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

Cul4 ubiquitin ligase cofactor DCAF12 promotes neurotransmitter release and homeostatic plasticity

Patrón, L. A., Nagatomo, K., Eves, D. T., Imad, M., Young, K., Torvund, M., Guo, X., Rogers, G. C., & Zinsmaier, K. E. (2019) · The Journal of Cell Biology · doi:10.1083/jcb.201805099 · Cited by 21

The RhoGAPcrossveinless-cInteracts withDystrophinand Is Required for Synaptic Homeostasis at theDrosophilaNeuromuscular Junction

Pilgram, G. S. K., Potikanond, S., van der Plas, M. C., Fradkin, L. G., & Noordermeer, J. N. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4732-10.2011 · Cited by 21

Functional adaptation of cortical interneurons to attenuated activity is subtype-specific

Karayannis, T., García, N. V. D. M., & Fishell, G. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00066 · Cited by 20

NMDA receptors regulate the firing rate set point of hippocampal circuits without altering single-cell dynamics

Ruggiero, A., Heim, L. R., Susman, L., Hreaky, D., Shapira, I., Katsenelson, M., Rosenblum, K., & Slutsky, I. (2024) · Neuron · doi:10.1016/j.neuron.2024.10.014 · Cited by 19

Subunit-specific and homeostatic regulation of glutamate receptor localization by CaMKII in Drosophila neuromuscular junctions

Morimoto, T., Nobechi, M., Komatsu, A., Miyakawa, H., & Nose, A. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.11.059 · Cited by 19

The kinase activity of EphA4 mediates homeostatic scaling-down of synaptic strength via activation of Cdk5

Peng, Y., Hou, Z.-H., & Yu, X. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.10.012 · Cited by 20

Enhanced Transmission at a Spinal Synapse TriggeredIn Vivoby an Injury Signal Independent of Altered Synaptic Activity

Bichler, E. K., Nakanishi, S. T., Wang, Q.-B., Pinter, M. J., Rich, M. M., & Cope, T. C. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1997-07.2007 · Cited by 19

Recent progress in memristors for stimulating synaptic plasticity

Zhang, C., Yan, C. H. E. N., Yi, M., Ying, Z. H. U., Li, T., Liu, L., Laiyuan, W. A. N. G., Xie, L., & Huang, W. (2018) · Scientia Sinica Informationis · doi:10.1360/n112017-00022 · Cited by 19

The Perineuronal Net Protein Brevican Acts in Nucleus Accumbens Parvalbumin-Expressing Interneurons of Adult Mice to Regulate Excitatory Synaptic Inputs and Motivated Behaviors

Hazlett, M. F., Hall, V. L., Patel, E. M., Halvorsen, A. T., Calakos, N., & West, A. E. (2024) · Biological Psychiatry · doi:10.1016/j.biopsych.2024.02.003 · Cited by 18

Ménage à Trio during BMP-Mediated Retrograde Signaling at the NMJ

Fuentes-Medel, Y., & Budnik, V. (2010) · Neuron · doi:10.1016/j.neuron.2010.05.016 · Cited by 18

Altered Mesolimbic Dopamine System in THC Dependence

Spiga, S., Lintas, A., & Diana, M. (2011) · Current Neuropharmacology · doi:10.2174/157015911795017083 · Cited by 18

Competition from newborn granule cells does not drive axonal retraction of silenced old granule cells in the adult hippocampus

Lopez, C. M., Pelkey, K. A., Chittajallu, R., Nakashiba, T., Tóth, K., Tonegawa, S., & McBain, C. J. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00085 · Cited by 18

Lesioning alters functional properties in isolated spinal cord hemisegmental networks

Hoffman, N., & Parker, D. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.04.014 · Cited by 18

Regulated lysosomal trafficking as a mechanism for regulating GABAA receptor abundance at synapses in Caenorhabditis elegans

Davis, K. M., Sturt, B. L., Friedmann, A. J., Richmond, J. E., Bessereau, J., Grant, B. D., & Bamber, B. A. (2010) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2010.04.002 · Cited by 18

