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 · see citing works

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 · see citing works

Synaptic scaling mediated by glial TNF-α

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

Robustness in simple biochemical networks

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

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 · see citing works

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 · see citing works

Robustness in bacterial chemotaxis

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

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 · see citing works

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 · see citing works

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 · see citing works

Differential Regulation of AMPA Receptor and GABA Receptor Trafficking by Tumor Necrosis Factor-α

Stellwagen, D., Beattie, E. C., Seo, J. Y., & Malenka, R. C. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.4486-04.2005 · Cited by 985 · cited 1× · see citing works

Plasticity in the intrinsic excitability of cortical pyramidal neurons

Desai, N. S., Rutherford, L. C., & Turrigiano, G. G. (1999) · Nature Neuroscience · doi:10.1038/9165 · Cited by 806 · see citing works

The Roles of APC and Axin Derived from Experimental and Theoretical Analysis of the Wnt Pathway

Lee, E., Salic, A., Krüger, R., Heinrich, R., & Kirschner, M. W. (2003) · PLoS Biology · doi:10.1371/journal.pbio.0000010 · Cited by 708 · see citing works

Hebb and homeostasis in neuronal plasticity

Turrigiano, G. G., & Nelson, S. B. (2000) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00091-x · Cited by 687 · see citing works

Inactivity produces increases in neurotransmitter release and synapse size

Murthy, V. N., Schikorski, T., Stevens, C. F., & Zhu, Y. (2001) · Neuron · doi:10.1016/s0896-6273(01)00500-1 · Cited by 612 · see citing works

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 · see citing works

THE TWO-COMPONENT SIGNALING PATHWAY OF BACTERIAL CHEMOTAXIS: A Molecular View of Signal Transduction by Receptors, Kinases, and Adaptation Enzymes

Falke, J. J., Bass, R. B., Butler, S. L., Chervitz, S. A., & Danielson, M. A. (1997) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.13.1.457 · Cited by 534 · see citing works

Eukaryotic zinc transporters and their regulation

Gaither, L. A., & Eide, D. J. (2001) · BioMetals · doi:10.1023/a:1012988914300 · Cited by 526 · see citing works

wishful thinking Encodes a BMP Type II Receptor that Regulates Synaptic Growth in Drosophila

Aberle, H., Haghighi, A. P., Fetter, R. D., McCabe, B. D., Magalhães, T. R., & Goodman, C. S. (2002) · Neuron · doi:10.1016/s0896-6273(02)00589-5 · Cited by 525 · see citing works

Multiple forms of synaptic plasticity triggered by selective suppression of activity in individual neurons

Burrone, J., O'Byrne, M., & Murthy, V. N. (2002) · Nature · doi:10.1038/nature01242 · Cited by 487 · see citing works

Stargazin modulates AMPA receptor gating and trafficking by distinct domains

Tomita, S., Adesnik, H., Sekiguchi, M., Zhang, W., Wada, K., Howe, J. R., Nicoll, R. A., & Bredt, D. S. (2005) · Nature · doi:10.1038/nature03624 · Cited by 486 · see citing works

Activity-Dependent Changes in the Intrinsic Properties of Cultured Neurons

Turrigiano, G. G., Abbott, L. F., & Marder, E. E. (1994) · Science · doi:10.1126/science.8178157 · Cited by 484 · see citing works

Adaptation to Synaptic Inactivity in Hippocampal Neurons

Thiagarajan, T. C., Lindskog, M., & Tsien, R. W. (2005) · Neuron · doi:10.1016/j.neuron.2005.06.037 · Cited by 482 · see citing works

Genetic Analysis of Glutamate Receptors in Drosophila Reveals a Retrograde Signal Regulating Presynaptic Transmitter Release

Petersen, S. A., Fetter, R. D., Noordermeer, J. N., Goodman, C. S., & DiAntonio, A. (1997) · Neuron · doi:10.1016/s0896-6273(00)80415-8 · Cited by 476 · see citing works

