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

Homeostatic Control of Sensory Output in Basal Vomeronasal Neurons: Activity-Dependent Expression ofEther-à-Go-Go-Related Gene Potassium Channels

Hagendorf, S., Fluegge, D., Engelhardt, C., & Spehr, M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3656-08.2009 · Cited by 43

Linking activity dyshomeostasis and sleep disturbances in Alzheimer disease

Slutsky, I. (2024) · Nature reviews. Neuroscience · doi:10.1038/s41583-024-00797-y · Cited by 43

Deficiency of AMPAR–Palmitoylation Aggravates Seizure Susceptibility

Itoh, M., Yamashita, M., Kaneko, M., Okuno, H., Abe, M., Yamazaki, M., Natsume, R., Yamada, D., Kaizuka, T., Suwa, R., et al. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1590-18.2018 · Cited by 40

Impaired GABAergic transmission disrupts normal homeostatic plasticity in rat cortical networks

Roux, N. L., Amar, M., Moreau, A. W., Baux, G., & Fossier, P. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06288.x · Cited by 42

Ionic Current Variability and Functional Stability in the Nervous System

Golowasch, J. (2014) · BioScience · doi:10.1093/biosci/biu070 · Cited by 41

Spontaneous Hemodynamic Oscillations during Human Sleep and Sleep Stage Transitions Characterized with Near-Infrared Spectroscopy

Näsi, T., Virtanen, J., Noponen, T., Toppila, J. P., Salmi, T. K., & Ilmoniemi, R. J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025415 · Cited by 44

Minimal requirements for a neuron to coregulate many properties and the implications for ion channel correlations and robustness

Yang, J., Shakil, H., Ratté, S., & Prescott, S. A. (2022) · eLife · doi:10.7554/elife.72875 · Cited by 41

Caspase-3 Deficiency Results in Disrupted Synaptic Homeostasis and Impaired Attention Control

Lo, S., Wang, Y. Y., Weber, M., Larson, J. L., Scearce-Levie, K. A., & Sheng, M. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.3280-14.2015 · Cited by 44

Emotion: the Self-regulatory Sense

Kauffman, K. P. (2014) · Global Advances in Health and Medicine · doi:10.7453/gahmj.2013.058 · Cited by 48

Krüppel Mediates the Selective Rebalancing of Ion Channel Expression

Parrish, J. Z., Kim, C. C., Tang, L. S., Bergquist, S. H., Wang, T., DeRisi, J. L., Jan, L. Y., Jan, Y. N., & Davis, G. W. (2014) · Neuron · doi:10.1016/j.neuron.2014.03.015 · Cited by 41

Tonic Nanomolar Dopamine Enables an Activity-Dependent Phase Recovery Mechanism That Persistently Alters the Maximal Conductance of the Hyperpolarization-Activated Current in a Rhythmically Active Neuron

Rodgers, E. W., Fu, J. J., Krenz, W. C., & Baro, D. J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.3770-11.2011 · Cited by 40

Dynamic bi-directional phosphorylation events associated with the reciprocal regulation of synapses during homeostatic up- and down-scaling

Desch, K., Langer, J. D., & Schuman, E. M. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109583 · Cited by 34

Nemo kinase interacts with Mad to coordinate synaptic growth at the Drosophila neuromuscular junction

Merino, C., Penney, J., González, M., Tsurudome, K., Moujahidine, M., O’Connor, M. B., Verheyen, E. M., & Haghighi, A. P. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200809127 · Cited by 41

Early Visuomotor Integration Processes Induce LTP/LTD-Like Plasticity in the Human Motor Cortex

Suppa, A., Voti, P. L., Rocchi, L., Papazachariadis, O., & Berardelli, A. (2013) · Cerebral Cortex · doi:10.1093/cercor/bht264 · Cited by 39

Synaptic Dysfunction and Plasticity in Amyotrophic Lateral Sclerosis

Gulino, R. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054613 · Cited by 38

