HOMEOSTATIC CONTROL OF NEURAL ACTIVITY: From Phenomenology to Molecular Design

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

Activity-dependent scaling of quantal amplitude in neocortical neurons

Turrigiano, G. G., Leslie, K. R., Desai, N. S., Rutherford, L. C., & Nelson, S. B. (1998) · Nature · doi:10.1038/36103 · Cited by 2,226

Synaptic scaling mediated by glial TNF-α

Stellwagen, D., & Malenka, R. C. (2006) · Nature · doi:10.1038/nature04671 · Cited by 1,715

Robustness in simple biochemical networks

Barkai, N., & Leibler, S. (1997) · Nature · doi:10.1038/43199 · Cited by 1,513

Control of Synaptic Strength by Glial TNFα

Beattie, E. C., Stellwagen, D., Morishita, W., Bresnahan, J. C., Ha, B. K., Von Zastrow, M., Beattie, M. S., & Malenka, R. C. (2002) · Science · doi:10.1126/science.1067859 · Cited by 1,344

AMPA receptor trafficking at excitatory synapses

Bredt, D. S., & Nicoll, R. A. (2003) · Neuron · doi:10.1016/s0896-6273(03)00640-8 · Cited by 1,150

Robustness in bacterial chemotaxis

Alon, U. S., Surette, M. G., Barkai, N., & Leibler, S. (1999) · Nature · doi:10.1038/16483 · Cited by 1,129

Similar network activity from disparate circuit parameters

Prinz, A. A., Bucher, D., & Marder, E. (2004) · Nature Neuroscience · doi:10.1038/nn1352 · Cited by 1,091

Robustness of cellular functions

Stelling, J., Sauer, U., Szallasi, Z., Doyle, F. J., & Doyle, J. (2004) · Cell · doi:10.1016/j.cell.2004.09.008 · Cited by 1,049

Robust perfect adaptation in bacterial chemotaxis through integral feedback control

Yi, T., Huang, Y. H., Simon, M. I., & Doyle, J. C. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.9.4649 · Cited by 1,038

Continual lifelong learning with neural networks: A review

Parisi, G. I., Kemker, R., Part, J. L., Kanan, C., & Wermter, S. (2019) · Neural Networks · doi:10.1016/j.neunet.2019.01.012 · Cited by 3,117

The self-tuning neuron: synaptic scaling of excitatory synapses

Turrigiano, G. G. (2008) · Cell · doi:10.1016/j.cell.2008.10.008 · Cited by 1,533

Variability, compensation and homeostasis in neuron and network function

Marder, E., & Goaillard, J.-M. (2006) · Nature Reviews Neuroscience · doi:10.1038/nrn1949 · Cited by 1,212

Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function

Turrigiano, G. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005736 · Cited by 1,139

Excitatory/Inhibitory Balance and Circuit Homeostasis in Autism Spectrum Disorders

Nelson, S. B., & Valakh, V. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.033 · Cited by 1,001

Synaptic AMPA receptor plasticity and behavior

Kessels, H. W., & Malinow, R. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.015 · Cited by 993

Too many cooks? Intrinsic and synaptic homeostatic mechanisms in cortical circuit refinement

Turrigiano, G. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-060909-153238 · Cited by 671

Unraveling mechanisms of homeostatic synaptic plasticity

Pozo, K., & Goda, Y. (2010) · Neuron · doi:10.1016/j.neuron.2010.04.028 · Cited by 565

MeCP2 Controls Excitatory Synaptic Strength by Regulating Glutamatergic Synapse Number

Chao, H.-T., Zoghbi, H. Y., & Rosenmund, C. (2007) · Neuron · doi:10.1016/j.neuron.2007.08.018 · Cited by 511

An integrative model of tinnitus based on a central gain controlling neural sensitivity

Noreña, A. J. (2010) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2010.11.003 · Cited by 460

Multiple models to capture the variability in biological neurons and networks

Marder, E., & Taylor, A. L. (2011) · Nature Neuroscience · doi:10.1038/nn.2735 · Cited by 451

Synaptic Signaling by All-Trans Retinoic Acid in Homeostatic Synaptic Plasticity

Aoto, J., Nam, C. I., Poon, M. M., Ting, P., & Chen, L. (2008) · Neuron · doi:10.1016/j.neuron.2008.08.012 · Cited by 397

Mechanisms Underlying the Rapid Induction and Sustained Expression of Synaptic Homeostasis