Using the hierarchical temporal memory spatial pooler for short-term forecasting of electrical load time series

Osegi, E. N. (2018) · Applied Computing and Informatics · doi:10.1016/j.aci.2018.09.002 · Cited by 18

The less things change, the more they are different: contributions of long-term synaptic plasticity and homeostasis to memoryPreprint

Schacher, S., & Hu, J. (2014) · Learning & Memory · doi:10.1101/lm.027326.112 · Cited by 18

Homeostasis of a representational map in the neocortex

Noda, T., Kienle, E., Eppler, J.-B., Aschauer, D. F., Kaschube, M., Loewenstein, Y., & Rumpel, S. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-01982-7 · Cited by 19

What the Escherichia Coli Tells Neurons about Learning

Gómez‐Ramírez, J., & Sanz, R. (2012) · Springer eBooks · doi:10.1007/978-3-642-28111-2_5 · Cited by 17

Altered synaptic homeostasis: a key factor in the pathophysiology of depression

Wang, B., He, T., Qiu, G., Li, C., Xue, S., Zheng, Y., Wang, T., Xia, Y., Yao, L., Yan, J., et al. (2025) · Cell & Bioscience · doi:10.1186/s13578-025-01369-y · Cited by 19

Lola regulates glutamate receptor expression at the Drosophila neuromuscular junction

Fukui, A., Inaki, M., Tonoe, G., Hamatani, H., Homma, M., Morimoto, T., Aburatani, H., & Nose, A. (2012) · Biology Open · doi:10.1242/bio.2012448 · Cited by 19

Signature Neural Networks: Definition and Application to Multidimensional Sorting Problems

Latorre, R., Rodrı́guez, F. B., & Varona, P. (2010) · IEEE Transactions on Neural Networks · doi:10.1109/tnn.2010.2060495 · Cited by 17

Animal-to-animal variability in the phasing of the crustacean cardiac motor pattern: an experimental and computational analysis

Williams, A. H., Kwiatkowski, M. A., Mortimer, A. L., Marder, E. E., Zeeman, M. L., & Dickinson, P. S. (2013) · Journal of Neurophysiology · doi:10.1152/jn.01010.2012 · Cited by 18

Adaptive information processing of network modules to dynamic and spatial stimuli

Krishnan, J., & Floros, I. (2019) · BMC Systems Biology · doi:10.1186/s12918-019-0703-1 · Cited by 17

The Photoparoxysmal Response Reflects Abnormal Early Visuomotor Integration in the Human Motor Cortex

Suppa, A., Rocchi, L., Voti, P. L., Papazachariadis, O., Casciato, S., Bonaventura, C. D., Giallonardo, A. T., & Berardelli, A. (2015) · Brain stimulation · doi:10.1016/j.brs.2015.05.013 · Cited by 18

Prolongation of Evoked and Spontaneous Synaptic Currents at the Neuromuscular Junction after Activity Blockade Is Caused by the Upregulation of Fetal Acetylcholine Receptors

Wang, X., Engisch, K. L., Teichert, R. W., Olivera, B. M., Pinter, M. J., & Rich, M. M. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2493-06.2006 · Cited by 17

Fully Integrated Memristive Hodgkin-Huxley Neurons With Homeostatic Plasticity

Yang, Y., Zhang, X., Chen, P., Cheng, L., Ding, Y., Li, C., Yu, J., & Liu, Q. (2024) · IEEE Electron Device Letters · doi:10.1109/led.2024.3456816 · Cited by 16

Neuronal Homeostasis: Voltage Brings It All Together

Golowasch, J. (2019) · Current Biology · doi:10.1016/j.cub.2019.05.029 · Cited by 16

Photoreceptor Cells With Profound Structural Deficits Can Support Useful Vision in Mice

Thompson, S., Blodi, F. R., Lee, S., Welder, C. R., Mullins, R. F., Tucker, B. A., Stasheff, S. F., & Stone, E. M. (2014) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.13-13661 · Cited by 16

Denervated mouse dentate granule cells adjust their excitatory but not inhibitory synapses following in vitro entorhinal cortex lesion