A genetic approach to dissect sexually dimorphic behaviors

Juntti, S. A., Coats, J., & Shah, N. M. (2008) · Hormones and Behavior · doi:10.1016/j.yhbeh.2007.12.012 · Cited by 39

Cerebellar continuous theta‐burst stimulation affects motor learning of voluntary arm movements in humans

Voti, P. L., Conte, A., Rocchi, L., Bologna, M., Khan, N., Leodori, G., & Berardelli, A. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12391 · Cited by 39

New Approaches for Studying Synaptic Development, Function, and Plasticity UsingDrosophilaas a Model System

Frank, C. A., Wang, X., Collins, C. A., Rodal, A. A., Yuan, Q., Verstreken, P., & Dickman, D. K. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.3261-13.2013 · Cited by 37

Inactivity-induced increase in nAChRs upregulates Shal K+ channels to stabilize synaptic potentials

Ping, Y., & Tsunoda, S. (2011) · Nature Neuroscience · doi:10.1038/nn.2969 · Cited by 37

Mitochondria: new players in homeostatic regulation of firing rate set points

Ruggiero, A., Katsenelson, M., & Slutsky, I. (2021) · Trends in Neurosciences · doi:10.1016/j.tins.2021.03.002 · Cited by 37

The Redistribution of Drosophila Vesicular Monoamine Transporter Mutants from Synaptic Vesicles to Large Dense-Core Vesicles Impairs Amine-Dependent Behaviors

Grygoruk, A., Chen, A., Martin, C. A., Lawal, H. O., Fei, H., Gutierrez, G., Biedermann, T., Najibi, R., Hadi, R., Chouhan, A. K., et al. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0694-14.2014 · Cited by 37

Wherefore Art Thou, Homeo(stasis)? Functional Diversity in Homeostatic Synaptic Plasticity

Queenan, B. N., Lee, K. J., & Pak, D. T. S. (2012) · Neural Plasticity · doi:10.1155/2012/718203 · Cited by 38

Activity and Neuromodulatory Input Contribute to the Recovery of Rhythmic Output After Decentralization in a Central Pattern Generator

Zhang, Y., Khorkova, O., Rodríguez, R., & Golowaschi, J. (2008) · Journal of Neurophysiology · doi:10.1152/jn.01290.2007 · Cited by 37

Functional Recovery after Lesion of a Central Pattern Generator

Sakurai, A., & Katz, P. S. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3485-09.2009 · Cited by 37

Age dependence of excitatory-inhibitory balance following stroke

Schmidt, S., Bruehl, C., Frahm, C., Redecker, C., & Witte, O. W. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2010.11.019 · Cited by 36

Rod‐cone crossover connectome of mammalian bipolar cells

Lauritzen, J. S., Sigulinsky, C., Anderson, J. R., Kalloniatis, M., Nelson, N. T., Emrich, D. P., Rapp, C. N., McCarthy, N., Kerzner, E., Meyer, M., et al. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.24084 · Cited by 35

REST-Dependent Presynaptic Homeostasis Induced by Chronic Neuronal Hyperactivity

Bisogni, F. P., Lignani, G., Contestabile, A., Castroflorio, E., Pozzi, D., Rocchi, A., Prestigio, C., Orlando, M., Valente, P., Massacesi, M., et al. (2017) · Molecular Neurobiology · doi:10.1007/s12035-017-0698-9 · Cited by 37

Peripheral and Central Glutamate Dyshomeostasis in Neurodegenerative Disorders

Onaolapo, A. Y., & Onaolapo, O. J. (2020) · Current Neuropharmacology · doi:10.2174/1570159x18666201015161919 · Cited by 37

Plasticity and metaplasticity of adult rat hippocampal mossy fibers induced by neurotrophin‐3

Ramos-Languren, L. E., & Escobar, M. L. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12141 · Cited by 36

An essential postsynaptic role for the ubiquitin proteasome system in slow homeostatic synaptic plasticity in cultured hippocampal neurons

Jakawich, S. K., Neely, R., Djakovic, S. N., Patrick, G. N., & Sutton, M. A. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.09.061 · Cited by 36

