Cited by 691Visual perception and processing mechanismsNeurogenesis and neuroplasticity mechanismsNeuroscience and Neuropharmacology Research

The DOI matches its Crossref record; 32 of the 32 references it cites were found in a registry or an index.

Ocular dominance in layer IV of the cat's visual cortex and the effects of monocular deprivation.

Open access

Shatz, C J, Stryker, M P·1978·The Journal of Physiology

DOI 10.1113/jphysiol.1978.sp012421PMC PMC1282696

Open this paper in CoChat — free account

Abstract

1. The relation between the physiological pattern of ocular dominance and the anatomical distribution of geniculocortical afferents serving each eye was studied in layer IV of the primary visual cortex of normal and monocularly deprived cats. 2. One eye was injected with radioactive label. After allowing sufficient time for transeuronal transport, micro‐electrode recordings were made, and the geniculocoritcal afferents serving the injected eye were located autoradiographically. 3. In layer IV of normal cats, cell were clustered according to eye preference, and fewer cells were binocularly driven than in other layers. Points of transition between groups of cells dominated by one eye and those dominated by the other were marked with electrolytic lesions. A good correspondence was found between the location of cells dominated by the injected eye and the patches of radioactively labelled geniculocortical afferents. 4. Following prolonged early monocular deprivation, the patches of geniculocortical afferents in layer IV serving the deprived eye were smaller, and those serving the non‐deprived eye larger, than normal. Again there was a coincidence between the patches of radioactively labelled afferents and the location of cells dominated by the injected eye. 5. The deprived eye was found to dominate a substantial fraction (22%) of cortical cells in the fourth layer. In other cortical layers, only 7% of the cells were dominated by the deprived eye. 6. These findings suggest that the thalamocortical projection is physically rearranged as a consequence of monocular deprivation, as has been demonstrated for layer IVc of the monkey's visual cortex (Hubel, Wiesel & Le Vay, 1977).

Integrity signals

Registry

Crossref · 10.1113/jphysiol.1978.sp012421

Cites

32 of 32 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

We couldn’t retrieve this paper’s full text, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Receptive fields, binocular interaction and functional architecture in the cat’s visual cortex
Hubel, D. H., & Wiesel, T. N. (1962) · The Journal of Physiology · doi:10.1113/jphysiol.1962.sp006837 · Cited by 13,680
Receptive fields and functional architecture of monkey striate cortex
Hubel, D. H., & Wiesel, T. N. (1968) · The Journal of Physiology · doi:10.1113/jphysiol.1968.sp008455 · Cited by 6,685
The period of susceptibility to the physiological effects of unilateral eye closure in kittens
Hubel, D. H., & Wiesel, T. N. (1970) · The Journal of Physiology · doi:10.1113/jphysiol.1970.sp009022 · Cited by 3,030
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
RECEPTIVE FIELDS AND FUNCTIONAL ARCHITECTURE IN TWO NONSTRIATE VISUAL AREAS (18 AND 19) OF THE CAT
Hubel, D. H., & Wiesel, T. N. (1965) · Journal of Neurophysiology · doi:10.1152/jn.1965.28.2.229 · Cited by 2,615
COMPARISON OF THE EFFECTS OF UNILATERAL AND BILATERAL EYE CLOSURE ON CORTICAL UNIT RESPONSES IN KITTENS
Wiesel, T. N., & Hubel, D. H. (1965) · Journal of Neurophysiology · doi:10.1152/jn.1965.28.6.1029 · Cited by 1,598
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
Laminar and columnar distribution of geniculo‐cortical fibers in the macaque monkey
Hubel, D. H., & Wiesel, T. N. (1972) · The Journal of Comparative Neurology · doi:10.1002/cne.901460402 · Cited by 945
Integrative action in the cat's lateral geniculate body
Hubel, D. H., & Wiesel, T. N. (1961) · The Journal of Physiology · doi:10.1113/jphysiol.1961.sp006635 · Cited by 789
Prenatal genesis of connections subserving ocular dominance in the rhesus monkey
Rakic, P. (1976) · Nature · doi:10.1038/261467a0 · Cited by 677

