin as a sleep modulator: circadian gating of the direct effects of light on sleep and altered sleep homeostasis in Opn4(-/-) mice}, Volume = {7}, @@ -29726,7 +29725,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {12}, Pages = {1013-9}, - pubmed = {14682362}, + pmid = {14682362}, Pst = {ppublish}, Title = {The legacy of Donald O. Hebb: more than the Hebb synapse}, Volume = {4}, @@ -29747,7 +29746,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {3}, Pages = {e1000334}, Pmc = {PMC2655718}, - pubmed = {19325892}, + pmid = {19325892}, Pst = {ppublish}, Title = {A proposal for a coordinated effort for the determination of brainwide neuroanatomical connectivity in model organisms at a mesoscopic scale}, Volume = {5}, @@ -29766,7 +29765,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {4}, Pages = {276-89}, - pubmed = {12671644}, + pmid = {12671644}, Pst = {ppublish}, Title = {Thalamocortical development: how are we going to get there?}, Volume = {4}, @@ -29783,7 +29782,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Journal of neurophysiology}, Keywords = {fmri;in vivo;optogenetics;imaging;21 Neurophysiology;23 Technique;frontiers review}, Month = {Dec}, - pubmed = {21160013}, + pmid = {21160013}, Pst = {aheadofprint}, Title = {Mapping Brain Networks in Awake Mice Using Combined Optical Neural Control and fMRI}, Year = {2010}, @@ -29802,7 +29801,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {4}, Pages = {472-9}, - pubmed = {20188652}, + pmid = {20188652}, Pst = {ppublish}, Title = {Modulation of visual responses by behavioral state in mouse visual cortex}, Volume = {65}, @@ -29823,7 +29822,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {3}, Pages = {400-12}, Pmc = {PMC2820366}, - pubmed = {19447095}, + pmid = {19447095}, Pst = {ppublish}, Title = {Motor behavior activates Bergmann glial networks}, Volume = {62}, @@ -29845,7 +29844,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {39}, Pages = {12070-8}, - pubmed = {19793965}, + pmid = {19793965}, Pst = {ppublish}, Title = {Nasal airflow rate affects the sensitivity and pattern of glomerular odorant responses in the mouse olfactory bulb}, Volume = {29}, @@ -29862,7 +29861,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {development;neocortex;21 Activity-development;10 circuit formation;axon guidance;review}, Mesh = {Afferent Pathways; Animals; Axons; Cell Division; Cerebral Cortex; Humans; Neuronal Plasticity; Thalamus}, Pages = {419-39}, - pubmed = {8210182}, + pmid = {8210182}, Pst = {ppublish}, Title = {Specification of neocortical areas and thalamocortical connections}, Volume = {17}, @@ -29880,7 +29879,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {21 Activity-development;axon guidance;Optic Nerve;retina;development;LGN;visual system;review}, Mesh = {Animals; Brain; Functional Laterality; Gene Expression Regulation, Developmental; Growth Cones; Humans; Intercellular Signaling Peptides and Proteins; Optic Chiasm; Retina; Retinal Ganglion Cells; Vision, Binocular; Visual Pathways}, Pages = {295-315}, - pubmed = {18558857}, + pmid = {18558857}, Pst = {ppublish}, Title = {Retinal axon growth at the optic chiasm: to cross or not to cross}, Volume = {31}, @@ -29900,7 +29899,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Animals; Fluorescent Dyes; Humans; Immune System; Immunologic Techniques; Lasers; Mice; Microscopy, Fluorescence, Multiphoton; Research}, Number = {4}, Pages = {438-44}, - pubmed = {20066001}, + pmid = {20066001}, Pst = {ppublish}, Title = {Practical intravital two-photon microscopy for immunological research: faster, brighter, deeper}, Volume = {88}, @@ -29921,7 +29920,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {7}, Pages = {596-601}, Pmc = {PMC2709730}, - pubmed = {19361999}, + pmid = {19361999}, Pst = {ppublish}, Title = {Retinotopically specific reorganization of visual cortex for tactile pattern recognition}, Volume = {19}, @@ -29942,7 +29941,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {47}, Pages = {14855-63}, Pmc = {PMC2829946}, - pubmed = {19940181}, + pmid = {19940181}, Pst = {ppublish}, Title = {Switching retinogeniculate axon laterality leads to normal targeting but abnormal eye-specific segregation that is activity dependent}, Volume = {29}, @@ -29962,7 +29961,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {33}, Pages = {10309-20}, - pubmed = {19692605}, + pmid = {19692605}, Pst = {ppublish}, Title = {Neocortical networks entrain neuronal circuits in cerebellar cortex}, Volume = {29}, @@ -29982,7 +29981,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {15}, Pages = {2309-11}, Pmc = {PMC2826365}, - pubmed = {19649080}, + pmid = {19649080}, Pst = {ppublish}, Title = {In vivo brain imaging using a portable 2.9 g two-photon microscope based on a microelectromechanical systems scanning mirror}, Volume = {34}, @@ -30000,7 +29999,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {5}, Pages = {565-6}, - pubmed = {18093825}, + pmid = {18093825}, Pst = {ppublish}, Title = {New technologies for neuroscience}, Volume = {17}, @@ -30021,7 +30020,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {11}, Pages = {935-8}, Pmc = {PMC2828344}, - pubmed = {18836457}, + pmid = {18836457}, Pst = {ppublish}, Title = {High-speed, miniaturized fluorescence microscopy in freely moving mice}, Volume = {5}, @@ -30040,7 +30039,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {neuroinformatics;Image Processing;Software;Computational Biology;Computer Graphics}, Pages = {13}, Pmc = {PMC2478650}, - pubmed = {18611266}, + pmid = {18611266}, Pst = {epublish}, Title = {Wndchrm - an open source utility for biological image analysis}, Volume = {3}, @@ -30060,7 +30059,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {39}, Pages = {12131-44}, - pubmed = {19793971}, + pmid = {19793971}, Pst = {ppublish}, Title = {Spontaneous bursting activity in the developing entorhinal cortex}, Volume = {29}, @@ -30079,7 +30078,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {10}, Pages = {798-9}, - pubmed = {20885441}, + pmid = {20885441}, Pst = {ppublish}, Title = {Optogenetics meets optical wavefront shaping}, Volume = {7}, @@ -30100,7 +30099,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {31}, Pages = {13034-9}, Pmc = {PMC2713389}, - pubmed = {19620732}, + pmid = {19620732}, Pst = {ppublish}, Title = {Bilateral visual field maps in a patient with only one hemisphere}, Volume = {106}, @@ -30123,7 +30122,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Nov}, Number = {5237}, Pages = {758-64}, - pubmed = {7481762}, + pmid = {7481762}, Pst = {ppublish}, Title = {Development and plasticity of cortical processing architectures}, Volume = {270}, @@ -30142,7 +30141,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {3}, Pages = {311-8}, - pubmed = {11516321}, + pmid = {11516321}, Pst = {ppublish}, Title = {Resolution of multiple green fluorescent protein color variants and dyes using two-photon microscopy and imaging spectroscopy}, Volume = {6}, @@ -30162,7 +30161,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Nov}, Number = {5}, Pages = {484-92}, - pubmed = {18983964}, + pmid = {18983964}, Pst = {ppublish}, Title = {Stem cell regulation via dynamic interactions of the nervous and immune systems with the microenvironment}, Volume = {3}, @@ -30182,7 +30181,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {5}, Pages = {978-90}, - pubmed = {21145009}, + pmid = {21145009}, Pst = {ppublish}, Title = {Spiral wave dynamics in neocortex}, Volume = {68}, @@ -30202,7 +30201,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {5}, Pages = {843-56}, - pubmed = {21144999}, + pmid = {21144999}, Pst = {ppublish}, Title = {Superresolution imaging of chemical synapses in the brain}, Volume = {68}, @@ -30222,7 +30221,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Nov}, Number = {7270}, Pages = {218-21}, - pubmed = {19907494}, + pmid = {19907494}, Pst = {ppublish}, Title = {Bidirectional plasticity in fast-spiking GABA circuits by visual experience}, Volume = {462}, @@ -30243,7 +30242,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {Pt 18}, Pages = {4347-55}, Pmc = {PMC2614011}, - pubmed = {18669531}, + pmid = {18669531}, Pst = {ppublish}, Title = {Synaptic activity, visual experience and the maturation of retinal synaptic circuitry}, Volume = {586}, @@ -30263,7 +30262,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {2}, Pages = {209-18}, - pubmed = {19743469}, + pmid = {19743469}, Pst = {ppublish}, Title = {Inhibitory actions of the gamma-aminobutyric acid in pediatric Sturge-Weber syndrome}, Volume = {66}, @@ -30284,7 +30283,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {24}, Pages = {9866-71}, Pmc = {PMC2687997}, - pubmed = {19478071}, + pmid = {19478071}, Pst = {ppublish}, Title = {The development of neural synchrony reflects late maturation and restructuring of functional networks in humans}, Volume = {106}, @@ -30305,7 +30304,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {15}, Pages = {5404-14}, Pmc = {PMC2885289}, - pubmed = {20392962}, + pmid = {20392962}, Pst = {ppublish}, Title = {Neuronal pentraxins mediate silent synapse conversion in the developing visual system}, Volume = {30}, @@ -30326,7 +30325,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {6}, Pages = {456-81}, Pmc = {PMC2919849}, - pubmed = {19672982}, + pmid = {19672982}, Pst = {ppublish}, Title = {Viral strategies for studying the brain, including a replication-restricted self-amplifying delta-G vesicular stomatis virus that rapidly expresses transgenes in brain and can generate a multicolor golgi-like expression}, Volume = {516}, @@ -30346,7 +30345,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Animals; Brain Mapping; Cerebral Cortex; Macaca; Mental Processes}, Number = {1}, Pages = {1-47}, - pubmed = {1822724}, + pmid = {1822724}, Pst = {ppublish}, Title = {Distributed hierarchical processing in the primate cerebral cortex}, Volume = {1}, @@ -30365,7 +30364,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Algorithms; Animals; Brain Mapping; Cerebral Cortex; Image Processing, Computer-Assisted; Macaca; Models, Anatomic; Statistics as Topic}, Number = {6}, Pages = {506-17}, - pubmed = {8590824}, + pmid = {8590824}, Pst = {ppublish}, Title = {Computational methods for reconstructing and unfolding the cerebral cortex}, Volume = {5}, @@ -30384,7 +30383,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {2}, Pages = {150-5}, - pubmed = {1638145}, + pmid = {1638145}, Pst = {ppublish}, Title = {Visual cortex: cartography, connectivity, and concurrent processing}, Volume = {2}, @@ -30403,7 +30402,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {5043}, Pages = {419-23}, - pubmed = {1734518}, + pmid = {1734518}, Pst = {ppublish}, Title = {Information processing in the primate visual system: an integrated systems perspective}, Volume = {255}, @@ -30420,7 +30419,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {Spontaneous activity; 21 Cortical oscillations; 21 Neurophysiology; 20 Networks; Theoretical; Computational Biology; graph theory}, Mesh = {Action Potentials; Animals; Humans; Nerve Net; Neural Networks (Computer); Nonlinear Dynamics; Signal Processing, Computer-Assisted; Time Factors}, Pages = {357-76}, - pubmed = {16022600}, + pmid = {16022600}, Pst = {ppublish}, Title = {Neural network dynamics}, Volume = {28}, @@ -30441,7 +30440,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1}, Pages = {69-84}, Pmc = {PMC2872122}, - pubmed = {20399730}, + pmid = {20399730}, Pst = {ppublish}, Title = {The apical complex couples cell fate and cell survival to cerebral cortical development}, Volume = {66}, @@ -30462,7 +30461,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1}, Pages = {21-31}, Pmc = {PMC2948651}, - pubmed = {20152110}, + pmid = {20152110}, Pst = {ppublish}, Title = {Cortical maps and white matter tracts following long period of visual deprivation and retinal image restoration}, Volume = {65}, @@ -30482,7 +30481,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {7231}, Pages = {901-5}, - pubmed = {19118385}, + pmid = {19118385}, Pst = {ppublish}, Title = {Calcium flickers steer cell migration}, Volume = {457}, @@ -30502,7 +30501,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {12}, Pages = {1541-8}, - pubmed = {17115045}, + pmid = {17115045}, Pst = {ppublish}, Title = {Simple fall-off pattern of correlated neural activity in the developing lateral geniculate nucleus}, Volume = {9}, @@ -30522,7 +30521,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {6626}, Pages = {680-5}, - pubmed = {9109486}, + pmid = {9109486}, Pst = {ppublish}, Title = {Disruption of orientation tuning in visual cortex by artificially correlated neuronal activity}, Volume = {386}, @@ -30542,7 +30541,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {4}, Pages = {563-75}, - pubmed = {16476665}, + pmid = {16476665}, Pst = {ppublish}, Title = {Spontaneous network activity in the embryonic spinal cord regulates AMPAergic and GABAergic synaptic strength}, Volume = {49}, @@ -30562,7 +30561,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {3 Pt 1}, Pages = {999-1010}, - pubmed = {8120639}, + pmid = {8120639}, Pst = {ppublish}, Title = {Growth cone "collapse" in vivo: are inhibitory interactions mediated by gap junctions?}, Volume = {14}, @@ -30581,7 +30580,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jun}, Number = {6}, Pages = {3437-48}, - pubmed = {8207465}, + pmid = {8207465}, Pst = {ppublish}, Title = {Calcium wave fronts that cross gap junctions may signal neuronal death during development}, Volume = {14}, @@ -30601,7 +30600,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {3}, Pages = {456-69}, Pmc = {PMC2966532}, - pubmed = {20933261}, + pmid = {20933261}, Pst = {ppublish}, Title = {Imaging activity-dependent regulation of neurexin-neuroligin interactions using trans-synaptic enzymatic biotinylation}, Volume = {143}, @@ -30621,7 +30620,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jun}, Number = {26}, Pages = {8745-58}, - pubmed = {20592196}, + pmid = {20592196}, Pst = {ppublish}, Title = {Visual function in mice with photoreceptor degeneration and transgenic expression of channelrhodopsin 2 in ganglion cells}, Volume = {30}, @@ -30641,7 +30640,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jun}, Number = {7247}, Pages = {698-702}, - pubmed = {19396159}, + pmid = {19396159}, Pst = {ppublish}, Title = {Parvalbumin neurons and gamma rhythms enhance cortical circuit performance}, Volume = {459}, @@ -30660,7 +30659,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {1}, Pages = {39-42}, - pubmed = {21191371}, + pmid = {21191371}, Pst = {ppublish}, Title = {Channelrhodopsin engineering and exploration of new optogenetic tools}, Volume = {8}, @@ -30680,7 +30679,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {4}, Pages = {183-92}, - pubmed = {20153060}, + pmid = {20153060}, Pst = {ppublish}, Title = {Learning to see: patterned visual activity and the development of visual function}, Volume = {33}, @@ -30701,7 +30700,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {10}, Pages = {512-20}, Pmc = {PMC2845908}, - pubmed = {18775572}, + pmid = {18775572}, Pst = {ppublish}, Title = {Cracking neural circuits in a tiny brain: new approaches for understanding the neural circuitry of Drosophila}, Volume = {31}, @@ -30721,7 +30720,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {6004}, Pages = {669-73}, - pubmed = {21030657}, + pmid = {21030657}, Pst = {ppublish}, Title = {Filtering of visual information in the tectum by an identified neural circuit}, Volume = {330}, @@ -30742,7 +30741,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {3}, Pages = {903-14}, - pubmed = {2230933}, + pmid = {2230933}, Pst = {ppublish}, Title = {Event-related potentials in the retina and optic tectum of fish}, Volume = {64}, @@ -30761,7 +30760,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {5}, Pages = {552-4}, - pubmed = {17450138}, + pmid = {17450138}, Pst = {ppublish}, Title = {Detection and prediction of periodic patterns by the retina}, Volume = {10}, @@ -30782,7 +30781,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {3}, Pages = {480-98}, Pmc = {PMC2946625}, - pubmed = {20696384}, + pmid = {20696384}, Pst = {ppublish}, Title = {A conserved switch in sensory processing prepares developing neocortex for vision}, Volume = {67}, @@ -30803,7 +30802,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {3}, Pages = {e61}, Pmc = {PMC1808114}, - pubmed = {17341130}, + pmid = {17341130}, Pst = {ppublish}, Title = {A burst-based "Hebbian" learning rule at retinogeniculate synapses links retinal waves to activity-dependent refinement}, Volume = {5}, @@ -30823,7 +30822,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {9}, Pages = {3580-93}, - pubmed = {10212317}, + pmid = {10212317}, Pst = {ppublish}, Title = {Retinal waves are governed by collective network properties}, Volume = {19}, @@ -30842,7 +30841,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {3}, Pages = {961-73}, - pubmed = {11157082}, + pmid = {11157082}, Pst = {ppublish}, Title = {The information content of spontaneous retinal waves}, Volume = {21}, @@ -30861,7 +30860,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jun}, Number = {3}, Pages = {243-53}, - pubmed = {12061504}, + pmid = {12061504}, Pst = {ppublish}, Title = {Retinal waves: implications for synaptic learning rules during development}, Volume = {8}, @@ -30880,7 +30879,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Animals; Axons; Cats; Immunohistochemistry; Optic Nerve; Rabbits; Rats; Retina; Tissue Distribution; gamma-Aminobutyric Acid}, Number = {6}, Pages = {1143-9}, - pubmed = {8962833}, + pmid = {8962833}, Pst = {ppublish}, Title = {Immunocytochemical evidence for an axonal localization of GABA in the optic nerves of rabbits, rats, and cats}, Volume = {12}, @@ -30898,7 +30897,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {3}, Pages = {339-42}, - pubmed = {10936491}, + pmid = {10936491}, Pst = {ppublish}, Title = {Modulation of gamma-aminobutyric acid responses in the rat optic nerve}, Volume = {401}, @@ -30917,7 +30916,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {8}, Pages = {1797-802}, - pubmed = {9223054}, + pmid = {9223054}, Pst = {ppublish}, Title = {GABAergic retinocollicular projection in the New World monkey Cebus apella}, Volume = {8}, @@ -30936,7 +30935,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {10}, Pages = {1357-63}, - pubmed = {8762755}, + pmid = {8762755}, Pst = {ppublish}, Title = {GABA immunopositive axons in the optic nerve and optic tract of macaque monkeys}, Volume = {36}, @@ -30955,7 +30954,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Nov}, Number = {1}, Pages = {19-26}, - pubmed = {1777820}, + pmid = {1777820}, Pst = {ppublish}, Title = {Localization of GAD- and GABA-like immunoreactivity in ground squirrel retina: retrograde labeling demonstrates GAD-positive ganglion cells}, Volume = {564}, @@ -30974,7 +30973,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {1}, Pages = {129-34}, - pubmed = {2914207}, + pmid = {2914207}, Pst = {ppublish}, Title = {GABA-immunoreactivity in ganglion cells of the rat retina}, Volume = {476}, @@ -30991,7 +30990,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {optic tectum;Superior Colliculus;connectivity;function;retina gaba paper}, Mesh = {Animals; Arousal; Auditory Perception; Brain Stem; Cerebellum; Cerebral Cortex; Ear, External; Eye Movements; Fixation, Ocular; Haplorhini; Mammals; Neural Pathways; Neurons; Rats; Retina; Spinal Cord; Superior Colliculi; Thalamus; Visual Perception}, Pages = {321-78}, - pubmed = {16221594}, + pmid = {16221594}, Pst = {ppublish}, Title = {The mammalian superior colliculus: laminar structure and connections}, Volume = {151}, @@ -31011,7 +31010,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {1}, Pages = {10-8}, - pubmed = {162939}, + pmid = {162939}, Pst = {ppublish}, Title = {Projections of extraocular, neck muscle, and retinal afferents to superior colliculus in the cat: their connections to cells of origin of tectospinal tract}, Volume = {38}, @@ -31030,7 +31029,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Feb}, Number = {4687}, Pages = {657-9}, - pubmed = {3969558}, + pmid = {3969558}, Pst = {ppublish}, Title = {Descending efferents from the superior colliculus relay integrated multisensory information}, Volume = {227}, @@ -31050,7 +31049,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {4}, Pages = {e41}, Pmc = {PMC1215388}, - pubmed = {16184189}, + pmid = {16184189}, Pst = {ppublish}, Title = {A digital atlas to characterize the mouse brain transcriptome}, Volume = {1}, @@ -31068,7 +31067,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {21 Calcium imaging;21 Circuit structure-function;21 Neurophysiology;Visual Cortex;Behavior;23 Technique;optogenetics;frontiers review}, Pages = {3}, Pmc = {PMC2854571}, - pubmed = {20407583}, + pmid = {20407583}, Pst = {epublish}, Title = {Chronic cellular imaging of mouse visual cortex during operant behavior and passive viewing}, Volume = {4}, @@ -31091,7 +31090,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1}, Pages = {49-60}, Pmc = {PMC2904318}, - pubmed = {20624591}, + pmid = {20624591}, Pst = {ppublish}, Title = {Melanopsin-expressing retinal ganglion-cell photoreceptors: cellular diversity and role in pattern vision}, Volume = {67}, @@ -31111,7 +31110,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jun}, Number = {7301}, Pages = {1070-4}, - pubmed = {20543823}, + pmid = {20543823}, Pst = {ppublish}, Title = {Activity-dependent relocation of the axon initial segment fine-tunes neuronal excitability}, Volume = {465}, @@ -31131,7 +31130,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {6}, Pages = {633-8}, - pubmed = {12490252}, + pmid = {12490252}, Pst = {ppublish}, Title = {The central complex and the genetic dissection of locomotor behaviour}, Volume = {12}, @@ -31151,7 +31150,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {18}, Pages = {1511-8}, Pmc = {PMC2755619}, - pubmed = {19765988}, + pmid = {19765988}, Pst = {ppublish}, Title = {Cell-cycle control by physiological matrix elasticity and in vivo tissue stiffening}, Volume = {19}, @@ -31172,7 +31171,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {7}, Pages = {889-95}, Pmc = {PMC2893238}, - pubmed = {20526331}, + pmid = {20526331}, Pst = {ppublish}, Title = {Stimulus-driven competition in a cholinergic midbrain nucleus}, Volume = {13}, @@ -31192,7 +31191,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {15}, Pages = {R650-R651}, - pubmed = {18682202}, + pmid = {18682202}, Pst = {ppublish}, Title = {The sound of change: visually-induced auditory synesthesia}, Volume = {18}, @@ -31212,7 +31211,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {1}, Pages = {7-8}, - pubmed = {18940583}, + pmid = {18940583}, Pst = {ppublish}, Title = {Walk this way}, Volume = {60}, @@ -31233,7 +31232,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {31}, Pages = {10575-85}, Pmc = {PMC2934783}, - pubmed = {20686000}, + pmid = {20686000}, Pst = {ppublish}, Title = {In vivo activation of channelrhodopsin-2 reveals that normal patterns of spontaneous activity are required for motoneuron guidance and maintenance of guidance molecules}, Volume = {30}, @@ -31253,7 +31252,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {5965}, Pages = {584-7}, - pubmed = {20110506}, + pmid = {20110506}, Pst = {ppublish}, Title = {Decorrelated neuronal firing in cortical microcircuits}, Volume = {327}, @@ -31273,7 +31272,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {5988}, Pages = {181}, - pubmed = {20616271}, + pmid = {20616271}, Pst = {ppublish}, Title = {Firefly synchrony: a behavioral strategy to minimize visual clutter}, Volume = {329}, @@ -31292,7 +31291,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {8}, Pages = {643-9}, - pubmed = {20622860}, + pmid = {20622860}, Pst = {ppublish}, Title = {Imaging brain electric signals with genetically targeted voltage-sensitive fluorescent proteins}, Volume = {7}, @@ -31309,7 +31308,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Current opinion in neurobiology}, Keywords = {optical physiology; frontiers review; calcium imaging; Technique;connectivity}, Month = {May}, - pubmed = {20570133}, + pmid = {20570133}, Pst = {aheadofprint}, Title = {Chasing the cell assembly}, Year = {2010;c}, @@ -31329,7 +31328,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {5}, Pages = {639-47}, Pmc = {PMC2629495}, - pubmed = {17329205}, + pmid = {17329205}, Pst = {ppublish}, Title = {Monosynaptic restriction of transsynaptic tracing from single, genetically targeted neurons}, Volume = {53}, @@ -31350,7 +31349,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {7304}, Pages = {373-7}, Pmc = {PMC2904843}, - pubmed = {20574422}, + pmid = {20574422}, Pst = {ppublish}, Title = {Blindsight depends on the lateral geniculate nucleus}, Volume = {466}, @@ -31371,7 +31370,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {5}, Pages = {1727-38}, Pmc = {PMC2828882}, - pubmed = {20130182}, + pmid = {20130182}, Pst = {ppublish}, Title = {Global inhibition and stimulus competition in the owl optic tectum}, Volume = {30}, @@ -31392,7 +31391,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {18}, Pages = {6342-54}, Pmc = {PMC2919315}, - pubmed = {20445060}, + pmid = {20445060}, Pst = {ppublish}, Title = {Functional identification of a pulvinar path from superior colliculus to cortical area MT}, Volume = {30}, @@ -31413,7 +31412,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {22}, Pages = {10244-9}, Pmc = {PMC2890467}, - pubmed = {20479225}, + pmid = {20479225}, Pst = {ppublish}, Title = {Circuit topology for synchronizing neurons in spontaneously active networks}, Volume = {107}, @@ -31434,7 +31433,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {25}, Pages = {11163-70}, Pmc = {PMC2895137}, - pubmed = {20484679}, + pmid = {20484679}, Pst = {ppublish}, Title = {Functional specificity in the human brain: a window into the functional architecture of the mind}, Volume = {107}, @@ -31455,7 +31454,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {25}, Pages = {8502-11}, Pmc = {PMC2905738}, - pubmed = {20573897}, + pmid = {20573897}, Pst = {ppublish}, Title = {Neural correlates of active avoidance behavior in superior colliculus}, Volume = {30}, @@ -31475,7 +31474,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jun}, Number = {3}, Pages = {429-50}, - pubmed = {2754044}, + pmid = {2754044}, Pst = {ppublish}, Title = {Recovery from cortical blindness mediated by destruction of nontectotectal fibers in the commissure of the superior colliculus in the cat}, Volume = {284}, @@ -31495,7 +31494,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jun}, Number = {1-2}, Pages = {161-74}, - pubmed = {16458361}, + pmid = {16458361}, Pst = {ppublish}, Title = {Ultrafast random-access scanning in two-photon microscopy using acousto-optic deflectors}, Volume = {154}, @@ -31513,7 +31512,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {Add Keywords}, Number = {8}, Pmc = {PMC2924383}, - pubmed = {20808861}, + pmid = {20808861}, Pst = {epublish}, Title = {Sounds move a static visual object}, Volume = {5}, @@ -31531,7 +31530,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {Add Keywords}, Number = {8}, Pmc = {PMC2923157}, - pubmed = {20808911}, + pmid = {20808911}, Pst = {epublish}, Title = {A transposon in comt generates mRNA variants and causes widespread expression and behavioral differences among mice}, Volume = {5}, @@ -31550,7 +31549,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {34}, Pages = {15264-8}, - pubmed = {20679218}, + pmid = {20679218}, Pst = {ppublish}, Title = {A mammalian neural tissue opsin (Opsin 5) is a deep brain photoreceptor in birds}, Volume = {107}, @@ -31570,7 +31569,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Nov}, Number = {10}, Pages = {2932-44}, - pubmed = {17156216}, + pmid = {17156216}, Pst = {ppublish}, Title = {Visual functions without the occipital lobe or after cerebral hemispherectomy in infancy}, Volume = {24}, @@ -31590,7 +31589,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Aug}, Number = {3}, Pages = {497-506}, - pubmed = {15223196}, + pmid = {15223196}, Pst = {ppublish}, Title = {Subcortical modulation of spatial attention including evidence that the Sprague effect extends to man}, Volume = {55}, @@ -31610,7 +31609,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {5}, Pages = {506-18}, - pubmed = {17901259}, + pmid = {17901259}, Pst = {ppublish}, Title = {Neural substrates of blindsight after hemispherectomy}, Volume = {13}, @@ -31631,7 +31630,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {5}, Pages = {775-85}, Pmc = {PMC2894573}, - pubmed = {20510925}, + pmid = {20510925}, Pst = {ppublish}, Title = {Hematopoietic origin of pathological grooming in Hoxb8 mutant mice}, Volume = {141}, @@ -31650,7 +31649,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {5}, Pages = {858-71}, - pubmed = {20826316}, + pmid = {20826316}, Pst = {ppublish}, Title = {Broadly tuned response properties of diverse inhibitory neuron subtypes in mouse visual cortex}, Volume = {67}, @@ -31671,7 +31670,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {2}, Pages = {110-4}, - pubmed = {19879331}, + pmid = {19879331}, Pst = {ppublish}, Title = {Cyan fluorescent protein (CFP) expressing cells in the retina of Thy1-CFP transgenic mice before and after optic nerve injury}, Volume = {468}, @@ -31691,7 +31690,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {1}, Pages = {1-8}, - pubmed = {19427523}, + pmid = {19427523}, Pst = {ppublish}, Title = {Imaging synaptically mediated responses produced by brainstem inputs onto identified spinal neurons in the neonatal mouse}, Volume = {180}, @@ -31712,7 +31711,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {2}, Pages = {178-84}, Pmc = {PMC2582024}, - pubmed = {18539336}, + pmid = {18539336}, Pst = {ppublish}, Title = {Two-photon imaging of spatially extended neuronal network dynamics with high temporal resolution}, Volume = {172}, @@ -31732,7 +31731,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {1}, Pages = {75-82}, Pmc = {PMC2934901}, - pubmed = {20659501}, + pmid = {20659501}, Pst = {ppublish}, Title = {Simultaneous multi-electrode array recording and two-photon calcium imaging of neural activity}, Volume = {192}, @@ -31752,7 +31751,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {2}, Pages = {191-8}, - pubmed = {16531040}, + pmid = {16531040}, Pst = {ppublish}, Title = {Neural basis of quasi-rational decision making}, Volume = {16}, @@ -31771,7 +31770,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {9}, Pages = {1098-106}, - pubmed = {20694002}, + pmid = {20694002}, Pst = {ppublish}, Title = {GABAergic circuits control stimulus-instructed