Cited by 784Neuroscience and Neuropharmacology ResearchVisual perception and processing mechanismsNeurogenesis and neuroplasticity mechanisms

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Patterned Activity, Synaptic Convergence, and the NMDA Receptor in Developing Visual Pathways

Constantine-Paton, M, Cline, H T, Debski, E·1990·Annual Review of Neuroscience

DOI 10.1146/annurev.ne.13.030190.001021

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Abstract

The brain's default mode network consists of discrete, bilateral and symmetrical cortical areas, in the medial and lateral parietal, medial prefrontal, and medial and lateral temporal cortices of the human, nonhuman primate, cat, and rodent brains. Its ...Read More

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Magnesium gates glutamate-activated channels in mouse central neurones
Nowak, L. M., Bregestovski, P. D., Ascher, P., Herbet, A., & Prochiantz, A. (1984) · Nature · doi:10.1038/307462a0 · Cited by 4,116
Voltage-dependent block by Mg2+ of NMDA responses in spinal cord neurones
Mayer, M. L., Westbrook, G. L., & Guthrie, P. B. (1984) · Nature · doi:10.1038/309261a0 · Cited by 2,941
SINGLE-CELL RESPONSES IN STRIATE CORTEX OF KITTENS DEPRIVED OF VISION IN ONE EYE
Wiesel, T. N., & Hubel, D. H. (1963) · Journal of Neurophysiology · doi:10.1152/jn.1963.26.6.1003 · Cited by 2,628
Plasticity of ocular dominance columns in monkey striate cortex
Hubel, D. H., Wiesel, T. N., LeVay, S., Barlow, H. B., & Gaze, R. M. (1977) · Philosophical transactions of the Royal Society of London. Series B, Biological sciences · doi:10.1098/rstb.1977.0050 · Cited by 1,629
Selective stabilisation of developing synapses as a mechanism for the specification of neuronal networks
Changeux, J.-P., & Danchin, A. (1976) · Nature · doi:10.1038/264705a0 · Cited by 1,448
BINOCULAR INTERACTION IN STRIATE CORTEX OF KITTENS REARED WITH ARTIFICIAL SQUINT
Hubel, D. H., & Wiesel, T. N. (1965) · Journal of Neurophysiology · doi:10.1152/jn.1965.28.6.1041 · Cited by 1,369
The development of ocular dominance columns in normal and visually deprived monkeys
Le Vay, S., Wiesel, T. N., & Hubel, D. H. (1980) · Journal of Comparative Neurology · doi:10.1002/cne.901910102 · Cited by 1,123
Organization of Behavior.
Kaplan, S. J. (1950) · PubMed Central · Cited by 1,050
The Biochemistry of Memory: A New and Specific Hypothesis
LYNCH, G. S., & Baudry, M. (1984) · Science · doi:10.1126/science.6144182 · Cited by 1,041
Long-term potentiation and NMDA receptors in rat visual cortex
Artola, A., & Singer, W. (1987) · Nature · doi:10.1038/330649a0 · Cited by 967