Flagged first, then by citations

Show all 32 references

Sorted by citations

Synaptic Activity and the Construction of Cortical Circuits
Katz, L. C., & Shatz, C. J. (1996) · Science · doi:10.1126/science.274.5290.1133 · Cited by 3,048
Self-citation
Critical period plasticity in local cortical circuits
Hensch, T. K. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1787 · Cited by 2,323
Sensitive periods in the development of the brain and behavior
Knudsen, E. I. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/0898929042304796 · Cited by 1,842
Developmental mechanisms that generate precise patterns of neuronal connectivity
Goodman, C. S., & Shatz, C. J. (1993) · Cell · doi:10.1016/s0092-8674(05)80030-3 · Cited by 1,425
Self-citation
Long-term dendritic spine stability in the adult cortex
Grutzendler, J., Kasthuri, N., & Gan, W.-B. (2002) · Nature · doi:10.1038/nature01276 · Cited by 1,198
Stably maintained dendritic spines are associated with lifelong memories
Yang, G., Pan, F., & Gan, W.-B. (2009) · Nature · doi:10.1038/nature08577 · Cited by 1,182
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
Local GABA Circuit Control of Experience-Dependent Plasticity in Developing Visual Cortex
Hensch, T. K., Fagiolini, M., Mataga, N., Stryker, M. P., Baekkeskov, S., & Kash, S. F. (1998) · Science · doi:10.1126/science.282.5393.1504 · Cited by 910
Self-citation
Experience-Dependent Plasticity of Binocular Responses in the Primary Visual Cortex of the Mouse
Gordon, J. A., & Stryker, M. P. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-10-03274.1996 · Cited by 856
Self-citation
The neural basis of cognitive development: A constructivist manifesto
Quartz, S. R., & B, T. J. S. A. (1997) · Behavioral and Brain Sciences · doi:10.1017/s0140525x97001581 · Cited by 865
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 · Cited by 784
Impulse activity and the patterning of connections during cns development
Shatz, C. J. (1990) · Neuron · doi:10.1016/0896-6273(90)90333-b · Cited by 766
Self-citation
Patterning and plasticity of the cerebral cortex
Sur, M., & Rubenstein, J. L. R. (2005) · Science · doi:10.1126/science.1112070 · Cited by 677
Binocular impulse blockade prevents the formation of ocular dominance columns in cat visual cortex
Stryker, M., & Harris, W. (1986) · The Journal of Neuroscience · doi:10.1523/jneurosci.06-08-02117.1986 · Cited by 687
Self-citation
Neural Mechanisms of Orientation Selectivity in the Visual Cortex
Ferster, D., & Miller, K. D. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.441 · Cited by 665
Ocular dominance columns and their development in layer IV of the cat's visual cortex: A quantitative study
LeVay, S., Stryker, M. P., & Shatz, C. J. (1978) · The Journal of Comparative Neurology · doi:10.1002/cne.901790113 · Cited by 658
Self-citation
Ocular Dominance Column Development: Analysis and Simulation
Miller, K. D., Keller, J. B., & Stryker, M. P. (1989) · Science · doi:10.1126/science.2762813 · Cited by 645
Self-citation
Removing brakes on adult brain plasticity: From molecular to behavioral interventions
Bavelier, D., Levi, D. M., Li, R. W., Dan, Y., & Hensch, T. K. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4812-10.2010 · Cited by 589
Inhibition of Ocular Dominance Column Formation by Infusion of NT-4/5 or BDNF
Cabelli, R. J., Hohn, A., & Shatz, C. J. (1995) · Science · doi:10.1126/science.7886458 · Cited by 566
Self-citation
Retinal waves and visual system development
Wong, R. O. L. (1999) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.22.1.29 · Cited by 544
Rapid Remodeling of Axonal Arbors in the Visual Cortex
Antonini, A., & Stryker, M. P. (1993) · Science · doi:10.1126/science.8511592 · Cited by 559
Self-citation
Immune proteins in brain development and synaptic plasticity
Boulanger, L. M. (2009) · Neuron · doi:10.1016/j.neuron.2009.09.001 · Cited by 555
Induction of visual orientation modules in auditory cortex
Sharma, J., Angelucci, A., & Sur, M. (2000) · Nature · doi:10.1038/35009043 · Cited by 551
A Physiological Basis for a Theory of Synapse Modification
Bear, M. F., Cooper, L. N., & Ebner, F. F. (1987) · Science · doi:10.1126/science.3037696 · Cited by 528
A role for synaptic plasticity in the adolescent development of executive function
Selemon, L. D. (2013) · Translational Psychiatry · doi:10.1038/tp.2013.7 · Cited by 439
“of plasticity during postnatal development that permits rewiring in response to altered sensory environments.(43,46,47) It is noteworthy that critical periods for sensory plasticity occur in the same preadolescent period in which remodeling of connectivity occurs.”
Background
Long-term sensory deprivation prevents dendritic spine loss in primary somatosensory cortex
Zuo, Y., Yang, G., Kwon, E., & Gan, W.-B. (2005) · Nature · doi:10.1038/nature03715 · Cited by 436
Selective reconfiguration of layer 4 visual cortical circuitry by visual deprivation
Maffei, A., Nelson, S. B., & Turrigiano, G. G. (2004) · Nature Neuroscience · doi:10.1038/nn1351 · Cited by 415