Synapse Formation between Central Neurons Requires Postsynaptic Expression of theMEN1Tumor Suppressor Gene

van Kesteren, R. E., Syed, N. I., Munno, D. W., Bouwman, J., Feng, Z., Geraerts, W. P. M., & Smit, A. B. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-16-j0004.2001 · Cited by 471 · see citing works

GATA-3 Is Involved in the Development of Serotonergic Neurons in the Caudal Raphe Nuclei

van Doorninck, J. H., van der Wees, J., Karis, A., Sabel-Goedknegt, E., Coesmans, M., Rutteman, M., Grosveld, F. G., & Zeeuw, C. I. D. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-12-j0002.1999 · Cited by 416 · see citing works

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 · see citing works

Activity-dependent homeostatic specification of transmitter expression in embryonic neurons

Borodinsky, L. N., Root, C. M., Cronin, J. A., Sann, S. B., Gu, X., & Spitzer, N. C. (2004) · Nature · doi:10.1038/nature02518 · Cited by 396 · see citing works

The BMP Homolog Gbb Provides a Retrograde Signal that Regulates Synaptic Growth at the Drosophila Neuromuscular Junction

McCabe, B. D., Marqués, G., Haghighi, A. P., Fetter, R. D., Crotty, M. L., Haerry, T. E., Goodman, C. S., & O’Connor, M. B. (2003) · Neuron · doi:10.1016/s0896-6273(03)00426-4 · Cited by 390 · see citing works

Alternative to Hand-Tuning Conductance-Based Models: Construction and Analysis of Databases of Model Neurons

Prinz, A. A., Billimoria, C. P., & Marder, E. E. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00641.2003 · Cited by 380 · see citing works

Global structure, robustness, and modulation of neuronal models

Goldman, M. S., Golowasch, J., Marder, E., & Abbott, L. F. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-14-05229.2001 · Cited by 371 · see citing works

Activity Deprivation Reduces Miniature IPSC Amplitude by Decreasing the Number of Postsynaptic GABA _A Receptors Clustered at Neocortical Synapses

Kilman, V., van Rossum, M. C. W., & Turrigiano, G. G. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-04-01328.2002 · Cited by 362 · see citing works

DnaK, DnaJ, and GrpE heat shock proteins negatively regulate heat shock gene expression by controlling the synthesis and stability of sigma 32.Preprint

Straus, D. B., Walter, W. A., & Gross, C. A. (1990) · Genes & Development · doi:10.1101/gad.4.12a.2202 · Cited by 361 · see citing works

Homeostatic plasticity and NMDA receptor trafficking

Pérez-Otaño, I., & Ehlers, M. D. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.03.004 · Cited by 356 · see citing works

Activity Coregulates Quantal AMPA and NMDA Currents at Neocortical Synapses

Watt, A. J., van Rossum, M. C. W., MacLeod, K. M., Nelson, S. B., & Turrigiano, G. G. (2000) · Neuron · doi:10.1016/s0896-6273(00)81202-7 · Cited by 350 · see citing works

Systems-Level Dissection of the Cell-Cycle Oscillator: Bypassing Positive Feedback Produces Damped Oscillations

Pomerening, J. R., Kim, S. Y., & Ferrell, J. E. (2005) · Cell · doi:10.1016/j.cell.2005.06.016 · Cited by 345 · see citing works

Increased Expression of the Drosophila Vesicular Glutamate Transporter Leads to Excess Glutamate Release and a Compensatory Decrease in Quantal Content

Daniels, R. W., Collins, C. A., Gelfand, M. V., Dant, J., Brooks, E. S., Krantz, D. E., & DiAntonio, A. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3001-04.2004 · Cited by 333 · see citing works

Translational induction of heat shock transcription factor sigma 32: evidence for a built-in RNA thermosensorPreprint

