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

Invertebrate Models for the Study of the Effects of Age on Neurotransmitter Release

Eaton, B. A. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811353-0.00033-6

Stress monitoring in captive vervet monkeys (Chlorocebus pygerythrus) co-housed with domestic cats (Felis silvestris catus)

Chipangura, J. K. (2017) · UpSpace Institutional Repository (University of Pretoria)

Cellular- and network-level regulation of place cell activity mediated by activity-dependent gene, Arc

Yuan, L. (2019) · doi:10.32657/10220/49828

Regulation of dendritic morphology and synapse formation by the intellectual disability associated palmitoyl acyl transferases zDHHC15 and zDHHC9

Shimell, J. J. (2019) · cIRcle (University of British Columbia) · doi:10.14288/1.0384822

Correction of disorders of neuronal homeostatic mechanisms in case of neuropsychiatric diseases as a probable direction of drug exposure

Абрамец, И. И., Евдокимов, Д. В., Kuznetsov, Y. V., & Сидорова, Ю. В. (2020) · Человек и его здоровье · doi:10.21626/vestnik/2020-3/09

Continuous Learning and Adaptation with Membrane Potential and Activation Threshold HomeostasisPreprint

Hadjiivanov, A. (2021) · arXiv (Cornell University) · doi:10.48550/arxiv.2104.10851 · Cited by 1

Melanin Concentrating Hormone- and sleep-dependent synaptic downscaling is impaired in Alzheimer’s DiseasePreprint

Calafate, S., Özturan, G., Thrupp, N., Vanderlinden, J., Chen, W.-T., Fiers, M. W. E. J., Lu, A., Creemers, E., Craessaerts, K., Vandenbempt, J., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.05.21.445007

Neuro-electronic Hybrid Systems

George, J. B. (2021)

Transcriptional adaptation of sensory neurons to GPCR identity and activityPreprint

Horgue, L. F., Assens, A., Fodoulian, L., Marconi, L., Tuberosa, J., Haider, A., Boillat, M., Carleton, A., & Rodríguez, I. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.11.29.468971

Activity Regulates Neuronal Connectivity and Function in the C. elegans Motor Circuit: A Dissertation

Barbagallo, B. (2014) · eScholarship@UMassChan · doi:10.13028/m2jw2t

Faculty Opinions recommendation of Excitatory/inhibitory synaptic imbalance leads to hippocampal hyperexcitability in mouse models of tuberous sclerosis.

Johnston, M. V., & Gipson, T. (2013) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.718008457.793476208

References

(2011) · CRC Press eBooks · doi:10.1201/b10562-22

Peer Review #1 of "CA1 pyramidal cells have diverse biophysical properties, affected by development, experience, and aging (v0.1)"

(2017) · PeerJ · doi:10.7287/peerj.3836v0.1/reviews/1

Membrantransport kleiner Moleküle und elektrische Eigenschaften von Membranen

(2017) · Wiley-VCH eBooks · doi:10.1002/9783527698448.ch11

Peer Review #2 of "CA1 pyramidal cells have diverse biophysical properties, affected by development, experience, and aging (v0.1)"

(2017) · PeerJ · doi:10.7287/peerj.3836v0.1/reviews/2

Faculty Opinions recommendation of Two distinct mechanisms for experience-dependent homeostasis.

Chen, L. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733231111.793546551

Peer Review #2 of "CA1 pyramidal cells have diverse biophysical properties, affected by development, experience, and aging (v0.2)"

(2017) · PeerJ · doi:10.7287/peerj.3836v0.2/reviews/2

Neuroinflammation, Glia, and Cytokines: Networks of Networks

Anderson, W. D., & Vadigepalli, R. (2019) · Encyclopedia of Computational Neuroscience · doi:10.1007/978-1-4614-7320-6_100694-1

Faculty Opinions recommendation of Decrease in calcium concentration triggers neuronal retinoic acid synthesis during homeostatic synaptic plasticity.

Kavalali, E. T., & Reese, A. L. (2012) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.13476957.14857055

Synapses

Harrigan, J., & Schweizer, F. E. (2021) · Wiley eBooks · doi:10.1002/9780470015902.a0029259

Faculty Opinions recommendation of Synaptic signaling by all-trans retinoic acid in homeostatic synaptic plasticity.

Hell, J. W. (2008) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1124578.581789

Faculty Opinions recommendation of CDK5 serves as a major control point in neurotransmitter release.