Lenz, M., Galanis, C., Kleidonas, D., Fellenz, M., Deller, T., & Vlachos, A. (2018) · Experimental Neurology · doi:10.1016/j.expneurol.2018.10.013 · Cited by 16

Homeostatic Plasticity in the Nervous System

Maffei, A., Bucher, D. M., & Fontanini, A. (2012) · Neural Plasticity · doi:10.1155/2012/913472 · Cited by 18

Excitatory and inhibitory neural dynamics jointly tune motion detection

Gonzalez-Suarez, A. D., Zavatone-Veth, J. A., Chen, J., Matulis, C. A., Badwan, B. A., & Clark, D. A. (2022) · Current Biology · doi:10.1016/j.cub.2022.06.075 · Cited by 13

Exact Distribution of the Quantal Content in Synaptic Transmission

Rijal, K., Müller, N. I. C., Friauf, E., Singh, A., Prasad, A., & Das, D. (2024) · Physical Review Letters · doi:10.1103/physrevlett.132.228401 · Cited by 15

Distinct expression of potassium channels regulates visual response properties of lamina neurons in Drosophila melanogaster

Gür, B., Šporar, K., Lopez-Behling, A., & Silies, M. (2019) · Journal of Comparative Physiology A · doi:10.1007/s00359-019-01385-7 · Cited by 15

Mechanisms and Functional Consequences of Presynaptic Homeostatic Plasticity at Auditory Nerve Synapses

Zhuang, X., Wong, N. F., Sun, W., & Xu‐Friedman, M. A. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1175-19.2020 · Cited by 17

Smn-Deficiency Increases the Intrinsic Excitability of Motoneurons

Arumugam, S., Garcerá, A., Soler, R. M., & Tabares, L. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00269 · Cited by 15

Homeostatic scaling is driven by a translation-dependent degradation axis that recruits miRISC remodeling

Srinivasan, B., Samaddar, S., Mylavarapu, S. V. S., Clement, J. P., & Banerjee, S. (2021) · PLoS Biology · doi:10.1371/journal.pbio.3001432 · Cited by 15

Efficient fitting of conductance-based model neurons from somatic current clamp

Lepora, N. F., Overton, P. G., & GURNEY, K. N. (2011) · Journal of Computational Neuroscience · doi:10.1007/s10827-011-0331-2 · Cited by 15

Coordinating Different Homeostatic Processes

Marder, E. E., & Tang, L. S. (2010) · Neuron · doi:10.1016/j.neuron.2010.04.022 · Cited by 16

Compensatory plasticity in the olfactory epithelium: age, timing, and reversibility

Barber, C. N., & Coppola, D. M. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00076.2015 · Cited by 14

The Contribution of TNFα to Synaptic Plasticity and Nervous System Function

Stellwagen, D. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-6612-4_57 · Cited by 15

Homeostatic plasticity and external input shape neural network dynamicsPreprint

Zierenberg, J., Wilting, J., & Priesemann, V. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/362152 · Cited by 16

Overview on cognitive impairment in psychotic disorders: From impaired microcircuits to dysconnectivity

Mana, L., Schwartz-Palleja, M., Vila‐Vidal, M., & Deco, G. (2024) · Schizophrenia Research · doi:10.1016/j.schres.2024.05.008 · Cited by 13

Developmental changes in expression of inhibitory neuronal proteins in the Fragile X Syndrome mouse basolateral amygdala

Kratovac, S., & Corbin, J. G. (2013) · Brain Research · doi:10.1016/j.brainres.2013.08.052 · Cited by 14

The role of cAMP in synaptic homeostasis in response to environmental temperature challenges and hyperexcitability mutations

Ueda, A., & Wu, C. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00010 · Cited by 15

Visuo-motor integration in unresponsive wakefulness syndrome: A piece of the puzzle towards consciousness detection?

