The DOI matches its Crossref record; 116 of the 116 references it cites were found in a registry or an index.
Homeostatic plasticity and NMDA receptor trafficking
Abstract
Learning, memory and brain development are associated with long-lasting modifications of synapses that are guided by specific patterns of neuronal activity. Such modifications include classical Hebbian plasticities (such as long-term potentiation and long-term depression), which are rapid and synapse-specific, and others, such as synaptic scaling and metaplasticity, that work over longer timescales and are crucial for maintaining and orchestrating neuronal network function. The cellular mechanisms underlying Hebbian plasticity have been well studied and involve rapid changes in the trafficking of highly mobile AMPA receptors. An emerging concept is that activity-dependent alterations in NMDA receptor trafficking contribute to homeostatic plasticity at central glutamatergic synapses.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Interestingly, synaptic scaling protocols homeostatically regulate both the NMDA and the AMPA component of glutamatergic synaptic currents, and the change in AMPA and NMDA currents are proportional at individual synapses (Watt et al. 2000;Perez-Otano and Ehlers 2005).”
From Homeostatic Synaptic Plasticity: Local and Global Mechanisms for Stabilizing Neuronal Function (2012) · cites this paper as Perez-Otano and Ehlers 2005
In the citing paper
“In this model, Ab accumulates along the endosomal/lysomal pathway that leads to dysfunction of multivesicular bodies, causing impairment of the ubiquitin-proteasome system, 9 which also controls the fate of NMDARs undergoing endocytic vesicular trafficking.50”
From Blocking the Interaction between Apolipoprotein E and Aβ Reduces Intraneuronal Accumulation of Aβ and Inhibits Synaptic Degeneration (2013) · cites this paper as [50]
Citations
Cites
The molecular biology of memory storage: a dialogue between genes and synapses
Kandel, E. R. (2001) · Science · doi:10.1126/science.1067020 · Cited by 3,917
Bienenstock, E., Cooper, L., & Munro, P. (1982) · The Journal of Neuroscience · doi:10.1523/jneurosci.02-01-00032.1982 · Cited by 2,896
AMPA Receptor Trafficking and Synaptic Plasticity
Malinow, R., & Malenka, R. C. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.112701.142758 · Cited by 2,588
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
Genetic enhancement of learning and memory in mice
Tang, Y., Shimizu, E., Dubé, G., Rampon, C., Kerchner, G. A., Zhuo, M., Liu, G., & Tsien, J. Z. (1999) · Nature · doi:10.1038/43432 · Cited by 1,878
Metaplasticity: the plasticity of synaptic plasticity
Abraham, W. C., & Bear, M. F. (1996) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)80018-x · Cited by 1,833
Extrasynaptic NMDARs oppose synaptic NMDARs by triggering CREB shut-off and cell death pathways
Hardingham, G. E., Fukunaga, Y., & Bading, H. (2002) · Nature Neuroscience · doi:10.1038/nn835 · Cited by 1,686
Cho, K.-O., Hunt, C. A., & Kennedy, M. B. (1992) · Neuron · doi:10.1016/0896-6273(92)90245-9 · Cited by 1,188
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
Cited by
Sorted by citations
Synaptic Plasticity: Multiple Forms, Functions, and Mechanisms
Citri, A., & Malenka, R. C. (2008) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301559 · Cited by 2,323
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
Metaplasticity: tuning synapses and networks for plasticity
Abraham, W. C. (2008) · Nature reviews. Neuroscience · doi:10.1038/nrn2356 · Cited by 1,166
Dopamine-mediated regulation of corticostriatal synaptic plasticity
Calabresi, P., Picconi, B., Tozzi, A., & Di Filippo, M. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.03.001 · Cited by 865