Sullivan, J. (2010) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.5589959.5555058

Cooperative Action of Neuroligins and Brain-Derived Neurotrophic Factor Mediates Presynaptic Maturation

Petkova-Tuffy, A. (2022) · doi:10.53846/goediss-9434

Cumulative dose responses for adapting biological systemsPreprint

Gupta, A., & Sontag, E. D. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.11.22.624851

Neuronal Network Inactivity Potentiates Neuropeptide Release from Mouse Cortical Neurons

Priebe, T., Subkhangulova, A., Toonen, R. F. G., & Verhage, M. (2025) · eNeuro · doi:10.1523/eneuro.0555-24.2024

Key mechanisms regulating synaptic and cell wide forms of homeostatic plasticity

Jakawich, S. K. (2011) · Deep Blue (University of Michigan)

Presynaptic Substrates Mediating Fos- and Jun-dependent Plasticity at the Drosophila Neuromuscular Junction

Kim, S. M. (2007) · UA Campus Repository (The University of Arizona)

Homeostatic preservation of action potential waveform by Notch and Nerfin-1

Karmelic, D., Steinberg, Y., Jones, R., Genç, Ö., & Davis, G. W. (2026) · Current Biology · doi:10.1016/j.cub.2026.01.044 · Cited by 1

Biological detail and graph structure in network neuroscience

Papo, D., & Buldú, J. M. (2025) · Institutional Research Information System University of Ferrara (University of Ferrara) · doi:10.3389/fnetp.2025.1667656/full

Alzheimer’s pathology enhances excitatory synaptic input and integration in VTA dopamine neurons

Blankenship, H. E., Higgs, M. H., Harold, K. M., Humphries, K. M., & Beckstead, M. J. (2026) · Journal of Neuroscience · doi:10.1523/jneurosci.2085-25.2026

Photochemical nanomotors reverse anxiety- and depressive-related behaviors in rodents via spatiotemporal polarity dynamics tuning

Chen, B., Ding, M., Feng, Y., Gao, C., Rong, J., Tan, H., Tian, H., Wilson, D. A., Zhou, Y., Tu, Y., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-70003-3

Effets de la modulation des canaux potassium SK et Kv4 sur les déficits moteurs et cognitifs de la maladie de Parkinson

Aidi-Knani, S. (2014) · theses.fr (ABES) · doi:10.70675/9bcb3ccfzbea9z4555z8ab9zebc1216c5e8b

Rôle du microARN miR-124 dans la plasticité homéostatique via le contrôle de l’expression de la synaptopodine et des récepteurs AMPA dans les neurones de l'hippocampe

Dubes, S. (2019) · theses.fr (ABES) · doi:10.70675/275d3182za2b9z4513z9941z62d044306e33

Hebbian and Homeostatic plasticity in the adult visual cortex

Prosper, A. (2025) · theses.fr (ABES) · doi:10.70675/62138cf3zacbdz46b0z8e1azecbeaf4bb955

Binding as an enabling mechanism for cross-modal plasticity

Park, W. J., & Celikel, T. (2026) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2026.106695 · Cited by 2

When can neuronal activity-dependent homeostatic plasticity maintain circuit-level properties?

Stolting, L., & Beer, R. D. (2026) · Journal of Computational Neuroscience · doi:10.1007/s10827-026-00936-7

Dissociation between hemodynamic and neurochemical responses during chemogenetic modulation of cortical circuits in ratsPreprint

Vind, F. A., & Just, N. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.22.733828

Reorganization of synchronous and asynchronous release in developing hippocampal autaptic neurons of mice

Uchino, K., Kawano, H., Fujikawa, R., Watanabe, T., Iwasaki, K., Kawaguchi, S., & Katsurabayashi, S. (2026) · Physiological Reports · doi:10.14814/phy2.71062

HERMES: Experience replay and operator plasticity in evolutionary UAV path planning

Darlan, D., Ajani, O. S., Adedigba, A. P., & Mallipeddi, R. (2026) · Expert Systems with Applications · doi:10.1016/j.eswa.2026.134407

Apparent dissociation between hemodynamic and neurochemical responses during chemogenetic modulation of cortical circuits in rats

Vind, F. A., & Just, N. (2026) · Frontiers in Neuroscience · doi:10.3389/fnins.2026.1916498

Calcium permeability–enhancing mutations in GluRIIC suppress sustained presynaptic homeostatic plasticity triggered by loss of GluRIIA

Malak, O. A., Gray, L. A., Aly, A., Ball, R. W., Gustin-Murray, J., Moujahidine, M., Carrasco, G., Rosko, A., Isacoff, E. Y., & Haghighi, A. P. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2625954123

Modulation and Robustness of Endogenous Neuronal SpikingPreprint

Drion, G., Franci, A., Seutin, V., & Sepulchre, R. J. (2013) · arXiv (Cornell University) · doi:10.48550/arxiv.1311.2200

MODELING LEARNING ON DYNAMIC BEHAVIOUR OF SYNAPSES

Fernando, S., Cho, Y. I., Nakamura, Y., Matsuzaki, S., & Marasinghe, A. (2009) · Journal of Medical Informatics & Technologies

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

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 693

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)