Developmental Remodeling of the Retinogeniculate Synapse
Chen, C., & Regehr, W. G. (2000) · Neuron · doi:10.1016/s0896-6273(00)00166-5 · Cited by 439
Hierarchical and parallel mechanisms in the organization of visual cortex
Stone, J., Dreher, B., & Leventhal, A. G. (1979) · Brain Research Reviews · doi:10.1016/0165-0173(79)90010-9 · Cited by 402
Critical-Period Plasticity in the Visual Cortex
Levelt, C. N., & Hübener, M. (2012) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113813 · Cited by 402
MECHANISMS OF VERTEBRATE SYNAPTOGENESIS
Waites, C. L., Craig, A. M., & Garner, C. C. (2005) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144336 · Cited by 483
The development of topography in the visual cortex: a review of models
Swindale, N. V. (1996) · Network Computation in Neural Systems · doi:10.1088/0954-898x/7/2/002 · Cited by 393
Experience-dependent pruning of dendritic spines in visual cortex by tissue plasminogen activator
Mataga, N., Mizuguchi, Y., & Hensch, T. K. (2004) · Neuron · doi:10.1016/j.neuron.2004.11.028 · Cited by 371
Critical Period Window for Spectral Tuning Defined in the Primary Auditory Cortex (A1) in the Rat
de Villers‐Sidani, E., Chang, E. F., Bao, S., & Merzenich, M. M. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3227-06.2007 · Cited by 378
Spatial Relationships among Three Columnar Systems in Cat Area 17
Hübener, M., Shoham, D., Grinvald, A., & Bonhoeffer, T. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-23-09270.1997 · Cited by 372
Anatomical Correlates of Functional Plasticity in Mouse Visual Cortex
Antonini, A., Fagiolini, M., & Stryker, M. P. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-11-04388.1999 · Cited by 337
Self-citation
Massive restructuring of neuronal circuits during functional reorganization of adult visual cortex
Keck, T., Mrsic-Flogel, T. D., Vaz Afonso, M., Eysel, U. T., Bonhoeffer, T., & Hübener, M. (2008) · Nature Neuroscience · doi:10.1038/nn.2181 · Cited by 315
Cognitive Training in Mental Disorders: Update and Future Directions
Keshavan, M. S., Vinogradov, S., Rumsey, J. M., Sherrill, J. T., & Wagner, A. (2014) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2013.13081075 · Cited by 315
Physiological Correlates of Perceptual Learning in Monkey V1 and V2
Ghose, G. M., Yang, T., & Maunsell, J. H. R. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00690.2001 · Cited by 310
Can regenerating axons recapitulate developmental guidance during recovery from spinal cord injury?
Harel, N. Y., & Strittmatter, S. M. (2006) · Nature reviews. Neuroscience · doi:10.1038/nrn1957 · Cited by 304
Mechanisms of Synapse Assembly and Disassembly
Goda, Y., & Davis, G. W. (2003) · Neuron · doi:10.1016/s0896-6273(03)00608-1 · Cited by 305
Dendritic Spine Dynamics Are Regulated by Monocular Deprivation and Extracellular Matrix Degradation
Oray, S., Majewska, A., & Sur, M. (2004) · Neuron · doi:10.1016/j.neuron.2004.12.001 · Cited by 296
Critical Periods and Amblyopia
Daw, N. W. (1998) · Archives of Ophthalmology · doi:10.1001/archopht.116.4.502 · Cited by 293
Projection patterns of individual X‐ and Y‐cell axons from the lateral geniculate nucleus to cortical area 17 in the cat
Humphrey, A. L., Sur, M., Uhlrich, D. J., & Sherman, S. M. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902330203 · Cited by 293
A functional role for REM sleep in brain maturation.
Marks, G. A., Shaffery, J., Oksenberg, A., Speciale, S., & Roffwarg, H. (1995) · Behavioural Brain Research · doi:10.1016/0166-4328(95)00018-o · Cited by 276
Profile of the sensitive period for monocular deprivation in kittens
Olson, C. R., & Freeman, R. D. (1980) · Experimental Brain Research · doi:10.1007/bf00237065 · Cited by 277
Is hemiplegic cerebral palsy equivalent to amblyopia of the corticospinal system?
Eyre, J. A., Smith, M. J., Dabydeen, L., Clowry, G. J., Petacchi, E., Battini, R., Guzzetta, A., & Cioni, G. (2007) · Annals of Neurology · doi:10.1002/ana.21108 · Cited by 266
Neural plasticity without postsynaptic action potentials: less-active inputs become dominant when kitten visual cortical cells are pharmacologically inhibited.
Reiter, H. O., & Stryker, M. P. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.10.3623 · Cited by 266
Self-citation
Stages of Synapse Development Defined by Dependence on F-Actin
Zhang, W., & Benson, D. L. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-14-05169.2001 · Cited by 262
Critical periods in amblyopia
Hensch, T. K., & Quinlan, E. M. (2018) · Visual Neuroscience · doi:10.1017/s0952523817000219 · Cited by 271
Nerve growth factor (NGF) prevents the shift in ocular dominance distribution of visual cortical neurons in monocularly deprived rats
Maffei, L., Berardi, N., Domenici, L., Parisi, V, & Pizzorusso, T. (1992) · The Journal of Neuroscience · doi:10.1523/jneurosci.12-12-04651.1992 · Cited by 252
Functional Considerations of the Operation of GABAergic Inhibitory Processes in the Visual Cortex