Naro, A., Leo, A., Filoni, S., Bramanti, P., & Calabrò, R. S. (2015) · Restorative Neurology and Neuroscience · doi:10.3233/rnn-150525 · Cited by 14

Extensive morphological divergence and rapid evolution of the larval neuromuscular junction in Drosophila

Campbell, M., & Ganetzky, B. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1201176109 · Cited by 14

Artificial synaptic modification reveals a dynamical invariant in the pyloric CPG

Reyes, M. B., Huerta, R., Rabinovich, M. I., & Selverston, A. I. (2007) · European Journal of Applied Physiology · doi:10.1007/s00421-007-0635-0 · Cited by 14

Synaptic Commitment: Developmentally Regulated Reciprocal Changes in Hippocampal Granule Cell NMDA and AMPA Receptors Over the Lifespan

Yang, Z., Krause, M., Rao, G., McNaughton, B. L., & Barnes, C. A. (2008) · Journal of Neurophysiology · doi:10.1152/jn.01276.2007 · Cited by 16

Glycinergic synapse development, plasticity, and homeostasis in zebrafish

Ganser, L. R. (2009) · Frontiers in Molecular Neuroscience · doi:10.3389/neuro.02.030.2009 · Cited by 13

Activity-Dependent Structural Plasticity of Dendritic Spines

Chapleau, C. A., & Pozzo‐Miller, L. D. (2008) · Elsevier eBooks · doi:10.1016/b978-012370509-9.00039-5 · Cited by 14

Neuromodulation

Katz, P. S., & Calin-Jageman, R. J. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.01964-1 · Cited by 14

Mechanisms Involved in Neuroprotective Effects of Transcranial Magnetic Stimulation

Caballero‐Villarraso, J., Medina, F. J., Escribano, B. M., Agüera, E., Santamarı́a, A., Pascual‐Leone, Á., & Túnez, I. (2021) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/1871527320666210809121922 · Cited by 14

The Uniform and Nonuniform Nature of Slow and Rapid Scaling in Embryonic Motoneurons

Pękala, D., & Wenner, P. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.0899-21.2021 · Cited by 13

An ultra-short-acting benzodiazepine in thalamic nucleus reuniens undermines fear extinction via intermediation of hippocamposeptal circuits

Cheung, H., Yu, T.-Z., Yi, X., Wu, Y., Wang, Q., Gu, X., Xu, M., Cai, M., Wen, W., Li, X.-N., et al. (2024) · Communications Biology · doi:10.1038/s42003-024-06417-w · Cited by 13

Pyramidal cell activity levels affect the polarity of activity-induced gene transcription changes in interneurons

Parrish, R. R., Codadu, N. K., Racca, C., & Trevelyan, A. J. (2018) · Journal of Neurophysiology · doi:10.1152/jn.00287.2018 · Cited by 13

New Insights on Retrieval-Induced and Ongoing Memory Consolidation: Lessons from Arc

Morin, J., Guzmán-Ramos, K. R., & Bermúdez‐Rattoni, F. (2015) · Neural Plasticity · doi:10.1155/2015/184083 · Cited by 12

Decrease in CA3 inhibitory network activity during Theiler’s virus encephalitis

Smeal, R. M., Fujinami, R. S., White, H. S., & Wilcox, K. S. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.10.032 · Cited by 13

Cell Adhesion Molecules at Synapses

Reichardt, L. F., & Lee, S.-H. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.00355-7 · Cited by 13

Cholinergic Synaptic Homeostasis Is Tuned by an NFAT-Mediated α7 nAChR-Kv4/Shal Coupled Regulatory System

Eadaim, A., Hahm, E.-T., Justice, E. D., & Tsunoda, S. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.108119 · Cited by 11

Specific Sets of Intrinsic and Extrinsic Factors Drive Excitatory and Inhibitory Circuit Formation

Terauchi, A., & Umemori, H. (2011) · The Neuroscientist · doi:10.1177/1073858411404228 · Cited by 12

Activity-regulated growth of motoneurons at the neuromuscular junction is mediated by NADPH oxidases

Sobrido‐Cameán, D., Oswald, M. C. W., Bailey, D. M., Mukherjee, A., & Landgraf, M. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.1106593 · Cited by 11

A unifying mechanism for presynaptic homeostatic plasticity at mammalian peripheral and central synapses