Morita, M. T., Tanaka, Y., Kodama, T. S., Kyogoku, Y., Yanagi, H., & Yura, T. (1999) · Genes & Development · doi:10.1101/gad.13.6.655 · Cited by 309 · see citing works

Maintaining the Stability of Neural Function: A Homeostatic Hypothesis

Davis, G. W., & Bezprozvanny, I. (2001) · Annual Review of Physiology · doi:10.1146/annurev.physiol.63.1.847 · Cited by 302 · see citing works

Glutamate Receptor Expression Regulates Quantal Size and Quantal Content at theDrosophilaNeuromuscular Junction

DiAntonio, A., Petersen, S. A., Heckmann, M., & Goodman, C. S. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-08-03023.1999 · Cited by 300 · see citing works

Failure of averaging in the construction of a conductance-based neuron model

Golowasch, J., Goldman, M. S., Abbott, L. F., & Marder, E. (2002) · Journal of Neurophysiology · doi:10.1152/jn.00412.2001 · Cited by 290 · see citing works

α- and βCaMKII

Thiagarajan, T. C., Piedras-Renterı́a, E. S., & Tsien, R. W. (2002) · Neuron · doi:10.1016/s0896-6273(02)01049-8 · Cited by 288 · see citing works

Surviving heat shock: Control strategies for robustness and performance

El‐Samad, H., Kurata, H., Doyle, J. C., Gross, C. A., & Khammash, M. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0403510102 · Cited by 279 · see citing works

Maintenance of Acetylcholine Receptor Number by Neuregulins at the Neuromuscular Junction in Vivo

Sandrock, A. W., Dryer, S. E., Rosen, K. M., Gozani, S. N., Kramer, R., Theill, L. E., & Fischbach, G. D. (1997) · Science · doi:10.1126/science.276.5312.599 · Cited by 274 · see citing works

Activity-Independent Homeostasis in Rhythmically Active Neurons

MacLean, J. N., Zhang, Y., Johnson, B. R., & Harris‐Warrick, R. M. (2003) · Neuron · doi:10.1016/s0896-6273(02)01104-2 · Cited by 272 · see citing works

Calcium-Permeable AMPA Receptor Plasticity Is Mediated by Subunit-Specific Interactions with PICK1 and NSF

Gardner, S. M., Takamiya, K., Xia, J., Suh, J., Johnson, R. C., Yu, S., & Huganir, R. L. (2005) · Neuron · doi:10.1016/j.neuron.2005.02.026 · Cited by 245 · see citing works

A Model Neuron with Activity-Dependent Conductances Regulated by Multiple Calcium Sensors

Liu, Z., Golowasch, J., Marder, E. E., & Abbott, L. F. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-07-02309.1998 · Cited by 243 · see citing works

Homeostatic Control of Presynaptic Release Is Triggered by Postsynaptic Membrane Depolarization

Paradis, S., Sweeney, S. T., & Davis, G. W. (2001) · Neuron · doi:10.1016/s0896-6273(01)00326-9 · Cited by 242 · see citing works

Activity-Dependent mRNA Splicing Controls ER Export and Synaptic Delivery of NMDA Receptors

Mu, Y., Otsuka, T., Horton, A. C., Scott, D. B., & Ehlers, M. (2003) · Neuron · doi:10.1016/s0896-6273(03)00676-7 · Cited by 240 · see citing works

Synapse-specific control of synaptic efficacy at the terminals of a single neuron

Davis, G. W., & Goodman, C. S. (1998) · Nature · doi:10.1038/32176 · Cited by 234 · see citing works

Synaptic gain control and homeostasis

Burrone, J., & Murthy, V. N. (2003) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2003.09.007 · Cited by 230 · see citing works

Modeling stability in neuron and network function: the role of activity in homeostasis

Marder, E. E., & Prinz, A. A. (2002) · BioEssays · doi:10.1002/bies.10185 · Cited by 224 · see citing works