receptive field development in the optic tectum}, Volume = {13}, @@ -31790,7 +31789,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Sep}, Number = {9}, Pages = {1144-9}, - pubmed = {20711183}, + pmid = {20711183}, Pst = {ppublish}, Title = {Parallel processing of visual space by neighboring neurons in mouse visual cortex}, Volume = {13}, @@ -31811,7 +31810,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {2}, Pages = {786-92}, - pubmed = {18029199}, + pmid = {18029199}, Pst = {ppublish}, Title = {Imaging human supraspinal locomotor centers in brainstem and cerebellum}, Volume = {39}, @@ -31830,7 +31829,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {7}, Pages = {R306-7}, - pubmed = {20392416}, + pmid = {20392416}, Pst = {ppublish}, Title = {Levels of selection}, Volume = {20}, @@ -31850,7 +31849,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {7}, Pages = {R314-6}, - pubmed = {20392420}, + pmid = {20392420}, Pst = {ppublish}, Title = {Cooperation: the secret society of sperm}, Volume = {20}, @@ -31870,7 +31869,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Number = {2}, Pages = {e1000301}, Pmc = {PMC2817711}, - pubmed = {20161719}, + pmid = {20161719}, Pst = {epublish}, Title = {Paleovirology--modern consequences of ancient viruses}, Volume = {8}, @@ -31890,7 +31889,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jan}, Number = {5961}, Pages = {84-7}, - pubmed = {20044575}, + pmid = {20044575}, Pst = {ppublish}, Title = {The Tasmanian devil transcriptome reveals Schwann cell origins of a clonally transmissible cancer}, Volume = {327}, @@ -31910,7 +31909,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {May}, Number = {5010}, Pages = {1177-9}, - pubmed = {2031188}, + pmid = {2031188}, Pst = {ppublish}, Title = {Interhemispheric synchronization of oscillatory neuronal responses in cat visual cortex}, Volume = {252}, @@ -31927,7 +31926,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Keywords = {21 Neurophysiology; Models; Computational Biology}, Pages = {9}, Pmc = {PMC2870944}, - pubmed = {20485451}, + pmid = {20485451}, Pst = {epublish}, Title = {Pooling and correlated neural activity}, Volume = {4}, @@ -31947,7 +31946,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {12}, Pages = {4325-37}, - pubmed = {20335468}, + pmid = {20335468}, Pst = {ppublish}, Title = {"Slow activity transients" in infant rat visual cortex: a spreading synchronous oscillation patterned by retinal waves}, Volume = {30}, @@ -31967,7 +31966,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {9}, Pages = {3438-49}, - pubmed = {20203203}, + pmid = {20203203}, Pst = {ppublish}, Title = {Neocortical Activation of the Hippocampus during Sleep in Infant Rats}, Volume = {30}, @@ -31983,7 +31982,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Annual review of neuroscience}, Mesh = {Animals; Auditory Cortex; Cats; Cerebral Cortex; Eye Movements; Motor Cortex; Movement; Neural Pathways; Neurons; Retina; Somatosensory Cortex; Strabismus; Superior Colliculi; Vision, Ocular; Visual Cortex; Visual Fields; Visual Perception}, Pages = {95-125}, - pubmed = {6370084}, + pmid = {6370084}, Pst = {ppublish}, Title = {Development of the superior colliculus}, Volume = {7}, @@ -32001,7 +32000,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Animals; Animals, Laboratory; Animals, Newborn; Behavior, Animal; Body Weight; Brain; Circadian Rhythm; Female; Housing, Animal; Locomotion; Male; Rats; Sleep; Startle Reaction; Wakefulness}, Number = {4}, Pages = {267-80}, - pubmed = {5527425}, + pmid = {5527425}, Pst = {ppublish}, Title = {The postnatal development of behavioral states in the rat}, Volume = {3}, @@ -32021,7 +32020,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {6944}, Pages = {72-5}, - pubmed = {12840761}, + pmid = {12840761}, Pst = {ppublish}, Title = {Spontaneous muscle twitches during sleep guide spinal self-organization}, Volume = {424}, @@ -32041,7 +32040,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {2}, Pages = {200-12}, - pubmed = {19874788}, + pmid = {19874788}, Title = {Spatial-temporal patterns of retinal waves underlying activity-dependent refinement of retinofugal projections}, Volume = {64}, Year = {2009}, @@ -32061,7 +32060,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {41}, Pages = {12909-18}, - pubmed = {19828805}, + pmid = {19828805}, Title = {Direction-specific disruption of subcortical visual behavior and receptive fields in mice lacking the beta2 subunit of nicotinic acetylcholine receptor}, Volume = {29}, Year = {2009}, @@ -32080,7 +32079,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jun}, Number = {5}, Pages = {785-96}, - pubmed = {12797962}, + pmid = {12797962}, Title = {Functional differentiation of multiple climbing fiber inputs during synapse elimination in the developing cerebellum}, Volume = {38}, Year = {2003}, @@ -32098,7 +32097,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {1}, Pages = {106-18}, - pubmed = {19607796}, + pmid = {19607796}, Title = {Translocation of a "winner" climbing fiber to the Purkinje cell dendrite and subsequent elimination of "losers" from the soma in developing cerebellum}, Volume = {63}, Year = {2009}, @@ -32119,7 +32118,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Mar}, Number = {2}, Pages = {227-38}, - pubmed = {3513902}, + pmid = {3513902}, Title = {The development of the corticotectal pathway in the albino rat}, Volume = {390}, Year = {1986}} @@ -32136,7 +32135,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Oct}, Number = {3}, Pages = {275-82}, - pubmed = {2446211}, + pmid = {2446211}, Title = {The development of the corticotectal pathway in the albino rat: transient projections from the visual and motor cortices}, Volume = {80}, Year = {1987}, @@ -32154,7 +32153,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jun}, Number = {6}, Pages = {3578-82}, - pubmed = {10848574}, + pmid = {10848574}, Title = {Onset of cross-modal synthesis in the neonatal superior colliculus is gated by the development of cortical influences}, Volume = {83}, Year = {2000}, @@ -32177,7 +32176,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Neural development}, Keywords = {21 Activity-development; 21 Cortical oscillations;21 Neurophysiology; retinal wave paper}, Pages = {24}, - pubmed = {19580682}, + pmid = {19580682}, Title = {Retinal waves are likely to instruct the formation of eye-specific retinogeniculate projections}, Volume = {4}, Year = {2009}, @@ -32193,7 +32192,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Journal-Full = {Neural development}, Keywords = {21 Activity-development; 21 Cortical oscillations; 21 Neurophysiology; retinal wave paper}, Pages = {25}, - pubmed = {19580684}, + pmid = {19580684}, Title = {Retinal waves are unlikely to instruct the formation of eye-specific retinogeniculate projections}, Volume = {4}, Year = {2009}, @@ -32210,7 +32209,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Dec}, Number = {4}, Pages = {301-22}, - pubmed = {7169027}, + pmid = {7169027}, Title = {The emergence of fetal behaviour. I. Qualitative aspects}, Volume = {7}, Year = {1982}, @@ -32227,7 +32226,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Mesh = {Aging; Animals; Body Patterning; Brain; Cell Differentiation; Cell Division; Humans; Mammals; Models, Neurological; Phylogeny; Reproducibility of Results; Statistical Distributions}, Number = {1}, Pages = {7-17}, - pubmed = {11483296}, + pmid = {11483296}, Title = {Translating developmental time across mammalian species}, Volume = {105}, Year = {2001}, @@ -32245,7 +32244,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jun}, Number = {3}, Pages = {255-61}, - pubmed = {11337194}, + pmid = {11337194}, Title = {Early onset of glutamatergic and GABAergic synaptic activity in the visual layers of the rodent superior colliculus}, Volume = {19}, Year = {2001}} @@ -32262,7 +32261,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Nov}, Number = {2}, Pages = {117-20}, - pubmed = {8110999}, + pmid = {8110999}, Title = {Two stages in the development of a mammalian retinocollicular projection}, Volume = {5}, Year = {1993}} @@ -32279,7 +32278,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Jul}, Number = {5427}, Pages = {599-604}, - pubmed = {10417392}, + pmid = {10417392}, Title = {Correlational structure of spontaneous neuronal activity in the developing lateral geniculate nucleus in vivo}, Volume = {285}, Year = {1999}, @@ -32298,7 +32297,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Apr}, Number = {6524}, Pages = {716-8}, - pubmed = {7715725}, + pmid = {7715725}, Title = {Early functional neural networks in the developing retina}, Volume = {374}, Year = {1995}, @@ -32317,7 +32316,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Month = {Nov}, Number = {5}, Pages = {923-38}, - pubmed = {8240814}, + pmid = {8240814}, Title = {Transient period of correlated bursting activity during development of the mammalian retina}, Volume = {11}, Year = {1993}, @@ -32350,7 +32349,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2003/02/19 {$[$}received{$]$}; 2003/04/23 {$[$}accepted{$]$}}, Pii = {nature01698}, Pl = {England}, - pubmed = {12827201}, + pmid = {12827201}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Parvalbumins); 56-12-2 (gamma-Aminobutyric Acid)}, @@ -32388,7 +32387,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {3855--3868}, Pii = {23/9/3855}, Pl = {United States}, - pubmed = {12736356}, + pmid = {12736356}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Proto-Oncogene Proteins c-fos); 0 (RNA, Messenger)}, @@ -32426,7 +32425,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {11--18}, Pl = {United States}, Pmc = {PMC2442722}, - pubmed = {18604307}, + pmid = {18604307}, Pst = {ppublish}, Pt = {Journal Article}, Sb = {IM}, @@ -32464,7 +32463,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2002/12/12 {$[$}received{$]$}; 2003/03/28 {$[$}accepted{$]$}}, Pii = {nature01616}, Pl = {England}, - pubmed = {12748642}, + pmid = {12748642}, Pst = {ppublish}, Pt = {In Vitro; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -32537,7 +32536,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {3284--3299}, Pl = {UNITED STATES}, - pubmed = {8340808}, + pmid = {8340808}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -32573,7 +32572,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {3266--3283}, Pl = {UNITED STATES}, - pubmed = {8340807}, + pmid = {8340807}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Rn = {487-79-6 (Kainic Acid); 51-79-6 (Urethane); 6740-88-1 (Ketamine)}, @@ -32610,7 +32609,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {3252--3265}, Pl = {UNITED STATES}, - pubmed = {8340806}, + pmid = {8340806}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Rn = {10024-97-2 (Nitrous Oxide); 137-58-6 (Lidocaine); 21306-56-9 (QX-314); 6740-88-1 (Ketamine); 7361-61-7 (Xylazine)}, @@ -32652,7 +32651,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pii = {jphysiol.2006.113050}, Pl = {England}, Pmc = {PMC2000673}, - pubmed = {16931555}, + pmid = {16931555}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -32693,7 +32692,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pl = {United States}, Pmc = {PMC2637308}, Pmcr = {2010/03/01}, - pubmed = {18632738}, + pmid = {18632738}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural}, Sb = {IM}, @@ -32733,7 +32732,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2006/06/07 {$[$}received{$]$}; 2006/09/28 {$[$}revised{$]$}; 2006/10/24 {$[$}accepted{$]$}}, Pii = {S0896-6273(06)00822-1}, Pl = {United States}, - pubmed = {17145507}, + pmid = {17145507}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -32773,7 +32772,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2007/08/23 {$[$}aheadofprint{$]$}}, Pii = {bhm137}, Pl = {United States}, - pubmed = {17720684}, + pmid = {17720684}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -32810,7 +32809,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {748--749}, Pii = {S0896-6273(06)00909-3}, Pl = {United States}, - pubmed = {17145497}, + pmid = {17145497}, Pst = {ppublish}, Pt = {Comment; Journal Article}, Sb = {IM}, @@ -32848,7 +32847,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2004/12/20 {$[$}received{$]$}; 2005/04/25 {$[$}revised{$]$}; 2005/06/15 {$[$}accepted{$]$}}, Pii = {S0896-6273(05)00521-0}, Pl = {United States}, - pubmed = {16055065}, + pmid = {16055065}, Pst = {ppublish}, Pt = {In Vitro; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -32888,7 +32887,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2005/12/30 {$[$}received{$]$}; 2006/03/16 {$[$}accepted{$]$}; 2006/04/12 {$[$}aheadofprint{$]$}}, Pii = {nature04720}, Pl = {England}, - pubmed = {16625207}, + pmid = {16625207}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -32925,7 +32924,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {4535--4545}, Pii = {26/17/4535}, Pl = {United States}, - pubmed = {16641233}, + pmid = {16641233}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -32962,7 +32961,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {375--378}, Pii = {S0896627303000564}, Pl = {United States}, - pubmed = {12575946}, + pmid = {12575946}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review}, Rf = {23}, @@ -33004,7 +33003,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pii = {101120998}, Pl = {United States}, Pmc = {PMC33489}, - pubmed = {11344259}, + pmid = {11344259}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Receptors, Nicotinic); 0 (nicotinic acetylcholine receptor alpha4 subunit); 0 (nicotinic receptor alpha4beta2); 0 (nicotinic receptor beta2)}, @@ -33040,7 +33039,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {65--67}, Pl = {ENGLAND}, - pubmed = {7870173}, + pmid = {7870173}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Receptors, Nicotinic); 54-11-5 (Nicotine); 9007-49-2 (DNA)}, @@ -33078,7 +33077,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {1179--1194}, Pl = {United States}, - pubmed = {11535668}, + pmid = {11535668}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Excitatory Amino Acid Agonists); 0 (Excitatory Amino Acid Antagonists); 0 (Receptors, N-Methyl-D-Aspartate); 115066-14-3 (6-Cyano-7-nitroquinoxaline-2,3-dione); 6384-92-5 (N-Methylaspartate); 76726-92-6 (2-Amino-5-phosphonovalerate); 77521-29-0 (alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid)}, @@ -33116,7 +33115,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {6760--6770}, Pii = {27/25/6760}, Pl = {United States}, - pubmed = {17581963}, + pmid = {17581963}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -33156,7 +33155,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2004/04/21 {$[$}received{$]$}; 2005/01/28 {$[$}accepted{$]$}}, Pii = {nature03409}, Pl = {England}, - pubmed = {15846347}, + pmid = {15846347}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Kir2.1 channel); 0 (Membrane Proteins); 0 (Potassium Channels, Inwardly Rectifying); 0 (R-SNARE Proteins); 7440-70-2 (Calcium)}, @@ -33196,7 +33195,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2002/07/16 {$[$}received{$]$}; 2002/10/23 {$[$}accepted{$]$}}, Pii = {nature01242}, Pl = {England}, - pubmed = {12459783}, + pmid = {12459783}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Potassium Channels, Inwardly Rectifying); 4368-28-9 (Tetrodotoxin)}, @@ -33237,7 +33236,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2006/03/15 {$[$}aheadofprint{$]$}}, Pii = {JNC3741}, Pl = {England}, - pubmed = {16539672}, + pmid = {16539672}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Rn = {0 (Anticonvulsants); 0 (GABA Antagonists); 0 (Isoenzymes); 0 (Protein Isoforms); 485-49-4 (Bicuculline); 56-12-2 (gamma-Aminobutyric Acid); 60643-86-9 (Vigabatrin); EC 2.6.1.19 (4-Aminobutyrate Transaminase); EC 4.1.1.15 (Glutamate Decarboxylase); EC 4.1.1.15 (glutamate decarboxylase 2)}, @@ -33277,7 +33276,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {177--194}, Pii = {10.1002/(SICI)1096-9861(19980601)395:2<177::AID-CNE3>3.0.CO;2-{\#}}, Pl = {UNITED STATES}, - pubmed = {9603371}, + pmid = {9603371}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Isoenzymes); 56-12-2 (gamma-Aminobutyric Acid); EC 4.1.1.15 (Glutamate Decarboxylase)}, @@ -33315,7 +33314,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {2725--2731}, Pl = {UNITED STATES}, - pubmed = {1880546}, + pmid = {1880546}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Apoenzymes); 54-47-7 (Pyridoxal Phosphate); EC 3.4.21.1 (Chymotrypsin); EC 4.1.1.15 (Glutamate Decarboxylase)}, @@ -33354,7 +33353,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {14060--14065}, Pl = {UNITED STATES}, Pmc = {PMC28432}, - pubmed = {9391152}, + pmid = {9391152}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Isoenzymes); 56-12-2 (gamma-Aminobutyric Acid); EC 4.1.1.15 (Glutamate Decarboxylase)}, @@ -33391,7 +33390,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {60--79}, Pl = {United States}, - pubmed = {14574680}, + pmid = {14574680}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Calcium-Binding Protein, Vitamin D-Dependent); 0 (Isoenzymes); 0 (Luminescent Proteins); 0 (Parvalbumins); 0 (calretinin); 147336-22-9 (Green Fluorescent Proteins); 51110-01-1 (Somatostatin); 56-12-2 (gamma-Aminobutyric Acid); EC 4.1.1.15 (Glutamate Decarboxylase); EC 4.1.1.15 (glutamate decarboxylase 1)}, @@ -33429,7 +33428,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {861--870}, Pii = {S0306452203003385}, Pl = {United States}, - pubmed = {12895526}, + pmid = {12895526}, Pst = {ppublish}, Pt = {In Vitro; Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Isoenzymes); 56-12-2 (gamma-Aminobutyric Acid); EC 4.1.1.15 (Glutamate Decarboxylase); EC 4.1.1.15 (glutamate decarboxylase 1)}, @@ -33466,7 +33465,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {81--84}, Pii = {S0304394003005706}, Pl = {Ireland}, - pubmed = {12850553}, + pmid = {12850553}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Luminescent Proteins); 147336-22-9 (Green Fluorescent Proteins); 56-12-2 (gamma-Aminobutyric Acid)}, @@ -33504,7 +33503,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {6496--6499}, Pl = {UNITED STATES}, Pmc = {PMC21078}, - pubmed = {9177246}, + pmid = {9177246}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Isoenzymes); 0 (RNA, Messenger); 56-12-2 (gamma-Aminobutyric Acid); EC 4.1.1.15 (Glutamate Decarboxylase)}, @@ -33539,7 +33538,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {21--32}, Pii = {0006-8993(72)90039-X}, Pl = {NETHERLANDS}, - pubmed = {5047191}, + pmid = {5047191}, Pst = {ppublish}, Pt = {Journal Article}, Sb = {IM}, @@ -33574,7 +33573,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {1--20}, Pii = {0006-8993(72)90038-8}, Pl = {NETHERLANDS}, - pubmed = {5047186}, + pmid = {5047186}, Pst = {ppublish}, Pt = {Journal Article}, Sb = {IM}, @@ -33610,7 +33609,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {1580--1591}, Pl = {UNITED STATES}, - pubmed = {10712481}, + pmid = {10712481}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Carrier Proteins); 0 (Coloring Agents); 0 (GABA Plasma Membrane Transport Proteins); 0 (Membrane Proteins); 0 (Membrane Transport Proteins); 0 (Organic Anion Transporters); 56-12-2 (gamma-Aminobutyric Acid); 56-87-1 (Lysine); 576-19-2 (biocytin); 6384-92-5 (N-Methylaspartate); EC 4.1.1.15 (Glutamate Decarboxylase)}, @@ -33648,7 +33647,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {6264--6276}, Pl = {UNITED STATES}, - pubmed = {9236237}, + pmid = {9236237}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (RNA, Messenger); 0 (Receptors, N-Methyl-D-Aspartate); 56-12-2 (gamma-Aminobutyric Acid)}, @@ -33685,7 +33684,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {1123--1134}, Pii = {S089662730200867X}, Pl = {United States}, - pubmed = {12354401}, + pmid = {12354401}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -33722,7 +33721,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {863-874}, Pii = {S0896-6273(00)80218-4}, Pl = {UNITED STATES}, - pubmed = {8938119}, + pmid = {8938119}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Anesthetics); 0 (Excitatory Amino Acid Antagonists); 0 (Receptors, AMPA); 0 (Receptors, N-Methyl-D-Aspartate); 115066-14-3 (6-Cyano-7-nitroquinoxaline-2,3-dione); 76726-92-6 (2-Amino-5-phosphonovalerate)}, @@ -33758,7 +33757,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {5694--5705}, Pii = {27/21/5694}, Pl = {United States}, - pubmed = {17522314}, + pmid = {17522314}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Cholinergic Agents); 0 (Cholinergic Agonists); 0 (Cholinergic Antagonists); 0 (Receptors, Muscarinic)}, @@ -33797,7 +33796,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {6570--6577}, Pii = {20/17/6570}, Pl = {UNITED STATES}, - pubmed = {10964962}, + pmid = {10964962}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Bungarotoxins); 0 (Excitatory Amino Acid Antagonists); 0 (Fluorescent Dyes); 0 (Muscarinic Antagonists); 0 (Neurotransmitter Agents); 0 (Nicotinic Antagonists); 0 (Piperidines); 105344-37-4 (fura-2-am); 115066-14-3 (6-Cyano-7-nitroquinoxaline-2,3-dione); 300-54-9 (Muscarine); 51-55-8 (Atropine); 54-77-3 (Dimethylphenylpiperazinium Iodide); 60-26-4 (Hexamethonium); 7440-70-2 (Calcium); 8063-06-7 (Curare); 81405-11-0 (4-diphenylacetoxy-1,1-dimethylpiperidinium); 96314-98-6 (Fura-2)}, @@ -33837,7 +33836,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2005/12/21 {$[$}aheadofprint{$]$}}, Pii = {00578.2005}, Pl = {United States}, - pubmed = {16371454}, + pmid = {16371454}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural}, Rn = {0 (Calcium Channels); 0 (Chlorides); 0 (Quinolinium Compounds); 0 (Receptors, GABA); 134907-10-1 (6-methoxy-N-ethylquinolinium); 1405-97-6 (Gramicidin); 56-12-2 (gamma-Aminobutyric Acid); 7440-70-2 (Calcium); 96314-98-6 (Fura-2)}, @@ -33878,7 +33877,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2005/12/08 {$[$}received{$]$}; 2006/01/24 {$[$}accepted{$]$}; 2006/02/12 {$[$}aheadofprint{$]$}}, Pii = {nn1649}, Pl = {United States}, - pubmed = {16474391}, + pmid = {16474391}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Rn = {0 (Excitatory Amino Acid Agonists); 0 (Excitatory Amino Acid Antagonists); 0 (Receptors, N-Methyl-D-Aspartate); 56-12-2 (gamma-Aminobutyric Acid); 56-86-0 (Glutamic Acid)}, @@ -33917,7 +33916,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {2861-2864}, Pl = {UNITED STATES}, Pmc = {PMC53791}, - pubmed = {2320593}, + pmid = {2320593}, Pst = {ppublish}, Pt = {Journal Article}, Sb = {IM}, @@ -33956,7 +33955,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2005/10/11 {$[$}received{$]$}; 2006/02/02 {$[$}revised{$]$}; 2006/03/01 {$[$}accepted{$]$}}, Pii = {S0896-6273(06)00177-2}, Pl = {United States}, - pubmed = {16600860}, + pmid = {16600860}, Pst = {ppublish}, Pt = {Comparative Study; In Vitro; Journal Article; Research Support, N.I.H., Extramural}, Rn = {0 (Carbazoles); 0 (Enzyme Inhibitors); 0 (Excitatory Amino Acid Antagonists); 0 (Indole Alkaloids); 50903-99-6 (NG-Nitroarginine Methyl Ester); 76726-92-6 (2-Amino-5-phosphonovalerate); 97161-97-2 (K 252)}, @@ -33998,7 +33997,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2005/10/28 {$[$}received{$]$}; 2005/12/21 {$[$}revised{$]$}; 2006/02/06 {$[$}accepted{$]$}}, Pii = {S0896-6273(06)00133-4}, Pl = {United States}, - pubmed = {16600859}, + pmid = {16600859}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -34037,7 +34036,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2002/05/06 {$[$}received{$]$}; 2002/07/12 {$[$}accepted{$]$}}, Pii = {nature00988}, Pl = {England}, - pubmed = {12368854}, + pmid = {12368854}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -34075,7 +34074,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {93--99}, Pii = {S0959438802002957}, Pl = {England}, - pubmed = {11861170}, + pmid = {11861170}, Pst = {ppublish}, Pt = {Journal Article; Review}, Rf = {71}, @@ -34113,7 +34112,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {3542--3548}, Pii = {21/10/3542}, Pl = {United States}, - pubmed = {11331383}, + pmid = {11331383}, Pst = {ppublish}, Pt = {Journal Article}, Rn = {0 (Fluorescent Dyes); 4368-28-9 (Tetrodotoxin); 7440-23-5 (Sodium)}, @@ -34147,7 +34146,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {129--154}, Pl = {UNITED STATES}, - pubmed = {2183671}, + pmid = {2183671}, Pst = {ppublish}, Pt = {Journal Article; Review}, Rf = {142}, @@ -34186,7 +34185,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {3837--3843}, Pl = {UNITED STATES}, - pubmed = {2573697}, + pmid = {2573697}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Anticonvulsants); 0 (Piperazines); 0 (Receptors, N-Methyl-D-Aspartate); 0 (Receptors, Neurotransmitter); 100828-16-8 (3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid); 56-84-8 (Aspartic Acid); 6384-92-5 (N-Methylaspartate); 76726-92-6 (2-Amino-5-phosphonovalerate)}, @@ -34223,7 +34222,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {65--84}, Pl = {UNITED STATES}, - pubmed = {2992788}, + pmid = {2992788}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {4368-28-9 (Tetrodotoxin)}, @@ -34260,7 +34259,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {293--298}, Pl = {NETHERLANDS}, - pubmed = {6831250}, + pmid = {6831250}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Rn = {4368-28-9 (Tetrodotoxin)}, @@ -34296,7 +34295,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {336--338}, Pl = {ENGLAND}, - pubmed = {6823306}, + pmid = {6823306}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -34331,7 +34330,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {639--641}, Pl = {UNITED STATES}, - pubmed = {309179}, + pmid = {309179}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -34381,7 +34380,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {R842-4}, Pii = {S0960-9822(06)02150-6}, Pl = {England}, - pubmed = {17027479}, + pmid = {17027479}, Pst = {ppublish}, Pt = {Comment; Journal Article}, Rn = {0 (Pheromones)}, @@ -34420,7 +34419,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2005/01/30 {$[$}received{$]$}; 2005/03/28 {$[$}revised{$]$}; 2005/04/13 {$[$}accepted{$]$}}, Pii = {S0092-8674(05)00407-1}, Pl = {United States}, - pubmed = {15935764}, + pmid = {15935764}, Pst = {ppublish}, Pt = {Journal Article}, Rn = {0 (Drosophila Proteins); 0 (Nerve Tissue Proteins); 0 (Transcription Factors); 0 (fru protein, Drosophila)}, @@ -34492,7 +34491,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {782--788}, Pii = {nature03012}, Pl = {England}, - pubmed = {15483599}, + pmid = {15483599}, Pst = {ppublish}, Pt = {Journal Article; Review}, Rf = {90}, @@ -34526,7 +34525,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {489--490}, Pl = {ENGLAND}, - pubmed = {7566144}, + pmid = {7566144}, Pst = {ppublish}, Pt = {Letter}, Sb = {IM}, @@ -34562,7 +34561,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {1603--1630}, Pl = {ENGLAND}, - pubmed = {9762952}, + pmid = {9762952}, Pst = {ppublish}, Pt = {Lectures; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review}, Rf = {160}, @@ -34597,7 +34596,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {1003--1017}, Pl = {UNITED STATES}, - pubmed = {14084161}, + pmid = {14084161}, Pst = {ppublish}, Pt = {Journal Article}, Sb = {OM}, @@ -34629,7 +34628,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {307--318}, Pl = {UNITED STATES}, - pubmed = {4215829}, + pmid = {4215829}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article}, Sb = {IM}, @@ -34664,7 +34663,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {1041--1059}, Pl = {UNITED STATES}, - pubmed = {5883731}, + pmid = {5883731}, Pst = {ppublish}, Pt = {Journal Article}, Sb = {IM}, @@ -34698,7 +34697,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {567--631}, Pl = {UNITED STATES}, - pubmed = {10202549}, + pmid = {10202549}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review}, Rf = {220}, @@ -34734,7 +34733,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {563--590}, Pl = {United States}, - pubmed = {18558867}, + pmid = {18558867}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review}, Rf = {150}, @@ -34773,7 +34772,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {642--649}, Pl = {Canada}, - pubmed = {16970864}, + pmid = {16970864}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review}, Rf = {77}, @@ -34809,7 +34808,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {896--900}, Pii = {322/5903/896}, Pl = {United States}, - pubmed = {18988841}, + pmid = {18988841}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Review}, Rf = {44}, @@ -34848,7 +34847,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2006/02/09 {$[$}received{$]$}; 2006/05/09 {$[$}revised{$]$}; 2006/06/02 {$[$}accepted{$]$}; 2006/06/27 {$[$}aheadofprint{$]$}}, Pii = {S0166-2236(06)00113-5}, Pl = {England}, - pubmed = {16806513}, + pmid = {16806513}, Pst = {ppublish}, Pt = {Journal Article; Review}, Rf = {65}, @@ -34887,7 +34886,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2006/02/08 {$[$}received{$]$}; 2006/05/03 {$[$}revised{$]$}; 2006/05/26 {$[$}accepted{$]$}}, Pii = {S0166-2236(06)00110-X}, Pl = {England}, - pubmed = {16769131}, + pmid = {16769131}, Pst = {ppublish}, Pt = {Journal Article; Review}, Rf = {47}, @@ -34928,7 +34927,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2006/01/18 {$[$}received{$]$}; 2006/04/18 {$[$}revised{$]$}; 2006/05/26 {$[$}accepted{$]$}; 2006/06/30 {$[$}aheadofprint{$]$}}, Pii = {S0166-2236(06)00111-1}, Pl = {England}, - pubmed = {16808981}, + pmid = {16808981}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Review}, Rf = {133}, @@ -34973,7 +34972,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pii = {300/5621/994}, Pl = {United States}, Pmc = {PMC2647844}, - pubmed = {12738869}, + pmid = {12738869}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Carrier Proteins); 0 (Immunotoxins); 0 (Membrane Transport Proteins); 0 (Plant Proteins); 0 (Ribosome Inactivating Proteins, Type 1); 0 (Vesicular Acetylcholine Transport Proteins); 0 (Vesicular Transport Proteins); 7440-70-2 (Calcium); EC 3.2.2.