Sillito, A. M. (1984) · Cerebral cortex · doi:10.1007/978-1-4615-6610-6_4 · Cited by 251
Involvement of Subplate Neurons in the Formation of Ocular Dominance Columns
Ghosh, A., & Shatz, C. J. (1992) · Science · doi:10.1126/science.1542795 · Cited by 249
Self-citation
Subplate Neurons Regulate Maturation of Cortical Inhibition and Outcome of Ocular Dominance Plasticity
Kanold, P. O., & Shatz, C. J. (2006) · Neuron · doi:10.1016/j.neuron.2006.07.008 · Cited by 245
Self-citation
Computational Maps in the Visual Cortex
Miikkulainen, R., Sirosh, J., Choe, Y., & Bednar, J. A. (2005) · Springer eBooks · doi:10.1007/0-387-28806-6 · Cited by 247
A model for the formation of ocular dominance stripes
Swindale, N. V. (1980) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1980.0051 · Cited by 244
The critical period for ocular dominance plasticity in the Ferret's visual cortex
Issa, N. P., Trachtenberg, J. T., Chapman, B., Zahs, K. R., & Stryker, M. P. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-16-06965.1999 · Cited by 243
Self-citation
Rapid Extragranular Plasticity in the Absence of Thalamocortical Plasticity in the Developing Primary Visual Cortex
Trachtenberg, J. T., Trepel, C., & Stryker, M. P. (2000) · Science · doi:10.1126/science.287.5460.2029 · Cited by 235
Self-citation
Multiple periods of functional ocular dominance plasticity in mouse visual cortex
Tagawa, Y., Kanold, P. O., Majdan, M., & Shatz, C. J. (2005) · Nature Neuroscience · doi:10.1038/nn1410 · Cited by 239
Self-citation
Regulation of axon growth in vivo by activity-based competition
Hua, J. Y., Smear, M. C., Baier, H., & Smith, S. J. (2005) · Nature · doi:10.1038/nature03409 · Cited by 234
Dendritic Spine Plasticity: Function and Mechanisms
Runge, K., Cardoso, C., & de Chevigny, A. (2020) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2020.00036 · Cited by 248
Critical Period Mechanisms in Developing Visual Cortex
Hensch, T. K. (2005) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(05)69008-4 · Cited by 237
Gene expression changes and molecular pathways mediating activity-dependent plasticity in visual cortex
Tropea, D., Kreiman, G., Lyckman, A., Mukherjee, S., Yu, H., Horng, S., & Sur, M. (2006) · Nature Neuroscience · doi:10.1038/nn1689 · Cited by 226
The effect of dark rearing on the time course of the critical period in cat visual cortex
Mower, G. D. (1991) · Developmental Brain Research · doi:10.1016/0165-3806(91)90001-y · Cited by 220
Prior experience enhances plasticity in adult visual cortex
Hofer, S. B., Mrsic‐Flogel, T. D., Bonhoeffer, T., & Hübener, M. (2005) · Nature Neuroscience · doi:10.1038/nn1610 · Cited by 234
Recovery of visual responses in foveal V1 neurons following bilateral foveal lesions in adult monkey
Heinen, S. J., & Skavenski, A. A. (1991) · Experimental Brain Research · doi:10.1007/bf00229845 · Cited by 212
Afferents to the medial nucleus of the trapezoid body and their collateral projections
Kuwabara, N., DiCaprio, R. A., & Zook, J. M. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903140405 · Cited by 204
Rapid Anatomical Plasticity of Horizontal Connections in the Developing Visual Cortex
Trachtenberg, J. T., & Stryker, M. P. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-10-03476.2001 · Cited by 203
Self-citation
Elimination of Inhibitory Synapses Is a Major Component of Adult Ocular Dominance Plasticity
van Versendaal, D., Rajendran, R., Saiepour, M. H., Klooster, J., Smit‐Rigter, L. A., Sommeijer, J.-P., Zeeuw, C. I. D., Hofer, S. B., Heimel, J. A., & Levelt, C. N. (2012) · Neuron · doi:10.1016/j.neuron.2012.03.015 · Cited by 197
The Role of the Subplate in the Development of the Mammalian Telencephalon
Shatz, C. J., Chun, J. J. M., & Luskin, M. B. (1988) · Cerebral cortex · doi:10.1007/978-1-4615-6619-9_2 · Cited by 192
Self-citation
Beyond faithful conduction: Short-term dynamics, neuromodulation, and long-term regulation of spike propagation in the axon
Bucher, D. M., & Goaillard, J. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.06.001 · Cited by 189
Tetrodotoxin Blocks the Formation of Ocular Dominance Columns in Goldfish
Meyer, R. L. (1982) · Science · doi:10.1126/science.7123262 · Cited by 186
Tetrodotoxin inhibits the formation of refined retinotopography in goldfish
Meyer, R. L. (1983) · Developmental Brain Research · doi:10.1016/0165-3806(83)90068-8 · Cited by 186
Experience-dependent plasticity in the inferior colliculus: a site for visual calibration of the neural representation of auditory space in the barn owl
Brainard, M. S., & Knudsen, E. I. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-11-04589.1993 · Cited by 186
Receptive-Field Modification in Rat Visual Cortex Induced by Paired Visual Stimulation and Single-Cell Spiking
Meliza, C. D., & Dan, Y. (2006) · Neuron · doi:10.1016/j.neuron.2005.12.009 · Cited by 177
Organization of primary visual cortex (area 17) in the ferret