Show all 77 references

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Items 101–200 of 780

LTP and activity-dependent synaptogenesis: the more alike they are, the more different they become
Constantine‐Paton, M., & Cline, H. T. (1998) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(98)80017-2 · Cited by 226
Self-citation
Development of individual geniculocortical arbors in cat striate cortex and effects of binocular impulse blockade
Antonini, A., & Stryker, M. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-08-03549.1993 · Cited by 220
Dual Palmitoylation of NR2 Subunits Regulates NMDA Receptor Trafficking
Hayashi, T., Thomas, G. M., & Huganir, R. L. (2009) · Neuron · doi:10.1016/j.neuron.2009.08.017 · Cited by 220
Thalamic Relay of Spontaneous Retinal Activity Prior to Vision
MOONEY, R. D., Penn, A. A., Gallego, R., & Shatz, C. J. (1996) · Neuron · doi:10.1016/s0896-6273(00)80218-4 · Cited by 218
Promotion of Dendritic Growth by CPG15, an Activity-Induced Signaling Molecule
Nedivi, E., Wu, G., & Cline, H. T. (1998) · Science · doi:10.1126/science.281.5384.1863 · Cited by 210
Self-citation
Spine Loss and Other Persistent Alterations of Hippocampal Pyramidal Cell Dendrites in a Model of Early-Onset Epilepsy
Jiang, M., Lee, C. L., Smith, K. L., & Swann, J. W. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-20-08356.1998 · Cited by 207
SynGAP regulates spine formation
Vazquez, L. E., Chen, H.-J., Sokolova, I., Knuesel, I., & Kennedy, M. B. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.3213-04.2004 · Cited by 203
Ionotropic Glutamate Receptors & CNS Disorders
Bowie, D. (2008) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/187152708784083821 · Cited by 207
A developmental handshake: Neuronal control of ionic currents and their control of neuronal differentiation
Spitzer, N. C. (1991) · Journal of Neurobiology · doi:10.1002/neu.480220702 · Cited by 202
Neuronal activity during development: permissive or instructive?
Crair, M. C. (1999) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(99)80011-7 · Cited by 203
Glutamate receptor blockade at cortical synapses disrupts development of thalamocortical and columnar organization in somatosensory cortex.
Fox, K. D., Schlaggar, B. L., Glazewski, S., & O'Leary, D. D. M. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.11.5584 · Cited by 198
Synapse elimination accompanies functional plasticity in hippocampal neurons
Bastrikova, N., Gardner, G. A., Reece, J. M., Jeromin, A., & Dudek, S. M. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800027105 · Cited by 202
Characterization of GABAergic neurons in hippocampal cell cultures
Benson, D. L., Watkins, F. H., Steward, O., & Banker, G. (1994) · Journal of Neurocytology · doi:10.1007/bf01188497 · Cited by 195
NMDA receptor agonist and antagonists alter retinal ganglion cell arbor structure in the developing frog retinotectal projection
Cline, H., & Constantine‐Paton, M. (1990) · Journal of Neuroscience · doi:10.1523/jneurosci.10-04-01197.1990 · Cited by 190
Self-citation
Evidence for Direct Protein Kinase-C Mediated Modulation of N-Methyl-d-aspartate Receptor Current
Liao, G.-Y., Wagner, D. A., Hsu, M. H., & Leonard, J. P. (2001) · Molecular Pharmacology · doi:10.1124/mol.59.5.960 · Cited by 192
Depolarizing GABAergic Conductances Regulate the Balance of Excitation to Inhibition in the Developing Retinotectal Circuit In Vivo
Akerman, C. J., & Cline, H. T. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0319-06.2006 · Cited by 197
Self-citation
Role of pro-brain-derived neurotrophic factor (proBDNF) to mature BDNF conversion in activity-dependent competition at developing neuromuscular synapses
Je, H. S., Yang, F., Ji, Y., Nagappan, G., Hempstead, B. L., & Lu, B. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1207767109 · Cited by 188
Developmentally Regulated Spontaneous Activity in the Embryonic Chick Retina
Wong, W. T., Sanes, J. R., & Wong, R. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-21-08839.1998 · Cited by 189
Developmental changes in NMDA and non-NMDA receptor-mediated synaptic potentials in rat neocortex
Burgard, E. C., & Hablitz, J. J. (1993) · Journal of Neurophysiology · doi:10.1152/jn.1993.69.1.230 · Cited by 187
Neuroserpin, an axonally secreted serine protease inhibitor.
Osterwalder, T., Contartese, J., Stoeckli, E. T., Kuhn, T. B., & Sonderegger, P. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00657.x · Cited by 184