Synaptic plasticity and dysconnection in schizophrenia
Stephan, K. E., Baldeweg, T., & Friston, K. J. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.10.005 · Cited by 841
Arc/Arg3.1 Is Essential for the Consolidation of Synaptic Plasticity and Memories
Plath, N., Ohana, O., Dammermann, B., Errington, M. L., Schmitz, D., Gross, C., Mao, X., Engelsberg, A., Mahlke, C., Welzl, H., et al. (2006) · Neuron · doi:10.1016/j.neuron.2006.08.024 · Cited by 827
Evidence for a cytokine model of cognitive function
McAfoose, J., & Baune, B. T. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.10.005 · Cited by 760
Chubykin, A. A., Atasoy, D., Etherton, M. R., Brose, N., Kavalali, E. T., Gibson, J. R., & Südhof, T. C. (2007) · Neuron · doi:10.1016/j.neuron.2007.05.029 · Cited by 594
Unraveling mechanisms of homeostatic synaptic plasticity
Pozo, K., & Goda, Y. (2010) · Neuron · doi:10.1016/j.neuron.2010.04.028 · Cited by 565
HOMEOSTATIC CONTROL OF NEURAL ACTIVITY: From Phenomenology to Molecular Design
Davis, G. W. (2006) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.28.061604.135751 · Cited by 543
Mechanism of action of memantine
Johnson, J. M., & Kotermanski, S. E. (2005) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2005.09.007 · Cited by 500
Glutamatergic substrates of drug addiction and alcoholism
Gass, J. T., & Olive, M. F. (2007) · Biochemical Pharmacology · doi:10.1016/j.bcp.2007.06.039 · Cited by 502
Decay happens: the role of active forgetting in memory
Hardt, O., Nader, K., & Nadel, L. (2013) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2013.01.001 · Cited by 416
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
Synaptic plasticity of NMDA receptors: mechanisms and functional implications
Hunt, D. L., & Castillo, P. E. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.01.007 · Cited by 405
Neuronal regulation of alternative pre-mRNA splicing
Li, Q., Lee, J.-A., & Black, D. L. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2237 · Cited by 376
ORGANELLES AND TRAFFICKING MACHINERY FOR POSTSYNAPTIC PLASTICITY
Kennedy, M. J., & Ehlers, M. D. (2006) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.112808 · Cited by 346
Self-citationInfluence of glutamate and GABA transport on brain excitatory/inhibitory balance
Sears, S. M. S., & Hewett, S. J. (2021) · Experimental Biology and Medicine · doi:10.1177/1535370221989263 · Cited by 371
NMDA receptor function: subunit composition versus spatial distribution
Köhr, G. (2006) · Cell and Tissue Research · doi:10.1007/s00441-006-0273-6 · Cited by 357
Kim, J., Jung, S., Clemens, A. M., Petralia, R. S., & Hoffman, D. A. (2007) · Neuron · doi:10.1016/j.neuron.2007.05.026 · Cited by 312
Role of the brain‐derived neurotrophic factor at glutamatergic synapses
Carvalho, A. L., Caldeira, M. V., Santos, S. D., & Duarte, C. B. (2008) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0707509 · Cited by 290
Prenatal stressors in rodents: Effects on behavior
Weinstock, M. (2017) · Neurobiology of Stress · doi:10.1016/j.ynstr.2016.08.004 · Cited by 264
Development and Regulation of Dendritic Spine Synapses
Calabrese, B., Wilson, M. S., & Halpain, S. (2006) · Physiology · doi:10.1152/physiol.00042.2005 · Cited by 287
Brain Plasticity Mechanisms and Memory: A Party of Four
Bruel‐Jungerman, E., Davis, S., & Laroche, S. (2007) · The Neuroscientist · doi:10.1177/1073858407302725 · Cited by 267
The DLGAP family: neuronal expression, function and role in brain disorders
Rasmussen, A. H., Rasmussen, H. B., & Silahtaroglu, A. (2017) · Molecular Brain · doi:10.1186/s13041-017-0324-9 · Cited by 234