Law, M. I., Zahs, K. R., & Stryker, M. P. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902780202 · Cited by 175
Self-citation
Structural neuroplasticity in expert pianists depends on the age of musical training onset
Vaquero, L., Hartmann, K., Ripollés, P., Rojo, N., Sierpowska, J., Clément, F., Càmara, E., van Vugt, F. T., Mohammadi, B., Samii, A., et al. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.11.008 · Cited by 186
Postnatal changes in the number of neurons and synapses in the visual cortex (area 17) of the macaque monkey: A stereological analysis in normal and monocularly deprived animals
OʼKusky, J. R., & Colonnier, M. (1982) · The Journal of Comparative Neurology · doi:10.1002/cne.902100308 · Cited by 169
Dark rearing prolongs physiological but not anatomical plasticity of the cat visual cortex
Mower, G. D., Caplan, C. J., Christen, W. G., & Duffy, F. H. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902350404 · Cited by 169
On and off sublaminae in the lateral geniculate nucleus of the ferret
Stryker, M. P., & Zahs, K. R. (1983) · Journal of Neuroscience · doi:10.1523/jneurosci.03-10-01943.1983 · Cited by 164
Self-citation
Brain Plasticity and Disease: A Matter of Inhibition
Baroncelli, L., Braschi, C., Spolidoro, M., Begenisic, T., Maffei, L., & Sale, A. (2011) · Neural Plasticity · doi:10.1155/2011/286073 · Cited by 173
GABABReceptors, Monoamine Receptors, and Postsynaptic Inositol Trisphosphate-Induced Ca2+Release Are Involved in the Induction of Long-Term Potentiation at Visual Cortical Inhibitory Synapses
Komatsu, Y. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-20-06342.1996 · Cited by 159
Developmental neuroimaging of the human ventral visual cortex
Grill-Spector, K., Golarai, G., & Gabrieli, J. (2008) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2008.01.009 · Cited by 147
Control of Thalamocortical Afferent Rearrangement by Postsynaptic Activity in Developing Visual Cortex
Hata, Y., & Stryker, M. P. (1994) · Science · doi:10.1126/science.8085163 · Cited by 156
Self-citation
Perinatal Subplate Neuron Injury: Implications for Cortical Development and Plasticity
McQuillen, P. S., & Ferriero, D. M. (2005) · Brain Pathology · doi:10.1111/j.1750-3639.2005.tb00528.x · Cited by 155
Pairing-Induced Changes of Orientation Maps in Cat Visual Cortex
Schuett, S., Bonhoeffer, T., & Hübener, M. (2001) · Neuron · doi:10.1016/s0896-6273(01)00472-x · Cited by 153
Timing of the Critical Period for Plasticity of Ocular Dominance Columns in Macaque Striate Cortex
Horton, J. C., & Hocking, D. R. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-10-03684.1997 · Cited by 156
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
Early speech perception and later language development: implications for the “critical period”
Kuhl, P. K., Conboy, B. T., Padden, D., Nelson, T., & Pruitt, J. (2005) · Language Learning and Development · doi:10.1080/15475441.2005.9671948 · Cited by 482
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
The overall pattern of ocular dominance bands in cat visual cortex
Anderson, P., Olavarría, J. F., & Sluyters, R. C. V. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-06-02183.1988 · Cited by 139
Recovery from monocular deprivation in the monkey. III. Reversal of anatomical effects in the visual cortex
Swindale, N. V., Vital‐Durand, F., & Blakemore, C. B. (1981) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1981.0074 · Cited by 132
VGluT2 immunochemistry identifies thalamocortical terminals in layer 4 of adult and developing visual cortex
Nahmani, M., & Erişir, A. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20505 · Cited by 132
Monocular deprivation decreases the expression of messenger RNA for brain-derived neurotrophic factor in the rat visual cortex
Bozzi, Y., Pizzorusso, T., Cremisi, F., Rossi, F., Barsacchi, G., & Maffei, L. (1995) · Neuroscience · doi:10.1016/0306-4522(95)00321-9 · Cited by 129
Molecular mechanisms of experience-dependent plasticity in visual cortex
Tropea, D., Wart, A. V., & Sur, M. (2008) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2008.0269 · Cited by 130
Arrangement of Ocular Dominance Columns in Human Visual Cortex
Horton, J. C. (1990) · Archives of Ophthalmology · doi:10.1001/archopht.1990.01070090127054 · Cited by 125
The effect of impulse blockage on cytochrome oxidase activity in the cat visual system
Wong‐Riley, M. T. T., & Riley, D. A. (1983) · Brain Research · doi:10.1016/0006-8993(83)90622-4 · Cited by 125
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
The sharpening of frequency tuning curves requires patterned activity during development in the mouse, Mus musculus
Sanes, D., & Constantine‐Paton, M. (1985) · Journal of Neuroscience · doi:10.1523/jneurosci.05-05-01152.1985 · Cited by 123
Topographic organization of the orientation column system in large flat‐mounts of the cat visual cortex: A 2‐deoxyglucose study
Löwel, S., Freeman, B., & Singer, W. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902550307 · Cited by 123