Activity-Dependent Regulation of Potassium Currents in an Identified Neuron of the Stomatogastric Ganglion of the CrabCancer borealis

Golowasch, J., Abbott, L. F., & Marder, E. E. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-20-j0004.1999 · Cited by 208 · see citing works

Postsynaptic PKA Controls Quantal Size and Reveals a Retrograde Signal that Regulates Presynaptic Transmitter Release in Drosophila

Davis, G. W., DiAntonio, A., Petersen, S. A., & Goodman, C. S. (1998) · Neuron · doi:10.1016/s0896-6273(00)80458-4 · Cited by 205 · see citing works

Calcium Homeostasis and Parturient Hypocalcemia: An Integral Feedback Perspective

El‐Samad, H., Goff, J. P., & Khammash, M. (2002) · Journal of Theoretical Biology · doi:10.1006/jtbi.2001.2422 · Cited by 201 · see citing works

BDNF Regulates the Intrinsic Excitability of Cortical NeuronsPreprint

Desai, N. S., Rutherford, L. C., & Turrigiano, G. G. (1999) · Learning & Memory · doi:10.1101/lm.6.3.284 · Cited by 199 · see citing works

The Stability of a Stochastic CaMKII Switch: Dependence on the Number of Enzyme Molecules and Protein Turnover

Miller, P., Zhabotinsky, A. M., Lisman, J. E., & Wang, X.-J. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030107 · Cited by 199 · see citing works

Animal-to-Animal Variability in Motor Pattern Production in Adults and during Growth

Bucher, D. M., Prinz, A. A., & Marder, E. E. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3679-04.2005 · Cited by 195 · see citing works

Phosphorylation of an N-terminal Regulatory Domain Activates the CheB Methylesterase in Bacterial Chemotaxis

Lupas, A. N., & Stock, J. B. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)71497-x · Cited by 194 · see citing works

Distinct triggering and expression mechanisms underlie LTD of AMPA and NMDA synaptic responses

Morishita, W., Marie, H., & Malenka, R. C. (2005) · Nature Neuroscience · doi:10.1038/nn1506 · Cited by 188 · see citing works

LIM Kinase1 Controls Synaptic Stability Downstream of the Type II BMP Receptor

Eaton, B. A., & Davis, G. W. (2005) · Neuron · doi:10.1016/j.neuron.2005.08.010 · Cited by 168 · see citing works

Retrograde Control of Synaptic Transmission by Postsynaptic CaMKII at the Drosophila Neuromuscular Junction

Haghighi, A. P., McCabe, B. D., Fetter, R. D., Palmer, J. E., Hom, S., & Goodman, C. S. (2003) · Neuron · doi:10.1016/s0896-6273(03)00427-6 · Cited by 161 · see citing works

Activity-Independent Coregulation of IA and Ih in Rhythmically Active Neurons

MacLean, J. N., Zhang, Y., Goeritz, M. L., Casey, R., Oliva, R. A., Guckenheimer, J. M., & Harris‐Warrick, R. M. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00281.2005 · Cited by 145 · see citing works

Hippocalcin functions as a calcium sensor in hippocampal LTD.

Palmer, C. L., Lim, W., Hastie, P. G. R., Toward, M., Korolchuk, V. I., Burbidge, S. A., Banting, G., Collingridge, G. L., Isaac, J. T. R., & Henley, J. M. (2005) · Neuron · doi:10.1016/j.neuron.2005.06.014 · Cited by 144 · see citing works

Synapse-Specific Downregulation of NMDA Receptors by Early Experience: A Critical Period for Plasticity of Sensory Input to Olfactory Cortex

Franks, K. M., & Isaacson, J. S. (2005) · Neuron · doi:10.1016/j.neuron.2005.05.024 · Cited by 138 · see citing works

Regulation of Neuronal Excitability through Pumilio-Dependent Control of a Sodium Channel Gene