Frank, C. A., Kennedy, M. J., Goold, C. P., Marek, K. W., & Davis, G. W. (2006) · Neuron · doi:10.1016/j.neuron.2006.09.029 · Cited by 384

Firing Rate Homeostasis in Visual Cortex of Freely Behaving Rodents

Hengen, K. B., Lambo, M. E., Hooser, S. D. V., Katz, D. B., & Turrigiano, G. G. (2013) · Neuron · doi:10.1016/j.neuron.2013.08.038 · Cited by 362

Depression of Human Corticospinal Excitability Induced by Magnetic Theta-burst Stimulation: Evidence of Rapid Polarity-Reversing Metaplasticity

Gentner, R., Wankerl, K., Reinsberger, C., Zeller, D., & Claßen, J. (2007) · Cerebral Cortex · doi:10.1093/cercor/bhm239 · Cited by 350

Shaping the Optimal Repetition Interval for Cathodal Transcranial Direct Current Stimulation (tDCS)

Monte-Silva, K. K., Kuo, M., Liebetanz, D., Paulus, W., & Nitsche, M. A. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00924.2009 · Cited by 350

Excitatory/Inhibitory Synaptic Imbalance Leads to Hippocampal Hyperexcitability in Mouse Models of Tuberous Sclerosis

Bateup, H. S., Johnson, C. A., Denefrio, C. L., Saulnier, J. L., Kornacker, K., & Sabatini, B. L. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.017 · Cited by 343

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

Imbalance between firing homeostasis and synaptic plasticity drives early-phase Alzheimer’s disease

Styr, B., & Slutsky, I. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0080-x · Cited by 327

Neurotransmitter Switching in the Adult Brain Regulates Behavior

Dulcis, D., Jamshidi, P., Leutgeb, S., & Spitzer, N. C. (2013) · Science · doi:10.1126/science.1234152 · Cited by 322

Dopamine neurons share common response function for reward prediction error

Eshel, N., Tian, J., Bukwich, M., & Uchida, N. (2016) · Nature Neuroscience · doi:10.1038/nn.4239 · Cited by 321

Neuromodulation of Circuits with Variable Parameters: Single Neurons and Small Circuits Reveal Principles of State-Dependent and Robust Neuromodulation

Marder, E., O'Leary, T., & Shruti, S. (2014) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071013-013958 · Cited by 262

Homeostatic signaling: the positive side of negative feedback

Turrigiano, G. G. (2007) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2007.04.004 · Cited by 284

Activity-Dependent Regulation of Synapses by Retrograde Messengers

Regehr, W. G., Carey, M. R., & Best, A. R. (2009) · Neuron · doi:10.1016/j.neuron.2009.06.021 · Cited by 298

Cell Types, Network Homeostasis, and Pathological Compensation from a Biologically Plausible Ion Channel Expression Model

O’Leary, T., Williams, A. H., Franci, A., & Marder, E. E. (2014) · Neuron · doi:10.1016/j.neuron.2014.04.002 · Cited by 286

SAM68 Regulates Neuronal Activity-Dependent Alternative Splicing of Neurexin-1

Iijima, T., Wu, K., Witte, H., Hanno-Iijima, Y., Glatter, T., Richard, S., & Scheiffele, P. (2011) · Cell · doi:10.1016/j.cell.2011.11.028 · Cited by 279

CDK5 Serves as a Major Control Point in Neurotransmitter Release

Kim, S. H., & Ryan, T. A. (2010) · Neuron · doi:10.1016/j.neuron.2010.08.003 · Cited by 277

Homeostatic Control of Presynaptic Neurotransmitter Release

Davis, G. W., & Müller, M. (2015) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021014-071740 · Cited by 261

Homeostatic Signaling and the Stabilization of Neural Function

Davis, G. W. (2013) · Neuron · doi:10.1016/j.neuron.2013.09.044 · Cited by 276

Diffusional trapping of GluR1 AMPA receptors by input-specific synaptic activity

Ehlers, M. D., Heine, M., Groc, L., Lee, M.-C., & Choquet, D. (2007) · Neuron · doi:10.1016/j.neuron.2007.04.010 · Cited by 300

The dialectic of Hebb and homeostasis

Turrigiano, G. G. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0258 · Cited by 251