- (N-Glycosyl Hydrolases); EC 3.2.2.22 (saporin)}, @@ -35014,7 +35013,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pl = {United States}, Pmc = {PMC2604840}, Pmcr = {2009/12/01}, - pubmed = {18922954}, + pmid = {18922954}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural}, Sb = {IM}, @@ -35057,7 +35056,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pii = {0807178105}, Pl = {United States}, Pmc = {PMC2527347}, - pubmed = {18757739}, + pmid = {18757739}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Rn = {0 (Chrnb2 protein, mouse); 0 (Receptors, Nicotinic)}, @@ -35099,7 +35098,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2006/12/12 {$[$}received{$]$}; 2007/03/07 {$[$}revised{$]$}; 2007/03/07 {$[$}accepted{$]$}; 2007/03/13 {$[$}aheadofprint{$]$}}, Pii = {S0165-0173(07)00039-2}, Pl = {Netherlands}, - pubmed = {17433447}, + pmid = {17433447}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.; Review}, Rf = {46}, @@ -35139,7 +35138,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {357-367}, Pii = {S0896627302005779}, Pl = {United States}, - pubmed = {11832224}, + pmid = {11832224}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Bicyclo Compounds, Heterocyclic); 0 (Fluorescent Dyes); 0 (Nicotinic Agonists); 0 (Pyridines); 140111-52-0 (epibatidine); 60-92-4 (Cyclic AMP); 66428-89-5 (Forskolin); 9012-63-9 (Cholera Toxin)}, @@ -35177,7 +35176,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {491--501}, Pl = {ENGLAND}, - pubmed = {10349970}, + pmid = {10349970}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.}, Rn = {4368-28-9 (Tetrodotoxin)}, @@ -35215,7 +35214,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {2108-2112}, Pl = {UNITED STATES}, - pubmed = {9516112}, + pmid = {9516112}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Bicyclo Compounds, Heterocyclic); 0 (Bungarotoxins); 0 (Conotoxins); 0 (Nicotinic Agonists); 0 (Peptides); 0 (Pyridines); 0 (alpha-conotoxin MII); 140111-52-0 (epibatidine)}, @@ -35251,7 +35250,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {855--877}, Pl = {UNITED STATES}, - pubmed = {7288468}, + pmid = {7288468}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -35288,7 +35287,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {383--399}, Pl = {ENGLAND}, Pmc = {PMC1279405}, - pubmed = {7411438}, + pmid = {7411438}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -35322,7 +35321,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {1276--1286}, Pl = {UNITED STATES}, - pubmed = {4436700}, + pmid = {4436700}, Pst = {ppublish}, Pt = {Journal Article}, Sb = {IM}, @@ -35358,7 +35357,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {1405--1416}, Pii = {EJN4683}, Pl = {France}, - pubmed = {16553604}, + pmid = {16553604}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Chlorides); 0 (Excitatory Amino Acid Antagonists); 0 (Fluorescent Dyes); 0 (Receptors, GABA); 0 (Receptors, Glutamate); 0 (Receptors, N-Methyl-D-Aspartate); 115066-14-3 (6-Cyano-7-nitroquinoxaline-2,3-dione); 4368-28-9 (Tetrodotoxin); 7440-70-2 (Calcium); 76726-92-6 (2-Amino-5-phosphonovalerate)}, @@ -35396,7 +35395,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {94--104}, Pii = {S0959-4388(99)80012-9}, Pl = {ENGLAND}, - pubmed = {10072366}, + pmid = {10072366}, Pst = {ppublish}, Pt = {Journal Article; Review}, Rf = {75}, @@ -35433,7 +35432,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {25--38}, Pl = {NETHERLANDS}, - pubmed = {9554940}, + pmid = {9554940}, Pst = {ppublish}, Pt = {In Vitro; Journal Article; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -35469,7 +35468,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {1372--1377}, Pl = {CANADA}, - pubmed = {8748987}, + pmid = {8748987}, Pst = {ppublish}, Pt = {Journal Article}, Sb = {IM}, @@ -35504,7 +35503,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {300--304}, Pl = {NETHERLANDS}, - pubmed = {8485851}, + pmid = {8485851}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -35540,7 +35539,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {3767--3778}, Pl = {UNITED STATES}, - pubmed = {9570807}, + pmid = {9570807}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (GABA Antagonists); 0 (Glycine Agents); 0 (Pyridazines); 0 (Receptors, GABA-A); 104104-50-9 (gabazine); 124-87-8 (Picrotoxin); 485-49-4 (Bicuculline); 56-12-2 (gamma-Aminobutyric Acid); 56-40-6 (Glycine); 57-24-9 (Strychnine)}, @@ -35576,7 +35575,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {351--360}, Pl = {UNITED STATES}, - pubmed = {10627612}, + pmid = {10627612}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Excitatory Amino Acid Antagonists); 0 (GABA Antagonists); 0 (Glycine Agents); 0 (Quinoxalines); 118876-58-7 (2,3-dioxo-6-nitro-7-sulfamoylbenzo(f)quinoxaline); 485-49-4 (Bicuculline); 56-12-2 (gamma-Aminobutyric Acid); 56-40-6 (Glycine); 56-86-0 (Glutamic Acid); 57-24-9 (Strychnine); 76726-92-6 (2-Amino-5-phosphonovalerate)}, @@ -35616,7 +35615,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2003/09/17 {$[$}received{$]$}; 2004/06/28 {$[$}revised{$]$}; 2005/01/27 {$[$}accepted{$]$}}, Pii = {S0896-6273(05)00115-7}, Pl = {United States}, - pubmed = {15797545}, + pmid = {15797545}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (GABA Agonists); 0 (GABA Antagonists); 0 (Receptors, GABA-A); 56-12-2 (gamma-Aminobutyric Acid); 56-86-0 (Glutamic Acid)}, @@ -35654,7 +35653,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {3007--3022}, Pl = {UNITED STATES}, - pubmed = {10191318}, + pmid = {10191318}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (GABA Antagonists); 0 (Nipecotic Acids); 0 (Receptors, Nicotinic); 147-85-3 (Proline); 485-49-4 (Bicuculline); 498-95-3 (nipecotic acid); 51-84-3 (Acetylcholine); 56-12-2 (gamma-Aminobutyric Acid); 56-86-0 (Glutamic Acid); 56879-46-0 (homoproline)}, @@ -35694,7 +35693,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2006/01/17 {$[$}received{$]$}; 2006/05/11 {$[$}revised{$]$}; 2006/07/06 {$[$}accepted{$]$}}, Pii = {S0896-6273(06)00548-4}, Pl = {United States}, - pubmed = {16950160}, + pmid = {16950160}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural}, Rn = {0 (RNA, Messenger); 0 (Receptors, GABA); 0 (Symporters); 0 (potassium-chloride symporters); 56-12-2 (gamma-Aminobutyric Acid)}, @@ -35732,7 +35731,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {524--526}, Pii = {S0896-6273(06)00644-1}, Pl = {United States}, - pubmed = {16950151}, + pmid = {16950151}, Pst = {ppublish}, Pt = {Comment; Journal Article; Review}, Rf = {18}, @@ -35771,7 +35770,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {10299--10310}, Pii = {27/38/10299}, Pl = {United States}, - pubmed = {17881536}, + pmid = {17881536}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, N.I.H., Extramural}, Sb = {IM}, @@ -35810,7 +35809,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2004/11/19 {$[$}received{$]$}; 2005/04/15 {$[$}revised{$]$}; 2005/06/02 {$[$}accepted{$]$}}, Pii = {S0896-6273(05)00516-7}, Pl = {United States}, - pubmed = {16039568}, + pmid = {16039568}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -35845,7 +35844,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {467--471}, Pl = {ENGLAND}, - pubmed = {819835}, + pmid = {819835}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -35882,7 +35881,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {8906--8914}, Pii = {21/22/8906}, Pl = {United States}, - pubmed = {11698602}, + pmid = {11698602}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -35919,7 +35918,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {1049--1052}, Pii = {35082568}, Pl = {England}, - pubmed = {11429605}, + pmid = {11429605}, Pst = {ppublish}, Pt = {Journal Article}, Sb = {IM}, @@ -35961,7 +35960,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pii = {10.1002/(SICI)1096-9861(19990503)407:2<151::AID-CNE1>3.0.CO;2-1}, Pl = {UNITED STATES}, Pmc = {PMC2453001}, - pubmed = {10213088}, + pmid = {10213088}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Wheat Germ Agglutinin-Horseradish Peroxidase Conjugate); 10028-17-8 (Tritium); 147-85-3 (Proline)}, @@ -35999,7 +35998,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {6443--6453}, Pl = {UNITED STATES}, - pubmed = {8815923}, + pmid = {8815923}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -36041,7 +36040,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pii = {S0896-6273(06)00625-8}, Pl = {United States}, Pmc = {PMC2647846}, - pubmed = {17046688}, + pmid = {17046688}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural}, Rn = {0 (Bicyclo Compounds, Heterocyclic); 0 (Nicotinic Agonists); 0 (Pyridines); 140111-52-0 (epibatidine)}, @@ -36083,7 +36082,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2006/01/20 {$[$}received{$]$}; 2006/03/16 {$[$}accepted{$]$}; 2006/04/09 {$[$}aheadofprint{$]$}}, Pii = {nn1684}, Pl = {United States}, - pubmed = {16604068}, + pmid = {16604068}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -36121,7 +36120,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {94--100}, Pii = {S0959-4388(05)00013-9}, Pl = {England}, - pubmed = {15721750}, + pmid = {15721750}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review}, Rf = {65}, @@ -36159,7 +36158,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {34--42}, Pii = {nrn703}, Pl = {England}, - pubmed = {11823803}, + pmid = {11823803}, Pst = {ppublish}, Pt = {Journal Article; Review}, Rf = {107}, @@ -36195,7 +36194,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {565--567}, Pl = {UNITED STATES}, - pubmed = {622560}, + pmid = {622560}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -36232,7 +36231,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {739--755}, Pii = {S0092-8674(00)81509-3}, Pl = {UNITED STATES}, - pubmed = {10499792}, + pmid = {10499792}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Brain-Derived Neurotrophic Factor); 0 (Parvalbumins); 0 (Receptors, GABA); 0 (Recombinant Proteins)}, @@ -36270,7 +36269,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {6695--6702}, Pii = {23/17/6695}, Pl = {United States}, - pubmed = {12890762}, + pmid = {12890762}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (GABA Modulators); 0 (Isoenzymes); 0 (Receptors, GABA-A); 439-14-5 (Diazepam); EC 4.1.1.15 (Glutamate Decarboxylase); EC 4.1.1.15 (glutamate decarboxylase 2)}, @@ -36306,7 +36305,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {183--186}, Pl = {ENGLAND}, - pubmed = {10724170}, + pmid = {10724170}, Pst = {ppublish}, Pt = {Journal Article}, Rn = {439-14-5 (Diazepam); 56-12-2 (gamma-Aminobutyric Acid)}, @@ -36341,7 +36340,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {549--579}, Pl = {United States}, - pubmed = {15217343}, + pmid = {15217343}, Pst = {ppublish}, Pt = {Journal Article; Review}, Rf = {234}, @@ -36380,7 +36379,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {293--296}, Pii = {nature01002}, Pl = {England}, - pubmed = {12239566}, + pmid = {12239566}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM; S}, @@ -36418,7 +36417,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {322--328}, Pii = {417322a}, Pl = {England}, - pubmed = {12015612}, + pmid = {12015612}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review}, Rf = {72}, @@ -36459,7 +36458,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {73--76}, Pii = {415073a}, Pl = {England}, - pubmed = {11780119}, + pmid = {11780119}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -36495,7 +36494,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {90--91}, Pl = {UNITED STATES}, - pubmed = {3175637}, + pmid = {3175637}, Pst = {ppublish}, Pt = {Journal Article}, Sb = {IM}, @@ -36531,7 +36530,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {939-943}, Pl = {UNITED STATES}, - pubmed = {2035024}, + pmid = {2035024}, Pst = {ppublish}, Pt = {In Vitro; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.}, Rn = {7440-70-2 (Calcium)}, @@ -36567,7 +36566,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {77--88}, Pii = {S0092-8674(00)00012-X}, Pl = {UNITED STATES}, - pubmed = {10929715}, + pmid = {10929715}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Eye Proteins); 0 (Homeodomain Proteins); 0 (Nerve Tissue Proteins); 0 (insulin gene enhancer binding protein Isl-1); EC 2.7.1.112 (Epha3 protein, mouse); EC 2.7.1.112 (Receptor Protein-Tyrosine Kinases); EC 2.7.1.112 (Receptor, EphA3); EC 2.7.1.112 (Receptor, EphA5)}, @@ -36605,7 +36604,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {5117--5130}, Pii = {26/19/5117}, Pl = {United States}, - pubmed = {16687503}, + pmid = {16687503}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.}, Rn = {0 (Chloride Channels); 56-12-2 (gamma-Aminobutyric Acid)}, @@ -36644,7 +36643,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2006/03/22 {$[$}received{$]$}; 2006/06/13 {$[$}accepted{$]$}}, Pii = {S095252380623013X}, Pl = {England}, - pubmed = {17020635}, + pmid = {17020635}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Rn = {0 (Anesthetics, Local); 0 (Chelating Agents); 0 (Excitatory Amino Acid Antagonists); 0 (GABA Antagonists); 0 (Pyridazines); 104104-50-9 (gabazine); 115066-14-3 (6-Cyano-7-nitroquinoxaline-2,3-dione); 124-87-8 (Picrotoxin); 139890-68-9 (1,2-bis(2-aminophenoxy)ethane N,N,N',N'-tetraacetic acid acetoxymethyl ester); 4368-28-9 (Tetrodotoxin); 56-12-2 (gamma-Aminobutyric Acid); 67-42-5 (Egtazic Acid); 7440-70-2 (Calcium); 76726-92-6 (2-Amino-5-phosphonovalerate)}, @@ -36681,7 +36680,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {703--710}, Pl = {UNITED STATES}, Pmc = {PMC221249}, - pubmed = {14077501}, + pmid = {14077501}, Pst = {ppublish}, Pt = {Journal Article}, Sb = {OM}, @@ -36716,7 +36715,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {150--152}, Pl = {ENGLAND}, - pubmed = {6823290}, + pmid = {6823290}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -36751,7 +36750,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {2117--2133}, Pl = {UNITED STATES}, - pubmed = {3746403}, + pmid = {3746403}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {4368-28-9 (Tetrodotoxin)}, @@ -36793,7 +36792,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pl = {United States}, Pmc = {PMC2629308}, Pmcr = {2009/06/23}, - pubmed = {19074264}, + pmid = {19074264}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Rn = {0 (Cpeb1 protein, Xenopus); 0 (RNA, Messenger); 0 (RNA, Small Interfering); 0 (RNA-Binding Proteins); 0 (Transcription Factors); 0 (Xenopus Proteins); 0 (mRNA Cleavage and Polyadenylation Factors)}, @@ -36838,7 +36837,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pl = {United States}, Pmc = {PMC2604980}, Pmcr = {2009/06/16}, - pubmed = {19066223}, + pmid = {19066223}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural}, Rn = {56-12-2 (gamma-Aminobutyric Acid)}, @@ -36881,7 +36880,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pii = {0802278105}, Pl = {United States}, Pmc = {PMC2504797}, - pubmed = {18663225}, + pmid = {18663225}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article}, Rn = {0 (Kaede protein, Trachyphyllia geoffroyi); 0 (Luminescent Proteins)}, @@ -36921,7 +36920,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {479--509}, Pl = {United States}, Pmc = {PMC2655105}, - pubmed = {18558864}, + pmid = {18558864}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review}, Rf = {200}, @@ -36961,7 +36960,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {983--991}, Pii = {00000542-200712000-00018}, Pl = {United States}, - pubmed = {18043067}, + pmid = {18043067}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, N.I.H., Extramural}, Rn = {26675-46-7 (Isoflurane)}, @@ -37000,7 +36999,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {655--661}, Pii = {S0166223603003412}, Pl = {England}, - pubmed = {14624849}, + pmid = {14624849}, Pst = {ppublish}, Pt = {Journal Article; Review}, Rf = {52}, @@ -37039,7 +37038,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {2947--2960}, Pii = {23/7/2947}, Pl = {United States}, - pubmed = {12684482}, + pmid = {12684482}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -37080,7 +37079,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pii = {152266799}, Pl = {United States}, Pmc = {PMC126634}, - pubmed = {12114537}, + pmid = {12114537}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (DNA Primers); 0 (Luminescent Proteins); 0 (Recombinant Fusion Proteins); 147336-22-9 (Green Fluorescent Proteins); EC 3.2.1.23 (beta-Galactosidase)}, @@ -37118,7 +37117,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {117--131}, Pii = {S0012160601905056}, Pl = {United States}, - pubmed = {11784099}, + pmid = {11784099}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Rn = {56-12-2 (gamma-Aminobutyric Acid); 56-86-0 (Glutamic Acid)}, @@ -37157,7 +37156,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {627--632}, Pii = {88450}, Pl = {United States}, - pubmed = {11369944}, + pmid = {11369944}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -37195,7 +37194,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {1585--1594}, Pl = {United States}, - pubmed = {11287482}, + pmid = {11287482}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -37231,7 +37230,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {1271--1273}, Pl = {UNITED STATES}, - pubmed = {11185393}, + pmid = {11185393}, Pst = {ppublish}, Pt = {Comment; News}, Sb = {IM}, @@ -37269,7 +37268,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {1321--1324}, Pii = {8992}, Pl = {UNITED STATES}, - pubmed = {11082053}, + pmid = {11082053}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -37304,7 +37303,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {1--37}, Pl = {UNITED STATES}, - pubmed = {10845057}, + pmid = {10845057}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.; Review}, Rf = {182}, @@ -37345,7 +37344,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {1125--1130}, Pl = {UNITED STATES}, - pubmed = {10570491}, + pmid = {10570491}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Fluorescent Dyes); 0 (biotinylated dextran amine); 58-85-5 (Biotin); 9004-54-0 (Dextrans)}, @@ -37383,7 +37382,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {1043--1045}, Pl = {UNITED STATES}, - pubmed = {10570475}, + pmid = {10570475}, Pst = {ppublish}, Pt = {Comment; News}, Sb = {IM; S}, @@ -37418,7 +37417,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {68--89}, Pl = {UNITED STATES}, - pubmed = {10415887}, + pmid = {10415887}, Pst = {ppublish}, Pt = {Journal Article}, Rn = {0 (Neurotransmitter Agents)}, @@ -37456,7 +37455,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {2429--2444}, Pl = {UNITED STATES}, - pubmed = {9065504}, + pmid = {9065504}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -37490,7 +37489,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {903--910}, Pl = {UNITED STATES}, - pubmed = {6396217}, + pmid = {6396217}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Review}, Rf = {56}, @@ -37528,7 +37527,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {527--530}, Pl = {UNITED STATES}, - pubmed = {6836298}, + pmid = {6836298}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Sb = {IM; S}, @@ -37563,7 +37562,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {91-101}, Pl = {UNITED STATES}, - pubmed = {1249606}, + pmid = {1249606}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -37598,7 +37597,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {690-713}, Pl = {UNITED STATES}, - pubmed = {1127462}, + pmid = {1127462}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Sulfur Radioisotopes); 63-68-3 (Methionine)}, @@ -37633,7 +37632,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {203--204}, Pl = {ENGLAND}, - pubmed = {1110771}, + pmid = {1110771}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -37672,7 +37671,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2007/02/15 {$[$}aheadofprint{$]$}}, Pii = {01207.2006}, Pl = {United States}, - pubmed = {17303810}, + pmid = {17303810}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Rn = {0 (Coloring Agents); 0 (Luminescent Proteins); 0 (yellow fluorescent protein, mouse); 147336-22-9 (Green Fluorescent Proteins); 56-12-2 (gamma-Aminobutyric Acid); EC 4.1.1.15 (Glutamate Decarboxylase)}, @@ -37715,7 +37714,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pl = {United States}, Pmc = {PMC2493472}, Pmcr = {2009/07/01 00:00}, - pubmed = {18497355}, + pmid = {18497355}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -37752,7 +37751,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {7520--7536}, Pii = {28/30/7520}, Pl = {United States}, - pubmed = {18650330}, + pmid = {18650330}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -37789,7 +37788,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {698--707}, Pii = {S0959-4388(99)00039-2}, Pl = {ENGLAND}, - pubmed = {10607648}, + pmid = {10607648}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -37828,7 +37827,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2006/02/02 {$[$}aheadofprint{$]$}}, Pii = {00409.2005}, Pl = {United States}, - pubmed = {16455771}, + pmid = {16455771}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Rn = {0 (Anesthetics, General); 0 (Biological Markers)}, @@ -37868,7 +37867,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2004/12/20 {$[$}received{$]$}; 2005/01/30 {$[$}revised{$]$}; 2005/02/10 {$[$}accepted{$]$}}, Pii = {S0092-8674(05)00157-1}, Pl = {United States}, - pubmed = {15882628}, + pmid = {15882628}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Genetic Markers); 0 (Luminescent Proteins); 0 (red fluorescent protein); 147336-22-9 (Green Fluorescent Proteins); EC 2.7.7.- (Cre recombinase); EC 2.7.7.- (Integrases)}, @@ -37911,7 +37910,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pii = {S0896-6273(07)00708-8}, Pl = {United States}, Pmc = {PMC2098835}, - pubmed = {17988631}, + pmid = {17988631}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Rn = {0 (Alexa594); 0 (Fluorescent Dyes); 0 (Organic Chemicals)}, @@ -37953,7 +37952,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pl = {England}, Pmc = {PMC2607365}, Pmcr = {2009/12/12}, - pubmed = {18829430}, + pmid = {18829430}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural}, Sb = {IM}, @@ -37996,7 +37995,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pii = {nn2065}, Pl = {United States}, Pmc = {PMC2413175}, - pubmed = {18368047}, + pmid = {18368047}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Review}, Rf = {100}, @@ -38034,7 +38033,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2007/10/19 {$[$}received{$]$}; 2008/08/04 {$[$}accepted{$]$}}, Pl = {United States}, Pmc = {PMC2518110}, - pubmed = {18725976}, + pmid = {18725976}, Pst = {epublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (enhanced green fluorescent protein); 147336-22-9 (Green Fluorescent Proteins); EC 2.7.7.- (Cre recombinase); EC 2.7.7.- (Integrases)}, @@ -38078,7 +38077,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pii = {S0896-6273(08)00105-0}, Pl = {United States}, Pmc = {PMC2322861}, - pubmed = {18341988}, + pmid = {18341988}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -38116,7 +38115,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2007/12/20 {$[$}received{$]$}; 2008/02/29 {$[$}revised{$]$}; 2008/03/14 {$[$}accepted{$]$}}, Pii = {S0896-6273(08)00257-2}, Pl = {United States}, - pubmed = {18498742}, + pmid = {18498742}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -38153,7 +38152,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2007/06/15 {$[$}received{$]$}; 2007/09/26 {$[$}revised{$]$}; 2008/01/07 {$[$}accepted{$]$}}, Pii = {S0896-6273(08)00044-5}, Pl = {United States}, - pubmed = {18341987}, + pmid = {18341987}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -38195,7 +38194,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pl = {United States}, Pmc = {PMC2588436}, Pmcr = {2009/04/22 00:00}, - pubmed = {18945909}, + pmid = {18945909}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural}, Rn = {0 (Ephrins); 0 (Receptors, Nicotinic)}, @@ -38237,7 +38236,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2004/01/30 {$[$}received{$]$}; 2004/06/15 {$[$}accepted{$]$}; 2004/07/18 {$[$}aheadofprint{$]$}}, Pii = {nn1287}, Pl = {United States}, - pubmed = {15258585}, + pmid = {15258585}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -38280,7 +38279,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pl = {United States}, Pmc = {PMC2474739}, Pmcr = {2009/05/22 00:00}, - pubmed = {18498732}, + pmid = {18498732}, Pst = {ppublish}, Pt = {In Vitro; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.}, Rn = {0 (Chrnb2 protein, mouse); 0 (Receptors, Nicotinic); 51-84-3 (Acetylcholine)}, @@ -38318,7 +38317,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {627--628}, Pii = {S0896-6273(08)00180-3}, Pl = {United States}, - pubmed = {18341982}, + pmid = {18341982}, Pst = {ppublish}, Pt = {Comment; Journal Article; Review}, Rf = {16}, @@ -38355,7 +38354,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {903--911}, Pii = {nature07456}, Pl = {England}, - pubmed = {18923512}, + pmid = {18923512}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review}, Rf = {91}, @@ -38394,7 +38393,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2008/05/16 {$[$}received{$]$}; 2008/09/18 {$[$}accepted{$]$}; 2008/10/15 {$[$}epublish{$]$}}, Pl = {United States}, Pmc = {PMC2566599}, - pubmed = {18923679}, + pmid = {18923679}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -38431,7 +38430,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {7376--7386}, Pii = {28/29/7376}, Pl = {United States}, - pubmed = {18632942}, + pmid = {18632942}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Ephrin-A2); 0 (Ephrin-A5)}, @@ -38473,7 +38472,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pii = {S0896-6273(08)00416-9}, Pl = {United States}, Pmc = {PMC2617787}, - pubmed = {18614029}, + pmid = {18614029}, Pst = {ppublish}, Pt = {In Vitro; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Rn = {EC 2.7.1.112 (Receptors, Eph Family)}, @@ -38509,7 +38508,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {38--52}, Pii = {S0092-8674(08)00386-3}, Pl = {United States}, - pubmed = {18394988}, + pmid = {18394988}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Review}, Rf = {94}, @@ -38549,7 +38548,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2007/12/20 {$[$}received{$]$}; 2008/03/17 {$[$}revised{$]$}; 2008/03/24 {$[$}accepted{$]$}}, Pii = {S0896-6273(08)00268-7}, Pl = {United States}, - pubmed = {18400161}, + pmid = {18400161}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Cadherins); 0 (Drosophila Proteins)}, @@ -38587,7 +38586,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {1--3}, Pii = {S0896-6273(08)00270-5}, Pl = {United States}, - pubmed = {18400154}, + pmid = {18400154}, Pst = {ppublish}, Pt = {Comment; Journal Article; Review}, Rf = {15}, @@ -38632,7 +38631,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pl = {United States}, Pmc = {PMC2494600}, Pmcr = {2009/04/10 00:00}, - pubmed = {18400160}, + pmid = {18400160}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Rn = {0 (Cadherins); 0 (Drosophila Proteins); 0 (stan protein, Drosophila)}, @@ -38676,7 +38675,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pl = {United States}, Pmc = {PMC2612727}, Pmcr = {2009/10/09}, - pubmed = {18940594}, + pmid = {18940594}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -38714,7 +38713,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {7--8}, Pii = {S0896-6273(08)00811-8}, Pl = {United States}, - pubmed = {18940583}, + pmid = {18940583}, Pst = {ppublish}, Pt = {Comment; Journal Article; Review}, Rf = {15}, @@ -38749,7 +38748,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {551--580}, Pl = {United States}, - pubmed = {16212507}, + pmid = {16212507}, Pst = {ppublish}, Pt = {Journal Article; Review}, Rf = {103}, @@ -38789,7 +38788,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {6921--6928}, Pii = {25/29/6921}, Pl = {United States}, - pubmed = {16033902}, + pmid = {16033902}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Chrnb2 protein, mouse); 0 (Receptors, Nicotinic)}, @@ -38826,7 +38825,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {43--65}, Pii = {S0079612304470058}, Pl = {Netherlands}, - pubmed = {15581697}, + pmid = {15581697}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.; Review}, Rf = {114}, @@ -38866,7 +38865,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2004/06/04 {$[$}received{$]$}; 2004/08/09 {$[$}accepted{$]$}}, Pii = {nature02957}, Pl = {England}, - pubmed = {15483613}, + pmid = {15483613}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (RNA, Messenger); EC 2.7.1.112 (Receptors, Eph Family)}, @@ -38902,7 +38901,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {361--366}, Pl = {Korea (South)}, - pubmed = {12521298}, + pmid = {12521298}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Calcium-Binding Protein, Vitamin D-Dependent); 0 (Fluorescent Dyes); 0 (Nerve Tissue Proteins); 0 (Parvalbumins); 0 (calretinin); 56-12-2 (gamma-Aminobutyric Acid)}, @@ -38935,7 +38934,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {3--19}, Pl = {Netherlands}, - pubmed = {12508579}, + pmid = {12508579}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Review}, Rf = {51}, @@ -38971,7 +38970,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {32--39}, Pii = {S0166-2236(00)01676-3}, Pl = {England}, - pubmed = {11163885}, + pmid = {11163885}, Pst = {ppublish}, Pt = {Journal Article; Review}, Rf = {79}, @@ -39009,7 +39008,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {210--230}, Pii = {10.1002/(SICI)1096-9861(19980406)393:2<210::AID-CNE6>3.0.CO;2-5}, Pl = {UNITED STATES}, - pubmed = {9548698}, + pmid = {9548698}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Antibodies, Monoclonal); 0 (Calcium-Binding Proteins); 0 (Parvalbumins)}, @@ -39046,7 +39045,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {1451--1452}, Pl = {UNITED STATES}, - pubmed = {9508718}, + pmid = {9508718}, Pst = {ppublish}, Pt = {Comment; News}, Sb = {IM}, @@ -39083,7 +39082,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {1531--1533}, Pl = {UNITED STATES}, - pubmed = {9488651}, + pmid = {9488651}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -39119,7 +39118,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {2732--2741}, Pl = {UNITED STATES}, - pubmed = {9356422}, + pmid = {9356422}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM; S}, @@ -39154,7 +39153,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {3763--3776}, Pl = {ENGLAND}, - pubmed = {8582286}, + pmid = {8582286}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Receptors, Cholinergic); 33507-63-0 (Substance P); EC 2.3.1.6 (Choline O-Acetyltransferase)}, @@ -39190,7 +39189,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {412--418}, Pl = {ENGLAND}, - pubmed = {7773438}, + pmid = {7773438}, Pst = {ppublish}, Pt = {Journal Article}, Sb = {IM}, @@ -39224,7 +39223,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {230--246}, Pl = {UNITED STATES}, - pubmed = {1397159}, + pmid = {1397159}, Pst = {ppublish}, Pt = {Journal Article}, Rn = {0 (Antibodies, Monoclonal); 0 (Calcium-Binding Protein, Vitamin D-Dependent); 0 (Parvalbumins); 0 (calbindin)}, @@ -39260,7 +39259,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {173--178}, Pl = {NETHERLANDS}, - pubmed = {1572062}, + pmid = {1572062}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -39294,7 +39293,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {219--248}, Pl = {NETHERLANDS}, - pubmed = {1321459}, + pmid = {1321459}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review}, Rf = {177}, @@ -39330,7 +39329,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {79--90}, Pl = {UNITED STATES}, - pubmed = {1714924}, + pmid = {1714924}, Pst = {ppublish}, Pt = {Journal Article}, Rn = {404-86-4 (Capsaicin)}, @@ -39367,7 +39366,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {51--57}, Pl = {NETHERLANDS}, - pubmed = {1914145}, + pmid = {1914145}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -39402,7 +39401,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {412--423}, Pl = {UNITED STATES}, - pubmed = {2007657}, + pmid = {2007657}, Pst = {ppublish}, Pt = {Journal Article}, Rn = {4368-28-9 (Tetrodotoxin)}, @@ -39439,7 +39438,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {513--529}, Pii = {0306-4522(91)90312-C}, Pl = {ENGLAND}, - pubmed = {1922782}, + pmid = {1922782}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Enkephalins); 0 (Neurotoxins)}, @@ -39475,7 +39474,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {197--200}, Pii = {0304-3940(90)90037-A}, Pl = {NETHERLANDS}, - pubmed = {1963482}, + pmid = {1963482}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Antibodies, Monoclonal); 0 (Parvalbumins); EC 1.9.3.1 (Electron Transport Complex IV); EC 3.1.1.7 (Acetylcholinesterase)}, @@ -39509,7 +39508,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {155--158}, Pl = {ENGLAND}, - pubmed = {2437459}, + pmid = {2437459}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {33507-63-0 (Substance P)}, @@ -39544,7 +39543,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {395--409}, Pl = {UNITED STATES}, - pubmed = {3722463}, + pmid = {3722463}, Pst = {ppublish}, Pt = {Journal Article}, Sb = {IM}, @@ -39579,7 +39578,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {365--369}, Pii = {0006-8993(86)90495-6}, Pl = {NETHERLANDS}, - pubmed = {3708332}, + pmid = {3708332}, Pst = {ppublish}, Pt = {Journal Article}, Rn = {EC 2.3.1.6 (Choline O-Acetyltransferase)}, @@ -39612,7 +39611,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {223--234}, Pl = {GERMANY, WEST}, - pubmed = {3985371}, + pmid = {3985371}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, Non-U.S. Gov't}, Rn = {EC 1.11.1.