Groc, L., Choquet, D., Stephenson, F. A., Verrier, D., Manzoni, O. J., & Chavis, P. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.1772-07.2007 · Cited by 225
Casein Kinase 2 Regulates the NR2 Subunit Composition of Synaptic NMDA Receptors
Sanz-Clemente, A., Matta, J. A., Isaac, J. T. R., & Roche, K. W. (2010) · Neuron · doi:10.1016/j.neuron.2010.08.011 · Cited by 223
Kristiansen, L. V., Beneyto, M., Haroutunian, V, & Meador-Woodruff, J. H. (2006) · Molecular Psychiatry · doi:10.1038/sj.mp.4001844 · Cited by 220
Synaptic plasticity and phosphorylation
Lee, H. (2006) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2006.06.003 · Cited by 222
Lerma, J. (2005) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2005.08.004 · Cited by 213
Ionotropic Glutamate Receptors & CNS Disorders
Bowie, D. (2008) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/187152708784083821 · Cited by 207
Molecular Neurobiology of Lead (Pb2+): Effects on Synaptic Function
Neal, A. P., & Guilarte, T. R. (2010) · Molecular Neurobiology · doi:10.1007/s12035-010-8146-0 · Cited by 204
Metabotropic Glutamate Receptor Ligands as Potential Therapeutics for Addiction
Olive, M. F. (2009) · Current Drug Abuse Reviews · doi:10.2174/1874473710902010083 · Cited by 207
Cytokines and Neuronal Ion Channels in Health and Disease
Viviani, B., Gardoni, F., & Marinovich, M. (2007) · International review of neurobiology · doi:10.1016/s0074-7742(07)82013-7 · Cited by 196
Insufficient Sleep Reversibly Alters Bidirectional Synaptic Plasticity and NMDA Receptor Function
Kopp, C., Longordo, F., Nicholson, J. R., & Lüthi, A. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.2702-06.2006 · Cited by 192
Wheeler, D., Knapp, E., Bandaru, V. V. R., Wang, Y., Knorr, D., Poirier, C., Mattson, M. P., Geiger, J. D., & Haughey, N. J. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06038.x · Cited by 201
De Gois, S., Schäfer, M. K.-H., Defamie, N., Chen, C., Ricci, A., Weihe, E., Varoqui, H., & Erickson, J. D. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.5221-04.2005 · Cited by 192
Gonzalez-Islas, C., & Wenner, P. (2006) · Neuron · doi:10.1016/j.neuron.2006.01.017 · Cited by 191
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
The role of metaplasticity mechanisms in regulating memory destabilization and reconsolidation
Finnie, P. S. B., & Nader, K. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.03.008 · Cited by 189
Visualization of NMDA receptor–dependent AMPA receptor synaptic plasticity in vivo
Zhang, Y., Cudmore, R. H., Lin, D., Linden, D. J., & Huganir, R. L. (2015) · Nature Neuroscience · doi:10.1038/nn.3936 · Cited by 185
Rommy von Bernhardi, M., Bernhardi, L. E.-V., & Eugenín, J. L. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-62817-2_1 · Cited by 214
Organization, control and function of extrasynaptic NMDA receptors
Papouin, T., & Oliet, S. H. R. (2014) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0601 · Cited by 189
Pathophysiology of complex regional pain syndrome
Schwartzman, R. J., Alexander, G. M., & Grothusen, J. R. (2006) · Expert Review of Neurotherapeutics · doi:10.1586/14737175.6.5.669 · Cited by 168
Sgambato, V., & Cenci, M. A. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.10.005 · Cited by 175
EphB Controls NMDA Receptor Function and Synaptic Targeting in a Subunit-Specific Manner
Nolt, M. J., Lin, Y., Hruska, M., Murphy, J. A., Sheffler-Collins, S. I., Kayser, M. S., Passer, J. Z., Bennett, M. V. L., Zukin, R. S., & Dalva, M. B. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0282-11.2011 · Cited by 169
Zhang, S., Edelmann, L., Liu, J., Crandall, J. E., & Morabito, M. A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.1900-07.2008 · Cited by 172
Frank, C. A., Pielage, J., & Davis, G. W. (2009) · Neuron · doi:10.1016/j.neuron.2008.12.028 · Cited by 167