Chipman, P. H., Lee, U., Orr, B. O., Fetter, R. D., & Davis, G. W. (2025) · Neuron · doi:10.1016/j.neuron.2025.05.030 · Cited by 12

Chronic Neuronal Inactivity Utilizes the mTOR-TFEB Pathway to Drive Transcription-Dependent Autophagy for Homeostatic Up-Scaling

Wang, Y., Lin, J., Li, J., Yan, A. L., Li, W., He, X., & Ma, H. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0146-23.2023 · Cited by 12

Glial Sphingosine-Mediated Epigenetic Regulation Stabilizes Synaptic Function inDrosophilaModels of Alzheimer's Disease

Yin, P., Cai, Y., Cui, T., Berg, A. J., Wang, T., Morency, D. T., Paganelli, P. M., Lok, C., Yang, X., Vicini, S., et al. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.0515-23.2023 · Cited by 11

Monoaminergic tone supports conductance correlations and stabilizes activity features in pattern generating neurons of the lobster, Panulirus interruptus

Krenz, W. C., Parker, A. R., Rodgers, E. W., & Baro, D. J. (2015) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00063 · Cited by 11

Molecular Mechanism of Tinnitus

Knipper, M., Müller, M. C., & Zimmermann, U. (2012) · Springer handbook of auditory research · doi:10.1007/978-1-4614-3728-4_3 · Cited by 11

Homeostatically regulated synchronized oscillations induced by short-term tetrodotoxin treatment in cultured neuronal network

Zhou, W., Li, X., Liu, M., Zhao, Y., Zhu, G., & Luo, Q. (2008) · Biosystems · doi:10.1016/j.biosystems.2008.06.008 · Cited by 12

BMP signaling modulates the probability of neurotransmitter release and readily releasable pools in Drosophila neuromuscular junction synapses

Lee, S., Kim, Y.-J., & Choi, S. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.09.072 · Cited by 11

Speed of processing in the primary motor cortex: A continuous theta burst stimulation study

Lakhani, B., Bolton, D. A. E., Miyasike-daSilva, V., Vette, A. H., & McIlroy, W. E. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.12.022 · Cited by 10

Calcium Oscillation Frequency-Sensitive Gene Regulation and Homeostatic Compensation in Pancreatic $$\upbeta $$-Cells

Yildirim, V., & Bertram, R. (2017) · Bulletin of Mathematical Biology · doi:10.1007/s11538-017-0286-1 · Cited by 8

Mitf Links Neuronal Activity and Long-Term Homeostatic Intrinsic Plasticity

Atacho, D. A. M., Reynisson, H., Pétursdóttir, A. Þ., Eysteinsson, Þ., Steingrı́msson, E., & Petersen, P. H. (2020) · eNeuro · doi:10.1523/eneuro.0412-19.2020 · Cited by 10

Transsynaptic Activity-Dependent Regulation of Axon Branching and Neurotrophin ExpressionIn Vivo

Calinescu, A., Liu, T., Wang, M. M., & Borjigin, J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2172-11.2011 · Cited by 10

Time Course of Activity-Dependent Changes in Auditory Nerve Synapses Reveals Multiple Underlying Cellular Mechanisms

Wong, N. F., & Xu‐Friedman, M. A. (2022) · Journal of Neuroscience · doi:10.1523/jneurosci.1583-21.2022 · Cited by 8

The Noonan syndrome-associated D61G variant of the protein tyrosine phosphatase SHP2 prevents synaptic down-scaling

Lu, W., Ai, H., Xue, F., Luan, Y., & Zhang, B. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.010331 · Cited by 9

Constraints of Metabolic Energy on the Number of Synaptic Connections of Neurons and the Density of Neuronal Networks

Yuan, Y., Huo, H., Zhao, P., Liu, J., Liu, J., Xing, F., & Fang, T. (2018) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2018.00091 · Cited by 9

An Introduction to In Vitro Slice Approaches for the Study of Neuronal Circuitry

Varela, C., Llano, D. A., & Theyel, B. B. (2011) · Neuromethods · doi:10.1007/7657_2011_19 · Cited by 8