- (Horseradish Peroxidase)}, @@ -39645,7 +39644,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {424--434}, Pl = {GERMANY, WEST}, - pubmed = {7238681}, + pmid = {7238681}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -39680,7 +39679,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {219--230}, Pii = {0006-8993(79)90103-3}, Pl = {NETHERLANDS}, - pubmed = {466408}, + pmid = {466408}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -39712,7 +39711,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {637--649}, Pl = {GERMANY, EAST}, - pubmed = {121134}, + pmid = {121134}, Pst = {ppublish}, Pt = {English Abstract; Journal Article}, Rn = {EC 1.1.- (Glycerolphosphate Dehydrogenase); EC 1.1.1.27 (L-Lactate Dehydrogenase); EC 1.3.99.1 (Succinate Dehydrogenase); EC 1.4.1.2 (Glutamate Dehydrogenase); EC 2.6.1.19 (4-Aminobutyrate Transaminase)}, @@ -39748,7 +39747,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {226--238}, Pl = {Not Available}, Pmc = {PMC1357023}, - pubmed = {14403678}, + pmid = {14403678}, Pst = {ppublish}, Pt = {Journal Article}, Sb = {OM}, @@ -39782,7 +39781,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {574--591}, Pl = {Not Available}, Pmc = {PMC1363130}, - pubmed = {14403679}, + pmid = {14403679}, Pst = {ppublish}, Pt = {Journal Article}, Sb = {OM}, @@ -39819,7 +39818,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {912--918}, Pii = {nature07457}, Pl = {England}, - pubmed = {18923513}, + pmid = {18923513}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review}, Rf = {69}, @@ -39856,7 +39855,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {10278--10286}, Pii = {28/41/10278}, Pl = {United States}, - pubmed = {18842887}, + pmid = {18842887}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Rn = {0 (Receptors, N-Methyl-D-Aspartate)}, @@ -39893,7 +39892,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {137--147}, Pii = {0166-2236(89)90052-0}, Pl = {ENGLAND}, - pubmed = {2470171}, + pmid = {2470171}, Pst = {ppublish}, Pt = {Journal Article; Review}, Rf = {66}, @@ -39928,7 +39927,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2006/12/12 {$[$}received{$]$}; 2007/05/15 {$[$}accepted{$]$}}, Pii = {06-PLBI-RA-2351}, Pmc = {PMC1914403}, - pubmed = {17622195}, + pmid = {17622195}, Pst = {aheadofprint}, Pt = {JOURNAL ARTICLE}, Status = {Publisher}, @@ -39966,7 +39965,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {1147-1160}, Pii = {S0896627303007906}, Pl = {United States}, - pubmed = {14687549}, + pmid = {14687549}, Pst = {ppublish}, Pt = {Comparative Study; In Vitro; Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Receptors, Nicotinic); 0 (nicotinic receptor beta2)}, @@ -39999,7 +39998,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Phst = {2008/10/22 {$[$}received{$]$}; 2008/12/11 {$[$}accepted{$]$}; 2009/02/08 {$[$}aheadofprint{$]$}}, Pii = {nature07722}, - pubmed = {19204731}, + pmid = {19204731}, Pst = {aheadofprint}, Pt = {JOURNAL ARTICLE}, Status = {Publisher}, @@ -40035,7 +40034,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {656--668}, Pii = {S0092-8674(09)00127-5}, Pl = {United States}, - pubmed = {19239887}, + pmid = {19239887}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Review}, Rf = {160}, @@ -40075,7 +40074,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2008/04/18 {$[$}received{$]$}; 2008/05/05 {$[$}revised{$]$}; 2008/05/08 {$[$}accepted{$]$}; 2008/05/29 {$[$}aheadofprint{$]$}}, Pii = {S0959-4388(08)00036-6}, Pl = {England}, - pubmed = {18513949}, + pmid = {18513949}, Pst = {ppublish}, Pt = {Journal Article; Review}, Rf = {64}, @@ -40112,7 +40111,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {805--811}, Phst = {2008/05/22 {$[$}received{$]$}; 2008/07/14 {$[$}accepted{$]$}; 2008/08/10 {$[$}aheadofprint{$]$}}, Pii = {nmeth.1243}, - pubmed = {18690223}, + pmid = {18690223}, Pst = {ppublish}, Pt = {JOURNAL ARTICLE}, Status = {Publisher}, @@ -40148,7 +40147,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {1550--1564}, Phst = {2008/05/01 {$[$}aheadofprint{$]$}}, Pl = {United States}, - pubmed = {18447377}, + pmid = {18447377}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Review}, Rf = {105}, @@ -40186,7 +40185,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {6268--6272}, Pii = {27/23/6268}, Pl = {United States}, - pubmed = {17554000}, + pmid = {17554000}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -40225,7 +40224,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2007/10/02 {$[$}aheadofprint{$]$}}, Pii = {1073858407306597}, Pl = {United States}, - pubmed = {17911223}, + pmid = {17911223}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Review}, Rf = {157}, @@ -40262,7 +40261,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {13828--13844}, Pii = {28/51/13828}, Pl = {United States}, - pubmed = {19091973}, + pmid = {19091973}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -40300,7 +40299,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {263--274}, Pii = {S0896-6273(01)00278-1}, Pl = {United States}, - pubmed = {11343660}, + pmid = {11343660}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -40335,7 +40334,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {1300--1311}, Pii = {29/5/1300}, Pl = {United States}, - pubmed = {19193877}, + pmid = {19193877}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Chemokine CXCL12); 0 (Cxcl12 protein, mouse); 147336-22-9 (Green Fluorescent Proteins); EC 4.1.1.15 (Glutamate Decarboxylase); EC 4.1.1.15 (glutamate decarboxylase 1)}, @@ -40375,7 +40374,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {1723--1725}, Pii = {315/5819/1723}, Pl = {United States}, - pubmed = {17379811}, + pmid = {17379811}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Rn = {0 (Retinal Pigments)}, @@ -40415,7 +40414,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2008/09/24 {$[$}received{$]$}; 2008/12/18 {$[$}accepted{$]$}; 2009/01/18 {$[$}aheadofprint{$]$}}, Pii = {nn.2262}, Pl = {United States}, - pubmed = {19151709}, + pmid = {19151709}, Pst = {ppublish}, Pt = {Journal Article}, Rn = {0 (Receptors, Odorant); 147336-22-9 (Green Fluorescent Proteins)}, @@ -40452,7 +40451,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {9560--9572}, Pii = {27/36/9560}, Pl = {United States}, - pubmed = {17804617}, + pmid = {17804617}, Pst = {ppublish}, Pt = {In Vitro; Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Receptors, Kainic Acid); 0 (enhanced green fluorescent protein); 147336-22-9 (Green Fluorescent Proteins); 56-86-0 (Glutamic Acid)}, @@ -40493,7 +40492,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2008/10/31 {$[$}received{$]$}; 2008/12/15 {$[$}accepted{$]$}; 2009/01/25 {$[$}aheadofprint{$]$}}, Pii = {nmeth.1296}, Pl = {United States}, - pubmed = {19169260}, + pmid = {19169260}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Fluorescent Dyes); 0 (Luminescent Proteins); 0 (Recombinant Fusion Proteins)}, @@ -40534,7 +40533,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2008/05/15 {$[$}received{$]$}; 2008/11/06 {$[$}accepted{$]$}; 2008/12/21 {$[$}aheadofprint{$]$}}, Pii = {nm.1897}, Pl = {United States}, - pubmed = {19098909}, + pmid = {19098909}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Rn = {0 (Microtubule-Associated Proteins); 0 (Neuropeptides); 0 (doublecortin protein)}, @@ -40574,7 +40573,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2008/04/02 {$[$}received{$]$}; 2008/09/15 {$[$}revised{$]$}; 2008/11/07 {$[$}accepted{$]$}}, Pii = {S0896-6273(08)01006-4}, Pl = {United States}, - pubmed = {19146811}, + pmid = {19146811}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.}, Sb = {IM}, @@ -40611,7 +40610,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {327--338}, Pii = {S0896-6273(07)00773-8}, Pl = {United States}, - pubmed = {17964249}, + pmid = {17964249}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Review}, Rating = {5}, @@ -40650,7 +40649,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {12623--12629}, Pii = {27/46/12623}, Pl = {United States}, - pubmed = {18003841}, + pmid = {18003841}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Rn = {0 (Intermediate Filament Proteins); 0 (Luminescent Proteins); 0 (Nerve Tissue Proteins); 0 (Recombinant Fusion Proteins); 0 (Selective Estrogen Receptor Modulators); 0 (nestin); 0 (yellow fluorescent protein, mouse); 10540-29-1 (Tamoxifen)}, @@ -40688,7 +40687,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2008/08/04 {$[$}received{$]$}; 2008/12/04 {$[$}revised{$]$}; 2008/12/04 {$[$}accepted{$]$}}, Pii = {S0896-6273(08)01092-1}, Pl = {United States}, - pubmed = {19186171}, + pmid = {19186171}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Fluorescent Dyes)}, @@ -40726,7 +40725,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2007/06/27 {$[$}received{$]$}; 2007/11/02 {$[$}revised{$]$}; 2007/11/05 {$[$}accepted{$]$}; 2007/11/12 {$[$}aheadofprint{$]$}}, Pii = {S0006-8993(07)02656-X}, Pl = {Netherlands}, - pubmed = {18155185}, + pmid = {18155185}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -40769,7 +40768,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pl = {United States}, Pmc = {PMC2640228}, Pmcr = {2009/11/26}, - pubmed = {19038224}, + pmid = {19038224}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.}, Sb = {IM}, @@ -40807,7 +40806,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2008/03/10 {$[$}received{$]$}; 2008/07/07 {$[$}revised{$]$}; 2008/08/26 {$[$}accepted{$]$}}, Pii = {S0896-6273(08)00767-8}, Pl = {United States}, - pubmed = {18957223}, + pmid = {18957223}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Rn = {0 (Fluorescent Dyes)}, @@ -40846,7 +40845,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2008/05/29 {$[$}received{$]$}; 2008/12/01 {$[$}accepted{$]$}; 2009/01/04 {$[$}aheadofprint{$]$}}, Pii = {nmeth.1292}, Pl = {United States}, - pubmed = {19122667}, + pmid = {19122667}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.}, Rn = {0 (Luminescent Proteins); 0 (red fluorescent protein); 147336-22-9 (Green Fluorescent Proteins)}, @@ -40885,7 +40884,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {766--773}, Phst = {2003/05/02 {$[$}received{$]$}; 2003/06/24 {$[$}accepted{$]$}; 2003/07/22 {$[$}aheadofprint{$]$}}, Pl = {Germany}, - pubmed = {12883893}, + pmid = {12883893}, Pst = {ppublish}, Pt = {In Vitro; Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Coloring Agents); 0 (Excitatory Amino Acids); 0 (Fluorescent Dyes); 0 (Glycine Agents); 57-24-9 (Strychnine); 7440-70-2 (Calcium)}, @@ -40924,7 +40923,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {10734--10745}, Pii = {28/42/10734}, Pl = {United States}, - pubmed = {18923048}, + pmid = {18923048}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -40960,7 +40959,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {66--70}, Pii = {301/5629/66}, Pl = {United States}, - pubmed = {12843386}, + pmid = {12843386}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Excitatory Amino Acid Antagonists); 0 (Receptors, N-Methyl-D-Aspartate); 77086-22-7 (Dizocilpine Maleate)}, @@ -40997,7 +40996,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {2535--2545}, Pl = {UNITED STATES}, - pubmed = {10509647}, + pmid = {10509647}, Pst = {ppublish}, Pt = {Journal Article}, Rn = {0 (Parvalbumins); 0 (RNA, Messenger); 487-79-6 (Kainic Acid)}, @@ -41036,7 +41035,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2008/05/05 {$[$}received{$]$}; 2008/05/08 {$[$}accepted{$]$}; 2008/06/03 {$[$}aheadofprint{$]$}}, Pii = {S0959-4388(08)00037-8}, Pl = {England}, - pubmed = {18534841}, + pmid = {18534841}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Review}, Rf = {73}, @@ -41076,7 +41075,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2008/09/24 {$[$}received{$]$}; 2008/11/05 {$[$}accepted{$]$}; 2008/12/07 {$[$}aheadofprint{$]$}}, Pii = {nn.2236}, Pl = {United States}, - pubmed = {19060895}, + pmid = {19060895}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural}, Rn = {0 (Luminescent Agents); 147336-22-9 (Green Fluorescent Proteins)}, @@ -41117,7 +41116,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2004/09/09 {$[$}received{$]$}; 2004/12/20 {$[$}revised{$]$}; 2005/01/27 {$[$}accepted{$]$}}, Pii = {S0896-6273(05)00116-9}, Pl = {United States}, - pubmed = {15797554}, + pmid = {15797554}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Fluorescent Dyes)}, @@ -41161,7 +41160,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pl = {England}, Pmc = {PMC2644578}, Pmcr = {2009/06/18}, - pubmed = {18946471}, + pmid = {18946471}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -41199,7 +41198,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {385--396}, Phst = {2006/07/07 {$[$}received{$]$}; 2006/08/02 {$[$}accepted{$]$}; 2006/10/18 {$[$}aheadofprint{$]$}}, Pl = {Germany}, - pubmed = {17047983}, + pmid = {17047983}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Review}, Rf = {49}, @@ -41240,7 +41239,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2008/05/24 {$[$}received{$]$}; 2008/12/31 {$[$}accepted{$]$}}, Pii = {nature07767}, Pl = {England}, - pubmed = {19225519}, + pmid = {19225519}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Rn = {0 (Amyloid beta-Protein Precursor); 0 (Bax protein, mouse); 0 (Ligands); 0 (Peptide Fragments); 0 (Receptors, Tumor Necrosis Factor); 0 (Tnfrsf21 protein, mouse); 0 (bcl-2-Associated X Protein); EC 3.4.22.- (Caspase 3); EC 3.4.22.- (Caspase 6); EC 3.4.22.- (Caspases)}, @@ -41279,7 +41278,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2007/10/27 {$[$}received{$]$}; 2008/08/07 {$[$}revised{$]$}; 2008/11/10 {$[$}accepted{$]$}}, Pii = {S0896-6273(08)00969-0}, Pl = {United States}, - pubmed = {19146814}, + pmid = {19146814}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't}, Rn = {0 (Cadherins); 0 (Receptors, AMPA); 0 (Sodium Channel Blockers); 0 (beta Catenin); 4368-28-9 (Tetrodotoxin)}, @@ -41318,7 +41317,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2008/04/16 {$[$}received{$]$}; 2008/07/02 {$[$}accepted{$]$}; 2008/08/31 {$[$}aheadofprint{$]$}}, Pii = {nn.2181}, Pl = {United States}, - pubmed = {18758460}, + pmid = {18758460}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -41351,7 +41350,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Phst = {2008/07/24 {$[$}received{$]$}; 2008/12/05 {$[$}accepted{$]$}; 2009/01/21 {$[$}aheadofprint{$]$}}, Pii = {nature07721}, - pubmed = {19158677}, + pmid = {19158677}, Pst = {aheadofprint}, Pt = {JOURNAL ARTICLE}, Status = {Publisher}, @@ -41391,7 +41390,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2003/11/04 {$[$}received{$]$}; 2004/01/14 {$[$}accepted{$]$}; 2004/02/01 {$[$}aheadofprint{$]$}}, Pii = {nn1191}, Pl = {United States}, - pubmed = {14758365}, + pmid = {14758365}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Biological Markers); 0 (Luminescent Proteins); 0 (Nerve Tissue Proteins); 0 (Recombinant Fusion Proteins); 0 (postsynaptic density proteins); 147336-22-9 (Green Fluorescent Proteins)}, @@ -41431,7 +41430,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2008/04/14 {$[$}received{$]$}; 2008/08/20 {$[$}accepted{$]$}; 2008/10/15 {$[$}aheadofprint{$]$}}, Pii = {nature07351}, Pl = {England}, - pubmed = {18923391}, + pmid = {18923391}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural}, Rn = {7440-70-2 (Calcium)}, @@ -41472,7 +41471,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {962--965}, Pl = {UNITED STATES}, - pubmed = {10320376}, + pmid = {10320376}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Receptors, GABA-A); 40709-69-1 (bicuculline methiodide); 485-49-4 (Bicuculline)}, @@ -41511,7 +41510,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2004/04/21 {$[$}received{$]$}; 2004/09/13 {$[$}accepted{$]$}; 2004/12/19 {$[$}aheadofprint{$]$}}, Pii = {nn1367}, Pl = {United States}, - pubmed = {15608636}, + pmid = {15608636}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -41548,7 +41547,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {227--233}, Pii = {0166-2236(90)90165-7}, Pl = {ENGLAND}, - pubmed = {1694329}, + pmid = {1694329}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review}, Rf = {60}, @@ -41584,7 +41583,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2008/04/17 {$[$}received{$]$}; 2008/08/11 {$[$}revised{$]$}; 2008/08/12 {$[$}accepted{$]$}; 2008/08/26 {$[$}aheadofprint{$]$}}, Pii = {S0165-0270(08)00491-3}, Pl = {Netherlands}, - pubmed = {18789968}, + pmid = {18789968}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Sb = {IM}, @@ -41627,7 +41626,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {289--327}, Pl = {UNITED STATES}, - pubmed = {3284443}, + pmid = {3284443}, Pst = {ppublish}, Pt = {Journal Article; Review}, Rf = {114}, @@ -41662,7 +41661,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {140--141}, Pl = {ENGLAND}, - pubmed = {692682}, + pmid = {692682}, Pst = {ppublish}, Pt = {Journal Article}, Sb = {IM}, @@ -41696,7 +41695,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Own = {NLM}, Pages = {37--44}, Pl = {ENGLAND}, - pubmed = {9738497}, + pmid = {9738497}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -41734,7 +41733,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2007/07/04 {$[$}aheadofprint{$]$}}, Pii = {dev.02870}, Pl = {England}, - pubmed = {17611227}, + pmid = {17611227}, Pst = {ppublish}, Pt = {Journal Article}, Rn = {0 (Basic Helix-Loop-Helix Transcription Factors); 0 (Helt protein, mouse); 0 (Nerve Tissue Proteins); 0 (Neurog2 protein, mouse); 0 (Repressor Proteins); 182238-50-2 (Neurog1 protein, mouse); 56-12-2 (gamma-Aminobutyric Acid); 56-86-0 (Glutamic Acid)}, @@ -41773,7 +41772,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2004/08/04 {$[$}received{$]$}; 2004/11/19 {$[$}revised{$]$}; 2004/11/24 {$[$}accepted{$]$}; 2005/01/07 {$[$}aheadofprint{$]$}}, Pii = {S0168-0102(04)00299-8}, Pl = {Ireland}, - pubmed = {15710488}, + pmid = {15710488}, Pst = {ppublish}, Pt = {Comparative Study; In Vitro; Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Amino Acids); 0 (Bearded protein, Drosophila); 0 (DNA-Binding Proteins); 0 (Drosophila Proteins); 0 (Isoenzymes); 0 (Neurofilament Proteins); 0 (dolaisoleucine); 147336-22-9 (Green Fluorescent Proteins); 56-12-2 (gamma-Aminobutyric Acid); EC 4.1.1.15 (Glutamate Decarboxylase); EC 4.1.1.15 (glutamate decarboxylase 1)}, @@ -41811,7 +41810,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2009/01/19 {$[$}aheadofprint{$]$}}, Pii = {jphysiol.2008.160952}, Pl = {England}, - pubmed = {19153163}, + pmid = {19153163}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural}, Sb = {IM}, @@ -41847,7 +41846,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {695--708}, Pii = {S0149763498000086}, Pl = {UNITED STATES}, - pubmed = {9809305}, + pmid = {9809305}, Pst = {ppublish}, Pt = {Journal Article; Review}, Rf = {167}, @@ -41885,7 +41884,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2003/01/15 {$[$}aheadofprint{$]$}}, Pii = {01029.2002}, Pl = {United States}, - pubmed = {12611963}, + pmid = {12611963}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Excitatory Amino Acid Antagonists); 0 (Receptors, N-Methyl-D-Aspartate); 76726-92-6 (2-Amino-5-phosphonovalerate)}, @@ -41924,7 +41923,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2006/03/14 {$[$}received{$]$}; 2006/03/30 {$[$}accepted{$]$}}, Pii = {S0952523806230062}, Pl = {England}, - pubmed = {17020630}, + pmid = {17020630}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.}, Rn = {0 (Excitatory Amino Acid Antagonists); 76726-92-6 (2-Amino-5-phosphonovalerate)}, @@ -41961,7 +41960,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {3847--3857}, Pii = {133/19/3847}, Pl = {England}, - pubmed = {16968817}, + pmid = {16968817}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't}, Rn = {0 (Basic Helix-Loop-Helix Transcription Factors); 0 (Biological Markers); 0 (Helt protein, mouse); 0 (Isoenzymes); 0 (Repressor Proteins); 56-12-2 (gamma-Aminobutyric Acid); EC 4.1.1.15 (Glutamate Decarboxylase); EC 4.1.1.15 (glutamate decarboxylase 1); EC 4.1.1.15 (glutamate decarboxylase 2)}, @@ -42001,7 +42000,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2005/05/25 {$[$}aheadofprint{$]$}}, Pii = {00166.2005}, Pl = {United States}, - pubmed = {15917326}, + pmid = {15917326}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -42043,7 +42042,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pii = {00816.2004}, Pl = {United States}, Pmc = {PMC1752200}, - pubmed = {16079191}, + pmid = {16079191}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.}, Sb = {IM}, @@ -42079,7 +42078,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {10358--10361}, Pii = {26/41/10358}, Pl = {United States}, - pubmed = {17035517}, + pmid = {17035517}, Pst = {ppublish}, Pt = {Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.; Review}, Rf = {50}, @@ -42119,7 +42118,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2005/10/13 {$[$}received{$]$}; 2006/04/11 {$[$}revised{$]$}; 2006/05/02 {$[$}accepted{$]$}}, Pii = {S0896-6273(06)00374-6}, Pl = {United States}, - pubmed = {16772171}, + pmid = {16772171}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, N.I.H., Extramural}, Rn = {0 (Cyclic AMP Response Element-Binding Protein); 0 (Wnt2 Protein); EC 2.7.11.17 (Calcium-Calmodulin-Dependent Protein Kinase Type 1); EC 2.7.11.17 (Calcium-Calmodulin-Dependent Protein Kinases); EC 2.7.11.17 (Camk1 protein, rat); EC 2.7.11.17 (Pnck protein, rat)}, @@ -42157,7 +42156,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pages = {9598--9611}, Pii = {24/43/9598}, Pl = {United States}, - pubmed = {15509747}, + pmid = {15509747}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Isoenzymes); 0 (Recombinant Fusion Proteins); 147336-22-9 (Green Fluorescent Proteins); 4368-28-9 (Tetrodotoxin); 56-12-2 (gamma-Aminobutyric Acid); EC 4.1.1.15 (Glutamate Decarboxylase); EC 4.1.1.15 (glutamate decarboxylase 1)}, @@ -42200,7 +42199,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pii = {1092436}, Pl = {United States}, Pmc = {PMC2405920}, - pubmed = {14671312}, + pmid = {14671312}, Pst = {ppublish}, Pt = {Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Histones); 0 (Luminescent Proteins); 0 (RNA, Messenger); 147336-22-9 (Green Fluorescent Proteins)}, @@ -42241,7 +42240,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Pii = {1734203100}, Pl = {United States}, Pmc = {PMC304094}, - pubmed = {12913119}, + pmid = {12913119}, Pst = {ppublish}, Pt = {Journal Article; Research Support, U.S. Gov't, P.H.S.; Review}, Rf = {64}, @@ -42281,7 +42280,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Phst = {2004/12/14 {$[$}received{$]$}; 2005/01/27 {$[$}accepted{$]$}; 2005/02/20 {$[$}aheadofprint{$]$}}, Pii = {nn1410}, Pl = {United States}, - pubmed = {15723060}, + pmid = {15723060}, Pst = {ppublish}, Pt = {Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.}, Rn = {0 (Anesthetics, Local); 0 (Cytoskeletal Proteins); 0 (Nerve Tissue Proteins); 0 (Proto-Oncogene Proteins c-fos); 0 (RNA, Messenger); 0 (activity regulated cytoskeletal-associated protein); 10028-17-8 (Tritium); 147-85-3 (Proline); 4368-28-9 (Tetrodotoxin)}, @@ -48241,8 +48240,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Uuid = {8FDA386E-7B7B-41E7-B2B8-20720BC5041E}, Volume = {30}, Year = {1989}, - url = {papers/Blanton_JNeurosciMethods1989.pdf}, - Bdsk-Url-1 = {http://www.ncbi.nlm.nih.gov/pubmed/?term=2607782&p%24a=&p%24l=DefaultSite&p%24st=m}} + url = {papers/Blanton_JNeurosciMethods1989.pdf}} @article{Blesch:2001, Abstract = {Vector systems for the regulated and reversible expression of therapeutic genes are likely to improve the safety and efficacy of gene therapy for medical disease. In the present study, we investigated whether the expression of genes transferred into the central nervous system by ex vivo gene therapy can be regulated in vivo leading to controlled neuronal survival and axonal growth. Primary rat fibroblasts were transfected with a retrovirus containing a tetracycline responsive promoter for the expression of the neurotrophin nerve growth factor (NGF) or green fluorescent protein as a control (GFP). After lesions of basal forebrain cholinergic neurons, NGF-mediated neuronal rescue and axonal growth could be completely controlled over a 2-week period by the addition or removal of the tetracycline modulator doxycycline in the animals' drinking water. Further, continued expression of the reporter gene GFP could be reliably and repeatedly turned on and off in the injured CNS for at least 3 months post-grafting, the longest time point investigated. These data constitute the first report of regulated neuronal rescue and axonal growth by controlled neurotrophin gene delivery and long-term, regulated expression using ex vivo CNS gene therapy.}, @@ -48363,8 +48361,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Title = {Increase of nestin-immunoreactive neural precursor cells in the dentate gyrus of pediatric patients with early-onset temporal lobe epilepsy}, Uuid = {AD8B01B1-A3E5-11DA-AB00-000D9346EC2A}, Volume = {11}, - Year = {2001}, - Bdsk-Url-1 = {http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=11769312&query_hl=0}} + Year = {2001}} @article{Blumenthal:1987, Abstract = {We have studied fusion between membranes of vesicular stomatitis virus (VSV) and Vero cells using an assay for lipid mixing based on the relief of self-quenching of octadecylrhodamine (R18) fluorescence. We could identify the two pathways of fusion by the kinetics of R18 dequenching, effects of inhibitors, temperature dependence, and dependence on osmotic pressure. Fusion at the plasma membrane began immediately after lowering the pH below 6 and showed an approximately exponential time course, whereas fusion via the endocytic pathway (pH 7.4) became apparent after a time delay of about 2 min. Fusion via the endocytic pathway was attenuated by treating cells with metabolic inhibitors and agents that raise the pH of the endocytic vesicle. A 10-fold excess of unlabeled virus arrested R18VSV entry via the endocytic pathway, whereas R18 dequenching below pH 6 (fusion at the plasma membrane) was not affected by the presence of unlabeled virus. The temperature dependence for fusion at pH 7.4 (in the endosome) was much steeper than that for fusion at pH 5.9 (with the plasma membrane). Fusion via the endocytic pathway was attenuated at hypo-osmotic pressures, whereas fusion at the plasma membrane was not affected by this treatment. The pH profile of Vero-VSV fusion at the plasma membrane, as measured by the dequenching method, paralleled that observed for VSV-induced cell-cell fusion. Fusion was blocked by adding neutralizing antibody to the Vero-VSV complexes. Activation of the fusion process by lowering the pH was reversible, in that the rate of fusion was arrested by raising the pH back to 7.4. The observation that pH-dependent fusion occurred at similar rates with fragments and with intact cells indicates that pH, voltage, or osmotic gradients are not required for viral fusion.}, @@ -50841,7 +50838,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a Organization = {W.M. Keck Foundation Center for Integrative Neuroscience, Department of Physiology, University of California, San Francisco, San Francisco, CA 94143-0444, USA.}, Pages = {511-23}, Pii = {S0896-6273(08)00028-7}, - pubmed = {18304481}, + pmid = {18304481}, Title = {Selective disruption of one Cartesian axis of cortical maps and receptive fields by deficiency in ephrin-As and structured activity}, Uuid = {99B7B73B-118F-485E-A0EB-4F16ADF49DC6}, Volume = {57}, @@ -111380,11 +111377,10 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a abstract = {Appropriate excitatory/inhibitory (E/I) balance is essential for normal cortical function and is altered in some psychiatric disorders, including autism spectrum disorders (ASDs). Cell-autonomous molecular mechanisms that control the balance of excitatory and inhibitory synapse function remain poorly understood; no proteins that regulate excitatory and inhibitory synapse strength in a coordinated reciprocal manner have been identified. Using super-resolution imaging, electrophysiology, and molecular manipulations, we show that cadherin-10, encoded by CDH10 within the ASD risk locus 5p14.1, maintains both excitatory and inhibitory synaptic scaffold structure in cultured cortical neurons from rats of both sexes. Cadherin-10 localizes to both excitatory and inhibitory synapses in neocortex, where it is organized into nanoscale puncta that influence the size of their associated PSDs. Knockdown of cadherin-10 reduces excitatory but increases inhibitory synapse size and strength, altering the E/I ratio in cortical neurons. Furthermore, cadherin-10 exhibits differential participation in complexes with PSD-95 and gephyrin, which may underlie its role in maintaining the E/I ratio. Our data provide a new mechanism whereby a protein encoded by a common ASD risk factor controls E/I ratios by regulating excitatory and inhibitory synapses in opposing directions.SIGNIFICANCE STATEMENT The correct balance between excitatory/inhibitory (E/I) is crucial for normal brain function and is altered in psychiatric disorders such as autism. However, the molecular mechanisms that underlie this balance remain elusive. To address this, we studied cadherin-10, an adhesion protein that is genetically linked to autism and understudied at the cellular level. Using a combination of advanced microscopy techniques and electrophysiology, we show that cadherin-10 forms nanoscale puncta at excitatory and inhibitory synapses, maintains excitatory and inhibitory synaptic structure, and is essential for maintaining the correct balance between excitation and inhibition in neuronal dendrites. These findings reveal a new mechanism by which E/I balance is controlled in neurons and may bear relevance to synaptic dysfunction in autism.