Synaptic basis for developmental plasticity in somatosensory cortex

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

Theory for the development of neuron selectivity: orientation specificity and binocular interaction in visual cortex

Bienenstock, E., Cooper, L., & Munro, P. (1982) · The Journal of Neuroscience · doi:10.1523/jneurosci.02-01-00032.1982 · Cited by 2,896

The structural organization of layer IV in the somatosensory region (S I) of mouse cerebral cortex

Woolsey, T. A., & Van der Loos, H. (1970) · Brain Research · doi:10.1016/0006-8993(70)90079-x · Cited by 2,254

CORTICAL PLASTICITY: From Synapses to Maps

Buonomano, D. V., & Merzenich, M. M. (1998) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.21.1.149 · Cited by 2,083

Long-term in vivo imaging of experience-dependent synaptic plasticity in adult cortex

Trachtenberg, J. T., Chen, B. E., Knott, G. W., Feng, G., Sanes, J. R., Welker, E., & Svoboda, K. (2002) · Nature · doi:10.1038/nature01273 · Cited by 1,927

Learning-Induced LTP in Neocortex

Rioult-Pedotti, M.-S., Friedman, D. J., & Donoghue, J. P. (2000) · Science · doi:10.1126/science.290.5491.533 · Cited by 1,014

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

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

Selection of Intrinsic Horizontal Connections in the Visual Cortex by Correlated Neuronal Activity

Löwel, S., & Singer, W. (1992) · Science · doi:10.1126/science.1372754 · Cited by 732

Nervous system reorganization following injury

Chen, R. E., Cohen, L. G., & Hallett, M. (2002) · Neuroscience · doi:10.1016/s0306-4522(02)00025-8 · Cited by 726

Neurotransmissão glutamatérgica e plasticidade sináptica: aspectos moleculares, clínicos e filogenéticos

Ruggiero, R. N., Bueno-Júnior, L. S., Ross, J. B. D., Fachim, H., Padovan‐Neto, F. E., Merlo, S., Rohner, C. J. S., Ikeda, E. T., Brusco, J., & Moreira, J. E. (2011) · Medicina (Ribeirão Preto) · doi:10.11606/issn.2176-7262.v44i2p143-156 · Cited by 9

Activity-Dependent Thalamocortical Axon Branching

Hayano, Y., & Yamamoto, N. (2008) · The Neuroscientist · doi:10.1177/1073858408317272 · Cited by 8

How Visual Body Perception Influences Somatosensory Plasticity

Kuehn, E., & Pleger, B. (2018) · Neural Plasticity · doi:10.1155/2018/7909684 · Cited by 9

Terminal Arbors of Callosal Axons Undergo Plastic Changes in Early-Amputated Rats

Bahia, C. P., Vianna-Barbosa, R. J., Tovar-Moll, F. F., & Lent, R. (2018) · Cerebral Cortex · doi:10.1093/cercor/bhy043 · Cited by 6

Erratum to “Consensus Paper: Probing Homeostatic Plasticity of Human Cortex With Non-invasive Transcranial Brain Stimulation”. Brain Stimulation 8 (2015) 442–454

Karabanov, A., Ziemann, U., Hamada, M., George, M. S., Quartarone, A., Classen, J., Massimini, M., Rothwell, J., & Siebner, H. R. (2015) · Brain Stimulation · doi:10.1016/j.brs.2015.06.016 · Cited by 5

Spontaneous Generation in Early Sensory Development. Focus on “Spontaneous Discharge Patterns in Cochlear Spiral Ganglion Cells Before the Onset of Hearing in Cats”

Köppl, C. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00844.2007 · Cited by 5

Metabolic barrel representations with various patterns of neonatal whisker deafferentation in rats

Shin, J. W., Lee, D., Jung, H., & Sohn, N. (2005) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2005.05.006 · Cited by 4

Reduction of cutaneous von Frey thresholds in boys with autism following a year of tactile and emotional stimulation