Naris occlusion alters the electro-olfactogram: Evidence for compensatory plasticity in the olfactory system

Waggener, C. T., & Coppola, D. M. (2007) · Neuroscience Letters · doi:10.1016/j.neulet.2007.09.013 · Cited by 36

Circadian control of neural excitability in an animal model of temporal lobe epilepsy

Talathi, S. S., Hwang, D., Ditto, W. L., Mareci, T., Sepulveda, H., Spano, M. L., & Carney, P. R. (2009) · Neuroscience Letters · doi:10.1016/j.neulet.2009.03.057 · Cited by 36

Dendritic refinement of an identified neuron in the Drosophila CNS is regulated by neuronal activity and Wnt signaling

Singh, A. P., VijayRaghavan, K., & Rodrigues, V. (2010) · Development · doi:10.1242/dev.044131 · Cited by 37

Spatio-temporal regulations and functions of neuronal alternative RNA splicing in developing and adult brains

Iijima, T., Hidaka, C., & Iijima, Y. (2016) · Neuroscience Research · doi:10.1016/j.neures.2016.01.010 · Cited by 35

Hyperpolarisation‐activated cyclic nucleotide‐gated channels regulate the spontaneous firing rate of olfactory receptor neurons and affect glomerular formation in mice

Nakashima, N., Ishii, T. M., Bessho, Y., Kageyama, R., & Ohmori, H. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2012.247361 · Cited by 34

Homeostatic Control of Synaptic Transmission by Distinct Glutamate Receptors

Yan, D., Yamasaki, M., Straub, C., Watanabe, M., & Tomita, S. (2013) · Neuron · doi:10.1016/j.neuron.2013.02.031 · Cited by 34

Synchronization in slowly switching networks of coupled oscillators

Zhou, J., Zou, Y., Guan, S., Liu, Z., & Boccaletti, S. (2016) · Scientific Reports · doi:10.1038/srep35979 · Cited by 33

Half a century legacy of long-term potentiation

Caya-Bissonnette, L., & Béïque, J.-C. (2024) · Current Biology · doi:10.1016/j.cub.2024.05.008 · Cited by 41

Reactive Neurogenesis and Down-Regulation of the Potassium-Chloride Cotransporter KCC2 in the Cochlear Nuclei after Cochlear Deafferentation

Tighilet, B., Dutheil, S., Siponen, M. I., & Noreña, A. J. (2016) · Frontiers in Pharmacology · doi:10.3389/fphar.2016.00281 · Cited by 31

Neuronal morphology enhances robustness to perturbations of channel densities

Zang, Y., & Marder, E. E. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2219049120 · Cited by 38

Geometry and dynamics of activity-dependent homeostatic regulation in neurons

Olypher, A. V., & Prinz, A. A. (2010) · Journal of Computational Neuroscience · doi:10.1007/s10827-010-0213-z · Cited by 35

Modeling the role of lateral membrane diffusion in AMPA receptor trafficking along a spiny dendrite

Earnshaw, B. A., & Bressloff, P. C. (2008) · Journal of Computational Neuroscience · doi:10.1007/s10827-008-0084-8 · Cited by 35

Homeostatic synaptic plasticity in developing spinal networks driven by excitatory GABAergic currents

Wenner, P. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.04.058 · Cited by 32

Homeostatic synaptic plasticity at the neuromuscular junction in myasthenia gravis

Wang, X., & Rich, M. M. (2017) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13472 · Cited by 31

Monaural conductive hearing loss alters the expression of the GluA3 AMPA and glycine receptor α1 subunits in bushy and fusiform cells of the cochlear nucleus

Wang, H., Yin, G.-D., Rogers, K., Miralles, C. M., Blas, A. L. D., & Rubio, M. E. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.10.021 · Cited by 30

Dendritic growth gated by a steroid hormone receptor underlies increases in activity in the developing Drosophila locomotor system

Zwart, M., Randlett, O., Evers, J. F., & Landgraf, M. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1311711110 · Cited by 31