}, keywords = {CDH10; PSD-95; adhesion; cadherin-10; dendritic spines; inhibitory synapses; }, mesh = {Animals; Cadherins; Cells, Cultured; Disks Large Homolog 4 Protein; Excitatory Postsynaptic Potentials; Female; HEK293 Cells; Humans; Inhibitory Postsynaptic Potentials; Male; Mice; Protein Binding; Rats; Rats, Sprague-Dawley; Synapses; }, - pubmed = {29030434}, + pmid = {29030434}, pii = {JNEUROSCI.1153-17.2017}, doi = {10.1523/JNEUROSCI.1153-17.2017}, pmc = {PMC5688522}, - eprint = {https://www.ncbi.nlm.nih.gov/pubmed/29030434}, url = {papers/Smith_JNeurosci2017-29030434.pdf}, nlmuniqueid = {8102140} } @@ -111400,12 +111396,10 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Mar}, abstract = {The structure of neuronal circuits that subserve cognitive functions in the brain is shaped and refined throughout development and into adulthood. Evidence from human and animal studies suggests that the cellular and synaptic substrates of these circuits are atypical in neuropsychiatric disorders, indicating that altered structural plasticity may be an important part of the disease biology. Advances in genetics have redefined our understanding of neuropsychiatric disorders and have revealed a spectrum of risk factors that impact pathways known to influence structural plasticity. In this Review, we discuss the importance of recent genetic findings on the different mechanisms of structural plasticity and propose that these converge on shared pathways that can be targeted with novel therapeutics.}, doi = {10.1038/nrn.2018.16}, - file = {papers/Forrest_NatRevNeurosci2018-29545546.pdf}, + url = {papers/Forrest_NatRevNeurosci2018-29545546.pdf}, nlmuniqueid = {100962781}, pii = {nrn.2018.16}, - pubmed = {29545546}, - url = {https://www.ncbi.nlm.nih.gov/pubmed/29545546}, -} + pmid = {29545546}} @article{Johnson1981, title = {Neural mechanisms of spatial tactile discrimination: neural patterns evoked by braille-like dot patterns in the monkey.}, @@ -111416,7 +111410,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Jan}, pages = {117-44}, abstract = {1. The experiments reported here were designed to investigate the responses of cutaneous mechanoreceptive afferents to spatially configured dot patterns scanned across the skin. Braille-like patterns were selected because the discrimination of Braille characters must depend on spatial patterning rather than some other facet of the afferent discharge. 2. A multifactorial experimental design was used in which each afferent fibre was studied using every combination of six dot patterns, two dot sizes, two dot spacings, two contact forces and two scanning velocities. Two other factors, scanning direction relative to the skin ridges and intermittent versus continuous scanning, were studied. 3. Beside the general question concerning the response properties of the mechanoreceptive afferents, three major questions were addressed here. (i) What is the critical spatial dimension at which neural spatial patterning breaks down and below which tactual discrimination must depend on facets of the afferent discharge other than spatial neural patterning? (ii) Which mechanoreceptive population sets this critical dimension? (iii) Why is tactual discrimination enhanced by lateral scanning? 4. The results presented here suggest that the critical dimension, below which spatial neural patterning breaks down, is of the order of 1.0 mm and that the slowly adapting (SA) afferent fibres are responsible for this limit. 5. At dimensions above approximately 1.0 mm the spatial contrast between peaks and troughs in the SA discharge is markedly enhanced during scanning. When the skin is stationary the discharge rates in the SA population drop rapidly to low levels. A second possible reason for enhanced tactual discrimination during scanning is related to the increased spatiotemporal information in a coherent pattern of neural activity moving across a discrete population of afferent fibres. 6. The effects of variations in conduction velocity are analysed and it is shown that they place serious constraints on the transmission of spatiotemporal information.}, - pubmed = {7230030}, + pmid = {7230030}, pmc = {PMC1274731}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/7230030}, url = {papers/Johnson_JPhysiol1981-7230030.pdf}, @@ -111433,7 +111427,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Nov}, pages = {1113-6}, abstract = {The brain's visual cortex processes information concerning form, pattern, and motion within functional maps that reflect the layout of neuronal circuits. We analyzed functional maps of orientation preference in the ferret, tree shrew, and galago--three species separated since the basal radiation of placental mammals more than 65 million years ago--and found a common organizing principle. A symmetry-based class of models for the self-organization of cortical networks predicts all essential features of the layout of these neuronal circuits, but only if suppressive long-range interactions dominate development. We show mathematically that orientation-selective long-range connectivity can mediate the required interactions. Our results suggest that self-organization has canalized the evolution of the neuronal circuitry underlying orientation preference maps into a single common design.}, - pubmed = {21051599}, + pmid = {21051599}, pii = {science.1194869}, doi = {10.1126/science.1194869}, pmc = {PMC3138194}, @@ -111452,7 +111446,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {48}, abstract = {The lack of a formal link between neural network structure and its emergent function has hampered our understanding of how the brain processes information. We have now come closer to describing such a link by taking the direction of synaptic transmission into account, constructing graphs of a network that reflect the direction of information flow, and analyzing these directed graphs using algebraic topology. Applying this approach to a local network of neurons in the neocortex revealed a remarkably intricate and previously unseen topology of synaptic connectivity. The synaptic network contains an abundance of cliques of neurons bound into cavities that guide the emergence of correlated activity. In response to stimuli, correlated activity binds synaptically connected neurons into functional cliques and cavities that evolve in a stereotypical sequence toward peak complexity. We propose that the brain processes stimuli by forming increasingly complex functional cliques and cavities.}, keywords = {Betti numbers; connectomics; correlations; directed networks; structure-function; topology; }, - pubmed = {28659782}, + pmid = {28659782}, doi = {10.3389/fncom.2017.00048}, pmc = {PMC5467434}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/28659782}, @@ -111469,7 +111463,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Dec}, pages = {42}, abstract = {In vertebrate development, the segmental pattern of the body axis is established as somites, masses of mesoderm distributed along the two sides of the neural tube, are formed sequentially in the anterior-posterior axis. This mechanism depends on waves of gene expression associated with the Notch, Fgf and Wnt pathways. The underlying transcriptional regulation has been studied by whole-transcriptome mRNA profiling; however, interpretation of the results is limited by poor resolution, noisy data, small sample size and by the absence of a wall clock to assign exact time for recorded points.}, - pubmed = {24304493}, + pmid = {24304493}, pii = {1471-213X-13-42}, doi = {10.1186/1471-213X-13-42}, pmc = {PMC4235037}, @@ -111488,7 +111482,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Dec}, pages = {1595-8}, abstract = {The segmental pattern of the spine is established early in development, when the vertebral precursors, the somites, are rhythmically produced from the presomitic mesoderm. Microarray studies of the mouse presomitic mesoderm transcriptome reveal that the oscillator associated with this process, the segmentation clock, drives the periodic expression of a large network of cyclic genes involved in cell signaling. Mutually exclusive activation of the notch-fibroblast growth factor and Wnt pathways during each cycle suggests that coordinated regulation of these three pathways underlies the clock oscillator.}, - pubmed = {17095659}, + pmid = {17095659}, pii = {1133141}, doi = {10.1126/science.1133141}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/17095659}, @@ -111505,7 +111499,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Dec}, pages = {3-8}, abstract = {It is currently thought that the mechanism underlying somitogenesis is linked to a molecular oscillator, the segmentation clock, and to gradients of signaling molecules within the paraxial mesoderm. Here, we review the current picture of this segmentation clock and gradients, and use this knowledge to critically ask: What is the basis for periodicity and directionality of somitogenesis?}, - pubmed = {17024300}, + pmid = {17024300}, doi = {10.1007/s00429-006-0124-y}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/17024300}, url = {papers/Aulehla_AnatEmbryol(Berl)2006-17024300.pdf}, @@ -111521,7 +111515,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a year = {1954}, month = {Oct}, pages = {1018-29}, - pubmed = {16589583}, + pmid = {16589583}, pmc = {PMC534216}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/16589583}, url = {papers/Pittendrigh_ProcNatlAcadSciUSA1954-16589583.pdf}, @@ -111539,7 +111533,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {123-135}, abstract = {Establishment of precise neuronal connectivity in the neocortex relies on activity-dependent circuit reorganization during postnatal development; however, the nature of cortical activity during this period remains largely unknown. Using two-photon calcium imaging of the barrel cortex in vivo during the first postnatal week, we reveal that layer 4 (L4) neurons within the same barrel fire synchronously in the absence of peripheral stimulation, creating a "patchwork" pattern of spontaneous activity corresponding to the barrel map. By generating transgenic mice expressing GCaMP6s in thalamocortical axons, we show that thalamocortical axons also demonstrate the spontaneous patchwork activity pattern. Patchwork activity is diminished by peripheral anesthesia but is mostly independent of self-generated whisker movements. The patchwork activity pattern largely disappeared during postnatal week 2, as even L4 neurons within the same barrel tended to fire asynchronously. This spontaneous L4 activity pattern has features suitable for thalamocortical (TC) circuit refinement in the neonatal barrel cortex.}, keywords = {activity-dependent development; awake; barrel cortex; in vivo calcium imaging; neonates; single-cell labeling; spontaneous activity; synchronized activity; thalamocortical axons; whisker monitoring; }, - pubmed = {29298415}, + pmid = {29298415}, pii = {S2211-1247(17)31808-9}, doi = {10.1016/j.celrep.2017.12.012}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/29298415}, @@ -111557,7 +111551,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Oct}, pages = {339-55}, abstract = {The tactile somatosensory pathway from whisker to cortex in rodents provides a well-defined system for exploring the link between molecular mechanisms, synaptic circuits, and behavior. The primary somatosensory cortex has an exquisite somatotopic map where each individual whisker is represented in a discrete anatomical unit, the "barrel," allowing precise delineation of functional organization, development, and plasticity. Sensory information is actively acquired in awake behaving rodents and processed differently within the barrel map depending upon whisker-related behavior. The prominence of state-dependent cortical sensory processing is likely to be crucial in our understanding of active sensory perception, experience-dependent plasticity and learning.}, - pubmed = {17964250}, + pmid = {17964250}, pii = {S0896-6273(07)00715-5}, doi = {10.1016/j.neuron.2007.09.017}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/17964250}, @@ -111576,7 +111570,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {15931-46}, abstract = {Transgenic mice expressing genetically encoded activity indicators are an attractive means of mapping mesoscopic regional functional cortical connectivity given widespread stable and cell-specific expression compatible with chronic recordings. Cortical functional connectivity was evaluated using wide-field imaging in lightly anesthetized Emx1-creXRosa26-GCaMP3 mice expressing calcium sensor in cortical neurons. Challenges exist because green fluorescence signals overlap with endogenous activity-dependent autofluorescence and are affected by changes in blood volume and oxygenation. Under the conditions used for imaging and analysis (0.1-1 Hz frequency band), autofluorescence and hemodynamic effects contributed 3% and 8% of the SD of spontaneous activity-dependent GCaMP3 fluorescence when signals were recorded through intact bone. To evaluate the accuracy and sensitivity of this approach, the topology of functional connections between somatomotor cortex (primary S1 and secondary S2 somatosensory, and primary motor cortex M1) was estimated. During sequences of spontaneous activity, calcium signals recorded at each location of area S1 were correlated with activity in contralateral area S1, ipsilateral area S2, and bilateral areas M1. Reciprocal results were observed when "seed pixels" were placed in S2 and M1. Coactivation of areas implies functional connections but could also be attributed to both regions receiving common upstream drive. These apparent connections revealed during spontaneous activity coactivation by GCaMP3 were confirmed by intracortical microstimulation but were more difficult to detect using intrinsic signals from reflected red light. We anticipate GCAMP wide-field imaging will enable longitudinal studies during plasticity paradigms or after models of CNS disease, such as stroke, where the weighting within these connectivity maps may be altered. }, keywords = {connectome; cortical stimulation; optogenetic; resting state; tracing; transgenic mice; Animals; Brain Mapping; Calcium Signaling; Female; Male; Mice; Mice, 129 Strain; Mice, Transgenic; Motor Cortex; Neural Pathways; Somatosensory Cortex; }, - pubmed = {25429135}, + pmid = {25429135}, pii = {34/48/15931}, doi = {10.1523/JNEUROSCI.1818-14.2014}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/25429135}, @@ -111593,7 +111587,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a year = {2019}, pages = {e0213924}, abstract = {Visual cortex is organized into discrete sub-regions or areas that are arranged into a hierarchy and serves different functions in the processing of visual information. In retinotopic maps of mouse cortex, there appear to be substantial mouse-to-mouse differences in visual area location, size and shape. Here we quantify the biological variation in the size, shape and locations of 11 visual areas in the mouse, after separating biological variation and measurement noise. We find that there is biological variation in the locations and sizes of visual areas.}, - pubmed = {31042712}, + pmid = {31042712}, doi = {10.1371/journal.pone.0213924}, pii = {PONE-D-18-29482}, pmc = {PMC6493719}, @@ -111612,7 +111606,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {04}, pages = {1500}, abstract = {Neural computations occurring simultaneously in multiple cerebral cortical regions are critical for mediating behaviors. Progress has been made in understanding how neural activity in specific cortical regions contributes to behavior. However, there is a lack of tools that allow simultaneous monitoring and perturbing neural activity from multiple cortical regions. We engineered 'See-Shells'-digitally designed, morphologically realistic, transparent polymer skulls that allow long-term (>300 days) optical access to 45 mm2 of the dorsal cerebral cortex in the mouse. We demonstrate the ability to perform mesoscopic imaging, as well as cellular and subcellular resolution two-photon imaging of neural structures up to 600 µm deep. See-Shells allow calcium imaging from multiple, non-contiguous regions across the cortex. Perforated See-Shells enable introducing penetrating neural probes to perturb or record neural activity simultaneously with whole cortex imaging. See-Shells are constructed using common desktop fabrication tools, providing a powerful tool for investigating brain structure and function.}, - pubmed = {30940809}, + pmid = {30940809}, doi = {10.1038/s41467-019-09488-0}, pii = {10.1038/s41467-019-09488-0}, pmc = {PMC6445105}, @@ -111632,7 +111626,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {2847-71}, abstract = {We have longitudinally assessed normative brain growth patterns in naturalistically reared Macaca mulatta monkeys. Postnatal to early adulthood brain development in two cohorts of rhesus monkeys was analyzed using magnetic resonance imaging. Cohort A consisted of 24 rhesus monkeys (12 male, 12 female) and cohort B of 21 monkeys (11 male, 10 female). All subjects were scanned at 1, 4, 8, 13, 26, 39, and 52 weeks; cohort A had additional scans at 156 weeks (3 years) and 260 weeks (5 years). Age-specific segmentation templates were developed for automated volumetric analyses of the T1-weighted magnetic resonance imaging scans. Trajectories of total brain size as well as cerebral and subcortical subdivisions were evaluated over this period. Total brain volume was about 64 % of adult estimates in the 1-week-old monkey. Brain volume of the male subjects was always, on average, larger than the female subjects. While brain volume generally increased between any two imaging time points, there was a transient plateau of brain growth between 26 and 39 weeks in both cohorts of monkeys. The trajectory of enlargement differed across cortical regions with the occipital cortex demonstrating the most idiosyncratic pattern of maturation and the frontal and temporal lobes showing the greatest and most protracted growth. A variety of allometric measurements were also acquired and body weight gain was most closely associated with the rate of brain growth. These findings provide a valuable baseline for the effects of fetal and early postnatal manipulations on the pattern of abnormal brain growth related to neurodevelopmental disorders.}, keywords = {Allometry; Development; Macaca mulatta; Nonhuman primate; Sexual dimorphism; Animals; Brain; Female; Functional Laterality; Image Processing, Computer-Assisted; Longitudinal Studies; Macaca mulatta; Magnetic Resonance Imaging; Male; }, - pubmed = {26159774}, + pmid = {26159774}, doi = {10.1007/s00429-015-1076-x}, pii = {10.1007/s00429-015-1076-x}, pmc = {PMC4884209}, @@ -111652,7 +111646,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {}, abstract = {Understanding the basis of brain function requires knowledge of cortical operations over wide-spatial scales, but also within the context of single neurons. In vivo, wide-field GCaMP imaging and sub-cortical/cortical cellular electrophysiology were used in mice to investigate relationships between spontaneous single neuron spiking and mesoscopic cortical activity. We make use of a rich set of cortical activity motifs that are present in spontaneous activity in anesthetized and awake animals. A mesoscale spike-triggered averaging procedure allowed the identification of motifs that are preferentially linked to individual spiking neurons by employing genetically targeted indicators of neuronal activity. Thalamic neurons predicted and reported specific cycles of wide-scale cortical inhibition/excitation. In contrast, spike-triggered maps derived from single cortical neurons yielded spatio-temporal maps expected for regional cortical consensus function. This approach can define network relationships between any point source of neuronal spiking and mesoscale cortical maps.}, keywords = {functional connectivity; mesoscale maps; mouse; neuroscience; spike triggered maps; thalamocortical; Action Potentials; Anesthesia; Animals; Brain Mapping; Calcium; Calcium Signaling; Cerebral Cortex; Electrodes, Implanted; Male; Mice; Mice, Transgenic; Molecular Probes; Nerve Net; Neurons; Optical Imaging; Stereotaxic Techniques; Thalamus; Wakefulness; }, - pubmed = {28160463}, + pmid = {28160463}, doi = {10.7554/eLife.19976}, pmc = {PMC5328594}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/28160463}, @@ -111682,7 +111676,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Jun}, pages = {1304-16}, abstract = {A fundamental issue in cortical processing of sensory information is whether top-down control circuits from higher brain areas to primary sensory areas not only modulate but actively engage in perception. Here, we report the identification of a neural circuit for top-down control in the mouse somatosensory system. The circuit consisted of a long-range reciprocal projection between M2 secondary motor cortex and S1 primary somatosensory cortex. In vivo physiological recordings revealed that sensory stimulation induced sequential S1 to M2 followed by M2 to S1 neural activity. The top-down projection from M2 to S1 initiated dendritic spikes and persistent firing of S1 layer 5 (L5) neurons. Optogenetic inhibition of M2 input to S1 decreased L5 firing and the accurate perception of tactile surfaces. These findings demonstrate that recurrent input to sensory areas is essential for accurate perception and provide a physiological model for one type of top-down control circuit. }, - pubmed = {26004915}, + pmid = {26004915}, pii = {S0896-6273(15)00413-4}, doi = {10.1016/j.neuron.2015.05.006}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/26004915}, @@ -111697,7 +111691,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a volume = {14}, year = {1991}, pages = {247-67}, - pubmed = {2031571}, + pmid = {2031571}, doi = {10.1146/annurev.ne.14.030191.001335}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/2031571}, url = {papers/Heiligenberg_AnnuRevNeurosci1991-2031571.pdf}, @@ -111714,7 +111708,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Oct}, pages = {16}, abstract = {Auditory hallucinations are among the most prevalent and most distressing symptoms of schizophrenia. Despite significant progress, it is still unclear whether auditory hallucinations arise from abnormalities in primary sensory processing or whether they represent failures of higher-order functions. To address this knowledge gap, we capitalized on the increased spatial resolution afforded by ultra-high field imaging at 7 Tesla to investigate the tonotopic organization of the auditory cortex in patients with schizophrenia with a history of recurrent hallucinations. Tonotopy is a fundamental feature of the functional organization of the auditory cortex that is established very early in development and predates the onset of symptoms by decades. Compared to healthy participants, patients showed abnormally increased activation and altered tonotopic organization of the auditory cortex during a purely perceptual task, which involved passive listening to tones across a range of frequencies (88-8000 Hz). These findings suggest that the predisposition to auditory hallucinations is likely to be predicated on abnormalities in the functional organization of the auditory cortex and which may serve as a biomarker for the early identification of vulnerable individuals.}, - pubmed = {31578332}, + pmid = {31578332}, doi = {10.1038/s41537-019-0084-x}, pii = {10.1038/s41537-019-0084-x}, pmc = {PMC6775081}, @@ -111733,7 +111727,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Jan}, pages = {45-61}, abstract = {An understanding of the diversity of cortical GABAergic interneurons is critical to understand the function of the cerebral cortex. Recent data suggest that neurons expressing three markers, the Ca2+-binding protein parvalbumin (PV), the neuropeptide somatostatin (SST), and the ionotropic serotonin receptor 5HT3a (5HT3aR) account for nearly 100% of neocortical interneurons. Interneurons expressing each of these markers have a different embryological origin. Each group includes several types of interneurons that differ in morphological and electrophysiological properties and likely have different functions in the cortical circuit. The PV group accounts for ∼40% of GABAergic neurons and includes fast spiking basket cells and chandelier cells. The SST group, which represents ∼30% of GABAergic neurons, includes the Martinotti cells and a set of neurons that specifically target layerIV. The 5HT3aR group, which also accounts for ∼30% of the total interneuronal population, is heterogeneous and includes all of the neurons that express the neuropeptide VIP, as well as an equally numerous subgroup of neurons that do not express VIP and includes neurogliaform cells. The universal modulation of these neurons by serotonin and acetylcholine via ionotropic receptors suggests that they might be involved in shaping cortical circuits during specific brain states and behavioral contexts.}, - pubmed = {21154909}, + pmid = {21154909}, doi = {10.1002/dneu.20853}, pmc = {PMC3556905}, mid = {NIHMS434044}, @@ -111752,7 +111746,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {}, abstract = {The medial prefrontal cortex plays a key role in higher order cognitive functions like decision making and social cognition. These complex behaviors emerge from the coordinated firing of prefrontal neurons. Fast-spiking interneurons (FSIs) control the timing of excitatory neuron firing via somatic inhibition and generate gamma (30-100 Hz) oscillations. Therefore, factors that regulate how FSIs respond to gamma-frequency input could affect both prefrontal circuit activity and behavior. Here, we show that serotonin (5HT), which is known to regulate gamma power, acts via 5HT2A receptors to suppress an inward-rectifying potassium conductance in FSIs. This leads to depolarization, increased input resistance, enhanced spiking, and slowed decay of excitatory post-synaptic potentials (EPSPs). Notably, we found that slowed EPSP decay preferentially enhanced temporal summation and firing elicited by gamma frequency inputs. These findings show how changes in passive membrane properties can affect not only neuronal excitability but also the temporal filtering of synaptic inputs.}, keywords = {fast-spiking interneurons; mouse; neuroscience; parvalbumin interneurons; prefrontal cortex; serotonin; synaptic integration; temporal summation; Action Potentials; Animals; Electric Conductivity; Gamma Rhythm; Interneurons; Mice; Models, Neurological; Optical Imaging; Potassium Channels; Prefrontal Cortex; Receptors, Serotonin; Serotonin; }, - pubmed = {29206101}, + pmid = {29206101}, doi = {10.7554/eLife.31991}, pmc = {PMC5746342}, pii = {31991}, @@ -111770,7 +111764,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {}, abstract = {Serotonin receptors of the 5-HT(2A) subtype are robustly expressed in the cerebral cortex where they have been implicated in the pathophysiology and therapeutics of mental disorders and the actions of hallucinogens. Much less is known, however, about the specific cell types expressing 5-HT(2A) receptors in cortex. In the current study we use immunohistochemical and electrophysiological approaches in genetically modified mice to address the expression of the Htr2a gene and 5-HT(2A) receptors in cortex. We first use an EGFP-expressing BAC transgenic mice and identify three main Htr2A gene expressing neuronal populations in cortex. The largest of these cell populations corresponds to layer V pyramidal cells of the anterior cortex, followed by GABAergic interneurons of the middle layers, and non-pyramidal cells of the subplate/Layer VIb. We then use 5-HT(2A) receptor knockout mice to identify an antibody capable of localizing 5-HT(2A) receptors in brain and use it to map these receptors. We find strong laminar expression of 5-HT(2A) receptors in cortex, especially along a diffuse band overlaying layer Va. This band exhibits a strong anteroposterior gradient that closely matches the localization of Htr2A expressing pyramidal cells of layer V. Finally we use electrophysiological and immunohistochemical approaches to show that most, but not all, GABAergic interneurons of the middle layers are parvalbumin expressing Fast-spiking interneurons and that these cells are depolarized and excited by serotonin, most likely through the activation of 5-HT(2A) receptors. These results clarify and extend our understanding of the cellular distribution of 5-HT(2A) receptors in the cerebral cortex.