Neurite outgrowth from progeny of epidermal growth factor-responsive hippocampal stem cells is significantly less robust than from fetal hippocampal cells following grafting onto organotypic hippocampal slice cultures: Effect of brain-derived neurotrophic factor
Shetty, A. K., & Turner, D. A. (1999) · Journal of Neurobiology · doi:10.1002/(sici)1097-4695(19990215)38:3 · Cited by 38
Self-citation
Activity- and Ca2+-Dependent Modulation of Surface Expression of Brain-Derived Neurotrophic Factor Receptors in Hippocampal Neurons
Du, J., Feng, L., Yang, F., & Lu, B. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.150.6.1423 · Cited by 178
Regulation of motor neuron dendrite growth by NMDA receptor activation
Kalb, R. G. (1994) · Development · doi:10.1242/dev.120.11.3063 · Cited by 177
Effects of experience and juvenile hormone on the organization of the mushroom bodies of honey bees
Withers, G. S., Fahrbach, S. E., & Robinson, G. E. (1995) · Journal of Neurobiology · doi:10.1002/neu.480260111 · Cited by 175
Glutamate receptor phosphorylation and synaptic plasticity.
Roche, K., Tingley, W., & Huganir, R. (1994) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(94)90100-7 · Cited by 179
Involvement of Serotonin in Developmental Plasticity of Kitten Visual Cortex
Gu, Q., & Singer, W. (1995) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1995.tb01104.x · Cited by 173
Nitric oxide mediates activity-dependent synaptic suppression at developing neuromuscular synapses
Wang, T., Xie, Z., & Lu, B. (1995) · Nature · doi:10.1038/374262a0 · Cited by 173
Uncoupling Dendrite Growth and Patterning: Single-Cell Knockout Analysis of NMDA Receptor 2B
Espinosa, J. S., Wheeler, D. G., Tsien, R. W., & Luo, L. (2009) · Neuron · doi:10.1016/j.neuron.2009.03.006 · Cited by 171
The contribution of NMDA and non-NMDA receptors to fast and slow transmission of sensory information in the rat SI barrel cortex
Armstrong‐James, M., Welker, E., & Callahan, C. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-05-02149.1993 · Cited by 171
Developmental regulation of cognitive abilities: Modified composition of a molecular switch turns on associative learning
Dumas, T. C. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2005.08.002 · Cited by 182
Influence of the NR3A subunit on NMDA receptor functions
Henson, M. A., Roberts, A. C., Pérez‐Otaño, I., & Philpot, B. D. (2010) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2010.01.004 · Cited by 195
Differential Regional Expression and Ultrastructural Localization of α-Actinin-2, a Putative NMDA Receptor-Anchoring Protein, in Rat Brain
Wyszynski, M., Kharazia, V., Shanghvi, R., Rao, A., Beggs, A. H., Craig, A. M., Weinberg, R., & Sheng, M. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-04-01383.1998 · Cited by 168
Are Adult Learning Mechanisms Also Used for Development?
Kandel, E. R., & O’Dell, T. J. (1992) · Science · doi:10.1126/science.1411522 · Cited by 168
Molecules, maps and synapse specificity
Benson, D. L., Colman, D., & Huntley, G. W. (2001) · Nature reviews. Neuroscience · doi:10.1038/35104078 · Cited by 170
Spike Timing-Dependent LTP/LTD Mediates Visual Experience-Dependent Plasticity in a Developing Retinotectal System
Mu, Y., & Poo, M.-M. (2006) · Neuron · doi:10.1016/j.neuron.2006.03.009 · Cited by 164
Distribution and synaptic localization of immunocytochemically identified NMDA receptor subunit proteins in sensory-motor and visual cortices of monkey and human
Huntley, G., Vickers, J., Janssen, W., Brose, N., Heinemann, S., & Morrison, J. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-06-03603.1994 · Cited by 161
Correlation of nitric oxide synthase expression with changing patterns of axonal projections in the developing visual system
Williams, C., Nordquist, D. T., & McLoon, S. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-03-01746.1994 · Cited by 161
Infantile amnesia reflects a developmental critical period for hippocampal learning
Travaglia, A., Bisaz, R., Sweet, E. S., Blitzer, R. D., & Alberini, C. M. (2016) · Nature Neuroscience · doi:10.1038/nn.4348 · Cited by 168
Synchronization of GABAergic interneuronal network in CA3 subfield of neonatal rat hippocampal slices.
Khazipov, R., Leinekugel, X., Khalilov, I., Gaïarsa, J., & Ben‐Ari, Y. (1997) · The Journal of Physiology · doi:10.1113/jphysiol.1997.sp021900 · Cited by 164