Mee, C., Pym, E. C. G., Moffat, K. G., & Baines, R. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2282-04.2004 · Cited by 137 · see citing works

Genetic analysis of synaptic development and plasticity: homeostatic regulation of synaptic efficacy

Davis, G. W., & Goodman, C. S. (1998) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(98)80018-4 · Cited by 128 · see citing works

Postsynaptic Depolarization Scales Quantal Amplitude in Cortical Pyramidal Neurons

Leslie, K. R., Nelson, S. B., & Turrigiano, G. G. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-19-j0005.2001 · Cited by 128 · see citing works

CPG2

Cottrell, J. R., Borók, E., Horváth, T. L., & Nedivi, E. (2004) · Neuron · doi:10.1016/j.neuron.2004.10.025 · Cited by 108 · see citing works

Elucidating mechanisms underlying robustness of morphogen gradients

Eldar, A., Shilo, B., & Barkai, N. (2004) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2004.06.009 · Cited by 95 · see citing works

Current Compensation in Neuronal Homeostasis

Marder, E., & Prinz, A. A. (2003) · Neuron · doi:10.1016/s0896-6273(02)01173-x · Cited by 80 · see citing works

Coordinating Structural and Functional Synapse Development: Postsynaptic p21-Activated Kinase Independently Specifies Glutamate Receptor Abundance and Postsynaptic Morphology

Albin, S. D., & Davis, G. W. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1538-04.2004 · Cited by 77 · see citing works

Space matters: local and global dendritic Ca2+ compartmentalization in cortical interneurons

Goldberg, J. H., & Yuste, R. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.01.005 · Cited by 65 · see citing works

Episodic Bouts of Activity Accompany Recovery of Rhythmic Output By a Neuromodulator- and Activity-Deprived Adult Neural Network

Luther, J. A., Robie, A. A., Yarotsky, J., Reina, C. P., Marder, E. E., & Golowasch, J. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00370.2003 · Cited by 61 · see citing works

Presynaptic homeostasis at CNS nerve terminals compensates for lack of a key Ca 2+ entry pathway

Piedras-Renterı́a, E. S., Pyle, J. L., Diehn, M., Glickfeld, L. L., Harata, N. C., Cao, Y. Q., Kavalali, E. T., Brown, P. O., & Tsien, R. W. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308188100 · Cited by 50 · see citing works

Clathrin-mediated endocytosis is required for compensatory regulation of GLR-1 glutamate receptors after activity blockade

Grunwald, M. E., Mellem, J. E., Strutz, N., Maricq, A. V., & Kaplan, J. M. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0306156101 · Cited by 41 · see citing works

Neuronal Homeostasis Through Translational Control

Baines, R. (2005) · Molecular Neurobiology · doi:10.1385/mn:32:2:113 · Cited by 31 · see citing works

Advances in the Pathophysiology of Developmental Epilepsies

Wong, M. L. (2005) · Seminars in Pediatric Neurology · doi:10.1016/j.spen.2005.03.002 · Cited by 20 · see citing works

Impaired synaptic scaling in mouse hippocampal neurones expressing NMDA receptors with reduced calcium permeability

Pawlak, V., Schupp, B. J., Single, F. N., Seeburg, P. H., & Köhr, G. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.076794 · Cited by 17 · see citing works

Constant amplitude of postsynaptic responses for single presynaptic action potentials but not bursting input during growth of an identified neuromuscular junction in the lobster, Homarus americanus

Pulver, S. R., Bucher, D. M., Simon, D. J., & Marder, E. E. (2004) · Journal of Neurobiology · doi:10.1002/neu.20066 · Cited by 16 · see citing works

An ER export signal accelerates the surface expression of shal potassium channels in pyloric neurons of the lobster stomatogastric ganglion

Zhang, Y., & Harris‐Warrick, R. M. (2004) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-003-1189-6 · Cited by 3 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

Synaptic AMPA receptor plasticity and behavior

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

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 · see citing works

Unraveling mechanisms of homeostatic synaptic plasticity

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

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 · see citing works

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 445 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 351 · see citing works

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 · see citing works

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 · see citing works

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 327 · see citing works

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 · see citing works

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 314 · see citing works

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 317 · see citing works

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 306 · see citing works

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 · see citing works

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 285 · see citing works

Activity-Dependent Regulation of Synapses by Retrograde Messengers

Regehr, W., Carey, M. R., & Best, A. R. (2009) · Neuron · doi:10.1016/j.neuron.2009.06.021 · Cited by 294 · see citing works

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 275 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

Homeostatic Signaling and the Stabilization of Neural Function

Davis, G. W. (2013) · Neuron · doi:10.1016/j.neuron.2013.09.044 · Cited by 271 · see citing works

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 · see citing works

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 242 · see citing works

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 246 · see citing works

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 · see citing works

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 230 · see citing works

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 · see citing works

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 230 · see citing works

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 224 · see citing works

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 · see citing works

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 228 · see citing works

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 · see citing works

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 212 · see citing works

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 · see citing works

The Schizophrenia Susceptibility Gene dysbindin Controls Synaptic Homeostasis

Dickman, D. K., & Davis, G. W. (2009) · Science · doi:10.1126/science.1179685 · Cited by 206 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 195 · see citing works

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 · see citing works

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 · see citing works

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 186 · see citing works

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 183 · see citing works

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 184 · see citing works

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 · see citing works

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 · see citing works

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 · see citing works

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 179 · see citing works

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 175 · see citing works

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 175 · see citing works

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 183 · see citing works

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 · see citing works

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 166 · see citing works

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 164 · see citing works

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 · see citing works

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 148 · see citing works

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 · see citing works

Modulation of stomatogastric rhythms

Stein, W. (2009) · Journal of Comparative Physiology A · doi:10.1007/s00359-009-0483-y · Cited by 144 · see citing works

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 · see citing works

Homeostatic plasticity at the Drosophila neuromuscular junction

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

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 · see citing works

Activity-dependent neurotransmitter respecification

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

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 132 · see citing works

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 · see citing works

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 · see citing works

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 132 · see citing works

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 135 · see citing works

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 128 · see citing works

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 124 · see citing works

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 · see citing works

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 124 · see citing works

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 · see citing works

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 126 · see citing works

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 123 · see citing works

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 121 · see citing works

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 117 · see citing works

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 · see citing works

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

Verstreken, P., Ohyama, T., Haueter, C. M., Habets, R. L. P., Qi, L. Y., 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 112 · see citing works

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 112 · see citing works

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 · see citing works

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 111 · see citing works

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 110 · see citing works

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 112 · see citing works

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 110 · see citing works

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 106 · see citing works

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 103 · see citing works

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 109 · see citing works

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 107 · see citing works

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 103 · see citing works

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

Müller, M., Pym, E. C. G., Tong, A., & Davis, G. (2011) · Neuron · doi:10.1016/j.neuron.2011.01.025 · Cited by 115 · see citing works

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

Hou, Q., Gilbert, J. P., & Man, H. (2011) · Neuron · doi:10.1016/j.neuron.2011.10.011 · Cited by 102 · see citing works

Synaptopodin regulates denervation-induced homeostatic synaptic plasticity

Vlachos, A., Ikenberg, B., Lenz, M., Becker, D., Reifenberg, K., Bas-Orth, C., & Deller, T. (2013) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.1213677110 · Cited by 105 · see citing works

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

Subramanian, J., & Dickman, D. K. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00380 · Cited by 1 · see citing works

Hebb and homeostasis in neuronal plasticity

Turrigiano, G. G., & Nelson, S. B. (2000) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00091-x · Cited by 687 · see citing works

Homeostatic and retrograde signaling mechanisms modulating presynaptic function and plasticity

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

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