Arc/Arg3.1: Linking Gene Expression to Synaptic Plasticity and Memory

Tzingounis, A. V., & Nicoll, R. A. (2006) · Neuron · doi:10.1016/j.neuron.2006.10.016 · Cited by 245

Single-Cell Optogenetic Excitation Drives Homeostatic Synaptic Depression

Goold, C. P., & Nicoll, R. A. (2010) · Neuron · doi:10.1016/j.neuron.2010.09.020 · Cited by 244

Alzheimer’s Disease: From Firing Instability to Homeostasis Network Collapse

Frère, S. G. A., & Slutsky, I. (2018) · Neuron · doi:10.1016/j.neuron.2017.11.028 · Cited by 242

Local Dendritic Activity Sets Release Probability at Hippocampal Synapses

Branco, T., Staras, K., Darcy, K. J., & Goda, Y. (2008) · Neuron · doi:10.1016/j.neuron.2008.07.006 · Cited by 230

Critical Role of CDK5 and Polo-like Kinase 2 in Homeostatic Synaptic Plasticity during Elevated Activity

Seeburg, D. P., Feliú-Mójer, M. I., Gaiottino, J., Pak, D. T. S., & Sheng, M. (2008) · Neuron · doi:10.1016/j.neuron.2008.03.021 · Cited by 239

Transsynaptic Signaling by Activity-Dependent Cleavage of Neuroligin-1

Peixoto, R. T., Kunz, P. A., Kwon, H., Mabb, A. M., Sabatini, B. L., Philpot, B. D., & Ehlers, M. (2012) · Neuron · doi:10.1016/j.neuron.2012.07.006 · Cited by 233

Spatiotemporally Graded NMDA Spike/Plateau Potentials in Basal Dendrites of Neocortical Pyramidal Neurons

Major, G., Poleg-Polsky, A., Denk, W. T., Schiller, J., & Tank, D. W. (2008) · Journal of Neurophysiology · doi:10.1152/jn.00011.2008 · Cited by 222

Targeted Intron Retention and Excision for Rapid Gene Regulation in Response to Neuronal Activity

Mauger, O., Lemoine, F., & Scheiffele, P. (2016) · Neuron · doi:10.1016/j.neuron.2016.11.032 · Cited by 233

Activity-Dependent Regulation of Synaptic AMPA Receptor Composition and Abundance by β3 Integrins

Cingolani, L. A., Thalhammer, A., Yu, L. M. Y., Catalano, M., Ramos, T., Colicos, M. A., & Goda, Y. (2008) · Neuron · doi:10.1016/j.neuron.2008.04.011 · Cited by 223

Genetics and Cell Biology of Building Specific Synaptic Connectivity

Shen, K., & Scheiffele, P. (2010) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.051508.135302 · Cited by 218

Communication between neurons and astrocytes: relevance to the modulation of synaptic and network activity

Fellin, T. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05830.x · Cited by 245

The Schizophrenia Susceptibility Gene dysbindin Controls Synaptic Homeostasis

Dickman, D. K., & Davis, G. W. (2009) · Science · doi:10.1126/science.1179685 · Cited by 212

Genetic controls balancing excitatory and inhibitory synaptogenesis in neurodevelopmental disorder models

Gatto (2010) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2010.00004 · Cited by 204

The temporal paradox of Hebbian learning and homeostatic plasticity

Zenke, F., Gerstner, W., & Ganguli, S. (2017) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2017.03.015 · Cited by 201

The Corneal Pain System. Part I: The Missing Piece of the Dry Eye Puzzle

Rosenthal, P., & Borsook, D. (2012) · The Ocular Surface · doi:10.1016/j.jtos.2012.01.002 · Cited by 199

Impaired Tuning of Neural Ensembles and the Pathophysiology of Schizophrenia: A Translational and Computational Neuroscience Perspective

Krystal, J. H., Anticevic, A., Yang, G., Dragoi, G., Driesen, N. R., Wang, X., & Murray, J. D. (2017) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.01.004 · Cited by 201

Correlations in ion channel expression emerge from homeostatic tuning rules

O'Leary, T., Williams, A. H., Caplan, J. S., & Marder, E. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1309966110 · Cited by 192

Homeostatic Matching and Nonlinear Amplification at Identified Central Synapses

Kazama, H., & Wilson, R. I. (2008) · Neuron · doi:10.1016/j.neuron.2008.02.030 · Cited by 190

A biologically plausible supervised learning method for spiking neural networks using the symmetric STDP rule

Hao, Y., Huang, X., Dong, M., & Xu, B. (2019) · Neural Networks · doi:10.1016/j.neunet.2019.09.007 · Cited by 196

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

cAMP Response Element-Binding Protein-Mediated Gene Expression Increases the Intrinsic Excitability of CA1 Pyramidal Neurons

de Armentia, M. L., Jančić, D., Olivares, R., Alarcón, J. M., Kandel, E. R., & Barco, Á. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3850-07.2007 · Cited by 190

Brain polarization enhances the formation and retention of motor memories.