The developmental onset of NMDA receptor-channel activity during neuronal migration
Rossi, D. J., & Slater, N. T. (1993) · Neuropharmacology · doi:10.1016/0028-3908(93)90018-x · Cited by 157
Homeostatic Regulation of Intrinsic Excitability and Synaptic Transmission in a Developing Visual Circuit
Pratt, K. G., & Aizenman, C. D. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1738-07.2007 · Cited by 161
Activity-Dependent Synaptic Competition in Vitro: Heterosynaptic Suppression of Developing Synapses
Lo, Y.-J., & Poo, M. (1991) · Science · doi:10.1126/science.1658939 · Cited by 155
Astrocyte subtypes in the rat olfactory bulb: Morphological heterogeneity and differential laminar distribution
Bailey, M. S., & Shipley, M. T. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903280405 · Cited by 153
The binaural auditory pathway: excitatory amino acid receptors mediate dual timecourse excitatory postsynaptic currents in the rat medial nucleus of the trapezoid body
Forsythe, I. D., & Barnes‐Davies, M. (1993) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1993.0022 · Cited by 152
Spatial Signaling in the Development and Function of Neural Connections
Montague, P. R., Gally, J. A., & Edelman, G. M. (1991) · Cerebral Cortex · doi:10.1093/cercor/1.3.199 · Cited by 150
Activity-Dependent Matching of Excitatory and Inhibitory Inputs during Refinement of Visual Receptive Fields
Tao, H. W., & Poo, M. (2005) · Neuron · doi:10.1016/j.neuron.2005.01.046 · Cited by 150
Activity-dependent plasticity in the visual systems of frogs and fish.
Cline, H. (1991) · Trends in Neurosciences · doi:10.1016/0166-2236(91)90071-2 · Cited by 159
Self-citation
BDNF in the development of the visual system of Xenopus
Cohen‐Cory, S., & Fraser, S. E. (1994) · Neuron · doi:10.1016/0896-6273(94)90328-x · Cited by 145
Reduced spontaneous activity of mice defective in the ε4 subunit of the NMDA receptor channel
Ikeda, K., Araki, K., Takayama, C., Inoue, Y., Yagi, T., Aizawa, S., & Mishina, M. (1995) · Molecular Brain Research · doi:10.1016/0169-328x(95)00107-4 · Cited by 147
Neuronal coupling in the developing mammalian retina
Penn, A. A., Wong, R., & Shatz, C. J. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-06-03805.1994 · Cited by 148
NGF and BDNF are differentially modulated by visual experience in the developing geniculocortical pathway
Schoups, A. A., Elliott, R. C., Friedman, W., & Black, I. B. (1995) · Developmental Brain Research · doi:10.1016/0165-3806(95)00043-d · Cited by 145
BDNF Modulates, But Does Not Mediate, Activity-Dependent Branching and Remodeling of Optic Axon ArborsIn Vivo
Cohen‐Cory, S. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-22-09996.1999 · Cited by 146
Gene regulation by patterned electrical activity during neural and skeletal muscle development
Buonanno, A., & Fields, R. D. (1999) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(99)80014-2 · Cited by 143
Development of neural selectivity for birdsong during vocal learning
Volman, S. F. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-11-04737.1993 · Cited by 144
Dynamics of Retinal Waves Are Controlled by Cyclic AMP
Stellwagen, D., Shatz, C. J., & Feller, M. B. (1999) · Neuron · doi:10.1016/s0896-6273(00)81121-6 · Cited by 145
Spontaneous Ca2+ spikes and waves in embryonic neurons: signaling systems for differentiation
Spitzer, N. C. (1994) · Trends in Neurosciences · doi:10.1016/0166-2236(94)90120-1 · Cited by 139
Neuronal activity differentially regulates NMDA receptor subunit expression in cerebellar granule cells
Vallano, M. L., Lambolez, B., Audinat, É., & Rossier, J. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-02-00631.1996 · Cited by 135
Suppression of NMDA Receptor Function Using Antisense DNA Blocks Ocular Dominance Plasticity While Preserving Visual Responses
Roberts, E. B., Meredith, M. A., & Ramoa, A. S. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.3.1021 · Cited by 137
Modification of NMDA Receptor Channels and Synaptic Transmission by Targeted Disruption of the NR2C Gene
Ebralidze, A. K., Rossi, D. J., Tonegawa, S., & Slater, N. T. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-16-05014.1996 · Cited by 136
Colocalization of ionotropic glutamate receptor subunits with NADPH-diaphorase-containing neurons in the rat mesopontine tegmentum
Inglis, W. L., & Semba, K. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960422)368:1 · Cited by 49
Activity-regulated genes as mediators of neural circuit plasticity
