The DOI matches its Crossref record; 190 of the 192 references it cites were found in a registry or an index.
CORTICAL PLASTICITY: From Synapses to Maps
Abstract
It has been clear for almost two decades that cortical representations in adult animals are not fixed entities, but rather, are dynamic and are continuously modified by experience. The cortex can preferentially allocate area to represent the particular peripheral input sources that are proportionally most used. Alterations in cortical representations appear to underlie learning tasks dependent on the use of the behaviorally important peripheral inputs that they represent. The rules governing this cortical representational plasticity following manipulations of inputs, including learning, are increasingly well understood. In parallel with developments in the field of cortical map plasticity, studies of synaptic plasticity have characterized specific elementary forms of plasticity, including associative long-term potentiation and long-term depression of excitatory postsynaptic potentials. Investigators have made many important strides toward understanding the molecular underpinnings of these fundamental plasticity processes and toward defining the learning rules that govern their induction. The fields of cortical synaptic plasticity and cortical map plasticity have been implicitly linked by the hypothesis that synaptic plasticity underlies cortical map reorganization. Recent experimental and theoretical work has provided increasingly stronger support for this hypothesis. The goal of the current paper is to review the fields of both synaptic and cortical map plasticity with an em…
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“These theoretical predictions are entirely consistent with empirical and computational characterisations of plasticity [56],[57].”
From Hierarchical Models in the Brain (2008) · cites this paper as [56]
Citations
Cites
A synaptic model of memory: long-term potentiation in the hippocampus
Bliss, T. V. P., & Collingridge, G. L. (1993) · Nature · doi:10.1038/361031a0 · Cited by 11,566
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 Organization of Behavior; A Neuropsychological Theory.
Attneave, F., B., M., & Hebb, D. O. (1950) · The American Journal of Psychology · doi:10.2307/1418888 · Cited by 5,146
The Organization of Behavior: A Neuropsychological Theory
(1950) · JAMA · doi:10.1001/jama.1950.02910470083028 · Cited by 4,272
Regulation of Synaptic Efficacy by Coincidence of Postsynaptic APs and EPSPs
Markram, H., Lübke, J., Frotscher, M., & Sakmann, B. (1997) · Science · doi:10.1126/science.275.5297.213 · Cited by 3,832
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
Bienenstock, E., Cooper, L., & Munro, P. (1982) · The Journal of Neuroscience · doi:10.1523/jneurosci.02-01-00032.1982 · Cited by 2,896
(1909) · Cited by 2,575
Increased Cortical Representation of the Fingers of the Left Hand in String Players
Elbert, T. R., Pantev, C., Wienbruch, C., Rockstroh, B. S., & Taub, E. (1995) · Science · doi:10.1126/science.270.5234.305 · Cited by 2,053
Dudek, S. M., & Bear, M. F. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.10.4363 · Cited by 1,708
Deficient Hippocampal Long-Term Potentiation in α-Calcium-Calmodulin Kinase II Mutant Mice
Silva, A. J., Stevens, C. F., Tonegawa, S., & Wang, Y. (1992) · Science · doi:10.1126/science.1378648 · Cited by 1,472
Self-organization of orientation sensitive cells in the striate cortex
Malsburg, C. V. D. (1973) · Kybernetik · doi:10.1007/bf00288907 · Cited by 1,444
Abeles, M. (1991) · Cambridge University Press eBooks · doi:10.1017/cbo9780511574566 · Cited by 1,341
Somatosensory cortical map changes following digit amputation in adult monkeys
Merzenich, M. M., Nelson, R. J., Stryker, M. P., Cynader, M. S., Schoppmann, A., & Zook, J. M. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902240408 · Cited by 1,326
Self-citationInhibition of Postsynaptic PKC or CaMKII Blocks Induction But Not Expression of LTP
Malinow, R., Schulman, H., & Tsien, R. W. (1989) · Science · doi:10.1126/science.2549638 · Cited by 1,325
Information processing in the primate visual system: an integrated systems perspective
Van Essen, D. C., Anderson, C. H., & Felleman, D. J. (1992) · Science · doi:10.1126/science.1734518 · Cited by 1,266
Recanzone, G., Schreiner, C., & Merzenich, M. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-01-00087.1993 · Cited by 1,266
Self-citationMechanisms underlying induction of homosynaptic long-term depression in area CA1 of the hippocampus
Mulkey, R. M., & Malenka, R. C. (1992) · Neuron · doi:10.1016/0896-6273(92)90248-c · Cited by 1,113
Massive Cortical Reorganization After Sensory Deafferentation in Adult Macaques
Pons, T. P., Garraghty, P. E., Ommaya, A. K., Kaas, J. H., Taub, E., & Mishkin, M. (1991) · Science · doi:10.1126/science.1843843 · Cited by 1,081
Merzenich, M. M., Kaas, J. H., Wall, J., Nelson, R. J., Sur, M., & Felleman, D. (1983) · Neuroscience · doi:10.1016/0306-4522(83)90024-6 · Cited by 1,042
Self-citationAn essential role for postsynaptic calmodulin and protein kinase activity in long-term potentiation
Malenka, R. C., Kauer, J. A., Perkel, D. J., Mauk, M. D., Kelly, P. T., Nicoll, R. A., & Waxham, M. N. (1989) · Nature · doi:10.1038/340554a0 · Cited by 1,025
Reshaping the Cortical Motor Map by Unmasking Latent Intracortical Connections
Jacobs, K. M., & Donoghue, J. P. (1991) · Science · doi:10.1126/science.2000496 · Cited by 1,004
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
Jenkins, W. M., Merzenich, M. M., Ochs, M. T., Allard, T., & Guic-Robles, E. (1990) · Journal of Neurophysiology · doi:10.1152/jn.1990.63.1.82 · Cited by 937
Self-citationPlasticity of Sensory and Motor Maps in Adult Mammals
Kaas, J. H. (1991) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.14.030191.001033 · Cited by 913
Artola, A., Bröcher, S., & Singer, W. (1990) · Nature · doi:10.1038/347069a0 · Cited by 880
Receptive field dynamics in adult primary visual cortex
Gilbert, C. D., & Wiesel, T. N. (1992) · Nature · doi:10.1038/356150a0 · Cited by 869
Redistribution of synaptic efficacy between neocortical pyramidal neurons
Markram, H., & Tsodyks, M. V. (1996) · Nature · doi:10.1038/382807a0 · Cited by 857
Somatosensory Cortex: Structural Alterations following Early Injury to Sense Organs
der Loos, H. V., & Woolsey, T. A. (1973) · Science · doi:10.1126/science.179.4071.395 · Cited by 819
Artola, A., & Singer, W. (1993) · Trends in Neurosciences · doi:10.1016/0166-2236(93)90081-v · Cited by 799
Response properties of vibrissa units in rat SI somatosensory neocortex
Simons, D. J. (1978) · Journal of Neurophysiology · doi:10.1152/jn.1978.41.3.798 · Cited by 780
Recanzone, G. H., Merzenich, M. M., Jenkins, W. M., Grajski, K. A., & Dinse, H. R. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.67.5.1031 · Cited by 778
Self-citationMerzenich, M. M., Kaas, J. H., Wall, J. T., Sur, M., Nelson, R. J., & Felleman, D. J. (1983) · Neuroscience · doi:10.1016/0306-4522(83)90208-7 · Cited by 735
Self-citationAn organizing principle for cerebral function : the unit module and the distributed system
Mountcastle, V. (1978) · Medical Entomology and Zoology · Cited by 734
A critical period for long-term potentiation at thalamocortical synapses
Crair, M. C., & Malenka, R. C. (1995) · Nature · doi:10.1038/375325a0 · Cited by 691
Laminar differences in receptive field properties of cells in cat primary visual cortex
Gilbert, C. D. (1977) · The Journal of Physiology · doi:10.1113/jphysiol.1977.sp011863 · Cited by 670
Experience-dependent modification of synaptic plasticity in visual cortex
Kirkwood, A., Rioult, M., & Bear, M. (1996) · Nature · doi:10.1038/381526a0 · Cited by 666
Reorganization of Retinotopic Cortical Maps in Adult Mammals After Lesions of the Retina
Kaas, J. H., Krubitzer, L. A., Chino, Y. M., Langston, A., Polley, E. H., & Blair, N. P. (1990) · Science · doi:10.1126/science.2326637 · Cited by 655
Plasticity of the sensorimotor cortex representation of the reading finger in Braille readers
Pascual‐Leone, Á., & Torres, F. (1993) · Brain · doi:10.1093/brain/116.1.39 · Cited by 654
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
Mechanisms Underlying Long-Term Potentiation of Synaptic Transmission
Madison, D. V., Malenka, R. C., & Nicoll, R. A. (1991) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.14.030191.002115 · Cited by 617
Long-Term Depression in Hippocampus
Bear, M. F., & Abraham, W. C. (1996) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.19.030196.002253 · Cited by 616
Heterosynaptic depression: a postsynaptic correlate of long-term potentiation
LYNCH, G. S., DUNWIDDIE, T., & GRIBKOFF, V. (1977) · Nature · doi:10.1038/266737a0 · Cited by 615
Robertson, D., & Irvine, D. R. F. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902820311 · Cited by 604
Axonal sprouting accompanies functional reorganization in adult cat striate cortex
Darian‐Smith, C., & Gilbert, C. D. (1994) · Nature · doi:10.1038/368737a0 · Cited by 603
Numbers and proportions of GABA-immunoreactive neurons in different areas of monkey cerebral cortex
Hendry, S., Schwark, H. D., Jones, E. G., & Yan, J. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-05-01503.1987 · Cited by 601
Gustafsson, B., Wigstrom, H., Abraham, W., & Huang, Y. (1987) · The Journal of Neuroscience · doi:10.1523/jneurosci.07-03-00774.1987 · Cited by 583
Horizontal integration and cortical dynamics
Gilbert, C. D. (1992) · Neuron · doi:10.1016/0896-6273(92)90215-y · Cited by 581
Hebbian synapses: biophysical mechanisms and algorithms.
Brown, T. H., Kairiss, E. W., & Keenan, C. L. (1990) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.13.030190.002355 · Cited by 577
Synapses as associative memory elements in the hippocampal formation
Levy, W. B., & Steward, O. (1979) · Brain Research · doi:10.1016/0006-8993(79)91003-5 · Cited by 557
Hebbian synapses in hippocampus.
Kelso, S. R., Ganong, A. H., & Brown, T. H. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.14.5326 · Cited by 555
Laminar patterns of geniculocortical projection in the cat
LeVay, S., & Gilbert, C. D. (1976) · Brain Research · doi:10.1016/0006-8993(76)90002-0 · Cited by 533
Martin, K. A. C., & Whitteridge, D. (1984) · The Journal of Physiology · doi:10.1113/jphysiol.1984.sp015347 · Cited by 529
Linden, D. J., & Connor, J. A. (1995) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.18.030195.001535 · Cited by 519
A canonical microcircuit for neocortex
Douglas, R. J., Martin, K. A. C., & Whitteridge, D. (1989) · Neural Computation · doi:10.1162/neco.1989.1.4.480 · Cited by 514
Cellular analysis of associative learning.
Byrne, J. H. (1987) · Physiological Reviews · doi:10.1152/physrev.1987.67.2.329 · Cited by 507
GABAergic Neurons and Their Role in Cortical Plasticity in Primates
Jones, E. G. (1993) · Cerebral Cortex · doi:10.1093/cercor/3.5.361-a · Cited by 500
Bear, M., Kleinschmidt, A., Gu, Q., & Singer, W. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-03-00909.1990 · Cited by 488
Common Forms of Synaptic Plasticity in the Hippocampus and Neocortex in Vitro
Kirkwood, A., Dudek, S. M., Gold, J. T., Aizenman, C. D., & Bear, M. F. (1993) · Science · doi:10.1126/science.8502997 · Cited by 483
Ca2+ Signaling Requirements for Long-Term Depression in the Hippocampus
Cummings, J., Mulkey, R. M., Nicoll, R. A., & Malenka, R. C. (1996) · Neuron · doi:10.1016/s0896-6273(00)80102-6 · Cited by 465
Anatomical demonstration of orientation columns in macaque monkey
Hubel, D. H., Wiesel, T. N., & Stryker, M. P. (1978) · The Journal of Comparative Neurology · doi:10.1002/cne.901770302 · Cited by 465
Temporal Information Transformed into a Spatial Code by a Neural Network with Realistic Properties
Buonomano, D. V., & Merzenich, M. M. (1995) · Science · doi:10.1126/science.7863330 · Cited by 457
Self-citationMerzenich, M. M., Kaas, J. H., Sur, M., & Lin, C. (1978) · The Journal of Comparative Neurology · doi:10.1002/cne.901810104 · Cited by 456
Self-citationThe Role of Constraints in Hebbian Learning
Miller, K. D., & MacKay, D. J. C. (1994) · Neural Computation · doi:10.1162/neco.1994.6.1.100 · Cited by 448
Remodelling of hand representation in adult cortex determined by timing of tactile stimulation
Wang, X., Merzenich, M. M., Sameshima, K., & Jenkins, W. M. (1995) · Nature · doi:10.1038/378071a0 · Cited by 436
Self-citationFlow of excitation within rat barrel cortex on striking a single vibrissa
Armstrong‐James, M., Fox, K. D., & Das-Gupta, A. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.68.4.1345 · Cited by 426
Hebbian synapses in visual cortex
Kirkwood, A., & Bear, M. F. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-03-01634.1994 · Cited by 418
Spatiotemporal convergence and divergence in the rat S1 “Barrel” cortex
Armstrong-James, M., & Fox, K. (1987) · The Journal of comparative neurology · doi:10.1002/cne.902630209 · Cited by 389
Bakin, J. S., & Weinberger, N. M. (1990) · Brain Research · doi:10.1016/0006-8993(90)90035-a · Cited by 387
Koch, C., & Zador, A. M. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-02-00413.1993 · Cited by 372
Rajan, R., Irvine, D. R. F., Wise, L. Z., & Heil, P. F. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903380104 · Cited by 359
Dependence of Cortical Plasticity on Correlated Activity of Single Neurons and on Behavioral Context
Ahissar, E., Vaadia, E., Ahissar, M., Bergman, H., Arieli, A., & Abeles, M. (1992) · Science · doi:10.1126/science.1529342 · Cited by 358
Calford, M. B., & Tweedale, R. (1988) · Nature · doi:10.1038/332446a0 · Cited by 355
Long-Term Potentiation in the Motor Cortex
Iriki, A., Pavlides, C., Keller, A., & Asanuma, H. (1989) · Science · doi:10.1126/science.2551038 · Cited by 349
Dykes, R. W., Landry, P., Metherate, R., & Hicks, T. P. (1984) · Journal of Neurophysiology · doi:10.1152/jn.1984.52.6.1066 · Cited by 345
Postsynaptic control of plasticity in developing somatosensory cortex
Schlaggar, B. L., Fox, K. D., & O'Leary, D. M. (1993) · Nature · doi:10.1038/364623a0 · Cited by 339
Florence, S. L., & Kaas, J. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-12-08083.1995 · Cited by 336
Development of orientation selectivity in ferret visual cortex and effects of deprivation
Chapman, B., & Stryker, M. P. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-12-05251.1993 · Cited by 332
Recanzone, G., Merzenich, M., & Schreiner, C. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.67.5.1071 · Cited by 325
Self-citationMalinow, R., & Miller, J. P. (1986) · Nature · doi:10.1038/320529a0 · Cited by 323
Dynamic Regulation of Receptive Fields and Maps in the Adult Sensory Cortex
Weinberger, N. M. (1995) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.18.030195.001021 · Cited by 311
Topographic reorganization in the striate cortex of the adult cat and monkey is cortically mediated
Darian‐Smith, C., & Gilbert, C. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-03-01631.1995 · Cited by 309
Experience-dependent plasticity in adult rat barrel cortex.
Diamond, M. E., Armstrong‐James, M., & Ebner, F. F. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.5.2082 · Cited by 309
The location and function of NMDA receptors in cat and kitten visual cortex
Fox, K., Sato, H., & Daw, N. (1989) · The Journal of Neuroscience · doi:10.1523/jneurosci.09-07-02443.1989 · Cited by 307
Rapid reorganization of cortical maps in adult cats following restricted deafferentation in retina
Chino, Y. M., Kaas, J. H., Smith, E. L., III, Langston, A., & Cheng, H. (1992) · Vision Research · doi:10.1016/0042-6989(92)90021-a · Cited by 307
Receptive fields in the body-surface map in adult cortex defined by temporally correlated inputs
Clark, S. A., Allard, T., Jenkins, W. M., & Merzenich, M. M. (1988) · Nature · doi:10.1038/332444a0 · Cited by 296
Self-citationPlasticity in the spinal cord sensory map following peripheral nerve injury in rats
Devor, M. G., & Wall, P. D. (1981) · Journal of Neuroscience · doi:10.1523/jneurosci.01-07-00679.1981 · Cited by 295
Allard, T., Clark, S. A., Jenkins, W. M., & Merzenich, M. M. (1991) · Journal of Neurophysiology · doi:10.1152/jn.1991.66.3.1048 · Cited by 295
Self-citationLaminar Comparison of Somatosensory Cortical Plasticity
Diamond, M. E., Huang, W. M., & Ebner, F. F. (1994) · Science · doi:10.1126/science.8091215 · Cited by 291
Wigström, H., Gustafsson, B., Huang, Y.-Y., & Abraham, W. C. (1986) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1986.tb07822.x · Cited by 284
Long-term potentiation and long-term depression in the neocortex.
Tsumoto, T. (1992) · Progress in neurobiology · doi:10.1016/0301-0082(92)90011-3 · Cited by 283
Kew, J., Ridding, M. C., Rothwell, J. C., Passingham, R. E., Leigh, P. N., Sooriakumaran, S., Frackowiak, R. S. J., & Brooks, D. J. (1994) · Journal of Neurophysiology · doi:10.1152/jn.1994.72.5.2517 · Cited by 283
Pharmacological Induction of Use-Dependent Receptive Field Modifications in the Visual Cortex
Greuel, J. M., Luhmann, H. J., & Singer, W. (1988) · Science · doi:10.1126/science.2902687 · Cited by 276
Activity-dependent regulation of GABA expression in the visual cortex of adult monkeys
Hendry, S. H. C. (1988) · Neuron · doi:10.1016/0896-6273(88)90169-9 · Cited by 273
Beaulieu, C., Kisvarday, Z., Somogyi, P., Cynader, M., & Cowey, A. (1992) · Cerebral Cortex · doi:10.1093/cercor/2.4.295 · Cited by 269
Recanzone, G. H., Merzenich, M. M., & Jenkins, W. M. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.67.5.1057 · Cited by 268
Self-citationSomatosensory cortical plasticity in adult humans revealed by magnetoencephalography.
Mogilner, A. Y., Grossman, J. A., Ribary, U., Joliot, M., Volkmann, J., Rapaport, D., Beasley, R. W., & Llinás, R. R. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.8.3593 · Cited by 267
White, E. L. (1989) · Birkhäuser Boston eBooks · doi:10.1007/978-1-4684-8721-3 · Cited by 256
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
A cellular analogue of visual cortical plasticity
Frégnac, Y., Shulz, D. E., Thorpe, S. J., & Bienenstock, E. (1988) · Nature · doi:10.1038/333367a0 · Cited by 248
Debanne, D., Gähwiler, B. H., & Thompson, S. M. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.3.1148 · Cited by 233
Basbaum, A. I., & Wall, P. D. (1976) · Brain Research · doi:10.1016/0006-8993(76)90899-4 · Cited by 233
Reorganization of raccoon somatosensory cortex following removal of the fifth digit
Rasmusson, D. D. (1982) · The Journal of Comparative Neurology · doi:10.1002/cne.902050402 · Cited by 217
Recanzone, G. H., Jenkins, W. M., Hradek, G. T., & Merzenich, M. M. (1992) · Journal of Neurophysiology · doi:10.1152/jn.1992.67.5.1015 · Cited by 215
Self-citationAssociative Induction of Posttetanic and Long-Term Potentiation in CA1 Neurons of Rat Hippocampus
Sastry, B. R., Goh, J. W., & Auyeung, A. (1986) · Science · doi:10.1126/science.3010459 · Cited by 214
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
Cortical plasticity and memory
Merzenich, M. M., & Sameshima, K. (1993) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(93)90209-h · Cited by 211
Self-citationNoninvasive detection of cerebral plasticity in adult human somatosensory cortex
Yang, T. T., Gallen, C. C., Ramachandran, V. S., Cobb, S., Schwartz, B. J., & Bloom, F. E. (1994) · Neuroreport · doi:10.1097/00001756-199402000-00010 · Cited by 201
Recanzone, G. H., Merzenich, M. M., & Dinse, H. R. (1992) · Cerebral Cortex · doi:10.1093/cercor/2.3.181 · Cited by 199
Self-citationLong-term retention of learning-induced receptive-field plasticity in the auditory cortex.
Weinberger, N. M., Javid, R., & Lepan, B. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.6.2394 · Cited by 198
Abraham, W. C., & Goddard, G. V. (1983) · Nature · doi:10.1038/305717a0 · Cited by 194
Wall, J., & Cusick, C. G. (1984) · Journal of Neuroscience · doi:10.1523/jneurosci.04-06-01499.1984 · Cited by 192
Pearson, J., Finkel, L., & Edelman, G. M. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-12-04209.1987 · Cited by 188
Diamond, D. M., & Weinberger, N. M. (1986) · Brain Research · doi:10.1016/0006-8993(86)91144-3 · Cited by 185
Bindman, L. J., Murphy, K. P., & Pockett, S. (1988) · Journal of Neurophysiology · doi:10.1152/jn.1988.60.3.1053 · Cited by 184
Hippocampal Interneurons Express a Novel Form of Synaptic Plasticity
McMahon, L. L., & Kauer, J. A. (1997) · Neuron · doi:10.1016/s0896-6273(00)80269-x · Cited by 182
Visual responses in adult cat visual cortex depend on N-methyl-D-aspartate receptors.
Miller, K. D., Chapman, B., & Stryker, M. P. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.13.5183 · Cited by 181
Neocortical long-term potentiation
Bear, M. F., & Kirkwood, A. (1993) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(93)90210-p · Cited by 180
Kalaska, J. F., & Pomeranz, B. H. (1979) · Journal of Neurophysiology · doi:10.1152/jn.1979.42.2.618 · Cited by 179
O’Leary, D. D. M., Ruff, N. L., & Dyck, R. H. (1994) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(94)90054-x · Cited by 174
Landry, P., & Deschênes, M. (1981) · The Journal of Comparative Neurology · doi:10.1002/cne.901990304 · Cited by 173
An innocuous bias in whisker use in adult rats modifies receptive fields of barrel cortex neurons
Armstrong‐James, M., Diamond, M. E., & Ebner, F. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-11-06978.1994 · Cited by 169
Welker, E., Soriano, E., & der Loos, H. V. (1989) · Experimental Brain Research · doi:10.1007/bf00247346 · Cited by 167
Alterations of the cortical representation of the rat ventrum induced by nursing behavior
Xerri, C., Stern, J. M., & Merzenich, M. M. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-03-01710.1994 · Cited by 167
Self-citationInjury-Induced Reorganization of Somatosensory Cortex Is Accompanied by Reductions in GABA Staining
Garraghty, P. E., Lachica, E. A., & Kaas, J. H. (1991) · Somatosensory & Motor Research · doi:10.3109/08990229109144757 · Cited by 160
Komatsu, Y. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-20-06342.1996 · Cited by 159
Functional reorganization in adult monkey thalamus after peripheral nerve injury
Garraghty, P. E., & Kaas, J. H. (1991) · Neuroreport · doi:10.1097/00001756-199112000-00004 · Cited by 158
Horizontal Propagation of Excitation in Rat Visual Cortical Slices Revealed by Optical Imaging
Tanifuji, M., Sugiyama, T., & Murase, K. (1994) · Science · doi:10.1126/science.7973662 · Cited by 155
Kelahan, A. M., & Doetsch, G. S. (1984) · Somatosensory Research · doi:10.3109/07367228409144560 · Cited by 150
Killackey, H. P., Belford, G. R., Ryugo, R., & Ryugo, D. K. (1976) · Brain Research · doi:10.1016/0006-8993(76)90623-5 · Cited by 150
Iriki, A., Pavlides, C., Keller, A., & Asanuma, H. (1991) · Journal of Neurophysiology · doi:10.1152/jn.1991.65.6.1435 · Cited by 148
Ren, J. Q., Aika, Y., Heizmann, C. W., & Kosaka, T. (1992) · Experimental Brain Research · doi:10.1007/bf00230378 · Cited by 148
Neuroplasticity of the adult primate auditory cortex following cochlear hearing loss.
Schwaber, M. K., Garraghty, P. E., & Kaas, J. H. (1993) · PubMed · Cited by 147
Physiological analysis of motor reorganization following lower limb amputation
Fuhr, P., Cohen, L. G., Dang, N., FINDLEY, T. W., Haghighi, S. S., Oro, J., & Hallett, M. (1992) · Electroencephalography and Clinical Neurophysiology/Evoked Potentials Section · doi:10.1016/0168-5597(92)90102-h · Cited by 146
Requirement for α-CaMKII in Experience-Dependent Plasticity of the Barrel Cortex
Glazewski, S., Chen, C.-M., Silva, A. J., & Fox, K. (1996) · Science · doi:10.1126/science.272.5260.421 · Cited by 142
Merzenich, M. M., Recanzone, G. H., Jenkins, W. M., & Grajski, K. A. (1990) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1990.055.01.082 · Cited by 138
Self-citationUnderstanding the cellular basis of memory and learning.
Woody, C. (1986) · Annual Review of Psychology · doi:10.1146/annurev.ps.37.020186.002245 · Cited by 136
Benshalom, G., & White, E. L. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902530303 · Cited by 131
Chino, Y., Smith, E., Kaas, J. H., Sasaki, Y., & Cheng, H. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-03-02417.1995 · Cited by 124
Baranyi, A., Szente, M. B., & Woody, C. D. (1991) · Neuroscience · doi:10.1016/0306-4522(91)90378-2 · Cited by 123
Chapin, J. K. (1986) · Experimental Brain Research · doi:10.1007/bf00236033 · Cited by 120
Role of intercellular interactions in heterosynaptic long-term depression
Scanziani, M., Malenka, R. C., & Nicoll, R. A. (1996) · Nature · doi:10.1038/380446a0 · Cited by 119
Age-dependent long-term potentiation of inhibitory synaptic transmission in rat visual cortex
Komatsu, Y. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-11-06488.1994 · Cited by 118
Long-term modification of inhibitory synaptic transmission in developing visual cortex
Komatsu, Y., & Iwakiri, M. (1993) · Neuroreport · doi:10.1097/00001756-199307000-00017 · Cited by 117
Wall, J. T. (1988) · Trends in Neurosciences · doi:10.1016/0166-2236(88)90184-1 · Cited by 116
Age-dependent decrease of synaptic plasticity in the neocortex of αCaMKII mutant mice
Kirkwood, A., Silva, A. J., & Bear, M. F. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.7.3380 · Cited by 113
Synaptic plasticity in visual cortex: comparison of theory with experiment
Clothiaux, E. E., Bear, M. F., & Cooper, L. N. (1991) · Journal of Neurophysiology · doi:10.1152/jn.1991.66.5.1785 · Cited by 112
Synaptic facilitation requires paired activation of convergent pathways in the neocortex
Baranyi, A., & Fehér, O. (1981) · Nature · doi:10.1038/290413a0 · Cited by 111
Neural Stem Cells Are Blasting Off
Stemple, D. L., & Mahanthappa, N. K. (1997) · Neuron · doi:10.1016/s0896-6273(01)80018-0 · Cited by 107
Dudek, S. M., & Friedlander, M. J. (1996) · Neuron · doi:10.1016/s0896-6273(00)80136-1 · Cited by 106
Cellular analogs of visual cortical epigenesis. I. Plasticity of orientation selectivity
Frégnac, Y., Shulz, D. E., Thorpe, S. J., & Bienenstock, E. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-04-01280.1992 · Cited by 106
Welker, E., Soriano, E., Dörfl, J., & der Loos, H. V. (1989) · Experimental Brain Research · doi:10.1007/bf00230256 · Cited by 106
Morphology of single intracellularly stained axons terminating in area 3b of macaque monkeys
Garraghty, P. E., & Sur, M. (1990) · The Journal of Comparative Neurology · doi:10.1002/cne.902940406 · Cited by 104
Receptive-field plasticity in the adult auditory cortex induced by Hebbian covariance
Cruikshank, S., & Weinberger, N. M. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-02-00861.1996 · Cited by 98
Welker, E., Rao, S., Dörfl, J., Melzer, P., & der Loos, H. V. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-01-00153.1992 · Cited by 95
Crook, J., & Eysel, U. T. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-05-01816.1992 · Cited by 93
Cortical reorganization in human amputees and mislocalization of painful stimuli to the phantom limb
Knecht, S., Henningsen, H., Elbert, T. R., Flor, H., Höhling, C., Pantev, C., Birbaumer, N., & Taub, E. (1995) · Neuroscience Letters · doi:10.1016/0304-3940(95)12186-2 · Cited by 93
Schmid, L. M., Rosa, M. G. P., Calford, M. B., & Ambler, J. S. (1996) · Cerebral Cortex · doi:10.1093/cercor/6.3.388 · Cited by 92
Neural representations, experience, and change.
Merzenich, M. M., & deCharms, R. C. (1996) · Cited by 88
Self-citationHuman fetal hippocampal development: II. The neuronal cytoskeleton
Arnold, S. E., & Trojanowski, J. Q. (1996) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(19960401)367:2 · Cited by 87
Plasticity in visual perception and physiology
Gilbert, C. D. (1996) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(96)80083-3 · Cited by 86
The distribution of intrinsic cortical axons in area 3b of cat primary somatosensory cortex
Schwark, H. D., & Jones, E. G. (1989) · Experimental Brain Research · doi:10.1007/bf00230238 · Cited by 85
Frégnac, Y., Burke, J. P., Smith, D. C., & Friedlander, M. J. (1994) · Journal of Neurophysiology · doi:10.1152/jn.1994.71.4.1403 · Cited by 82
Global plasticity in adult visual cortex following reversal of visual input
Sugita, Y. (1996) · Nature · doi:10.1038/380523a0 · Cited by 78
Pharmacological analysis of cortical circuitry
Bolz, J., Gilbert, C. D., & Wiesel, T. N. (1989) · Trends in Neurosciences · doi:10.1016/0166-2236(89)90009-x · Cited by 77
Welker, E., Armstrong‐James, M., der Loos, H. V., & Kraftsik, R. (1993) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1993.tb00534.x · Cited by 74
Functional reorganization of adult cat somatosensory cortex is dependent on NMDA receptors
Kano, M., lino, K., & Kano, M. (1991) · Neuroreport · doi:10.1097/00001756-199102000-00003 · Cited by 74
Sur, M., Garraghty, P. E., & Bruce, C. J. (1985) · Brain Research · doi:10.1016/0006-8993(85)91144-8 · Cited by 71
Eysel, U. T., González-Aguilar, F., & Mayer, U. (1981) · Experimental Brain Research · doi:10.1007/bf00238882 · Cited by 64
Pockett, S., Brookes, N. H., & Bindman, L. J. (1990) · Experimental Brain Research · doi:10.1007/bf00228861 · Cited by 62
Alterations in correlated activity parallel ICMS-induced representational plasticity
Dinse, H. R., Recanzone, G. H., & Merzenich, M. M. (1993) · Neuroreport · doi:10.1097/00001756-199311180-00020 · Cited by 60
Self-citationWhat should a biochemistry of learning and memory be about?
Rose, S. P. R. (1981) · Neuroscience · doi:10.1016/0306-4522(81)90164-0 · Cited by 59
Aou, S., Woody, C., & Birt, D. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-02-00549.1992 · Cited by 59
Long-term depression but not potentiation is induced in Ca2+-chelated visual cortex neurons
Kimura, F., Tsumoto, T., Nishigori, A., & Yoshimura, Y. (1990) · Neuroreport · doi:10.1097/00001756-199009000-00018 · Cited by 57
Grajski, K. A., & Merzenich, M. M. (1990) · Neural Computation · doi:10.1162/neco.1990.2.1.71 · Cited by 55
Self-citationHeterosynaptic correlates of long-term potentiation induction in hippocampal CA3 neurons
Bradler, J. E., & Barrionuevo, G. (1990) · Neuroscience · doi:10.1016/0306-4522(90)90080-n · Cited by 52
Cortical Map Reorganization as a Competitive Process
Sutton, G. G., Reggia, J. A., Armentrout, S. L., & D’Autrechy, C. L. (1994) · Neural Computation · doi:10.1162/neco.1994.6.1.1 · Cited by 50
Beňušková, Ľ., Diamond, M. E., & Ebner, F. F. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.11.4791 · Cited by 45
Ishizaki, H., & Suzuki, A. (1992) · Progress in brain research · doi:10.1016/s0079-6123(08)61160-7 · Cited by 42
Reversible relocation of representational boundaries of adult rats by intracortical microstimulation
Spengler, F., & Dinse, H. R. (1994) · Neuroreport · doi:10.1097/00001756-199404000-00024 · Cited by 36
Pubols, L. M. (1984) · Somatosensory Research · doi:10.3109/07367228409144558 · Cited by 36
Effects of hind limb nerve section on lumbosacral dorsal horn neurones in the cat.
Brown, A. G., Fyffe, R. E. W., Noble, R., & Rowe, M. J. (1984) · The Journal of Physiology · doi:10.1113/jphysiol.1984.sp015382 · Cited by 34
Induction of LTP and LTD in visual cortex neurones by intracellular tetanization
Volgushev, M., Voronin, L. L., Chistiakova, M., & Singer, W. (1994) · Neuroreport · doi:10.1097/00001756-199410270-00020 · Cited by 32
THE PHYSIOLOGY OF THE NERVOUS SYSTEM.
Hull, A. G. (1846) · The Lancet · doi:10.1016/s0140-6736(02)89373-4 · Cited by 30
Land, P. W., & Akhtar, N. D. (1987) · Brain Research · doi:10.1016/0006-8993(87)90497-5 · Cited by 28
Hirsch, J. C., Barrionuevo, G., & Crépel, F. (1992) · Synapse · doi:10.1002/syn.890120110 · Cited by 27
Wilson, P., & Snow, P. J. (1987) · Journal of Neurophysiology · doi:10.1152/jn.1987.57.3.803 · Cited by 21
Buonomano, D. V., & Merzenich, M. M. (1996) · Journal of Neurophysiology · doi:10.1152/jn.1996.76.1.631 · Cited by 19
Self-citationDynamic Regulation of Receptive Fields and Maps in the Adult Sensory Cortex
Weinberger, N. (1995) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.18.1.129 · Cited by 18
Lisney, S. J. W. (1983) · Brain Research · doi:10.1016/0006-8993(83)91379-3 · Cited by 16
Research works printed but not linked: 8
- Buonomano DV, 1996, Soc. Neurosci. Abstr., 22, 1743
- Clark SA, 1986, Soc. Neurosci. Abstr., 12, 391
- Heinen SJ, 1981, Exp. Brain Res., 83, 670
- Merzenich MM. 1987. Dynamic neocortical processes and the origins of higher brain functions. In The Neural and Molecular Bases of Learning , ed. JP Changeux, M Konishi, pp. 337–58. Chichester: Wiley
- Merzenich MM, Jenkins WM. 1992. Cortical plasticity, learning, and learning dysfunction. In Maturational Windows and Adult Cortical Plasticity , ed. B Julesz, I Kovacs, pp. 1–26. Reading: Addison-Wesley
- Merzenich MM, Recanzone GH, Jenkins WM, Nudo RJ. 1990b. How the brain functionally rewires itself. In Natural and Artificial Parallel Computation , ed. M Arbib, D Robinson, pp. 177–210. Cambridge: MIT Press
- Schwaber MK, 1993, Am. J. Otol., 14, 252
- Tyler T, 1990, Semin. Neurosci., 2, 365
Cited by
Sorted by citations
A theory of cortical responses.
Friston, K. (2005) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2005.1622 · Cited by 4,578
Spinal and Supraspinal Factors in Human Muscle Fatigue
Gandevia, S. C. (2001) · Physiological Reviews · doi:10.1152/physrev.2001.81.4.1725 · Cited by 3,855
Synaptic Plasticity and Memory: An Evaluation of the Hypothesis
Martin, S. J., Grimwood, P. D., & Morris, R. G. M. (2000) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.23.1.649 · Cited by 2,794
The human hippocampus and spatial and episodic memory
Burgess, N., Maguire, E. A., & O'Keefe, J. (2002) · Neuron · doi:10.1016/s0896-6273(02)00830-9 · Cited by 2,401
Proske, U., & Gandevia, S. C. (2012) · Physiological Reviews · doi:10.1152/physrev.00048.2011 · Cited by 2,223
Metadata
- Authors
- Buonomano, D. V., & Merzenich, M. M.
- Affiliations
- University of California, Los Angeles (US)
- University of California, San Francisco (US)
- Venue
- Annual Review of Neuroscience
- Publisher
- Annual Reviews
- Published
- 1998-03
- Volume
- 21
- Issue
- 1
- Pages
- 149-186
- ISSN
- 0147-006X (ISSN-L)
- 1545-4126
- OpenAlex
- W2158935809
- Cited by
- 2,083
- References
- 192
- Citations by year
- 2026: 21 · 2025: 27 · 2024: 43 · 2023: 40 · 2022: 45 · 2021: 58 · 2020: 49 · 2019: 73 · 2018: 67 · 2017: 61 · 2016: 61 · 2015: 78 · 2014: 72 · 2013: 95 · 2012: 98
- FWCI
- 8.24
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Public Health Service (10414)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- cortical plasticity, synaptic plasticity, long-term potentiation, long-term depression, excitatory postsynaptic potentials, learning rules
- MeSH terms
- Animals, Brain Mapping, Cerebral Cortex, Neuronal Plasticity, Synapses
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