Galea, J., & Celnik, P. (2009) · Journal of Neurophysiology · doi:10.1152/jn.00184.2009 · Cited by 202

Wnt Signaling Mediates Experience-Related Regulation of Synapse Numbers and Mossy Fiber Connectivities in the Adult Hippocampus

Gogolla, N., Galimberti, I., Deguchi, Y., & Caroni, P. (2009) · Neuron · doi:10.1016/j.neuron.2009.04.022 · Cited by 181

Homeostatic regulation of AMPA receptor expression at single hippocampal synapses

Hou, Q., Zhang, D., Jarzylo, L., Huganir, R. L., & Man, H.-Y. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706447105 · Cited by 179

RIM Controls Homeostatic Plasticity through Modulation of the Readily-Releasable Vesicle Pool

Müller, M., Liu, K. S. Y., Sigrist, S. J., & Davis, G. W. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0981-12.2012 · Cited by 183

Fragile X Protein FMRP Is Required for Homeostatic Plasticity and Regulation of Synaptic Strength by Retinoic Acid

Soden, M. E., & Chen, L. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.3660-10.2010 · Cited by 181

Homeostatic plasticity in human motor cortex demonstrated by two consecutive sessions of paired associative stimulation

Müller, J. F. M., Orekhov, Y., Liu, Y., & Ziemann, U. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05603.x · Cited by 178

What Is Neural Plasticity?

Rommy von Bernhardi, M., Bernhardi, L. E.-V., & Eugenín, J. L. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-62817-2_1 · Cited by 214

Local Presynaptic Activity Gates Homeostatic Changes in Presynaptic Function Driven by Dendritic BDNF Synthesis

Jakawich, S. K., Nasser, H. B., Strong, M. J., McCartney, A. J., Perez, A. S., Rakesh, N., Carruthers, C. J. L., & Sutton, M. A. (2010) · Neuron · doi:10.1016/j.neuron.2010.11.034 · Cited by 171

Long-Term Relationships between Synaptic Tenacity, Synaptic Remodeling, and Network Activity

Minerbi, A., Kahana, R., Goldfeld, L., Kaufman, M., Marom, S., & Ziv, N. E. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000136 · Cited by 170

A Presynaptic Homeostatic Signaling System Composed of the Eph Receptor, Ephexin, Cdc42, and CaV2.1 Calcium Channels

Frank, C. A., Pielage, J., & Davis, G. W. (2009) · Neuron · doi:10.1016/j.neuron.2008.12.028 · Cited by 167

Retrograde BMP Signaling Controls Synaptic Growth at the NMJ by Regulating Trio Expression in Motor Neurons

Ball, R. W., Warren-Paquin, M., Tsurudome, K., Liao, E. H., Elazzouzi, F., Cavanagh, C., An, B., Wang, T. T., White, J. H., & Haghighi, A. P. (2010) · Neuron · doi:10.1016/j.neuron.2010.04.011 · Cited by 153

Neuromodulators, Not Activity, Control Coordinated Expression of Ionic Currents

Khorkova, O., & Golowasch, J. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1274-07.2007 · Cited by 149

Phasic Voluntary Movements Reverse the Aftereffects of Subsequent Theta-Burst Stimulation in Humans

Iezzi, E., Conte, A., Suppa, A., Agostino, R., Dinapoli, L., Scontrini, A., & Berardelli, A. (2008) · Journal of Neurophysiology · doi:10.1152/jn.90521.2008 · Cited by 146

Modulation of stomatogastric rhythms

Stein, W. (2009) · Journal of Comparative Physiology A · doi:10.1007/s00359-009-0483-y · Cited by 142

GluA2-lacking, calcium-permeable AMPA receptors--inducers of plasticity?

Man, H.-Y. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.01.001 · Cited by 142

Homeostatic plasticity at the Drosophila neuromuscular junction

Frank, C. A. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.06.015 · Cited by 140

Retinoic acid regulates RARα-mediated control of translation in dendritic RNA granules during homeostatic synaptic plasticity

Maghsoodi, B., Poon, M. M., Nam, C. I., Aoto, J., Ting, P., & Chen, L. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804801105 · Cited by 138

Activity-dependent neurotransmitter respecification

Spitzer, N. C. (2012) · Nature reviews. Neuroscience · doi:10.1038/nrn3154 · Cited by 137

Semaphorins in Adult Nervous System Plasticity and Disease

Carulli, D., de Winter, F., & Verhaagen, J. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.672891 · Cited by 137

The Rett Syndrome Protein MeCP2 Regulates Synaptic Scaling

Qiu, Z., Sylwestrak, E., Lieberman, D. N., Zhang, Y., Liu, X., & Ghosh, A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0175-11.2012 · Cited by 136

A Screen of Cell-Surface Molecules Identifies Leucine-Rich Repeat Proteins as Key Mediators of Synaptic Target Selection

Kurusu, M., Cording, A., Taniguchi, M., Menon, K. P., Suzuki, E., & Zinn, K. (2008) · Neuron · doi:10.1016/j.neuron.2008.07.037 · Cited by 134

Emerging links between homeostatic synaptic plasticity and neurological disease

Wondolowski, J., & Dickman, D. K. (2013) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2013.00223 · Cited by 140

The HTM Spatial Pooler—A Neocortical Algorithm for Online Sparse Distributed Coding

Cui, Y., Ahmad, S., & Hawkins, J. (2017) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2017.00111 · Cited by 142

Synaptic retinoic acid signaling and homeostatic synaptic plasticity

Chen, L., Lau, A. G., & Sarti, F. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.12.004 · Cited by 134

The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders

Willsey, A. J., Morris, M. T., Wang, S., Willsey, H. R., Sun, N., Teerikorpi, N., Baum, T., Cagney, G., Bender, K. J., Desai, T. A., et al. (2018) · Cell · doi:10.1016/j.cell.2018.06.016 · Cited by 129

Morphological Differentiation Towards Neuronal Phenotype of SH-SY5Y Neuroblastoma Cells by Estradiol, Retinoic Acid and Cholesterol

Teppola, H., Sarkanen, J., Jalonen, T. O., & Linne, M. (2015) · Neurochemical Research · doi:10.1007/s11064-015-1743-6 · Cited by 125

Transsynaptic Control of Presynaptic Ca2+ Influx Achieves Homeostatic Potentiation of Neurotransmitter Release

Müller, M., & Davis, G. W. (2012) · Current Biology · doi:10.1016/j.cub.2012.04.018 · Cited by 129

Synapse-Specific Adaptations to Inactivity in Hippocampal Circuits Achieve Homeostatic Gain Control while Dampening Network Reverberation

Kim, J., & Tsien, R. W. (2008) · Neuron · doi:10.1016/j.neuron.2008.05.009 · Cited by 124

Mitochondrial Regulation of the Hippocampal Firing Rate Set Point and Seizure Susceptibility

Styr, B., Gonen, N., Zarhin, D., Ruggiero, A., Atsmon, R., Gazit, N., Braun, G., Frère, S. G. A., Vertkin, I., Shapira, I., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.03.045 · Cited by 122

Homeostatic Synapse-Driven Membrane Plasticity in Nucleus Accumbens Neurons

Ishikawa, M., Mu, P., Moyer, J. T., Wolf, J. A., Quock, R. M., Davies, N. M., Hu, X., Schlüter, O. M., & Dong, Y. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5703-08.2009 · Cited by 121

The BMP Ligand Gbb Gates the Expression of Synaptic Homeostasis Independent of Synaptic Growth Control

Goold, C. P., & Davis, G. W. (2007) · Neuron · doi:10.1016/j.neuron.2007.08.006 · Cited by 123

Neuronal activity regulates glutamate transporter dynamics in developing astrocytes

Benediktsson, A. M., Marrs, G. S., Tu, J. C., Worley, P. F., Rothstein, J. D., Bergles, D. E., & Dailey, M. E. (2011) · Glia · doi:10.1002/glia.21249 · Cited by 127

Pumilio BindsparamRNA and Requires Nanos and Brat to Regulate Sodium Current inDrosophilaMotoneurons

Muraro, N. I., Weston, A. J., Gerber, A. P., Luschnig, S., Moffat, K. G., & Baines, R. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.5092-07.2008 · Cited by 114

Tweek, an Evolutionarily Conserved Protein, Is Required for Synaptic Vesicle Recycling

Verstreken, P., Ohyama, T., Haueter, C. M., Habets, R. L. P., Lin, Y. Q., Swan, L. E., Ly, C. V., Venken, K. J. T., Camilli, P. V. D., & Bellen, H. J. (2009) · Neuron · doi:10.1016/j.neuron.2009.06.017 · Cited by 114

L-Type Voltage-Gated Ca2+Channels: A Single Molecular Switch for Long-Term Potentiation/Long-Term Depression-Like Plasticity and Activity-Dependent Metaplasticity in Humans

Wankerl, K., Weise, D., Gentner, R., Rumpf, J., & Claßen, J. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.4673-09.2010 · Cited by 119

PICK1 loss of function occludes homeostatic synaptic scaling

Anggono, V., Clem, R. L., & Huganir, R. L. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.5633-10.2011 · Cited by 111

Reactive oxygen species regulate activity-dependent neuronal plasticity in Drosophila

Oswald, M. C. W., Brooks, P. S., Zwart, M., Mukherjee, A., West, R. J. H., Giachello, C. N., Morarach, K., Baines, R., Sweeney, S. T., & Landgraf, M. (2018) · eLife · doi:10.7554/elife.39393 · Cited by 113

Compensation for Variable Intrinsic Neuronal Excitability by Circuit-Synaptic Interactions

Grashow, R. G., Brookings, T., & Marder, E. E. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0980-10.2010 · Cited by 112

Characterization of developmental and molecular factors underlying release heterogeneity at Drosophila synapses

Akbergenova, Y., Zhang, Y. V., Weiss, S., Cunningham, K. L., & Littleton, J. T. (2018) · eLife · doi:10.7554/elife.38268 · Cited by 109

Interplay between population firing stability and single neuron dynamics in hippocampal networks

Slomowitz, E., Styr, B., Vertkin, I., Milshtein-Parush, H., Nelken, I., Slutsky, M., & Slutsky, I. (2015) · eLife · doi:10.7554/elife.04378 · Cited by 108

Activity-Induced Polo-Like Kinase 2 Is Required for Homeostatic Plasticity of Hippocampal Neurons during Epileptiform Activity

Seeburg, D. P., & Sheng, M. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1853-08.2008 · Cited by 111

Correlated Connectivity and the Distribution of Firing Rates in the Neocortex

Koulakov, A. A., Hromádka, T., & Zador, A. M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4500-08.2009 · Cited by 104

Homeostatic Synaptic Plasticity through Changes in Presynaptic Calcium Influx

Zhao, C., Dreosti, E., & Lagnado, L. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6636-10.2011 · Cited by 112

Coordinated Changes in Dendritic Arborization and Synaptic Strength during Neural Circuit Development

Peng, Y., He, S., Marie, H., Zeng, S.-Y., Ma, J., Tan, Z.-J., Lee, S. Y., Malenka, R. C., & Yu, X. (2009) · Neuron · doi:10.1016/j.neuron.2008.11.015 · Cited by 111

MicroRNA miR124 is required for the expression of homeostatic synaptic plasticity

Hou, Q., Ruan, H., Gilbert, J. P., Wang, G., Ma, Q., Yao, W., & Man, H. (2015) · Nature Communications · doi:10.1038/ncomms10045 · Cited by 106

Rab3-GAP Controls the Progression of Synaptic Homeostasis at a Late Stage of Vesicle Release

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Homeostatic Regulation of AMPA Receptor Trafficking and Degradation by Light-Controlled Single-Synaptic Activation

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Synaptopodin regulates denervation-induced homeostatic synaptic plasticity

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Molecular mechanisms underlying the bi-directional control of presynaptic homeostatic plasticity

Li, X. (. (2020) · University of Southern California Digital Library · doi:10.25549/usctheses-c89-290112

Editorial: Homeostatic and retrograde signaling mechanisms modulating presynaptic function and plasticity

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Hebb and homeostasis in neuronal plasticity

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Homeostatic and retrograde signaling mechanisms modulating presynaptic function and plasticity

Sutton, M. A., Dickman, D., & Subramanian, J. (2016)

For a review, (q

Yin, J., Yuan, Q., & Subramanian, J. (2016)