Leslie, J. H., & Nedivi, E. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.05.002 · Cited by 136
Physiological effects of sustained blockade of excitatory synaptic transmission on spontaneously active developing neuronal networks—an inquiry into the reciprocal linkage between intrinsic biorhythms and neuroplasticity in early ontogeny
Corner, M. A., van Pelt, J., Wolters, P. S., Baker, R. E., & Nuytinck, R. H. (2002) · Neuroscience & Biobehavioral Reviews · doi:10.1016/s0149-7634(01)00062-8 · Cited by 133
Developmental analysis of hippocampal mossy fiber outgrowth in a mutant mouse with inherited spike-wave seizures
Qiao, X., & Noebels, J. L. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-11-04622.1993 · Cited by 134
Development of the retina and optic pathway
Reese, B. E. (2010) · Vision Research · doi:10.1016/j.visres.2010.07.010 · Cited by 140
Pro-BDNF–induced synaptic depression and retraction at developing neuromuscular synapses
Yang, F., Je, H.-S., Ji, Y., Nagappan, G., Hempstead, B., & Lu, B. (2009) · Journal of Cell Biology · doi:10.1083/jcb.200811147 · Cited by 130
Activity-dependent regulation of synaptic clustering in a hippocampal culture system
Kavalali, E. T., Klingauf, J., & Tsien, R. W. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.22.12893 · Cited by 129
Hebbian Depression of Isolated Neuromuscular Synapses in Vitro
Dan, Y., & Poo, M. (1992) · Science · doi:10.1126/science.1317971 · Cited by 128
Influence of spontaneous activity and visual experience on developing retinal receptive fields
Sernagor, E., & Grzywacz, N. M. (1996) · Current Biology · doi:10.1016/s0960-9822(96)00755-5 · Cited by 127
Nature versus nurture revisited: an old idea with a new twist
Krubitzer, L. A., & Kahn, D. M. (2003) · Progress in Neurobiology · doi:10.1016/s0301-0082(03)00088-1 · Cited by 126
Rapid remodeling of retinal arbors in the tectum with and without blockade of synaptic transmission
O’Rourke, N. A., Cline, H. T., & Fraser, S. E. (1994) · Neuron · doi:10.1016/0896-6273(94)90343-3 · Cited by 125
Self-citation
Effects of limb exercise after spinal cord injury on motor neuron dendrite structure
Gazula, V., Roberts, M., Luzzio, C. C., Jawad, A. F., & Kalb, R. G. (2004) · The Journal of Comparative Neurology · doi:10.1002/cne.20204 · Cited by 125
Diverse Distribution and Function of Fibrous Microtubule-Associated Proteins in the Nervous System
Schoenfeld, T. A., & Obar, R. A. (1994) · International review of cytology · doi:10.1016/s0074-7696(08)62631-5 · Cited by 128
A set of genes expressed in response to light in the adult cerebral cortex and regulated during development.
Nedivi, E., Fieldust, S., Theill, L. E., & Hevron, D. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.5.2048 · Cited by 124
Direct Participation of Starburst Amacrine Cells in Spontaneous Rhythmic Activities in the Developing Mammalian Retina
Zhou, Z. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-11-04155.1998 · Cited by 123
Brief visual experience induces immediate early gene expression in the cat visual cortex.
Rosen, K. M., McCormack, M., Villa‐Komaroff, L., & Mower, G. D. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.12.5437 · Cited by 124
D-serine as a gliotransmitter and its roles in brain development and disease
Horn, M. R. V., Sild, M., & Ruthazer, E. S. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00039 · Cited by 126
Sensorimotor stimulation to improve locomotor recovery after spinal cord injury
Muir, G. D., & Steeves, J. D. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)10068-0 · Cited by 122
Postsynaptic Calcium/Calmodulin-Dependent Protein Kinase II Is Required to Limit Elaboration of Presynaptic and Postsynaptic Neuronal Arbors
Zou, D., & Cline, H. T. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-20-08909.1999 · Cited by 124
Self-citation
Two-Stage, Input-Specific Synaptic Maturation in a Nucleus Essential for Vocal Production in the Zebra Finch
Stark, L. L., & Perkel, D. J. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-20-09107.1999 · Cited by 117
The development of synaptic function and integration in the central auditory system
Sanes, D. H. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-06-02627.1993 · Cited by 120
Pyramidal neurons in layer 5 of the rat visual cortex. II. Development of electrophysiological properties