Surface expression and distribution of voltage-gated potassium channels in neurons (Review)

McKeown, L., Swanton, L., Robinson, P. A., & Jones, O. (2008) · Molecular Membrane Biology · doi:10.1080/09687680801992470 · Cited by 33

Implementation of integral feedback control in biological systems

Somvanshi, P. R., Patel, A. K., Bhartiya, S., & Venkatesh, K. V. (2015) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1307 · Cited by 32

A Correspondence Between Normalization Strategies in Artificial and Biological Neural Networks

Shen, Y., Wang, J. H., & Navlakha, S. (2021) · Neural Computation · doi:10.1162/neco_a_01439 · Cited by 31

Novel Models for Studying the Blood-Brain and Blood-Eye Barriers in Drosophila

Pinsonneault, R. L., Mayer, N., Mayer, F., Tegegn, N., & Bainton, R. J. (2010) · Methods in molecular biology · doi:10.1007/978-1-60761-938-3_17 · Cited by 32

Heat shock response and homeostatic plasticity

Karunanithi, S., & Brown, I. R. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00068 · Cited by 31

Stability of Neuronal Networks with Homeostatic Regulation

Harnack, D., Pelko, M., Chaillet, A., Chitour, Y., & van Rossum, M. C. W. (2015) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004357 · Cited by 33

Disrupted neural correlates of anesthesia and sleep reveal early circuit dysfunctions in Alzheimer models

Zarhin, D., Atsmon, R., Ruggiero, A., Baeloha, H., Shoob, S., Scharf, O., Heim, L. R., Buchbinder, N., Shinikamin, O., Shapira, I., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2021.110268 · Cited by 32

Isolation rearing impairs wound healing and is associated with increased locomotion and decreased immediate early gene expression in the medial prefrontal cortex of juvenile rats

Levine, J. B., Leeder, A., Parekkadan, B., Berdichevsky, Y., Rauch, S. L., Smoller, J. W., Konradi, C. L., Francois Berthiaume, B., & Yarmush, M. L. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.10.014 · Cited by 30

Self-Organized Chaos through Polyhomeostatic Optimization

Marković, D., & Gros, C. (2010) · Physical Review Letters · doi:10.1103/physrevlett.105.068702 · Cited by 29

MicroRNA-8 promotes robust motor axon targeting by coordinate regulation of cell adhesion molecules during synapse development

Lu, C. S., Zhai, B., Mauss, A. S., Landgraf, M., Gygi, S. P., & Vactor, D. V. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0517 · Cited by 28

Disruption of Axonal Transport Perturbs Bone Morphogenetic Protein (BMP) - Signaling and Contributes to Synaptic Abnormalities in Two Neurodegenerative Diseases

Kang, M., Hansen, T. J., Mickiewicz, M., Kaczynski, T. J., Fye, S., & Gunawardena, S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0104617 · Cited by 29

Serotonin Transduction Cascades Mediate Variable Changes in Pyloric Network Cycle Frequency in Response to the Same Modulatory Challenge

Spitzer, N., Cymbalyuk, G., Zhang, H., Edwards, D. H., & Baro, D. J. (2008) · Journal of Neurophysiology · doi:10.1152/jn.00986.2007 · Cited by 29

Dual separable feedback systems govern firing rate homeostasis

Kulik, Y. D., Jones, R., Moughamian, A. J., Whippen, J., & Davis, G. W. (2019) · eLife · doi:10.7554/elife.45717 · Cited by 28

Comparison of Two Voltage-Sensitive Dyes and Their Suitability for Long-Term Imaging of Neuronal Activity

Preuß, S., & Stein, W. (2013) · PLoS ONE · doi:10.1371/journal.pone.0075678 · Cited by 28

Rapid feedback regulation of synaptic efficacy during high-frequency activity at the Drosophila larval neuromuscular junction

Kauwe, G., & Isacoff, E. Y. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1221314110 · Cited by 29