AMPA and NMDA glutamate receptor trafficking: multiple roads for reaching and leaving the synapse
Groc, L., & Choquet, D. (2006) · Cell and Tissue Research · doi:10.1007/s00441-006-0254-9 · Cited by 170
Lee, J.-A., Tang, Z., & Black, D. L. (2009) · Genes & Development · doi:10.1101/gad.1837009 · Cited by 162
Guidetti, P., Hoffman, G. E., Meléndez‐Ferro, M., Albuquerque, E. X., & Schwarcz, R. M. (2006) · Glia · doi:10.1002/glia.20432 · Cited by 156
Regulators of synaptic transmission: Roles in the pathogenesis and treatment of epilepsy
Casillas-Espinosa, P. M., Powell, K. L., & O'Brien, T. J. (2012) · Epilepsia · doi:10.1111/epi.12034 · Cited by 151
Development of Cortical Maps: Perspectives From the Barrel Cortex
Inan, M., & Crair, M. C. (2007) · The Neuroscientist · doi:10.1177/1073858406296257 · Cited by 152
Long-Term Potentiation Selectively Expressed by NMDA Receptors at Hippocampal Mossy Fiber Synapses
Kwon, H., & Castillo, P. E. (2008) · Neuron · doi:10.1016/j.neuron.2007.11.024 · Cited by 156
Unconventional NMDA Receptor Signaling
Doré, K., Stein, I. S., Brock, J. A., Castillo, P. E., Zito, K., & Sjöström, P. J. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1825-17.2017 · Cited by 148
Dual role of the exocyst in AMPA receptor targeting and insertion into the postsynaptic membrane
Gerges, N. Z., Backos, D. S., Rupasinghe, C. N., Spaller, M. R., & Esteban, J. A. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601065 · Cited by 147
Glutamate Dysfunction in Hippocampus: Relevance of Dentate Gyrus and CA3 Signaling
Tamminga, C. A., Southcott, S. A., Sacco, C., Wagner, A. D., & Ghose, S. (2012) · Schizophrenia Bulletin · doi:10.1093/schbul/sbs062 · Cited by 152
GluA2-lacking, calcium-permeable AMPA receptors--inducers of plasticity?
Man, H.-Y. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.01.001 · Cited by 142
Homeostatic plasticity at the Drosophila neuromuscular junction
Frank, C. A. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.06.015 · Cited by 140
Dendritic ion channel trafficking and plasticity
Shah, M. M., Hammond, R., & Hoffman, D. A. (2010) · Trends in Neurosciences · doi:10.1016/j.tins.2010.03.002 · Cited by 142
Regulation of NMDA receptor Ca2+ signalling and synaptic plasticity
Lau, C. G., Takeuchi, K., Rodenas-Ruano, A., Takayasu, Y., Murphy, J., Bennett, M. V. L., & Zukin, R. S. (2009) · Biochemical Society Transactions · doi:10.1042/bst0371369 · Cited by 138
Cytoskeleton Regulation of Glycine Receptor Number at Synapses and Diffusion in the Plasma Membrane
Charrier, C., Ehrensperger, M.-V., Dahan, M., Lévi, S., & Triller, A. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1758-06.2006 · Cited by 137
Surface trafficking of N-methyl-d-aspartate receptors: Physiological and pathological perspectives
Groc, L., Bard, L., & Choquet, D. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.05.029 · Cited by 135
Golgi fragmentation in Alzheimer's disease
Joshi, G. S., Bekier, M. E., & Wang, Y. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00340 · Cited by 129
Okuda, K., Kobayashi, S., Fukaya, M., Watanabe, A., Murakami, T., Hagiwara, M., Sato, T., Ueno, H., Ogonuki, N., Komano‐Inoue, S., et al. (2017) · Neurobiology of Disease · doi:10.1016/j.nbd.2017.07.002 · Cited by 121
Lead exposure during synaptogenesis alters NMDA receptor targeting via NMDA receptor inhibition
Neal, A. P., Worley, P. F., & Guilarte, T. R. (2010) · NeuroToxicology · doi:10.1016/j.neuro.2010.12.013 · Cited by 125
SNAP-25 is a target of protein kinase C phosphorylation critical to NMDA receptor trafficking
Lau, C. G., Takayasu, Y., Rodenas-Ruano, A., Paternain, A. V., Lerma, J., Bennett, M. V. L., & Zukin, R. S. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.4933-08.2010 · Cited by 120