}, keywords = {5-HT2A; cortex; interneuron; prefrontal; pyramidal cell; serotonin; serotonin receptors; }, - pubmed = {20802802}, + pmid = {20802802}, doi = {10.3389/fnins.2010.00036}, pmc = {PMC2928707}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/20802802}, @@ -111788,7 +111782,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Apr}, pages = {264-355}, abstract = {Psychedelics (serotonergic hallucinogens) are powerful psychoactive substances that alter perception and mood and affect numerous cognitive processes. They are generally considered physiologically safe and do not lead to dependence or addiction. Their origin predates written history, and they were employed by early cultures in many sociocultural and ritual contexts. After the virtually contemporaneous discovery of (5R,8R)-(+)-lysergic acid-N,N-diethylamide (LSD)-25 and the identification of serotonin in the brain, early research focused intensively on the possibility that LSD and other psychedelics had a serotonergic basis for their action. Today there is a consensus that psychedelics are agonists or partial agonists at brain serotonin 5-hydroxytryptamine 2A receptors, with particular importance on those expressed on apical dendrites of neocortical pyramidal cells in layer V. Several useful rodent models have been developed over the years to help unravel the neurochemical correlates of serotonin 5-hydroxytryptamine 2A receptor activation in the brain, and a variety of imaging techniques have been employed to identify key brain areas that are directly affected by psychedelics. Recent and exciting developments in the field have occurred in clinical research, where several double-blind placebo-controlled phase 2 studies of psilocybin-assisted psychotherapy in patients with cancer-related psychosocial distress have demonstrated unprecedented positive relief of anxiety and depression. Two small pilot studies of psilocybin-assisted psychotherapy also have shown positive benefit in treating both alcohol and nicotine addiction. Recently, blood oxygen level-dependent functional magnetic resonance imaging and magnetoencephalography have been employed for in vivo brain imaging in humans after administration of a psychedelic, and results indicate that intravenously administered psilocybin and LSD produce decreases in oscillatory power in areas of the brain's default mode network. }, - pubmed = {26841800}, + pmid = {26841800}, pii = {68/2/264}, doi = {10.1124/pr.115.011478}, pmc = {PMC4813425}, @@ -111807,7 +111801,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {11}, pages = {}, abstract = {Det er økt interesse for psykedeliske stoffer til bruk i behandling av psykiske lidelser. Stoffene regnes som trygge når de gis innenfor en klinisk ramme. Eldre studier fra før 1970 har metodologiske svakheter, men i de senere år har det kommet lovende resultater fra bruk ved unipolar depresjon, depresjon ved livstruende sykdom, angst og avhengighet. Formålet med denne litteraturgjennomgangen er å gi en oversikt over nyere resultater og disse studienes begrensninger.}, - pubmed = {30421744}, + pmid = {30421744}, pii = {17-1110}, doi = {10.4045/tidsskr.17.1110}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/30421744}, @@ -111824,7 +111818,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {20}, abstract = {Entropy is a dimensionless quantity that is used for measuring uncertainty about the state of a system but it can also imply physical qualities, where high entropy is synonymous with high disorder. Entropy is applied here in the context of states of consciousness and their associated neurodynamics, with a particular focus on the psychedelic state. The psychedelic state is considered an exemplar of a primitive or primary state of consciousness that preceded the development of modern, adult, human, normal waking consciousness. Based on neuroimaging data with psilocybin, a classic psychedelic drug, it is argued that the defining feature of "primary states" is elevated entropy in certain aspects of brain function, such as the repertoire of functional connectivity motifs that form and fragment across time. Indeed, since there is a greater repertoire of connectivity motifs in the psychedelic state than in normal waking consciousness, this implies that primary states may exhibit "criticality," i.e., the property of being poised at a "critical" point in a transition zone between order and disorder where certain phenomena such as power-law scaling appear. Moreover, if primary states are critical, then this suggests that entropy is suppressed in normal waking consciousness, meaning that the brain operates just below criticality. It is argued that this entropy suppression furnishes normal waking consciousness with a constrained quality and associated metacognitive functions, including reality-testing and self-awareness. It is also proposed that entry into primary states depends on a collapse of the normally highly organized activity within the default-mode network (DMN) and a decoupling between the DMN and the medial temporal lobes (which are normally significantly coupled). These hypotheses can be tested by examining brain activity and associated cognition in other candidate primary states such as rapid eye movement (REM) sleep and early psychosis and comparing these with non-primary states such as normal waking consciousness and the anaesthetized state. }, keywords = {5-HT2A receptor; REM sleep; consciousness; criticality; default mode network; entropy; metastability; serotonin; }, - pubmed = {24550805}, + pmid = {24550805}, doi = {10.3389/fnhum.2014.00020}, pmc = {PMC3909994}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/24550805}, @@ -111842,7 +111836,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {May}, pages = {5033-7}, abstract = {In brains of higher vertebrates, the functional segregation of local areas that differ in their anatomy and physiology contrasts sharply with their global integration during perception and behavior. In this paper, we introduce a measure, called neural complexity (CN), that captures the interplay between these two fundamental aspects of brain organization. We express functional segregation within a neural system in terms of the relative statistical independence of small subsets of the system and functional integration in terms of significant deviations from independence of large subsets. CN is then obtained from estimates of the average deviation from statistical independence for subsets of increasing size. CN is shown to be high when functional segregation coexists with integration and to be low when the components of a system are either completely independent (segregated) or completely dependent (integrated). We apply this complexity measure in computer simulations of cortical areas to examine how some basic principles of neuroanatomical organization constrain brain dynamics. We show that the connectivity patterns of the cerebral cortex, such as a high density of connections, strong local connectivity organizing cells into neuronal groups, patchiness in the connectivity among neuronal groups, and prevalent reciprocal connections, are associated with high values of CN. The approach outlined here may prove useful in analyzing complexity in other biological domains such as gene regulation and embryogenesis.}, - pubmed = {8197179}, + pmid = {8197179}, pmc = {PMC43925}, doi = {10.1073/pnas.91.11.5033}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/8197179}, @@ -111861,7 +111855,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {3170-3182}, abstract = {Atrophy of neurons in the prefrontal cortex (PFC) plays a key role in the pathophysiology of depression and related disorders. The ability to promote both structural and functional plasticity in the PFC has been hypothesized to underlie the fast-acting antidepressant properties of the dissociative anesthetic ketamine. Here, we report that, like ketamine, serotonergic psychedelics are capable of robustly increasing neuritogenesis and/or spinogenesis both in vitro and in vivo. These changes in neuronal structure are accompanied by increased synapse number and function, as measured by fluorescence microscopy and electrophysiology. The structural changes induced by psychedelics appear to result from stimulation of the TrkB, mTOR, and 5-HT2A signaling pathways and could possibly explain the clinical effectiveness of these compounds. Our results underscore the therapeutic potential of psychedelics and, importantly, identify several lead scaffolds for medicinal chemistry efforts focused on developing plasticity-promoting compounds as safe, effective, and fast-acting treatments for depression and related disorders.}, keywords = {DMT; LSD; MDMA; depression; ketamine; neural plasticity; noribogaine; psychedelic; spinogenesis; synaptogenesis; Animals; Antidepressive Agents; Brain-Derived Neurotrophic Factor; Cells, Cultured; Cerebral Cortex; Female; Male; Microscopy, Fluorescence; Neurogenesis; Neuronal Plasticity; Rats; Rats, Sprague-Dawley; Receptor, Serotonin, 5-HT2A; Receptor, trkB; Signal Transduction; TOR Serine-Threonine Kinases; }, - pubmed = {29898390}, + pmid = {29898390}, pii = {S2211-1247(18)30755-1}, doi = {10.1016/j.celrep.2018.05.022}, pmc = {PMC6082376}, @@ -111882,7 +111876,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {2475-2483}, abstract = {The West African iboga plant has been used for centuries by the Bwiti and Mbiri tribes to induce hallucinations during religious ceremonies. Ibogaine, the principal alkaloid responsible for iboga's psychedelic properties, was isolated and sold as an antidepressant in France for decades before its adverse effects precipitated its removal from the market. An ibogaine resurgence in the 1960s was driven by U.S. heroin addicts who claimed that ibogaine cured their opiate addictions. Behavioral pharmacologic studies in animal models provided evidence that ibogaine could blunt self-administration of not only opiates but cocaine, amphetamines, and nicotine. Ibogaine displays moderate-to-weak affinities for a wide spectrum of receptor and transporter proteins; recent work suggests that its actions at nicotinic acetylcholine receptor subtypes may underlie its reputed antiopiate effects. At micromolar levels, ibogaine is neurotoxic and cardiotoxic and has been linked to several deaths by cardiac arrest. Structure-activity studies led to the isolation of the ibogaine analog 18-methoxycoronaridine (18-MC), an α3β4 nicotinic receptor modulator that retains ibogaine's anticraving properties with few or no adverse effects. Clinical trials of 18-MC treatment of nicotine addiction are pending. Ibogaine analogs may also hold promise for treating anxiety and depression via the "psychedelic-assisted therapy" approach that employs hallucinogens including psilocybin and methylenedioxymethamphetamine ("ecstasy").}, keywords = {addiction; hallucinogen; iboga; nicotine; opioid; therapeutic; Cardiotoxicity; Hallucinogens; History, 20th Century; History, 21st Century; Humans; Ibogaine; Receptors, Nicotinic; Structure-Activity Relationship; Substance-Related Disorders; Tabernaemontana; }, - pubmed = {30216039}, + pmid = {30216039}, doi = {10.1021/acschemneuro.8b00294}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/30216039}, url = {papers/Wasko_ACSChemNeurosci2018-30216039.pdf}, @@ -111899,7 +111893,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Mar}, pages = {398-412}, abstract = {Ibogaine is a naturally occurring psychoactive plant alkaloid that is used globally in medical and nonmedical settings for opioid detoxification and other substance use indications. All available autopsy, toxicological, and investigative reports were systematically reviewed for the consecutive series of all known fatalities outside of West Central Africa temporally related to the use of ibogaine from 1990 through 2008. Nineteen individuals (15 men, four women between 24 and 54 years old) are known to have died within 1.5-76 h of taking ibogaine. The clinical and postmortem evidence did not suggest a characteristic syndrome of neurotoxicity. Advanced preexisting medical comorbidities, which were mainly cardiovascular, and/or one or more commonly abused substances explained or contributed to the death in 12 of the 14 cases for which adequate postmortem data were available. Other apparent risk factors include seizures associated with withdrawal from alcohol and benzodiazepines and the uninformed use of ethnopharmacological forms of ibogaine.}, - pubmed = {22268458}, + pmid = {22268458}, doi = {10.1111/j.1556-4029.2011.02008.x}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/22268458}, url = {papers/Alper_JForensicSci2012-22268458.pdf}, @@ -111917,7 +111911,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {513-517}, abstract = {Serotonin-norepinephrine reuptake inhibitors (SNRIs) are commonly used for various psychiatric conditions and neuropathic pain syndromes. SNRIs inhibit the reuptake of serotonin (5-HT) and norepinephrine (NE); however, NE reuptake inhibition is thought to be the primary mediator for their analgesic effect.}, keywords = {antidepressants; binding affinity; neuropathic pain; pain; serotonin-norepinephrine reuptake inhibitors; Analgesics; Dose-Response Relationship, Drug; Humans; Neuralgia; Norepinephrine; Serotonin; Serotonin and Noradrenaline Reuptake Inhibitors; }, - pubmed = {28503727}, + pmid = {28503727}, doi = {10.1111/jcpt.12534}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/28503727}, url = {papers/Raouf_JClinPharmTher2017-28503727.pdf}, @@ -111934,7 +111928,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Dec}, pages = {871-80}, abstract = {The blockade of serotonin (5-HT) and norepinephrine (NE) transporters in vitro and in vivo by the dual 5-HT/NE reuptake inhibitors duloxetine and venlafaxine was compared. Duloxetine inhibited binding to the human NE and 5-HT transporters with K(i) values of 7.5 and 0.8 nM, respectively, and with a K(i) ratio of 9. Venlafaxine inhibited binding to the human NE and 5-HT transporters with K(i) values of 2480 and 82 nM, respectively, and with a K(i) ratio of 30. Duloxetine inhibited ex vivo binding to rat 5-HT transporters and NE transporters with ED(50) values of 0.03 and 0.7 mg/kg, respectively, whereas venlafaxine had ED(50) values of 2 and 54 mg/kg, respectively. The depletion of rat brain 5-HT by p-chloramphetamine and depletion of rat hypothalamic NE by 6-hydroxydopamine was blocked by duloxetine with ED(50) values of 2.3 and 12 mg/kg, respectively. Venlafaxine had ED(50) values of 5.9 and 94 mg/kg for blocking p-chloramphetamine- and 6-hydroxydopamine-induced monoamine depletion, respectively. Thus, duloxetine more potently blocks 5-HT and NE transporters in vitro and in vivo than venlafaxine.}, - pubmed = {11750180}, + pmid = {11750180}, pii = {S0893133X01002986}, doi = {10.1016/S0893-133X(01)00298-6}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/11750180}, @@ -111952,7 +111946,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Feb}, pages = {e9019}, abstract = {We currently understand the mental effects of psychedelics to be caused by agonism or partial agonism of 5-HT(2A) (and possibly 5-HT(2C)) receptors, and we understand that psychedelic drugs, especially phenylalkylamines, are fairly selective for these two receptors. This manuscript is a reference work on the receptor affinity pharmacology of psychedelic drugs. New data is presented on the affinity of twenty-five psychedelic drugs at fifty-one receptors, transporters, and ion channels, assayed by the National Institute of Mental Health-Psychoactive Drug Screening Program (NIMH-PDSP). In addition, comparable data gathered from the literature on ten additional drugs is also presented (mostly assayed by the NIMH-PDSP). A new method is introduced for normalizing affinity (K(i)) data that factors out potency so that the multi-receptor affinity profiles of different drugs can be directly compared and contrasted. The method is then used to compare the thirty-five drugs in graphical and tabular form. It is shown that psychedelic drugs, especially phenylalkylamines, are not as selective as generally believed, interacting with forty-two of forty-nine broadly assayed sites. The thirty-five drugs of the study have very diverse patterns of interaction with different classes of receptors, emphasizing eighteen different receptors. This diversity of receptor interaction may underlie the qualitative diversity of these drugs. It should be possible to use this diverse set of drugs as probes into the roles played by the various receptor systems in the human mind.}, - pubmed = {20126400}, + pmid = {20126400}, doi = {10.1371/journal.pone.0009019}, pmc = {PMC2814854}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/20126400}, @@ -111969,7 +111963,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {240}, abstract = {Hallucinogen-persisting perception disorder (HPPD) is a syndrome characterized by prolonged or reoccurring perceptual symptoms, reminiscent of acute hallucinogen effects. HPPD was associated with a broader range of LSD (lysergic acid diethylamide)-like substances, cannabis, methylenedioxymethamphetamine (MDMA), psilocybin, mescaline, and psychostimulants. The recent emergence of novel psychoactive substances (NPS) posed a critical concern regarding the new onset of psychiatric symptoms/syndromes, including cases of HPPD. Symptomatology mainly comprises visual disorders (i.e., geometric pseudo-hallucinations, haloes, flashes of colors/lights, motion-perception deficits, afterimages, micropsia, more acute awareness of floaters, etc.), even though depressive symptoms and thought disorders may be comorbidly present. Although HPPD was first described in 1954, it was just established as a fully syndrome in 2000, with the revised fourth version of the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV-TR). HPPD neural substrates, risk factors, and aetiopathogenesys still largely remain unknown and under investigation, and many questions about its pharmacological targets remain unanswered too. A critical mini review on psychopathological bases, etiological hypothesis, and psychopharmacological approaches toward HPPD, including the association with some novel substances, are provided here, by means of a literature search on PubMed/Medline, Google Scholar, and Scopus databases without time restrictions, by using a specific set of keywords. Pharmacological and clinical issues are considered, and practical psychopharmacological recommendations and clinical guidelines are suggested.}, keywords = {flashbacks; hallucinations; hallucinogen-persisting perception disorder; hallucinogens; novel psychoactive substances; palinopsia; }, - pubmed = {29209235}, + pmid = {29209235}, doi = {10.3389/fpsyt.2017.00240}, pmc = {PMC5701998}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/29209235}, @@ -111987,7 +111981,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Oct}, pages = {2105-2113}, abstract = {Plant-based psychedelics, such as psilocybin, have an ancient history of medicinal use. After the first English language report on LSD in 1950, psychedelics enjoyed a short-lived relationship with psychology and psychiatry. Used most notably as aids to psychotherapy for the treatment of mood disorders and alcohol dependence, drugs such as LSD showed initial therapeutic promise before prohibitive legislature in the mid-1960s effectively ended all major psychedelic research programs. Since the early 1990s, there has been a steady revival of human psychedelic research: last year saw reports on the first modern brain imaging study with LSD and three separate clinical trials of psilocybin for depressive symptoms. In this circumspective piece, RLC-H and GMG share their opinions on the promises and pitfalls of renewed psychedelic research, with a focus on the development of psilocybin as a treatment for depression.}, - pubmed = {28443617}, + pmid = {28443617}, pii = {npp201784}, doi = {10.1038/npp.2017.84}, pmc = {PMC5603818}, @@ -112005,7 +111999,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {733}, abstract = {Mental disorders are rising while development of novel psychiatric medications is declining. This stall in innovation has also been linked with intense debates on the current diagnostics and explanations for mental disorders, together constituting a paradigmatic crisis. A radical innovation is psychedelic-assisted psychotherapy (PAP): professionally supervised use of ketamine, MDMA, psilocybin, LSD and ibogaine as part of elaborated psychotherapy programs. Clinical results so far have shown safety and efficacy, even for "treatment resistant" conditions, and thus deserve increasing attention from medical, psychological and psychiatric professionals. But more than novel treatments, the PAP model also has important consequences for the diagnostics and explanation axis of the psychiatric crisis, challenging the discrete nosological entities and advancing novel explanations for mental disorders and their treatment, in a model considerate of social and cultural factors, including adversities, trauma, and the therapeutic potential of some non-ordinary states of consciousness.}, keywords = {LSD; MDMA; explanation in neuroscience; ibogaine; ketamine; psilocybin; psychedelic-assisted psychotherapy; states of consciousness; }, - pubmed = {30026698}, + pmid = {30026698}, doi = {10.3389/fphar.2018.00733}, pmc = {PMC6041963}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/30026698}, @@ -112022,7 +112016,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {974}, abstract = {Introduction: It is a basic principle of the "psychedelic" treatment model that the quality of the acute experience mediates long-term improvements in mental health. In the present paper we sought to test this using data from a clinical trial assessing psilocybin for treatment-resistant depression (TRD). In line with previous reports, we hypothesized that the occurrence and magnitude of Oceanic Boundlessness (OBN) (sharing features with mystical-type experience) and Dread of Ego Dissolution (DED) (similar to anxiety) would predict long-term positive outcomes, whereas sensory perceptual effects would have negligible predictive value. Materials and Methods: Twenty patients with treatment resistant depression underwent treatment with psilocybin (two separate sessions: 10 and 25 mg psilocybin). The Altered States of Consciousness (ASC) questionnaire was used to assess the quality of experiences in the 25 mg psilocybin session. From the ASC, the dimensions OBN and DED were used to measure the mystical-type and challenging experiences, respectively. The Self-Reported Quick Inventory of Depressive Symptoms (QIDS-SR) at 5 weeks served as the endpoint clinical outcome measure, as in later time points some of the subjects had gone on to receive new treatments, thus confounding inferences. In a repeated measure ANOVA, Time was the within-subject factor (independent variable), with QIDS-SR as the within-subject dependent variable in baseline, 1-day, 1-week, 5-weeks. OBN and DED were independent variables. OBN-by-Time and DED-by-Time interactions were the primary outcomes of interest. Results: For the interaction of OBN and DED with Time (QIDS-SR as dependent variable), the main effect and the effects at each time point compared to baseline were all significant (p = 0.002 and p = 0.003, respectively, for main effects), confirming our main hypothesis. Furthermore, Pearson's correlation of OBN with QIDS-SR (5 weeks) was specific compared to perceptual dimensions of the ASC (p < 0.05). Discussion: This report further bolsters the view that the quality of the acute psychedelic experience is a key mediator of long-term changes in mental health. Future therapeutic work with psychedelics should recognize the essential importance of quality of experience in determining treatment efficacy and consider ways of enhancing mystical-type experiences and reducing anxiety. Trial Registration: ISRCTN, number ISRCTN14426797, http://www.isrctn.com/ISRCTN14426797.}, keywords = {depression; mystical experience; peak experience; psilocybin; psychedelics; serotonin; therapy; }, - pubmed = {29387009}, + pmid = {29387009}, doi = {10.3389/fphar.2017.00974}, pmc = {PMC5776504}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/29387009}, @@ -112040,7 +112034,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Jan}, pages = {2208-28}, abstract = {The plant indole alkaloid ibogaine has shown promising anti-addictive properties in animal studies. Ibogaine is also anti-addictive in humans as the drug alleviates drug craving and impedes relapse of drug use. Although not licensed as therapeutic drug and despite safety concerns, ibogaine is currently used as an anti-addiction medication in alternative medicine in dozens of clinics worldwide. In recent years, alarming reports of life-threatening complications and sudden death cases, temporally associated with the administration of ibogaine, have been accumulating. These adverse reactions were hypothesised to be associated with ibogaine's propensity to induce cardiac arrhythmias. The aim of this review is to recapitulate the current knowledge about ibogaine's effects on the heart and the cardiovascular system, and to assess the cardiac risks associated with the use of this drug in anti- addiction therapy. The actions of 18-methoxycoronaridine (18-MC), a less toxic ibogaine congener with anti-addictive properties, are also considered. }, - pubmed = {25642835}, + pmid = {25642835}, pii = {molecules20022208}, doi = {10.3390/molecules20022208}, pmc = {PMC4382526}, @@ -112060,7 +112054,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {04}, pages = {e1007791}, abstract = {Widefield calcium imaging enables recording of large-scale neural activity across the mouse dorsal cortex. In order to examine the relationship of these neural signals to the resulting behavior, it is critical to demix the recordings into meaningful spatial and temporal components that can be mapped onto well-defined brain regions. However, no current tools satisfactorily extract the activity of the different brain regions in individual mice in a data-driven manner, while taking into account mouse-specific and preparation-specific differences. Here, we introduce Localized semi-Nonnegative Matrix Factorization (LocaNMF), a method that efficiently decomposes widefield video data and allows us to directly compare activity across multiple mice by outputting mouse-specific localized functional regions that are significantly more interpretable than more traditional decomposition techniques. Moreover, it provides a natural subspace to directly compare correlation maps and neural dynamics across different behaviors, mice, and experimental conditions, and enables identification of task- and movement-related brain regions.}, - pubmed = {32282806}, + pmid = {32282806}, doi = {10.1371/journal.pcbi.1007791}, pii = {PCOMPBIOL-D-19-01682}, pmc = {PMC7179949}, @@ -112079,7 +112073,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {06}, pages = {84-88}, abstract = {Data analysis workflows in many scientific domains have become increasingly complex and flexible. Here we assess the effect of this flexibility on the results of functional magnetic resonance imaging by asking 70 independent teams to analyse the same dataset, testing the same 9 ex-ante hypotheses1. The flexibility of analytical approaches is exemplified by the fact that no two teams chose identical workflows to analyse the data. This flexibility resulted in sizeable variation in the results of hypothesis tests, even for teams whose statistical maps were highly correlated at intermediate stages of the analysis pipeline. Variation in reported results was related to several aspects of analysis methodology. Notably, a meta-analytical approach that aggregated information across teams yielded a significant consensus in activated regions. Furthermore, prediction markets of researchers in the field revealed an overestimation of the likelihood of significant findings, even by researchers with direct knowledge of the dataset2-5. Our findings show that analytical flexibility can have substantial effects on scientific conclusions, and identify factors that may be related to variability in the analysis of functional magnetic resonance imaging. The results emphasize the importance of validating and sharing complex analysis workflows, and demonstrate the need for performing and reporting multiple analyses of the same data. Potential approaches that could be used to mitigate issues related to analytical variability are discussed.}, - pubmed = {32483374}, + pmid = {32483374}, doi = {10.1038/s41586-020-2314-9}, pii = {10.1038/s41586-020-2314-9}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/32483374}, @@ -112097,7 +112091,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Aug}, pages = {757-64}, abstract = {Caret software is widely used for analyzing and visualizing many types of fMRI data, often in conjunction with experimental data from other modalities. This article places Caret's development in a historical context that spans three decades of brain mapping--from the early days of manually generated flat maps to the nascent field of human connectomics. It also highlights some of Caret's distinctive capabilities. This includes the ease of visualizing data on surfaces and/or volumes and on atlases as well as individual subjects. Caret can display many types of experimental data using various combinations of overlays (e.g., fMRI activation maps, cortical parcellations, areal boundaries), and it has other features that facilitate the analysis and visualization of complex neuroimaging datasets.}, - pubmed = {22062192}, + pmid = {22062192}, pii = {S1053-8119(11)01241-9}, doi = {10.1016/j.neuroimage.2011.10.077}, pmc = {PMC3288593}, @@ -112117,7 +112111,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Aug}, pages = {e124}, abstract = {There is increasing concern that most current published research findings are false. The probability that a research claim is true may depend on study power and bias, the number of other studies on the same question, and, importantly, the ratio of true to no relationships among the relationships probed in each scientific field. In this framework, a research finding is less likely to be true when the studies conducted in a field are smaller; when effect sizes are smaller; when there is a greater number and lesser preselection of tested relationships; where there is greater flexibility in designs, definitions, outcomes, and analytical modes; when there is greater financial and other interest and prejudice; and when more teams are involved in a scientific field in chase of statistical significance. Simulations show that for most study designs and settings, it is more likely for a research claim to be false than true. Moreover, for many current scientific fields, claimed research findings may often be simply accurate measures of the prevailing bias. In this essay, I discuss the implications of these problems for the conduct and interpretation of research.