Loss of Signal Transducer and Activator of Transcription 3 (STAT3) Signaling during Elevated Activity Causes Vulnerability in Hippocampal Neurons

Murase, S., Kim, E., Lin, L., Hoffman, D. A., & McKay, R. D. G. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2940-12.2012 · Cited by 30

Short-Term Synaptic Plasticity Compensates for Variability in Number of Motor Neurons at a Neuromuscular Junction

Daur, N., Bryan, A. S., Garcia, V. J., & Bucher, D. M. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2584-12.2012 · Cited by 24

Activity-dependent compensation of cell size is vulnerable to targeted deletion of ion channels

Gorur-Shandilya, S., Marder, E. E., & O’Leary, T. (2020) · Scientific Reports · doi:10.1038/s41598-020-72977-6 · Cited by 30

Inefficient neural system stabilization: a theory of spontaneous resolutions and recurrent relapses in psychosis

Palaniyappan, L. K. (2019) · Journal of Psychiatry and Neuroscience · doi:10.1503/jpn.180038 · Cited by 27

Homeostatic plasticity fails at the intersection of autism-gene mutations and a novel class of common genetic modifiers

Genç, Ö., An, J., Fetter, R. D., Kulik, Y. D., Zunino, G., Sanders, S., & Davis, G. W. (2020) · eLife · doi:10.7554/elife.55775 · Cited by 28

Homeostatic plasticity in the retina

Fitzpatrick, M. J., & Kerschensteiner, D. (2022) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2022.101131 · Cited by 31

Non-scaling regulation of AMPA receptors in homeostatic synaptic plasticity

Wang, G., Zhong, J., Guttieres, D., & Man, H. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.107700 · Cited by 25

Adaptive Synaptic Scaling in Spiking Networks for Continual Learning and Enhanced Robustness

Xu, M., Liu, F., Hu, Y., Li, H., Wei, Y., Zhong, S., Pei, J., & Deng, L. (2024) · IEEE Transactions on Neural Networks and Learning Systems · doi:10.1109/tnnls.2024.3373599 · Cited by 25

Motor neuronal activity varies least among individuals when it matters most for behavior

Cullins, M. J., Shaw, K. M., Gill, J. P., & Chiel, H. J. (2014) · Journal of Neurophysiology · doi:10.1152/jn.00729.2014 · Cited by 25

Mechanism of Notch Pathway Activation and Its Role in the Regulation of Olfactory Plasticity in Drosophila melanogaster

Kidd, S., & Lieber, T. (2016) · PLoS ONE · doi:10.1371/journal.pone.0151279 · Cited by 25

Homeostatic Activity-Dependent Tuning of Recurrent Networks for Robust Propagation of Activity

Gjorgjieva, J., Evers, J. F., & Eglen, S. J. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2511-15.2016 · Cited by 25

A transcriptional constraint mechanism limits the homeostatic response to activity deprivation in mammalian neocortex

Valakh, V., Wise, D. L., Zhu, X. A., Sha, M., Fok, J., Hooser, S. D. V., Schectman, R., Cepeda, I., Kirk, R., O'Toole, S. M., et al. (2023) · eLife · doi:10.7554/elife.74899 · Cited by 24

Tuning of synaptic responses: an organizing principle for optimization of neural circuits

O’Donnell, C., & Nolan, M. F. (2010) · Trends in Neurosciences · doi:10.1016/j.tins.2010.10.003 · Cited by 26

Intrinsic Spine Dynamics Are Critical for Recurrent Network Learning in Models With and Without Autism Spectrum Disorder

Humble, J., Hiratsuka, K., Kasai, H., & Toyoizumi, T. (2019) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2019.00038 · Cited by 23

Phospho-dependent Accumulation of GABABRs at Presynaptic Terminals after NMDAR Activation

Hannan, S. B., Gerrow, K., Triller, A., & Smart, T. G. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.07.021 · Cited by 21

Homeostatic Synaptic Plasticity

Turrigiano, G. G. (2008) · Springer eBooks · doi:10.1007/978-0-387-77232-5_18 · Cited by 25