Fernández-Lechuga, A. I., Nuñez-Arcos, L. Y., Carrillo, P., García, L. I., Coria‐Ávila, G. A., Toledo‐Cárdenas, M. R., Hernández‐Aguilar, M. E., & Manzo, J. G. (2021) · Revista de Fomento Social · doi:10.24875/rmn.20000002 · Cited by 3

Selective antagonists of calcium-permeable GluA1 AMPA-receptors as potential antiaddictive agents

Potapkin, A. M., Гмиро, В. Е., & Shabanov, P. D. (2023) · Психофармакология и биологическая наркология · doi:10.17816/phbn267069 · Cited by 4

CRYAA and GJA8 promote visual development after whisker tactile deprivation

Zhang, S., Liu, C., Wang, Q., Zhou, H., Wu, H., Zhuang, J., Cao, Y., Shi, H., Zhang, J., & Wang, J. (2023) · Heliyon · doi:10.1016/j.heliyon.2023.e13897 · Cited by 3

Effect of norepinephrine depletion on induction of experience dependent plasticity in male rats barrel cortex

Sheibani, V., Arabzadeh, S., Afarineshkhaki, M., Shamsizadeh, A., Aminizadeh, H., & Azizollahi, S. (2008) · Cited by 3

Long-Term Measurements

Graziane, N., & Dong, Y. (2015) · Neuromethods · doi:10.1007/978-1-4939-3274-0_12 · Cited by 3

Neurodevelopmental outcome, developmental trajectories, and management in 22q11.2 deletion syndrome

Swillen, A. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-816047-3.00013-7 · Cited by 2

4-EA-NBOMe, an amphetamine derivative, alters glutamatergic synaptic transmission through 5-HT1A receptors on cortical neurons from Sprague Dawley rat and pyramidal neurons from C57BL/6 mouse

Oh, H., Yoo, J. H., Kim, Y., Han, K., & Woo, D. H. (2023) · NeuroToxicology · doi:10.1016/j.neuro.2023.02.001 · Cited by 2

Rho Guanine Nucleotide Exchange Factors Regulate Horizontal Axon Branching of Cortical Upper Layer Neurons

Sasaki, K., Arimoto, K., Kankawa, K., Terada, C., Yamamori, T., Watakabe, A., & Yamamoto, N. (2019) · Cerebral Cortex · doi:10.1093/cercor/bhz256 · Cited by 3

Pattern selection in the visual cortex

Kaschube, M. (2006) · doi:10.53846/goediss-2890 · Cited by 2

Cooperative Multi-user Motor-Imagery BCI Based on the Riemannian Manifold and CSP Classifiers

Titaev, S. A. (2022) · Studies in computational intelligence · doi:10.1007/978-3-030-96993-6_60 · Cited by 1

Papel de las subunidades alfa del receptor GABAA en la regulación de la conducta agresiva

Martín‐López, M., & Navarro, J. F. (2009) · Psiquiatría Biológica · Cited by 1

Long-term cortical plasticity following sensory deprivation is reduced in male Rett model mice

Farhoomand, F., & Delaney, K. R. (2022) · Somatosensory & Motor Research · doi:10.1080/08990220.2022.2158799 · Cited by 1

Synaptic plasticity in drug abuse disorders : Studies of the human post-mortem brain

Ökvist, A. (2009) · Figshare · Cited by 1

Metabotropic signaling within somatostatin interneurons controls transient thalamocortical inputs during developmentPreprint

Dwivedi, D., Dumontier, D., Sherer, M., Lin, S., Mirow, A. M., Qiu, Y., Xu, Q., Liebman, S. A., Joseph, D., Datta, S. R., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.09.21.558862 · Cited by 1

Making Sense of Words through the Eyes of a Child

Gläser, C. (2011)

CircuitandPlasticityDefectsintheDeveloping SomatosensoryCortexofFmr1Knock-OutMice