Kasper, E. M., Larkman, A. U., Lübke, J. H. R., & Blakemore, C. B. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903390403 · Cited by 119
Activity-dependent mapping in the retinotectal projection
Debski, E. A., & Cline, H. T. (2002) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(02)00295-7 · Cited by 116
Self-citation
Control of Topographic Retinal Axon Branching by Inhibitory Membrane-Bound Molecules
Roskies, A. L., & O’Leary, D. D. M. (1994) · Science · doi:10.1126/science.8047886 · Cited by 119
Thalamocortical Assemblies
Alain Destexhe, A., & Sejknowski, T. (2023) · doi:10.1093/oso/9780198864998.001.0001 · Cited by 115
Running Changes the Brain: the Long and the Short of It
Vivar, C., & van Praag, H. (2017) · Physiology · doi:10.1152/physiol.00017.2017 · Cited by 114
Coordinated Transitions in Neurotransmitter Systems for the Initiation and Propagation of Spontaneous Retinal Waves
Zhou, Z., & Zhao, D. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-17-06570.2000 · Cited by 113
Linear pattern dynamics in nonlinear threshold systems
Rundle, J. B., Klein, W., Tiampo, K. F., & Gross, S. (2000) · Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics · doi:10.1103/physreve.61.2418 · Cited by 113
Learning from NMDA Receptor Trafficking: Clues to the Development and Maturation of Glutamatergic Synapses
Pérez‐Otaño, I., & Ehlers, M. (2004) · Neurosignals · doi:10.1159/000077524 · Cited by 118
A Role for Glial Cells in Activity-Dependent Development of the Vertebrate Nervous System
Fields, R. D., & Nelson, P. G. (1992) · International review of neurobiology · doi:10.1016/s0074-7742(08)60098-7 · Cited by 113
Enhancement of transmission at the developing retinogeniculate synapse
MOONEY, R. D., Madison, D. V., & Shatz, C. J. (1993) · Neuron · doi:10.1016/0896-6273(93)90198-z · Cited by 112
Axon regeneration and exercise‐dependent plasticity after spinal cord injury
Houlé, J. D., & Côté, M. (2013) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12052 · Cited by 111
Face Image Analysis by Unsupervised Learning
Bartlett, M. S. (2001) · Springer eBooks · doi:10.1007/978-1-4615-1637-8 · Cited by 111
Developmental changes in EPSC quantal size and quantal content at a central glutamatergic synapse in rat
Bellingham, M., Lim, R., & Walmsley, B. (1998) · Journal of Physiology · doi:10.1111/j.1469-7793.1998.861bg.x · Cited by 112
Ocular dominance column development: strabismus changes the spacing of adjacent columns in cat visual cortex
Löwel, S. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-12-07451.1994 · Cited by 109
Rapid BDNF-induced retrograde synaptic modification in a developing retinotectal system
Du, J., & Poo, M. (2004) · Nature · doi:10.1038/nature02618 · Cited by 109
Molecular evidence for nitric oxide-mediated motor neuron development
Kalb, R. G., & Agostini, J. V. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90107-q · Cited by 108
Relationships between dendritic fields and functional architecture in striate cortex of normal and visually deprived cats
Kossel, A. H., Löwel, S., & Bolz, J. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-05-03913.1995 · Cited by 107
Visual stimuli–induced LTD of GABAergic synapses mediated by presynaptic NMDA receptors
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Authors: Constantine-Paton, M., Cline, H. T., & Debski, E.
ORCID: Cline, H T
Venue: Annual Review of Neuroscience
Publisher: Annual Reviews
Published: 1990-03
Volume: 13
Issue: 1
Pages: 129-154
ISSN: 0147-006X (ISSN-L)
1545-4126
DOI: 10.1146/annurev.ne.13.030190.001021
OpenAlex: W1986240433
Cited by: 784
References: 77
Citations by year: 2025: 3 · 2024: 2 · 2023: 22 · 2022: 3 · 2021: 4 · 2020: 6 · 2019: 7 · 2018: 2 · 2017: 5 · 2016: 9 · 2015: 10 · 2014: 7 · 2013: 11 · 2012: 13
FWCI: 16.15
Type: journal article
Language: en
Open access: closed
Locations: Annual Review of Neuroscience (publishedVersion)
PubMed (publishedVersion)
Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) (acceptedVersion)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Keywords: NMDA receptor, synaptic convergence, visual pathway development, default mode network, visual cortex development
MeSH terms: Animals, Geniculate Bodies, Functional Laterality, Neuronal Plasticity, Retina, Visual Cortex, Visual Pathways

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Patterned Activity, Synaptic Convergence, and the NMDA Receptor in Developing Visual Pathways

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