A New Model for Developmental Neuronal Death and Excitatory/Inhibitory Balance in Hippocampus

Murase, S. (2013) · Molecular Neurobiology · doi:10.1007/s12035-013-8521-8 · Cited by 23

Serotonergic modulation of LTP at excitatory and inhibitory synapses in the developing rat visual cortex

Moreau, A. W., Amar, M., Callebert, J., & Fossier, P. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.02.013 · Cited by 25

Nonreciprocal homeostatic compensation in Drosophila potassium channel mutants

Kim, E. Z., Vienne, J., Rosbash, M., & Griffith, L. C. (2017) · Journal of Neurophysiology · doi:10.1152/jn.00002.2017 · Cited by 25

A postsynaptic PI3K-cII dependent signaling controller for presynaptic homeostatic plasticity

Hauswirth, A. G., Ford, K., Wang, T., Fetter, R. D., Tong, A., & Davis, G. W. (2018) · eLife · doi:10.7554/elife.31535 · Cited by 23

PACAP increases Arc/Arg 3.1 expression within the extended amygdala after fear conditioning in rats

Meloni, E. G., Kaye, K. T., Venkataraman, A., & Carlezon, W. A. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.11.011 · Cited by 21

M-Current Inhibition in Hippocampal Excitatory Neurons Triggers Intrinsic and Synaptic Homeostatic Responses at Different Temporal Scales

Lezmy, J., Gelman, H., Katsenelson, M., Styr, B., Tikochinsky, E., Lipinsky, M., Peretz, A. S., Slutsky, I., & Attali, B. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.1914-19.2020 · Cited by 24

Kismet Positively Regulates Glutamate Receptor Localization and Synaptic Transmission at the Drosophila Neuromuscular Junction

Ghosh, R., Vegesna, S., Safi, R., Bao, H., Zhang, B., Marenda, D. R., & Liebl, F. L. W. (2014) · PLoS ONE · doi:10.1371/journal.pone.0113494 · Cited by 22

Terminal Axonal Arborization and Synaptic Bouton Formation Critically Rely on Abp1 and the Arp2/3 Complex

Koch, N., Kobler, O., Thomas, U., Qualmann, B., & Kessels, M. M. (2014) · PLoS ONE · doi:10.1371/journal.pone.0097692 · Cited by 24

Importin 13 Regulates Neurotransmitter Release at theDrosophilaNeuromuscular Junction

Γιαγτζόγλου, Ν., Lin, Y. Q., Haueter, C. M., & Bellen, H. J. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0794-09.2009 · Cited by 24

In vivo and in vitro effects of vortioxetine on molecules associated with neuroplasticity

Kugathasan, P., Waller, J. A., Westrich, L., Abdourahman, A., Tamm, J. A., Pehrson, A. L., Dale, E., Gulinello, M. E., Sánchez, C., & Li, Y. (2016) · Journal of Psychopharmacology · doi:10.1177/0269881116667710 · Cited by 22

Calcium, synaptic plasticity and intrinsic homeostasis in Purkinje neuron models

Achard, P. (2008) · Frontiers in Computational Neuroscience · doi:10.3389/neuro.10.008.2008 · Cited by 23

Shifting attention to dynamics: Self-reconfiguration of neural networks

Kirst, C., Modes, C. D., & Magnasco, M. O. (2017) · Current Opinion in Systems Biology · doi:10.1016/j.coisb.2017.04.006 · Cited by 23

Cholinergic Homeostatic Synaptic Plasticity Drives the Progression of Aβ-Induced Changes in Neural Activity

Hahm, E.-T., Nagaraja, R. Y., Waro, G., & Tsunoda, S. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.06.029 · Cited by 24

Intrinsic plasticity and birdsong learning

Daou, A., & Margoliash, D. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107407 · Cited by 24

IGF-1 receptor regulates upward firing rate homeostasis via the mitochondrial calcium uniporter

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Activation and expansion of presynaptic signaling foci drives presynaptic homeostatic plasticity

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