Long-lasting changes in neural networks to compensate for altered nicotinic input

John, D., & Berg, D. K. (2015) · Biochemical Pharmacology · doi:10.1016/j.bcp.2015.07.020 · Cited by 9

The molecular diversity of plasticity mechanisms underlying memory: An evolutionary perspective

Zha, C., & Sossin, W. S. (2022) · Journal of Neurochemistry · doi:10.1111/jnc.15717 · Cited by 10

Channeling the Central Dogma

Calabrese, R. L. (2014) · Neuron · doi:10.1016/j.neuron.2014.05.008 · Cited by 8

Spinal cord - skeletal muscle cocultures detect muscle-relaxant action of botulinum neurotoxin A

Eckle, V. (2014) · ALTEX · doi:10.14573/altex.1304291 · Cited by 8

Excitatory and inhibitory hippocampal neurons differ in their homeostatic adaptation to chronic M-channel modulation

Bar, L., Shalom, L., Lezmy, J., Peretz, A. S., & Attali, B. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.972023 · Cited by 8

Dysregulated glial genes in Alzheimer's disease are essential for homeostatic plasticity: Evidence from integrative epigenetic and single cell analyses

Cai, Y., Cui, T., Yin, P., Paganelli, P. M., Vicini, S., & Wang, T. (2023) · Aging Cell · doi:10.1111/acel.13989 · Cited by 7

Downregulation of C entaurin gamma1 A increases synaptic transmission at D rosophila larval neuromuscular junctions

Homma, M., Nagashima, S., Fukuda, T., Yanagi, S., Miyakawa, H., Suzuki, E., & Morimoto, T. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12681 · Cited by 8

Sensory processing by motoneurons: a numerical model for low-level flight control in flies

Bartussek, J., & Lehmann, F. (2018) · Journal of The Royal Society Interface · doi:10.1098/rsif.2018.0408 · Cited by 8

Geometry and dynamics of activity-dependent homeostatic regulation in neurons

Prinz, A. A., & Olypher, A. V. (2009) · BMC Neuroscience · doi:10.1186/1471-2202-10-s1-p203 · Cited by 8

Daily light-induced transcription in visual cortex neurons drives downward firing rate homeostasis and stabilizes sensory processing

Kushinsky, D., Tsivourakis, E., Apelblat, D., Roethler, O., Breger-Mikulincer, M., Malina, K. C.-K., & Spiegel, I. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114701 · Cited by 7

A complex network perspective on brain disease

Papo, D., & Buldú, J. M. (2025) · Biological reviews/Biological reviews of the Cambridge Philosophical Society · doi:10.1111/brv.70086 · Cited by 10

The calcineurin regulator Sarah enables distinct forms of homeostatic plasticity at the Drosophila neuromuscular junction

Armstrong, N. S., & Frank, C. A. (2023) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2022.1033743 · Cited by 7

Cellular and Molecular Mechanisms of rTMS-induced Neural Plasticity

Lenz, M., Müller‐Dahlhaus, F., & Vlachos, A. (2015) · Springer eBooks · doi:10.1007/978-3-319-25721-1_2 · Cited by 7

Postsynaptic receptors regulate presynaptic transmitter stability through transsynaptic bridges

Godavarthi, S. K., Hiramoto, M., Ignatyev, Y., Levin, J. B., Li, H.-Q., Pratelli, M., Borchardt, J. S., Czajkowski, C., Borodinsky, L. N., Sweeney, L. B., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2318041121 · Cited by 6

Further insights into the effect of BDNF genotype on non-invasive brain stimulation

Suppa, A., & Cheeran, B. (2014) · Clinical Neurophysiology · doi:10.1016/j.clinph.2014.10.003 · Cited by 7

Horizons in LTP-like plasticity in human primary motor cortex

Suppa, A., & Berardelli, A. (2012) · Clinical Neurophysiology · doi:10.1016/j.clinph.2012.04.011 · Cited by 7

Barfly: Sculpting membranes at the Drosophila neuromuscular junction

Oh, E., & Robinson, I. M. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20923 · Cited by 7

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For a review, (q

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