Shepherd, G. M. (2008)

plasticidade sináptica: aspectos mo- plasticidade sináptica: aspectos mo- plasticidade sináptica: aspectos mo- plasticidade sináptica: aspectos mo- plasticidade sináptica: aspectos mo- lecular

Ruggiero, R. N., Bueno-Júnior, L. S., Ross, J. B. D., Fachim, H., Padovan‐Neto, F. E., Merlo, S., Rohner, C. J. S., Ikeda, E. T., Brusco, J., & Moreira, J. E. (2011)

Inter-trial Coherence as a Marker of Cortical Dys-synchrony in Children with Auditory Neuropathy Spectrum Disorder (ANSD)

Nash-Kille, A. (2013) · CU Scholar (University of Colorado Boulder)

Pre- and Postsynaptic Assembly and Maturation

Sigrist, S. J., & Wichmann, C. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397266-8.00008-9

Neuronal Activity-Dependent Development of the Nociceptive Circuit in Drosophila

Kaneko, T. (2018) · Deep Blue (University of Michigan)

Neurophysiologic and proteomic investigations of experience-dependent plasticity in the somatosensory cortex of the adult mouse following chronic whisker stimulation

Quairiaux, C. (2005) · reroDoc Digital Library · doi:10.22005/bcu.15965

Effects of Whisker-Trimming on GABAA Receptors in S1 Cortex

Salazar, E. (2004) · doi:10.12794/metadc4576

Darwinian computation with a functional map of the auditory cortex

Takahashi, H. (2020) · Nippon Onkyo Gakkaishi/Acoustical science and technology/Nihon Onkyo Gakkaishi · doi:10.1250/ast.41.39

TMS and TMS-EEG studies on the excitability, connectivity and plasticity of the human motor cortex

Ferreri, F. (2011) · UEF eRepo (University of Eastern Finland)

Pannexin-1-Dependent Long-Term Depression at the CA3-CA1 Synapse

Werner, A. C. (2021) · doi:10.11575/prism/38720

SPECIFICITY OF INHIBITORY CONTROL OF CORTICAL INTERNEURONS IN LAYER 4 OF MOUSE SOMATOSENSORY BARREL CORTEX

Krook-Magnuson, E. I. (2009) · DigitalGeorgetown (Georgetown University Library)

Long-Term Measurements

Graziane, N., & Dong, Y. (2022) · Neuromethods · doi:10.1007/978-1-0716-2589-7_12

Spike Timing-Dependent Plasticity at Layer 2/3 Horizontal Connections Between Neighboring Columns During Synapse Formation Before the Critical Period in the Developing Barrel Cortex

Itami, C., & Kimura, F. (2025) · Cells · doi:10.3390/cells14181459

Heterogeneity of interneuron circuit function in sensory processing and synaptic plasticity

Li, P. (2011) · DigitalGeorgetown (Georgetown University Library)

Synaptic mechanisms for plasticity in neocortex

Feldman, D. E. (2009) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.051508.135516 · Cited by 704

LTD, Spike Timing and Somatosensory Barrel Cortex Plasticity

Feldman, D. E., Allen, C. B., & Celikel, T. (2003) · Springer eBooks · doi:10.1007/978-1-4615-0039-1_15 · Cited by 3

Map Plasticity in Somatosensory Cortex

Okamoto, K., Nagai, T., Miyawaki, A., Hayashi, Y., Berardi, N., Pizzorusso, T., Ratto, G. M., & Maffei, L. (2005)

Plasticity and stability of somatosensory maps in thalamus and cortex

Fox, K. D., Glazewski, S., & Schulze, S. (2000) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00112-4 · Cited by 57

Sensory experience modifies the short-term dynamics of neocortical synapses

Finnerty, G. T., Roberts, L., & Connors, B. W. (1999) · Nature · doi:10.1038/22553 · Cited by 264