}, - pubmed = {16060722}, + pmid = {16060722}, pii = {04-PLME-E-0321R2}, doi = {10.1371/journal.pmed.0020124}, pmc = {PMC1182327}, @@ -112136,7 +112130,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Oct}, pages = {e1001747}, abstract = {In a 2005 paper that has been accessed more than a million times, John Ioannidis explained why most published research findings were false. Here he revisits the topic, this time to address how to improve matters. Please see later in the article for the Editors' Summary. }, - pubmed = {25334033}, + pmid = {25334033}, doi = {10.1371/journal.pmed.1001747}, pii = {PMEDICINE-D-14-01145}, pmc = {PMC4204808}, @@ -112152,7 +112146,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a volume = {57}, year = {1995}, pages = {355-85}, - pubmed = {7778872}, + pmid = {7778872}, doi = {10.1146/annurev.ph.57.030195.002035}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/7778872}, url = {papers/Barchi_AnnuRevPhysiol1995-7778872.pdf}, @@ -112169,7 +112163,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Feb}, pages = {20110534}, abstract = {Independent component analysis is a probabilistic method for learning a linear transform of a random vector. The goal is to find components that are maximally independent and non-Gaussian (non-normal). Its fundamental difference to classical multi-variate statistical methods is in the assumption of non-Gaussianity, which enables the identification of original, underlying components, in contrast to classical methods. The basic theory of independent component analysis was mainly developed in the 1990s and summarized, for example, in our monograph in 2001. Here, we provide an overview of some recent developments in the theory since the year 2000. The main topics are: analysis of causal relations, testing independent components, analysing multiple datasets (three-way data), modelling dependencies between the components and improved methods for estimating the basic model.}, - pubmed = {23277597}, + pmid = {23277597}, pii = {rsta.2011.0534}, doi = {10.1098/rsta.2011.0534}, pmc = {PMC3538438}, @@ -112208,7 +112202,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a number = {3}, year = {1982}, pages = {267-73}, - pubmed = {7153672}, + pmid = {7153672}, doi = {10.1007/BF00275687}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/7153672}, url = {papers/Oja_JMathBiol1982-7153672.pdf}, @@ -112248,7 +112242,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Jan}, pages = {83-7}, abstract = {The brain maintains internal models of its environment to interpret sensory inputs and to prepare actions. Although behavioral studies have demonstrated that these internal models are optimally adapted to the statistics of the environment, the neural underpinning of this adaptation is unknown. Using a Bayesian model of sensory cortical processing, we related stimulus-evoked and spontaneous neural activities to inferences and prior expectations in an internal model and predicted that they should match if the model is statistically optimal. To test this prediction, we analyzed visual cortical activity of awake ferrets during development. Similarity between spontaneous and evoked activities increased with age and was specific to responses evoked by natural scenes. This demonstrates the progressive adaptation of internal models to the statistics of natural stimuli at the neural level.}, - pubmed = {21212356}, + pmid = {21212356}, pii = {331/6013/83}, doi = {10.1126/science.1195870}, pmc = {PMC3065813}, @@ -112268,7 +112262,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Oct}, pages = {10742-50}, abstract = {Some movements that animals and humans make are highly stereotyped, repeated with little variation. The patterns of neural activity associated with repeats of a movement may be highly similar, or the same movement may arise from different patterns of neural activity, if the brain exploits redundancies in the neural projections to muscles. We examined the stability of the relationship between neural activity and behavior. We asked whether the variability in neural activity that we observed during repeated reaching was consistent with a noisy but stable relationship, or with a changing relationship, between neural activity and behavior. Monkeys performed highly similar reaches under tight behavioral control, while many neurons in the dorsal aspect of premotor cortex and the primary motor cortex were simultaneously monitored for several hours. Neural activity was predominantly stable over time in all measured properties: firing rate, directional tuning, and contribution to a decoding model that predicted kinematics from neural activity. The small changes in neural activity that we did observe could be accounted for primarily by subtle changes in behavior. We conclude that the relationship between neural activity and practiced behavior is reasonably stable, at least on timescales of minutes up to 48 h. This finding has significant implications for the design of neural prosthetic systems because it suggests that device recalibration need not be overly frequent, It also has implications for studies of neural plasticity because a stable baseline permits identification of nonstationary shifts.}, - pubmed = {17913908}, + pmid = {17913908}, pii = {27/40/10742}, doi = {10.1523/JNEUROSCI.0959-07.2007}, pmc = {PMC6672821}, @@ -112288,7 +112282,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {698-715.e10}, abstract = {The inter-areal wiring pattern of the mouse cerebral cortex was analyzed in relation to a refined parcellation of cortical areas. Twenty-seven retrograde tracer injections were made in 19 areas of a 47-area parcellation of the mouse neocortex. Flat mounts of the cortex and multiple histological markers enabled detailed counts of labeled neurons in individual areas. The observed log-normal distribution of connection weights to each cortical area spans 5 orders of magnitude and reveals a distinct connectivity profile for each area, analogous to that observed in macaques. The cortical network has a density of 97%, considerably higher than the 66% density reported in macaques. A weighted graph analysis reveals a similar global efficiency but weaker spatial clustering compared with that reported in macaques. The consistency, precision of the connectivity profile, density, and weighted graph analysis of the present data differ significantly from those obtained in earlier studies in the mouse.}, keywords = {anatomy; connectivity; log-normal; neocortex; retrograde; rodent; tract-tracing; Animals; Connectome; Female; Macaca; Male; Models, Neurological; Neocortex; Neural Pathways; Neuroanatomical Tract-Tracing Techniques; Species Specificity; }, - pubmed = {29420935}, + pmid = {29420935}, pii = {S0896-6273(17)31185-6}, doi = {10.1016/j.neuron.2017.12.037}, pmc = {PMC5958229}, @@ -112308,7 +112302,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {10}, pages = {25-36}, abstract = {Neuroscience needs behavior. However, it is daunting to render the behavior of organisms intelligible without suppressing most, if not all, references to life. When animals are treated as passive stimulus-response, disembodied and identical machines, the life of behavior perishes. Here, we distill three biological principles (materiality, agency, and historicity), spell out their consequences for the study of animal behavior, and illustrate them with various examples from the literature. We propose to put behavior back into context, with the brain in a species-typical body and with the animal's body situated in the world; stamp Newtonian time with nested ontogenetic and phylogenetic processes that give rise to individuals with their own histories; and supplement linear cause-and-effect chains and information processing with circular loops of purpose and meaning. We believe that conceiving behavior in these ways is imperative for neuroscience.}, - pubmed = {31600513}, + pmid = {31600513}, pii = {S0896-6273(19)30790-1}, doi = {10.1016/j.neuron.2019.09.017}, pmc = {PMC6873815}, @@ -112328,7 +112322,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {10}, pages = {184-185}, abstract = {A dot in this text can simultaneously stimulate thousands of neurons in primary visual cortex, a response that may seem unnecessarily redundant. Contrary to such a view, in this issue of Neuron, Nigam et al. (2019) demonstrate that these co-activated neurons generate abundant synergistic interactions that help to decode the stimulus.}, - pubmed = {31647891}, + pmid = {31647891}, pii = {S0896-6273(19)30844-X}, doi = {10.1016/j.neuron.2019.09.041}, url = {papers/Mazade_Neuron2019-31647891.pdf}, @@ -112345,7 +112339,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Oct}, pages = {153-65}, abstract = {Network oscillations support transient communication across brain structures. We show here, in rats, that task-related neuronal activity in the medial prefrontal cortex (PFC), the hippocampus, and the ventral tegmental area (VTA), regions critical for working memory, is coordinated by a 4 Hz oscillation. A prominent increase of power and coherence of the 4 Hz oscillation in the PFC and the VTA and its phase modulation of gamma power in both structures was present in the working memory part of the task. Subsets of both PFC and hippocampal neurons predicted the turn choices of the rat. The goal-predicting PFC pyramidal neurons were more strongly phase locked to both 4 Hz and hippocampal theta oscillations than nonpredicting cells. The 4 Hz and theta oscillations were phase coupled and jointly modulated both gamma waves and neuronal spikes in the PFC, the VTA, and the hippocampus. Thus, multiplexed timing mechanisms in the PFC-VTA-hippocampus axis may support processing of information, including working memory.}, - pubmed = {21982376}, + pmid = {21982376}, pii = {S0896-6273(11)00739-2}, doi = {10.1016/j.neuron.2011.08.018}, pmc = {PMC3235795}, @@ -112365,7 +112359,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {30033-30038}, abstract = {Deep learning networks have been trained to recognize speech, caption photographs, and translate text between languages at high levels of performance. Although applications of deep learning networks to real-world problems have become ubiquitous, our understanding of why they are so effective is lacking. These empirical results should not be possible according to sample complexity in statistics and nonconvex optimization theory. However, paradoxes in the training and effectiveness of deep learning networks are being investigated and insights are being found in the geometry of high-dimensional spaces. A mathematical theory of deep learning would illuminate how they function, allow us to assess the strengths and weaknesses of different network architectures, and lead to major improvements. Deep learning has provided natural ways for humans to communicate with digital devices and is foundational for building artificial general intelligence. Deep learning was inspired by the architecture of the cerebral cortex and insights into autonomy and general intelligence may be found in other brain regions that are essential for planning and survival, but major breakthroughs will be needed to achieve these goals.}, keywords = {artificial intelligence; deep learning; neural networks; }, - pubmed = {31992643}, + pmid = {31992643}, pii = {1907373117}, doi = {10.1073/pnas.1907373117}, pmc = {PMC7720171}, @@ -112398,7 +112392,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {01}, pages = {107-113}, abstract = {Spontaneous and sensory-evoked activity propagates across varying spatial scales in the mammalian cortex, but technical challenges have limited conceptual links between the function of local neuronal circuits and brain-wide network dynamics. We present a method for simultaneous cellular-resolution two-photon calcium imaging of a local microcircuit and mesoscopic widefield calcium imaging of the entire cortical mantle in awake mice. Our multi-scale approach involves a microscope with an orthogonal axis design where the mesoscopic objective is oriented above the brain and the two-photon objective is oriented horizontally, with imaging performed through a microprism. We also introduce a viral transduction method for robust and widespread gene delivery in the mouse brain. These approaches allow us to identify the behavioral state-dependent functional connectivity of pyramidal neurons and vasoactive intestinal peptide-expressing interneurons with long-range cortical networks. Our imaging system provides a powerful strategy for investigating cortical architecture across a wide range of spatial scales.}, - pubmed = {31686040}, + pmid = {31686040}, doi = {10.1038/s41592-019-0625-2}, pii = {10.1038/s41592-019-0625-2}, pmc = {PMC6946863}, @@ -112418,7 +112412,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {3017-3036}, abstract = {Widefield optical imaging of neuronal populations over large portions of the cerebral cortex in awake behaving animals provides a unique opportunity for investigating the relationship between brain function and behavior. In this paper, we demonstrate that the temporal characteristics of calcium dynamics obtained through widefield imaging can be utilized to infer the corresponding behavior. Cortical activity in transgenic calcium reporter mice (n=6) expressing GCaMP6f in neocortical pyramidal neurons is recorded during active whisking (AW) and no whisking (NW). To extract features related to the temporal characteristics of calcium recordings, a method based on visibility graph (VG) is introduced. An extensive study considering different choices of features and classifiers is conducted to find the best model capable of predicting AW and NW from calcium recordings. Our experimental results show that temporal characteristics of calcium recordings identified by the proposed method carry discriminatory information that are powerful enough for decoding behavior.}, keywords = {(170.2655) Functional monitoring and imaging; (170.3880) Medical and biological imaging; }, - pubmed = {29984080}, + pmid = {29984080}, doi = {10.1364/BOE.9.003017}, pii = {320299}, pmc = {PMC6033549}, @@ -112437,7 +112431,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {141-9}, abstract = {Craniotomy-based window implants are commonly used for microscopic imaging, in head-fixed rodents, however their field of view is typically small and incompatible with mesoscopic functional mapping of cortex.}, keywords = {GCaMP; Head-fixed; Optogenetics; Animals; Cerebral Cortex; Craniotomy; Dental Cements; Equipment Design; Glass; Grooming; Longitudinal Studies; Mice, Transgenic; Motor Activity; Neuroimaging; Optical Imaging; Optogenetics; Prostheses and Implants; Skull; Time Factors; Wakefulness; }, - pubmed = {27102043}, + pmid = {27102043}, pmc = {PMC5075450}, pii = {S0165-0270(16)30064-4}, doi = {10.1016/j.jneumeth.2016.04.012}, @@ -112456,7 +112450,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {570-584}, abstract = {The organization of brain areas in functionally connected networks, their dynamic changes, and perturbations in disease states are subject of extensive investigations. Research on functional networks in humans predominantly uses functional magnetic resonance imaging (fMRI). However, adopting fMRI and other functional imaging methods to mice, the most widely used model to study brain physiology and disease, poses major technical challenges and faces important limitations. Hence, there is great demand for alternative imaging modalities for network characterization. Here, we present a refined protocol for in vivo widefield calcium imaging of both cerebral hemispheres in mice expressing a calcium sensor in excitatory neurons. We implemented a stringent protocol for minimizing anesthesia and excluding movement artifacts which both imposed problems in previous approaches. We further adopted a method for unbiased identification of functional cortical areas using independent component analysis (ICA) on resting-state imaging data. Biological relevance of identified components was confirmed using stimulus-dependent cortical activation. To explore this novel approach in a model of focal brain injury, we induced photothrombotic lesions of the motor cortex, determined changes in inter- and intrahemispheric connectivity at multiple time points up to 56 days post-stroke and correlated them with behavioral deficits. We observed a severe loss in interhemispheric connectivity after stroke, which was partially restored in the chronic phase and associated with corresponding behavioral motor deficits. Taken together, we present an improved widefield calcium imaging tool accounting for anesthesia and movement artifacts, adopting an advanced analysis pipeline based on human fMRI algorithms and with superior sensitivity to recovery mechanisms in mouse models compared to behavioral tests. This tool will enable new studies on interhemispheric connectivity in murine models with comparability to human imaging studies for a wide spectrum of neuroscience applications in health and disease.}, keywords = {ICA; In vivo imaging; Mouse models; Neuronal network connectivity; Recovery; Stroke; Animals; Calcium; Cerebral Cortex; Connectome; Disease Models, Animal; Female; Male; Mice; Mice, Inbred C57BL; Motor Cortex; Nerve Net; Neuroimaging; Optical Imaging; Prosencephalon; Stroke; }, - pubmed = {31181333}, + pmid = {31181333}, pii = {S1053-8119(19)30499-9}, doi = {10.1016/j.neuroimage.2019.06.014}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/31181333}, @@ -112475,7 +112469,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {108303}, abstract = {Gain-of-function (GOF) variants in K+ channels cause severe childhood epilepsies, but there are no mechanisms to explain how increased K+ currents lead to network hyperexcitability. Here, we introduce a human Na+-activated K+ (KNa) channel variant (KCNT1-Y796H) into mice and, using a multiplatform approach, find motor cortex hyperexcitability and early-onset seizures, phenotypes strikingly similar to those of human patients. Although the variant increases KNa currents in cortical excitatory and inhibitory neurons, there is an increase in the KNa current across subthreshold voltages only in inhibitory neurons, particularly in those with non-fast-spiking properties, resulting in inhibitory-neuron-specific impairments in excitability and action potential (AP) generation. We further observe evidence of synaptic rewiring, including increases in homotypic synaptic connectivity, accompanied by network hyperexcitability and hypersynchronicity. These findings support inhibitory-neuron-specific mechanisms in mediating the epileptogenic effects of KCNT1 channel GOF, offering cell-type-specific currents and effects as promising targets for therapeutic intervention.}, keywords = {ADNFLE; K(Na) current; KCNT1; MEA; Slack; calcium imaging; electrocorticography; electrophysiology; epilepsy; synaptic transmission; }, - pubmed = {33113364}, + pmid = {33113364}, pii = {S2211-1247(20)31292-4}, doi = {10.1016/j.celrep.2020.108303}, pmc = {PMC7712469}, @@ -112494,7 +112488,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {}, abstract = {We report improved automated open-source methodology for head-fixed mesoscale cortical imaging and/or behavioral training of home cage mice using Raspberry Pi-based hardware. Staged partial and probabilistic restraint allows mice to adjust to self-initiated headfixation over 3 weeks' time with ~50% participation rate. We support a cue-based behavioral licking task monitored by a capacitive touch-sensor water spout. While automatically head-fixed, we acquire spontaneous, movement-triggered, or licking task-evoked GCaMP6 cortical signals. An analysis pipeline marked both behavioral events, as well as analyzed brain fluorescence signals as they relate to spontaneous and/or task-evoked behavioral activity. Mice were trained to suppress licking and wait for cues that marked the delivery of water. Correct rewarded go-trials were associated with widespread activation of midline and lateral barrel cortex areas following a vibration cue and delayed frontal and lateral motor cortex activation. Cortical GCaMP signals predicted trial success and correlated strongly with trial-outcome dependent body movements.}, keywords = {automation; cortex; homecage; imaging; mesoscale; mouse; neuroscience; Animals; Behavior, Animal; Brain Mapping; Calcium-Binding Proteins; Cues; Drinking; Equipment Design; Female; Head Movements; Luminescent Proteins; Male; Mice, Inbred C57BL; Mice, Transgenic; Motor Cortex; Optical Imaging; Restraint, Physical; Reward; Time Factors; }, - pubmed = {32412409}, + pmid = {32412409}, doi = {10.7554/eLife.55964}, pii = {55964}, pmc = {PMC7332290}, @@ -112513,7 +112507,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {12}, pages = {1262-1271}, abstract = {Achieving a comprehensive understanding of brain function requires multiple imaging modalities with complementary strengths. We present an approach for concurrent widefield optical and functional magnetic resonance imaging. By merging these modalities, we can simultaneously acquire whole-brain blood-oxygen-level-dependent (BOLD) and whole-cortex calcium-sensitive fluorescent measures of brain activity. In a transgenic murine model, we show that calcium predicts the BOLD signal, using a model that optimizes a gamma-variant transfer function. We find consistent predictions across the cortex, which are best at low frequency (0.009-0.08 Hz). Furthermore, we show that the relationship between modality connectivity strengths varies by region. Our approach links cell-type-specific optical measurements of activity to the most widely used method for assessing human brain function.}, - pubmed = {33139894}, + pmid = {33139894}, doi = {10.1038/s41592-020-00984-6}, pii = {10.1038/s41592-020-00984-6}, pmc = {PMC7704940}, @@ -112533,7 +112527,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {356-366}, abstract = {Wide-field calcium imaging is often used to measure brain dynamics in behaving mice. With a large field of view and a high sampling rate, wide-field imaging can monitor activity from several distant cortical areas simultaneously, revealing cortical interactions. Interpretation of wide-field images is complicated, however, by the absorption of light by hemoglobin, which can substantially affect the measured fluorescence. One approach to separating hemodynamics and calcium signals is to use multiwavelength backscatter recordings to measure light absorption by hemoglobin. Following this approach, we develop a spatially detailed regression-based method to estimate hemodynamics. This Spatial Model is based on a linear form of the Beer-Lambert relationship but is fit at every pixel in the image and does not rely on the estimation of physical parameters. In awake mice of three transgenic lines, the Spatial Model offers improved separation of hemodynamics and changes in GCaMP fluorescence. The improvement is pronounced near blood vessels and, in contrast with the Beer-Lambert equations, can remove vascular artifacts along the sagittal midline and in general permits more accurate fluorescence-based determination of neuronal activity across the cortex.NEW & NOTEWORTHY This paper addresses a well-known and strong source of contamination in wide-field calcium-imaging data: hemodynamics. To guide researchers toward the best method to separate calcium signals from hemodynamics, we compare the performance of several methods in three commonly used mouse lines and present a novel regression model that outperforms the other techniques we consider.}, keywords = {animal behavior; calcium imaging; hemodynamics; optical methods; systems neuroscience; }, - pubmed = {31747332}, + pmid = {31747332}, doi = {10.1152/jn.00304.2019}, eprint = {https://www.ncbi.nlm.nih.gov/pubmed/31747332}, url = {papers/Valley_JNeurophysiol2020-31747332.pdf}, @@ -112551,7 +112545,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {5443-5454}, abstract = {An essential feature of goal-directed behavior is the ability to selectively respond to the diverse stimuli in one's environment. However, the neural mechanisms that enable us to respond to target stimuli while ignoring distractor stimuli are poorly understood. To study this sensory selection process, we trained male and female mice in a selective detection task in which mice learn to respond to rapid stimuli in the target whisker field and ignore identical stimuli in the opposite, distractor whisker field. In expert mice, we used widefield Ca2+ imaging to analyze target-related and distractor-related neural responses throughout dorsal cortex. For target stimuli, we observed strong signal activation in primary somatosensory cortex (S1) and frontal cortices, including both the whisker region of primary motor cortex (wMC) and anterior lateral motor cortex (ALM). For distractor stimuli, we observed strong signal activation in S1, with minimal propagation to frontal cortex. Our data support only modest subcortical filtering, with robust, step-like attenuation in distractor processing between mono-synaptically coupled regions of S1 and wMC. This study establishes a highly robust model system for studying the neural mechanisms of sensory selection and places important constraints on its implementation.SIGNIFICANCE STATEMENT Responding to task-relevant stimuli while ignoring task-irrelevant stimuli is critical for goal-directed behavior. However, the neural mechanisms involved in this selection process are poorly understood. We trained mice in a detection task with both target and distractor stimuli. During expert performance, we measured neural activity throughout cortex using widefield imaging. We observed responses to target stimuli in multiple sensory and motor cortical regions. In contrast, responses to distractor stimuli were abruptly suppressed beyond sensory cortex. Our findings localize the sites of attenuation when successfully ignoring a distractor stimulus and provide essential foundations for further revealing the neural mechanism of sensory selection and distractor suppression.}, keywords = {attenuating filter; neocortex; sensorimotor; sensory selection; somatosensory; widefield imaging; Animals; Attention; Female; Male; Mice; Motor Cortex; Physical Stimulation; Reaction Time; Somatosensory Cortex; Touch Perception; Vibrissae; }, - pubmed = {32487695}, + pmid = {32487695}, pii = {JNEUROSCI.2993-19.2020}, doi = {10.1523/JNEUROSCI.2993-19.2020}, pmc = {PMC7343319}, @@ -112570,7 +112564,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {89-100}, abstract = {Imagine you were asked to investigate the workings of an engine, but to do so without ever opening the hood. Now imagine the engine fueled the human mind. This is the challenge faced by cognitive neuroscientists worldwide aiming to understand the neural bases of our psychological functions. Luckily, human ingenuity comes to the rescue. Around the same time as the Society for Neuroscience was being established in the 1960s, the first tools for measuring the human brain at work were becoming available. Noninvasive human brain imaging and neurophysiology have continued developing at a relentless pace ever since. In this 50 year anniversary, we reflect on how these methods have been changing our understanding of how brain supports mind.}, keywords = {Electroencephalograhy (EEG); Functional Magnetic Resonance Imaging (fMRI); Historical overview; Human brain imaging; Human neurophysiology; Selective attention; Attention; Brain Mapping; Cognition; Evoked Potentials; Forecasting; History, 19th Century; History, 20th Century; History, 21st Century; Humans; Machine Learning; Mental Processes; Neuroimaging; Neurophysiology; Neuropsychology; Psychophysiology; }, - pubmed = {31630115}, + pmid = {31630115}, pii = {JNEUROSCI.0742-19.2019}, doi = {10.1523/JNEUROSCI.0742-19.2019}, pmc = {PMC6939481}, @@ -112590,7 +112584,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {1601-1607}, abstract = {With ever-increasing advancements in technology, neuroscientists are able to collect data in greater volumes and with finer resolution. The bottleneck in understanding how the brain works is consequently shifting away from the amount and type of data we can collect and toward what we actually do with the data. There has been a growing interest in leveraging this vast volume of data across levels of analysis, measurement techniques, and experimental paradigms to gain more insight into brain function. Such efforts are visible at an international scale, with the emergence of big data neuroscience initiatives, such as the BRAIN initiative (Bargmann et al., 2014), the Human Brain Project, the Human Connectome Project, and the National Institute of Mental Health's Research Domain Criteria initiative. With these large-scale projects, much thought has been given to data-sharing across groups (Poldrack and Gorgolewski, 2014; Sejnowski et al., 2014); however, even with such data-sharing initiatives, funding mechanisms, and infrastructure, there still exists the challenge of how to cohesively integrate all the data. At multiple stages and levels of neuroscience investigation, machine learning holds great promise as an addition to the arsenal of analysis tools for discovering how the brain works.}, keywords = {explainable artificial intelligence; machine learning; reinforcement learning; Animals; Big Data; Brain; Connectome; Humans; Information Dissemination; Machine Learning; Neurosciences; Reproducibility of Results; }, - pubmed = {29374138}, + pmid = {29374138}, pii = {JNEUROSCI.0508-17.2018}, doi = {10.1523/JNEUROSCI.0508-17.2018}, pmc = {PMC5815449}, @@ -112608,7 +112602,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {08}, pages = {7551-7558}, abstract = {The vast majority of experiments examining perception and behavior are conducted using experimental paradigms that adhere to a rigid trial structure: each trial consists of a brief and discrete series of events and is regarded as independent from all other trials. The assumptions underlying this structure ignore the reality that natural behavior is rarely discrete, brain activity follows multiple time courses that do not necessarily conform to the trial structure, and the natural environment has statistical structure and dynamics that exhibit long-range temporal correlation. Modern advances in statistical modeling and analysis offer tools that make it feasible for experiments to move beyond rigid independent and identically distributed trial structures. Here we review literature that serves as evidence for the feasibility and advantages of moving beyond trial-based paradigms to understand the neural basis of perception and cognition. Furthermore, we propose a synthesis of these efforts, integrating the characterization of natural stimulus properties with measurements of continuous neural activity and behavioral outputs within the framework of sensory-cognitive-motor loops. Such a framework provides a basis for the study of natural statistics, naturalistic tasks, and/or slow fluctuations in brain activity, which should provide starting points for important generalizations of analytical tools in neuroscience and subsequent progress in understanding the neural basis of perception and cognition.