Authors: Shatz, C. J., & Stryker, M. P.
ORCID: Shatz, C J
Stryker, M P
Venue: The Journal of Physiology
Publisher: Wiley
Published: 1978-08
Volume: 281
Issue: 1
Pages: 267-283
ISSN: 0022-3751 (ISSN-L)
1469-7793
DOI: 10.1113/jphysiol.1978.sp012421
PMC: PMC1282696
OpenAlex: W2150471545
Cited by: 691
References: 32
Citations by year: 2026: 6 · 2025: 5 · 2024: 14 · 2023: 8 · 2022: 11 · 2021: 9 · 2020: 14 · 2019: 8 · 2018: 12 · 2017: 13 · 2016: 12 · 2015: 8 · 2014: 18 · 2013: 15 · 2012: 17
FWCI: 6.89
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor)
Locations: The Journal of Physiology (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Keywords: ocular dominance, layer 4, primary visual cortex, monocular deprivation, thalamocortical connections, binocular vision, eye preference, cortical reorganization, cats
MeSH terms: Animals, Autoradiography, Cats, Dominance, Cerebral, Eye, Geniculate Bodies, Neurons, Afferent, Ocular Physiological Phenomena, Sensory Deprivation, Visual Cortex

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Ocular dominance in layer IV of the cat's visual cortex and the effects of monocular deprivation.

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks