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Experience-Dependent Plasticity of Binocular Responses in the Primary Visual Cortex of the Mouse
Open accessAbstract
An activity-dependent form of synaptic plasticity underlies the fine tuning of connections in the developing primary visual cortex of mammals such as the cat and monkey. Studies of the effects of manipulations of visual experience during a critical period have demonstrated that a correlation-based competitive process governs this plasticity. The cellular mechanisms underlying this competition, however, are poorly understood. Transgenic and gene-targeting technologies have led to the development of a new category of reagents that have the potential to help answer questions of cellular mechanism, provided that the questions can be studied in a mouse model. The current study attempts to characterize a developmental plasticity in the mouse primary visual cortex and to demonstrate its relevance to that found in higher mammals. We found that 4 d of monocular lid suture at postnatal day 28 (P28) induced a maximal loss of responsiveness of cortical neurons to the deprived eye. These ocular dominance shifts occurred during a well-defined critical period, between P19 and P32. Furthermore, binocular deprivation during this critical period did not decrease visual cortical responses, and alternating monocular deprivation resulted in a decrease in the number of binocularly responsive neurons. Finally, a laminar analysis demonstrated plasticity of both geniculocortical and intracortical connections. These results demonstrate that an activity-dependent, competitive form of synaptic plasticity that obeys correlation-based rules operates in the developing primary visual cortex of the mouse.
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Citations
Cites
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
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
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
Ocular dominance in layer IV of the cat's visual cortex and the effects of monocular deprivation.
Shatz, C. J., & Stryker, M. P. (1978) · The Journal of Physiology · doi:10.1113/jphysiol.1978.sp012421 · Cited by 691
Self-citationMaffei, 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
Antonini, A., & Stryker, M. (1993) · The Journal of Neuroscience · doi:10.1523/jneurosci.13-08-03549.1993 · Cited by 220
Self-citation
Cited by
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
Homeostatic plasticity in the developing nervous system
Turrigiano, G. G., & Nelson, S. B. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1327 · Cited by 2,485
Critical period plasticity in local cortical circuits
Hensch, T. K. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1787 · Cited by 2,323
Microglial interactions with synapses are modulated by visual experience
Tremblay, M.-È., Lowery, R. L., & Majewska, A. K. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000527 · Cited by 1,542
Hensch, T. K. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144327 · Cited by 1,300
Huang, Z. J., Kirkwood, A., Pizzorusso, T., Porciatti, V., Morales, B., Bear, M. F., Maffei, L., & Tonegawa, S. (1999) · Cell · doi:10.1016/s0092-8674(00)81509-3 · Cited by 1,198
Adolescent cortical development: A critical period of vulnerability for addiction
Crews, F., He, J., & Hodge, C. (2007) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2006.12.001 · Cited by 1,091
Hippocampal GABAergic Inhibitory Interneurons
Pelkey, K. A., Chittajallu, R., Craig, M. T., Tricoire, L., Wester, J. C., & McBain, C. J. (2017) · Physiological Reviews · doi:10.1152/physrev.00007.2017 · Cited by 889
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-citationAdolescence as a neurobiological critical period for the development of higher-order cognition
Larsen, B., & Luna, B. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.09.005 · Cited by 853
Inhibitory threshold for critical-period activation in primary visual cortex
Fagiolini, M., & Hensch, T. K. (2000) · Nature · doi:10.1038/35004582 · Cited by 716
Development and plasticity of the primary visual cortex
Espinosa, J. S., & Stryker, M. P. (2012) · Neuron · doi:10.1016/j.neuron.2012.06.009 · Cited by 672
Self-citationExperience-driven plasticity of visual cortex limited by myelin and nogo receptor
McGee, A. W., Yang, Y., Fischer, Q. S., Daw, N. W., & Strittmatter, S. M. (2005) · Science · doi:10.1126/science.1114362 · Cited by 643
Regulation of NMDA receptor subunit expression and its implications for LTD, LTP, and metaplasticity
Yashiro, K., & Philpot, B. D. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.07.046 · Cited by 649
Chattopadhyaya, B., Di Cristo, G., Higashiyama, H., Knott, G. W., Kuhlman, S. J., Welker, E., & Huang, Z. J. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.1851-04.2004 · Cited by 596
The “quad‐partite” synapse: Microglia‐synapse interactions in the developing and mature CNS
Schafer, D. P., Lehrman, E. K., & Stevens, B. (2013) · Glia · doi:10.1002/glia.22389 · Cited by 570
Critical periods for experience-dependent synaptic scaling in visual cortex
Desai, N. S., Cudmore, R. H., Nelson, S. B., & Turrigiano, G. G. (2002) · Nature Neuroscience · doi:10.1038/nn878 · Cited by 582
Ultrastructure of dendritic spines: correlation between synaptic and spine morphologies
Arellano, J. I. (2007) · Frontiers in Neuroscience · doi:10.3389/neuro.01.1.1.010.2007 · Cited by 529
Animals lacking link protein have attenuated perineuronal nets and persistent plasticity
Carulli, D., Pizzorusso, T., Kwok, J. C. F., Putignano, E., Poli, A., Forostyak, S., Andrews, M. R., Deepa, S. S., Glant, T. T., & Fawcett, J. W. (2010) · Brain · doi:10.1093/brain/awq145 · Cited by 495
Neuromodulatory transmitter systems in the cortex and their role in cortical plasticity
Gu, Q. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00026-x · Cited by 518
Experience leaves a lasting structural trace in cortical circuits
Hofer, S. B., Mrsic-Flogel, T. D., Bonhoeffer, T., & Hübener, M. (2009) · Nature · doi:10.1038/nature07487 · Cited by 514
Microglial P2Y12 is necessary for synaptic plasticity in mouse visual cortex
Sipe, G. O., Lowery, Tremblay, M.-È., Kelly, E. A., Lamantia, C. E., & Majewska, A. K. (2016) · Nature Communications · doi:10.1038/ncomms10905 · Cited by 512
Sugiyama, S., Di Nardo, A. A., Aizawa, S., Matsuo, I., Volovitch, M., Prochiantz, A., & Hensch, T. K. (2008) · Cell · doi:10.1016/j.cell.2008.05.054 · Cited by 491
Specific GABA A Circuits for Visual Cortical Plasticity
Fagiolini, M., Fritschy, J.-M., Löw, K., Möhler, H., Rudolph, U., & Hensch, T. K. (2004) · Science · doi:10.1126/science.1091032 · Cited by 471
Brain-Derived Neurotrophic Factor Is Required for the Maintenance of Cortical Dendrites
Gorski, J. A., Zeiler, S. R., Tamowski, S., & Jones, K. R. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-17-06856.2003 · Cited by 411
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
A disinhibitory microcircuit initiates critical-period plasticity in the visual cortex
Kuhlman, S. J., Olivas, N. D., Tring, E., Ikrar, T., Xu, X., & Trachtenberg, J. T. (2013) · Nature · doi:10.1038/nature12485 · Cited by 412
How Monocular Deprivation Shifts Ocular Dominance in Visual Cortex of Young Mice
Frenkel, M. Y., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.12.003 · Cited by 412
Kaneko, M., Stellwagen, D., Malenka, R. C., & Stryker, M. P. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.023 · Cited by 405
Self-citationCritical-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
Otx2 Binding to Perineuronal Nets Persistently Regulates Plasticity in the Mature Visual Cortex
Beurdeley, M., Spatazza, J., Lee, H. H. C., Sugiyama, S., Bernard, C., Di Nardo, A. A., Hensch, T. K., & Prochiantz, A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0394-12.2012 · Cited by 398
Bhatt, D. H., Zhang, S., & Gan, W.-B. (2009) · Annual Review of Physiology · doi:10.1146/annurev.physiol.010908.163140 · Cited by 380
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
Persistent cortical plasticity by upregulation of chondroitin 6-sulfation
Miyata, S., Komatsu, Y., Yoshimura, Y., Taya, C., & Kitagawa, H. (2012) · Nature Neuroscience · doi:10.1038/nn.3023 · Cited by 365
Nurturing brain plasticity: Impact of environmental enrichment
Baroncelli, L., Braschi, C., Spolidoro, M., Begenisic, T., Sale, A., & Maffei, L. (2010) · Cell Death & Differentiation · doi:10.1038/cdd.2009.193 · Cited by 330
Ube3a is required for experience-dependent maturation of the neocortex
Yashiro, K., Riday, T. T., Condon, K. H., Roberts, A. C., Bernardo, D. R., Prakash, R., Weinberg, R. J., Ehlers, M. D., & Philpot, B. D. (2009) · Nature Neuroscience · doi:10.1038/nn.2327 · Cited by 328
Homeostatic Regulation of Eye-Specific Responses in Visual Cortex during Ocular Dominance Plasticity
Mrsic-Flogel, T. D., Hofer, S. B., Ohki, K., Reid, R. C., Bonhoeffer, T., & Hübener, M. (2007) · Neuron · doi:10.1016/j.neuron.2007.05.028 · Cited by 330
Stowell, R. D., Sipe, G. O., Dawes, R. P., Batchelor, H. N., Lordy, K. A., Whitelaw, B. S., Stoessel, M. B., Bidlack, J. M., Brown, E., Sur, M., et al. (2019) · Nature Neuroscience · doi:10.1038/s41593-019-0514-0 · Cited by 321
Critical period revisited: impact on vision
Morishita, H., & Hensch, T. K. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.05.009 · Cited by 311
Autism: A “Critical Period” Disorder?
LeBlanc, J. J., & Fagiolini, M. (2011) · Neural Plasticity · doi:10.1155/2011/921680 · Cited by 301
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
Multiple Modes of Network Homeostasis in Visual Cortical Layer 2/3
Maffei, A., & Turrigiano, G. G. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.5298-07.2008 · Cited by 282
Cortical Plasticity Induced by Inhibitory Neuron Transplantation
Southwell, D. G., Froemke, R. C., Alvarez-Buylla, A., Stryker, M. P., & Gandhi, S. P. (2010) · Science · doi:10.1126/science.1183962 · Cited by 271
Self-citationHanover, T. J. L., Huang, Z. J., Tonegawa, S., & Stryker, M. P. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-22-j0003.1999 · Cited by 265
Self-citationExcitatory-inhibitory balance and critical period plasticity in developing visual cortex
Hensch, T. K., & Fagiolini, M. (2005) · Progress in Brain Research · doi:10.1016/s0079-6123(04)47009-5 · Cited by 267
Mechanisms of sleep-dependent consolidation of cortical plasticity
Aton, S. J., Seibt, J., Dumoulin, M., Jha, S. K., Steinmetz, N., Coleman, T., Naidoo, N., & Frank, M. G. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.007 · 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-citationFunctional recovery with recombinant human IGF1 treatment in a mouse model of Rett syndrome
Castro, J., Garcia, R. I., Kwok, S., Banerjee, A., Petravicz, J., Woodson, J., Mellios, N., Tropea, D., & Sur, M. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1311685111 · Cited by 242
Neuronal Plasticity: Beyond the Critical Period
Hübener, M., & Bonhoeffer, T. (2014) · Cell · doi:10.1016/j.cell.2014.10.035 · Cited by 237
Reinhard, S. M., Razak, K., & Ethell, I. M. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00280 · Cited by 219
Tropea, D., Kreiman, G., Lyckman, A., Mukherjee, S., Yu, H., Horng, S., & Sur, M. (2006) · Nature Neuroscience · doi:10.1038/nn1689 · Cited by 226
Structural basis for the role of inhibition in facilitating adult brain plasticity
Chen, J. L., Lin, W. C., Cha, J. W., So, P. T., Kubota, Y., & Nedivi, E. (2011) · Nature Neuroscience · doi:10.1038/nn.2799 · Cited by 214
The visual physiology of the wild type mouse determined with pattern VEPs
Porciatti, V., Pizzorusso, T., & Maffei, L. (1999) · Vision Research · doi:10.1016/s0042-6989(99)00022-x · Cited by 202
Critical Period Plasticity Matches Binocular Orientation Preference in the Visual Cortex
Wang, B.-S., Sarnaik, R., & Cang, J. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.002 · Cited by 209
Rapid critical period induction by tonic inhibition in visual cortex
Iwai, Y., Fagiolini, M., Obata, K., & Hensch, T. K. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-17-06695.2003 · Cited by 201
HENSCH, T. K., & QUINLAN, E. M. (2018) · Visual Neuroscience · doi:10.1017/s0952523817000219 · Cited by 206
Visual cortex is rescued from the effects of dark rearing by overexpression of BDNF
Gianfranceschi, L., Siciliano, R., Walls, J., Morales, B., Kirkwood, A., Huang, Z. J., Tonegawa, S., & Maffei, L. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1934836100 · Cited by 201
Bidirectional plasticity in fast-spiking GABA circuits by visual experience
Yazaki-Sugiyama, Y., Kang, S., Câteau, H., Fukai, T., & Hensch, T. K. (2009) · Nature · doi:10.1038/nature08485 · Cited by 200
Reversing Neurodevelopmental Disorders in Adults
Ehninger, D., Li, W., Fox, K., Stryker, M. P., & Silva, A. J. (2008) · Neuron · doi:10.1016/j.neuron.2008.12.007 · Cited by 196
Self-citationPutignano, E., Lonetti, G., Cancedda, L., Ratto, G., Costa, M., Maffei, L., & Pizzorusso, T. (2007) · Neuron · doi:10.1016/j.neuron.2007.02.007 · Cited by 196
Sensory experience regulates cortical inhibition by inducing IGF1 in VIP neurons
Mardinly, A. R., Spiegel, I., Patrizi, A., Centofante, E., Bazinet, J. E., Tzeng, C. P., Mandel-Brehm, C., Harmin, D. A., Adesnik, H., Fagiolini, M., et al. (2016) · Nature · doi:10.1038/nature17187 · Cited by 176
miR-132, an experience-dependent microRNA, is essential for visual cortex plasticity
Mellios, N., Sugihara, H., Castro, J., Banerjee, A., Le, C., Kumar, A., Crawford, B., Strathmann, J., Tropea, D., Levine, S. S., et al. (2011) · Nature Neuroscience · doi:10.1038/nn.2909 · Cited by 189
Does puberty mark a transition in sensitive periods for plasticity in the associative neocortex?
Piekarski, D. J., Johnson, C. M., Boivin, J. R., Thomas, A. W., Lin, W. C., Delevich, K., M. Galarce, E., & Wilbrecht, L. (2017) · Brain Research · doi:10.1016/j.brainres.2016.08.042 · Cited by 175
Toyoizumi, T., Miyamoto, H., Yazaki-Sugiyama, Y., Atapour, N., Hensch, T. K., & Miller, K. D. (2013) · Neuron · doi:10.1016/j.neuron.2013.07.022 · Cited by 158
Loss of Arc renders the visual cortex impervious to the effects of sensory experience or deprivation
McCurry, C. L., Shepherd, J. D., Tropea, D., Wang, K. H., Bear, M. F., & Sur, M. (2010) · Nature Neuroscience · doi:10.1038/nn.2508 · Cited by 159
Ye, Q., & Miao, Q.-L. (2013) · Matrix Biology · doi:10.1016/j.matbio.2013.04.001 · Cited by 146
Krishnan, K., Wang, B.-S., Lu, J., Wang, L., Maffei, A., Cang, J., & Huang, Z. J. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1506499112 · Cited by 146
Greifzu, F., Pielecka-Fortuna, J., Kalogeraki, E., Krempler, K., Favaro, P. D., Schlüter, O. M., & Löwel, S. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1313385111 · Cited by 144
Venturino, A., Schulz, R., De Jesús-Cortés, H., Maes, M. E., Nagy, B., Reilly-Andújar, F., Colombo, G., Cubero, R. J. A., Schoot Uiterkamp, F. E., Bear, M. F., et al. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109313 · Cited by 140
Vetencourt, J. F. M., Tiraboschi, E., Spolidoro, M., Castrén, E., & Maffei, L. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07488.x · Cited by 138
Manipulating critical period closure across different sectors of the primary auditory cortex
de Villers-Sidani, E., Simpson, K. L., Lu, Y.-F., Lin, R. C. S., & Merzenich, M. M. (2008) · Nature Neuroscience · doi:10.1038/nn.2144 · Cited by 137
Sensory experience during locomotion promotes recovery of function in adult visual cortex
Kaneko, M., & Stryker, M. P. (2014) · eLife · doi:10.7554/elife.02798 · Cited by 126
Self-citationHensch, T. K., Gordon, J. A., Brandon, E. P., McKnight, G. S., Idzerda, R. L., & Stryker, M. P. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-06-02108.1998 · Cited by 117
Self-citationHe, L.-J., Liu, N., Cheng, T.-L., Chen, X.-J., Li, Y.-D., Shu, Y.-S., Qiu, Z.-L., & Zhang, X.-H. (2014) · Nature Communications · doi:10.1038/ncomms6036 · Cited by 107
Nowicka, D., Soulsby, S., Skangiel‐Kramska, J., & Glazewski, S. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06996.x · Cited by 110
Sleep-Dependent Plasticity Requires Cortical Activity
Jha, S. K., Jones, B. E., Coleman, T., Steinmetz, N., Law, C.-T., Griffin, G., Hawk, J., Dabbish, N., Kalatsky, V. A., & Frank, M. G. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2722-05.2005 · Cited by 96
Tropea, D., Majewska, A. K., Garcia, R., & Sur, M. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.1661-10.2010 · Cited by 92
A precritical period for plasticity in visual cortex
Feller, M. B., & Scanziani, M. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.01.012 · Cited by 92
Guire, E. S., Lickey, M. E., & Gordon, B. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.81.1.121 · Cited by 83
From brain formation to plasticity: Insights on Otx2 homeoprotein
Sugiyama, S., Prochiantz, A., & Hensch, T. K. (2009) · Development, Growth & Differentiation · doi:10.1111/j.1440-169x.2009.01093.x · Cited by 77
Kim, H., Kunz, P. A., Mooney, R., Philpot, B. D., & Smith, S. L. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.4204-15.2016 · Cited by 65
Subanesthetic Ketamine Reactivates Adult Cortical Plasticity to Restore Vision from Amblyopia
Grieco, S. F., Qiao, X., Zheng, X., Liu, Y., Chen, L., Zhang, H., Yu, Z., Gavornik, J. P., Lai, C., Gandhi, S. P., et al. (2020) · Current Biology · doi:10.1016/j.cub.2020.07.008 · Cited by 60
Rupert, D. D., & Shea, S. D. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2022.886629 · Cited by 58
The role of GABAergic inhibition in ocular dominance plasticity
Heimel, J. A., van Versendaal, D., & Levelt, C. N. (2011) · Neural Plasticity · doi:10.1155/2011/391763 · Cited by 57
Kaneko, M., Xie, Y., An, J. J., Stryker, M. P., & Xu, B. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.4462-11.2012 · Cited by 55
Self-citationKelly, E. A., Russo, A. S., Jackson, C. D., Lamantia, C. E., & Majewska, A. K. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00369 · Cited by 48
From pupil to the brain: New insights for studying cortical plasticity through pupillometry
Viglione, A., Mazziotti, R., & Pizzorusso, T. (2023) · Frontiers in Neural Circuits · doi:10.3389/fncir.2023.1151847 · Cited by 48
Brief dark exposure restored ocular dominance plasticity in aging mice and after a cortical stroke
Stodieck, S. K., Greifzu, F., Goetze, B., Schmidt, K.-F., & Löwel, S. (2014) · Experimental Gerontology · doi:10.1016/j.exger.2014.09.007 · Cited by 43
Myers, A. K., Ray, J., & Kulesza, R. J. (2012) · Brain Research · doi:10.1016/j.brainres.2012.05.024 · Cited by 34
Isochronic development of cortical synapses in primates and mice
Wildenberg, G., Li, H., Sampathkumar, V., Sorokina, A., & Kasthuri, N. (2023) · Nature Communications · doi:10.1038/s41467-023-43088-3 · Cited by 31
Enhancement of visual cortex plasticity by dark exposure
Erchova, I., Vasalauskaite, A., Longo, V., & Sengpiel, F. (2017) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2016.0159 · Cited by 32
Regional and temporal specificity of intrinsic plasticity mechanisms in rodent primary visual cortex
Nataraj, K., & Turrigiano, G. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.4455-11.2011 · Cited by 23
Pielecka-Fortuna, J., Kalogeraki, E., Fortuna, M. G., & Löwel, S. (2015) · eLife · doi:10.7554/elife.11290 · Cited by 21
Nagakura, I., Van Wart, A., Petravicz, J., Tropea, D., & Sur, M. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0189-14.2014 · Cited by 18
Cannarozzo, C., Rubiolo, A., Casarotto, P., & Castrén, E. (2022) · doi:10.1101/2022.04.06.487292 · Cited by 2
Metadata
- Authors
- Gordon, J. A., & Stryker, M. P.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 1996-05-15
- Volume
- 16
- Issue
- 10
- Pages
- 3274-3286
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- OpenAlex
- W1842266333
- Cited by
- 854
- References
- 6
- FWCI
- 6.17
- Type
- journal article
- Language
- en
- Open access
- hybrid
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 ›
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Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.