}, - pubmed = {30037835}, + pmid = {30037835}, pii = {JNEUROSCI.1920-17.2018}, doi = {10.1523/JNEUROSCI.1920-17.2018}, pmc = {PMC6113904}, @@ -112627,7 +112621,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {9042-9052}, abstract = {Multiphoton microscopy (MPM) has emerged as one of the most powerful and widespread technologies to monitor the activity of neuronal networks in awake, behaving animals over long periods of time. MPM development spanned across decades and crucially depended on the concurrent improvement of calcium indicators that report neuronal activity as well as surgical protocols, head fixation approaches, and innovations in optics and microscopy technology. Here we review the last decade of MPM development and highlight how in vivo imaging has matured and diversified, making it now possible to concurrently monitor thousands of neurons across connected brain areas or, alternatively, small local networks with sampling rates in the kilohertz range. This review includes different laser scanning approaches, such as multibeam technologies as well as recent developments to image deeper into neuronal tissues using new, long-wavelength laser sources. As future development will critically depend on our ability to resolve and discriminate individual neuronal spikes, we will also describe a simple framework that allows performing quantitative comparisons between the reviewed MPM instruments. Finally, we provide our own opinion on how the most recent MPM developments can be leveraged at scale to enable the next generation of discoveries in brain function.}, keywords = {imaging; in vivo; multiphoton; two-photon; Animals; Brain; Image Processing, Computer-Assisted; Microscopy, Confocal; Microscopy, Fluorescence, Multiphoton; Neurons; }, - pubmed = {31578235}, + pmid = {31578235}, pii = {JNEUROSCI.1527-18.2019}, doi = {10.1523/JNEUROSCI.1527-18.2019}, pmc = {PMC6855689}, @@ -112645,7 +112639,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Feb}, pages = {353-364}, abstract = {Despite substantial recent progress, our understanding of the principles and mechanisms underlying complex brain function and cognition remains incomplete. Network neuroscience proposes to tackle these enduring challenges. Approaching brain structure and function from an explicitly integrative perspective, network neuroscience pursues new ways to map, record, analyze and model the elements and interactions of neurobiological systems. Two parallel trends drive the approach: the availability of new empirical tools to create comprehensive maps and record dynamic patterns among molecules, neurons, brain areas and social systems; and the theoretical framework and computational tools of modern network science. The convergence of empirical and computational advances opens new frontiers of scientific inquiry, including network dynamics, manipulation and control of brain networks, and integration of network processes across spatiotemporal domains. We review emerging trends in network neuroscience and attempt to chart a path toward a better understanding of the brain as a multiscale networked system.}, - pubmed = {28230844}, + pmid = {28230844}, pii = {nn.4502}, doi = {10.1038/nn.4502}, pmc = {PMC5485642}, @@ -112663,7 +112657,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a number = {2}, pages = {}, keywords = {cognition; connectomics; levels of analysis; promissory materialism; }, - pubmed = {33648976}, + pmid = {33648976}, pii = {ENEURO.0521-20.2021}, doi = {10.1523/ENEURO.0521-20.2021}, url = {papers/Gomez-Marin_eNeuro-33648976.pdf}, @@ -112678,7 +112672,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a year = {2020}, month = {12}, pages = {1455}, - pubmed = {33230327}, + pmid = {33230327}, doi = {10.1038/s41593-020-00750-z}, pii = {10.1038/s41593-020-00750-z}, url = {papers/_NatNeurosci2020-33230327.pdf}, @@ -112695,7 +112689,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {12}, pages = {1456-1468}, abstract = {To understand the function of cortical circuits, it is necessary to catalog their cellular diversity. Past attempts to do so using anatomical, physiological or molecular features of cortical cells have not resulted in a unified taxonomy of neuronal or glial cell types, partly due to limited data. Single-cell transcriptomics is enabling, for the first time, systematic high-throughput measurements of cortical cells and generation of datasets that hold the promise of being complete, accurate and permanent. Statistical analyses of these data reveal clusters that often correspond to cell types previously defined by morphological or physiological criteria and that appear conserved across cortical areas and species. To capitalize on these new methods, we propose the adoption of a transcriptome-based taxonomy of cell types for mammalian neocortex. This classification should be hierarchical and use a standardized nomenclature. It should be based on a probabilistic definition of a cell type and incorporate data from different approaches, developmental stages and species. A community-based classification and data aggregation model, such as a knowledge graph, could provide a common foundation for the study of cortical circuits. This community-based classification, nomenclature and data aggregation could serve as an example for cell type atlases in other parts of the body.}, - pubmed = {32839617}, + pmid = {32839617}, doi = {10.1038/s41593-020-0685-8}, pii = {10.1038/s41593-020-0685-8}, pmc = {PMC7683348}, @@ -112728,7 +112722,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Mar}, pages = {}, abstract = {Neuronal activity results in increased blood flow in the brain, a response named functional hyperemia. Astrocytes play an important role in mediating this response. Neurotransmitters released from active neurons evoke Ca(2+) increases in astrocytes, leading to the release of vasoactive metabolites of arachidonic acid from astrocyte endfeet onto blood vessels. Synthesis of prostaglandin E2 (PGE2) and epoxyeicosatrienoic acids (EETs) dilate blood vessels, whereas 20-hydroxyeicosatetraenoic acid (20-HETE) constricts vessels. The release of K(+) from astrocyte endfeet may also contribute to vasodilation. Oxygen modulates astrocyte regulation of blood flow. Under normoxic conditions, astrocytic Ca(2+) signaling results in vasodilation, whereas under hyperoxic conditions, vasoconstriction is favored. Astrocytes also contribute to the generation of vascular tone. Tonic release of both 20-HETE and ATP from astrocytes constricts vascular smooth muscle cells, generating vessel tone. Under pathological conditions, including Alzheimer's disease and diabetic retinopathy, disruption of normal astrocyte physiology can compromise the regulation of blood flow. }, - pubmed = {25818565}, + pmid = {25818565}, pii = {cshperspect.a020388}, doi = {10.1101/cshperspect.a020388}, pmc = {PMC4448617}, @@ -112746,7 +112740,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Nov}, pages = {232-43}, abstract = {Blood flow in the brain is regulated by neurons and astrocytes. Knowledge of how these cells control blood flow is crucial for understanding how neural computation is powered, for interpreting functional imaging scans of brains, and for developing treatments for neurological disorders. It is now recognized that neurotransmitter-mediated signalling has a key role in regulating cerebral blood flow, that much of this control is mediated by astrocytes, that oxygen modulates blood flow regulation, and that blood flow may be controlled by capillaries as well as by arterioles. These conceptual shifts in our understanding of cerebral blood flow control have important implications for the development of new therapeutic approaches.}, - pubmed = {21068832}, + pmid = {21068832}, pii = {nature09613}, doi = {10.1038/nature09613}, pmc = {PMC3206737}, @@ -112766,7 +112760,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {10460-73}, abstract = {In terrestrial mammals, the oxygen storage capacity of the CNS is limited, and neuronal function is rapidly impaired if oxygen supply is interrupted even for a short period of time. However, oxygen tension monitored by the peripheral (arterial) chemoreceptors is not sensitive to regional CNS differences in partial pressure of oxygen (PO2 ) that reflect variable levels of neuronal activity or local tissue hypoxia, pointing to the necessity of a functional brain oxygen sensor. This experimental animal (rats and mice) study shows that astrocytes, the most numerous brain glial cells, are sensitive to physiological changes in PO2 . Astrocytes respond to decreases in PO2 a few millimeters of mercury below normal brain oxygenation with elevations in intracellular calcium ([Ca(2+)]i). The hypoxia sensor of astrocytes resides in the mitochondria in which oxygen is consumed. Physiological decrease in PO2 inhibits astroglial mitochondrial respiration, leading to mitochondrial depolarization, production of free radicals, lipid peroxidation, activation of phospholipase C, IP3 receptors, and release of Ca(2+) from the intracellular stores. Hypoxia-induced [Ca(2+)]i increases in astrocytes trigger fusion of vesicular compartments containing ATP. Blockade of astrocytic signaling by overexpression of ATP-degrading enzymes or targeted astrocyte-specific expression of tetanus toxin light chain (to interfere with vesicular release mechanisms) within the brainstem respiratory rhythm-generating circuits reveals the fundamental physiological role of astroglial oxygen sensitivity; in low-oxygen conditions (environmental hypoxia), this mechanism increases breathing activity even in the absence of peripheral chemoreceptor oxygen sensing. These results demonstrate that astrocytes are functionally specialized CNS oxygen sensors tuned for rapid detection of physiological changes in brain oxygenation. Significance statement: Most, if not all, animal cells possess mechanisms that allow them to detect decreases in oxygen availability leading to slow-timescale, adaptive changes in gene expression and cell physiology. To date, only two types of mammalian cells have been demonstrated to be specialized for rapid functional oxygen sensing: glomus cells of the carotid body (peripheral respiratory chemoreceptors) that stimulate breathing when oxygenation of the arterial blood decreases; and pulmonary arterial smooth muscle cells responsible for hypoxic pulmonary vasoconstriction to limit perfusion of poorly ventilated regions of the lungs. Results of the present study suggest that there is another specialized oxygen-sensitive cell type in the body, the astrocyte, that is tuned for rapid detection of physiological changes in brain oxygenation.}, keywords = {astrocyte; glia; hypoxia; oxygen; respiration; Animals; Astrocytes; Cell Hypoxia; Cells, Cultured; Chemoreceptor Cells; Immunohistochemistry; Male; Mice; Mice, Knockout; Organ Culture Techniques; Oxygen; Rats; Rats, Sprague-Dawley; Respiratory Physiological Phenomena; }, - pubmed = {26203141}, + pmid = {26203141}, pii = {35/29/10460}, doi = {10.1523/JNEUROSCI.0045-15.2015}, pmc = {PMC4510287}, @@ -112784,7 +112778,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a month = {Feb}, pages = {260-7}, abstract = {Local increase in blood flow during neural activity forms the basis for functional brain imaging, but its mechanism remains poorly defined. Here we show that cortical astrocytes in vivo possess a powerful mechanism for rapid vasodilation. We imaged the activity of astrocytes labeled with the calcium (Ca(2+))-sensitive indicator rhod-2 in somatosensory cortex of adult mice. Photolysis of caged Ca(2+) in astrocytic endfeet ensheathing the vessel wall was associated with an 18% increase in arterial cross-section area that corresponded to a 37% increase in blood flow. Vasodilation occurred with a latency of only 1-2 s, and both indomethacin and the cyclooxygenase-1 inhibitor SC-560 blocked the photolysis-induced hyperemia. These observations implicate astrocytes in the control of local microcirculation and suggest that one of their physiological roles is to mediate vasodilation in response to increased neural activity.}, - pubmed = {16388306}, + pmid = {16388306}, pii = {nn1623}, doi = {10.1038/nn1623}, url = {papers/Takano_NatNeurosci2006-16388306.pdf}, @@ -112802,7 +112796,7 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a pages = {6473-7}, abstract = {In the mammalian brain, astrocytes modulate neuronal function, in part, by synchronizing neuronal firing and coordinating synaptic networks. Little, however, is known about how this is accomplished from a structural standpoint. To investigate the structural basis of astrocyte-mediated neuronal synchrony and synaptic coordination, the three-dimensional relationships between cortical astrocytes and neurons was investigated. Using a transgenic and viral approach to label astrocytes with enhanced green fluorescent protein, we performed a three-dimensional reconstruction of astrocytes from tissue sections or live animals in vivo. We found that cortical astrocytes occupy nonoverlapping territories similar to those described in the hippocampus. Using immunofluorescence labeling of neuronal somata, a single astrocyte enwraps on average four neuronal somata with an upper limit of eight. Single-neuron dye-fills allowed us to estimate that one astrocyte contacts 300-600 neuronal dendrites. Together with the recent findings showing that glial Ca2+ signaling is restricted to individual astrocytes in vivo, and that Ca2+ signaling leads to gliotransmission, we propose the concept of functional islands of synapses in which groups of synapses confined within the boundaries of an individual astrocyte are modulated by the gliotransmitter environment controlled by that astrocyte. Our description offers a new structurally based conceptual framework to evaluate functional data involving interactions between neurons and astrocytes in the mammalian brain.}, keywords = {Animals; Astrocytes; Cell Communication; Cerebral Cortex; Dendrites; Glial Fibrillary Acidic Protein; Green Fluorescent Proteins; Humans; Imaging, Three-Dimensional; In Vitro Techniques; Mice; Mice, Transgenic; Neurons; Synapses; Synaptic Transmission; Transduction, Genetic; Vesicle-Associated Membrane Protein 2; }, - pubmed = {17567808}, + pmid = {17567808}, pii = {27/24/6473}, doi = {10.1523/JNEUROSCI.1419-07.2007}, pmc = {PMC6672436}, @@ -112810,3 +112804,163 @@ CONCLUSIONS: Centrifugal axons in the macaque retina are part of the system of a nlmuniqueid = {8102140} } +@article{Court2004, + title = {Restricted growth of Schwann cells lacking Cajal bands slows conduction in myelinated nerves.}, + author = {Court, Felipe A and Sherman, Diane L and Pratt, Thomas and Garry, Emer M and Ribchester, Richard R and Cottrell, David F and Fleetwood-Walker, Susan M and Brophy, Peter J}, + journal = {Nature}, + volume = {431}, + number = {7005}, + year = {2004}, + month = {Sep}, + pages = {191-5}, + abstract = {Nerve impulses are propagated at nodes of Ranvier in the myelinated nerves of vertebrates. Internodal distances have been proposed to affect the velocity of nerve impulse conduction; however, direct evidence is lacking, and the cellular mechanisms that might regulate the length of the myelinated segments are unknown. Ramón y Cajal described longitudinal and transverse bands of cytoplasm or trabeculae in internodal Schwann cells and suggested that they had a nutritive function. Here we show that internodal growth in wild-type nerves is precisely matched to nerve extension, but disruption of the cytoplasmic bands in Periaxin-null mice impairs Schwann cell elongation during nerve growth. By contrast, myelination proceeds normally. The capacity of wild-type and mutant Schwann cells to elongate is cell-autonomous, indicating that passive stretching can account for the lengthening of the internode during limb growth. As predicted on theoretical grounds, decreased internodal distances strikingly decrease conduction velocities and so affect motor function. We propose that microtubule-based transport in the longitudinal bands of Cajal permits internodal Schwann cells to lengthen in response to axonal growth, thus ensuring rapid nerve impulse transmission.}, + keywords = {Animals; Axons; Behavior, Animal; Cell Size; Cytoplasm; Gene Deletion; Membrane Proteins; Mice; Mice, Knockout; Microtubules; Muscle, Skeletal; Myelin Basic Protein; Nerve Fibers, Myelinated; RNA, Messenger; Schwann Cells; Sciatic Nerve; Synaptic Transmission; }, + pubmed = {15356632}, + doi = {10.1038/nature02841}, + pii = {nature02841}, + url = {papers/Court_Nature2004-15356632.pdf}, + nlmuniqueid = {0410462} +} + +@article{Otsu2015, + title = {Calcium dynamics in astrocyte processes during neurovascular coupling.}, + author = {Otsu, Yo and Couchman, Kiri and Lyons, Declan G and Collot, Mayeul and Agarwal, Amit and Mallet, Jean-Maurice and Pfrieger, Frank W and Bergles, Dwight E and Charpak, Serge}, + journal = {Nat Neurosci}, + volume = {18}, + number = {2}, + year = {2015}, + month = {Feb}, + pages = {210-8}, + abstract = {Enhanced neuronal activity in the brain triggers a local increase in blood flow, termed functional hyperemia, via several mechanisms, including calcium (Ca(2+)) signaling in astrocytes. However, recent in vivo studies have questioned the role of astrocytes in functional hyperemia because of the slow and sparse dynamics of their somatic Ca(2+) signals and the absence of glutamate metabotropic receptor 5 in adults. Here, we reexamined their role in neurovascular coupling by selectively expressing a genetically encoded Ca(2+) sensor in astrocytes of the olfactory bulb. We show that in anesthetized mice, the physiological activation of olfactory sensory neuron (OSN) terminals reliably triggers Ca(2+) increases in astrocyte processes but not in somata. These Ca(2+) increases systematically precede the onset of functional hyperemia by 1-2 s, reestablishing astrocytes as potential regulators of neurovascular coupling. }, + keywords = {Animals; Astrocytes; Calcium Signaling; Cerebrovascular Circulation; Mice; Mice, Transgenic; Olfactory Bulb; Olfactory Receptor Neurons; Receptor, Metabotropic Glutamate 5; Synapses; }, + pubmed = {25531572}, + pii = {nn.3906}, + doi = {10.1038/nn.3906}, + pmc = {PMC4651918}, + mid = {NIHMS671426}, + url = {papers/Otsu_NatNeurosci2015-25531572.pdf}, + nlmuniqueid = {9809671} +} + +@article{Kast2019, + title = {Precision in the development of neocortical architecture: From progenitors to cortical networks.}, + author = {Kast, Ryan J and Levitt, Pat}, + journal = {Prog Neurobiol}, + volume = {175}, + year = {2019}, + month = {04}, + pages = {77-95}, + abstract = {Of all brain regions, the 6-layered neocortex has undergone the most dramatic changes in size and complexity during mammalian brain evolution. These changes, occurring in the context of a conserved set of organizational features that emerge through stereotypical developmental processes, are considered responsible for the cognitive capacities and sensory specializations represented within the mammalian clade. The modern experimental era of developmental neurobiology, spanning 6 decades, has deciphered a number of mechanisms responsible for producing the diversity of cortical neuron types, their precise connectivity and the role of gene by environment interactions. Here, experiments providing insight into the development of cortical projection neuron differentiation and connectivity are reviewed. This current perspective integrates discussion of classic studies and new findings, based on recent technical advances, to highlight an improved understanding of the neuronal complexity and precise connectivity of cortical circuitry. These descriptive advances bring new opportunities for studies related to the developmental origins of cortical circuits that will, in turn, improve the prospects of identifying pathogenic targets of neurodevelopmental disorders.}, + keywords = {Axon guidance; Cell type specification; Cerebral cortex; Circuits; Connectivity; Excitatory neurons; Experience; Genetics; Histogenesis; Human; Microcircuit; Neural network; Refinement; Reprogramming; Rodent; Specification; Synaptic specificity; Synaptogenesis; Thalamus; Animals; Humans; Neocortex; Nerve Net; Neural Pathways; Neural Stem Cells; Neurogenesis; Neurons; }, + pubmed = {30677429}, + pii = {S0301-0082(18)30136-9}, + doi = {10.1016/j.pneurobio.2019.01.003}, + pmc = {PMC6402587}, + mid = {NIHMS1520766}, + url = {papers/Kast_ProgNeurobiol2019-30677429.pdf}, + nlmuniqueid = {0370121} +} + +@article{McGuire1991, + title = {Targets of horizontal connections in macaque primary visual cortex.}, + author = {McGuire, B A and Gilbert, C D and Rivlin, P K and Wiesel, T N}, + journal = {J Comp Neurol}, + volume = {305}, + number = {3}, + year = {1991}, + month = {Mar}, + pages = {370-92}, + abstract = {Pyramidal neurons within the cerebral cortex are known to make long-range horizontal connections via an extensive axonal collateral system. The synaptic characteristics and specificities of these connections were studied at the ultrastructural level. Two superficial layer pyramidal cells in the primate striate cortex were labeled by intracellular injections with horseradish peroxidase (HRP) and their axon terminals were subsequently examined with the technique of electron microscopic (EM) serial reconstruction. At the light microscopic level both cells showed the characteristic pattern of widespread, clustered axon collaterals. We examined collateral clusters located near the dendritic field (proximal) and approximately 0.5 mm away (distal). The synapses were of the asymmetric/round vesicle variety (type I), and were therefore presumably excitatory. Three-quarters of the postsynaptic targets were the dendritic spines of other pyramidal cells. A few of the axodendritic synapses were with the shafts of pyramidal cells, bringing the proportion of pyramidal cell targets to 80%. The remaining labeled endings were made with the dendritic shafts of smooth stellate cells, which are presumed to be (GABA)ergic inhibitory cells. On the basis of serial reconstruction of a few of these cells and their dendrites, a likely candidate for one target inhibitory cell is the small-medium basket cell. Taken together, this pattern of outputs suggests a mixture of postsynaptic effects mediated by consequence the horizontal connections may well be the substrate for the variety of influences observed between the receptive field center and its surround.}, + keywords = {Animals; Axonal Transport; Axons; Cerebral Cortex; Dendrites; Horseradish Peroxidase; Macaca fascicularis; Microscopy, Electron; Pyramidal Tracts; Synapses; Visual Cortex; }, + pubmed = {1709953}, + doi = {10.1002/cne.903050303}, + url = {papers/McGuire_JCompNeurol1991-1709953.pdf}, + nlmuniqueid = {0406041} +} + +@article{Wilson1973, + title = {A mathematical theory of the functional dynamics of cortical and thalamic nervous tissue.}, + author = {Wilson, H R and Cowan, J D}, + journal = {Kybernetik}, + volume = {13}, + number = {2}, + year = {1973}, + month = {Sep}, + pages = {55-80}, + keywords = {Animals; Cerebral Cortex; Cybernetics; Electrophysiology; Humans; Mathematics; Models, Neurological; Rabbits; Thalamus; }, + pubmed = {4767470}, + doi = {10.1007/BF00288786}, + url = {papers/Wilson_Kybernetik1973-4767470.pdf}, + nlmuniqueid = {7502604} +} + +@article{Rockland1982, + title = {Anatomical binding of intrinsic connections in striate cortex of tree shrews (Tupaia glis).}, + author = {Rockland, K S and Lund, J S and Humphrey, A L}, + journal = {J Comp Neurol}, + volume = {209}, + number = {1}, + year = {1982}, + month = {Jul}, + pages = {41-58}, + abstract = {The intrinsic connectivity of striate cortex was investigated by injecting horseradish peroxidase (HRP) into this area in tree shrews. Such HRP injections demonstrated periodically organized, stripelike connections within area 17. These stripes occur in layers I-IIIA and consist of a small number or retrogradely filled neurons, some clearly pyramidal, together with HRP-labeled axon terminals. HRP-filled axons trunks run between labeled stripes, interconnecting adjacent and distant regions of the stripe pattern. Correlation with Golgi-stained tissue suggests that these stripes are horizontally interconnected by pyramidal neurons with long intracortical axon collaterals (followed for distances over 1 mm from the soma). The HRP-labeled strips measure about 230 micrometers in width, with a center-to-center repeat distance of 450--500 micrometers. They have been mapped over an 8 mm2 area of striate cortex and would thus seem capable of effecting lateral interactions over considerable portions of the retinotopic map. In their dimensions and overall pattern, these anatomical stripes resemble the 2-deoxyglucose (2-DG) bands resulting from visual stimulation of trees shrews with stripes of a single orientation. While the functional role of the HRP-labeled stripes is unclear, their similarities with the 2-DG pattern raise the intriguing possibility that they may be related to orientation selectivity. The striking regularity of these extensive lateral interconnections emphasizes the importance of horizontal intralaminar connections within the cortex.}, + keywords = {Animals; Autoradiography; Brain Mapping; Corpus Callosum; Deoxyglucose; Genetic Variation; Horseradish Peroxidase; Tupaia; Tupaiidae; Visual Cortex; }, + pubmed = {7119173}, + doi = {10.1002/cne.902090105}, + url = {papers/Rockland_JCompNeurol1982-7119173.pdf}, + nlmuniqueid = {0406041} +} + +@article{Mallot1996, + title = {Population networks: a large-scale framework for modelling cortical neural networks.}, + author = {Mallot, H A and Giannakopoulos, F}, + journal = {Biol Cybern}, + volume = {75}, + number = {6}, + year = {1996}, + month = {Dec}, + pages = {441-52}, + abstract = {Artificial neural networks are usually built on rather few elements such as activation functions, learning rules, and the network topology. When modelling the more complex properties of realistic networks, however, a number of higher-level structural principles become important. In this paper we present a theoretical framework for modelling cortical networks at a high level of abstraction. Based on the notion of a population of neurons, this framework can accommodate the common features of cortical architecture, such as lamination, multiple areas and topographic maps, input segregation, and local variations of the frequency of different cell types (e.g., cytochrome oxidase blobs). The framework is meant primarily for the simulation of activation dynamics; it can also be used to model the neural environment of single cells in a multiscale approach.}, + keywords = {Animals; Cerebral Cortex; Cybernetics; Feedback; Humans; Mathematics; Models, Neurological; Nerve Net; Neural Networks, Computer; Thalamus; Visual Cortex; }, + pubmed = {9008348}, + doi = {10.1007/s004220050309}, + url = {papers/Mallot_BiolCybern1996-9008348.pdf}, + nlmuniqueid = {7502533} +} + +@article{Gilbert1983, + title = {Clustered intrinsic connections in cat visual cortex.}, + author = {Gilbert, C D and Wiesel, T N}, + journal = {J Neurosci}, + volume = {3}, + number = {5}, + year = {1983}, + month = {May}, + pages = {1116-33}, + abstract = {The intrinsic connections of the cortex have long been known to run vertically, across the cortical layers. In the present study we have found that individual neurons in the cat primary visual cortex can communicate over suprisingly long distances horizontally (up to 4 mm), in directions parallel to the cortical surface. For all of the cells having widespread projections, the collaterals within their axonal fields were distributed in repeating clusters, with an average periodicity of 1 mm. This pattern of extensive clustered projections has been revealed by combining the techniques of intracellular recording and injection of horseradish peroxidase with three-dimensional computer graphic reconstructions. The clustering pattern was most apparent when the cells were rotated to present a view parallel to the cortical surface. The pattern was observed in more than half of the pyramidal and spiny stellate cells in the cortex and was seen in all cortical layers. In our sample, cells made distant connections within their own layer and/or within another layer. The axon of one cell had clusters covering the same area in two layers, and the clusters in the deeper layer were located under those in the upper layer, suggesting a relationship between the clustering phenomenon and columnar cortical architecture. Some pyramidal cells did not project into the white matter, forming intrinsic connections exclusively. Finally, the axonal fields of all our injected cells were asymmetric, extending for greater distances along one cortical axis than along the orthogonal axis. The axons appeared to cover areas of cortex representing a larger part of the visual field than that covered by the excitatory portion of the cell's own receptive field. These connections may be used to generate larger receptive fields or to produce the inhibitory flanks in other cells' receptive fields.}, + keywords = {Animals; Axonal Transport; Cats; Horseradish Peroxidase; Pyramidal Tracts; Visual Cortex; }, + pubmed = {6188819}, + pmc = {PMC6564507}, + url = {papers/Gilbert_JNeurosci1983-6188819.pdf}, + nlmuniqueid = {8102140} +} + +@article{Destexhe2009, + title = {The Wilson-Cowan model, 36 years later.}, + author = {Destexhe, Alain and Sejnowski, Terrence J}, + journal = {Biol Cybern}, + volume = {101}, + number = {1}, + year = {2009}, + month = {Jul}, + pages = {1-2}, + abstract = {The Wilson-Cowan model of interacting neurons (1973) is one of the most influential papers published in Biological Cybernetics (Kybernetik). This paper and a companion paper published in 1972 have been cited over 1000 times. Rather than focus on the microscopic properties of neurons, Wilson and Cowan analyzed the collective properties of large numbers of neurons using methods from statistical mechanics, based on the mean-field approach. New experimental techniques to measure neuronal activity at the level of large populations are now available to test these models, including optical recording of brain activity with intrinsic signals and voltage sensitive dyes, and new methods for analyzing EEG and MEG. These measurement techniques have revealed patterns of coherent activity that span centimetres of tissue in the cerebral cortex. Here the underlying ideas are reviewed in a historic context.}, + keywords = {Animals; Humans; Models, Neurological; Nerve Net; Neurons; }, + pubmed = {19662434}, + doi = {10.1007/s00422-009-0328-3}, + pmc = {PMC2866289}, + mid = {HHMIMS199370}, + url = {papers/Destexhe_BiolCybern2009-19662434.pdf}, + nlmuniqueid = {7502533} +} + diff --git a/bibd-md.csl b/bibd-md.csl index 26c7317..5a8c5b5 100644 --- a/bibd-md.csl +++ b/bibd-md.csl @@ -212,7 +212,7 @@ - + @@ -274,7 +274,7 @@ - +