Aoki, C. J., Sekino, Y., Hanamura, K., Fujisawa, S., Mahadomrongkul, V., Ren, Y., & Shirao, T. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20449 · Cited by 119
N -Methyl-D-Aspartate Receptor Subunit Changes after Traumatic Injury to the Developing Brain
Giza, C. C., Maria, N. S. S., & Hovda, D. A. (2006) · Journal of Neurotrauma · doi:10.1089/neu.2006.23.950 · Cited by 123
Sensing and expressing homeostatic synaptic plasticity
Rich, M. M., & Wenner, P. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.01.004 · Cited by 118
Kumamaru, E., Numakawa, T., Adachi, N., Yagasaki, Y., Izumi, A., Niyaz, M., Kudo, M., & Kunugi, H. (2007) · Molecular Endocrinology · doi:10.1210/me.2007-0264 · Cited by 116
Carpenter‐Hyland, E. P., & Chandler, L. J. (2007) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2007.01.016 · Cited by 110
Spatial and temporal boundaries of NMDA receptor hypofunction leading to schizophrenia
Nakazawa, K., Jeevakumar, V., & Nakao, K. (2017) · npj Schizophrenia · doi:10.1038/s41537-016-0003-3 · Cited by 110
Modeling Synaptic Dynamics Driven by Receptor Lateral Diffusion
Holcman, D., & Triller, A. (2006) · Biophysical Journal · doi:10.1529/biophysj.106.081935 · Cited by 113
Miglio, G., Varsaldi, F., & Lombardi, G. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.10.164 · Cited by 106
Keeping your brain in balance: homeostatic regulation of network function
Wen, W., & Turrigiano, G. G. (2024) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-092523-110001 · Cited by 137
Dynamic and specific interaction between synaptic NR2-NMDA receptor and PDZ proteins
Bard, L., Sainlos, M., Bouchet, D., Cousins, S. L., Mikasová, L., Breillat, C., Stephenson, F. A., Imperiali, B., Choquet, D., & Groc, L. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1002690107 · Cited by 106
Organization of β-adrenoceptor signaling compartments by sympathetic innervation of cardiac myocytes
Shcherbakova, O. G., Hurt, C. M., Xiang, Y. K., Dell’Acqua, M. L., Zhang, Q., Tsien, R. W., & Kobilka, B. K. (2007) · The Journal of Cell Biology · doi:10.1083/jcb.200604167 · Cited by 105
Pharmacological insights obtained from structure–function studies of ionotropic glutamate receptors
Chen, P. E., & Wyllie, D. J. A. (2006) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0706689 · Cited by 101
Heise, C., Gardoni, F., Culotta, L., di Luca, M., Verpelli, C., & Sala, C. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00035 · Cited by 99
LTP and adaptation to inactivity: Overlapping mechanisms and implications for metaplasticity
Thiagarajan, T. C., Lindskog, M., Malgaroli, A., & Tsien, R. W. (2007) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.07.030 · Cited by 99
Advances in non-dopaminergic treatments for Parkinson's disease
Stayte, S., & Vissel, B. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00113 · Cited by 104
Takahashi, H., Mizui, T., & Shirao, T. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03536.x · Cited by 95
Dopamine receptors regulate NMDA receptor surface expression in prefrontal cortex neurons
Gao, C., & Wolf, M. E. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05597.x · Cited by 95
Jung, S., Kim, J., & Hoffman, D. A. (2008) · Neuron · doi:10.1016/j.neuron.2008.08.029 · Cited by 94
Fan, N., Yang, H., Zhang, J., & Chen, C. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06489.x · Cited by 92
Biochemical Fractionation of Brain Tissue for Studies of Receptor Distribution and Trafficking
Hallett, P. J., Collins, T. L., Standaert, D. G., & Dunah, A. W. (2008) · Current Protocols in Neuroscience · doi:10.1002/0471142301.ns0116s42 · Cited by 92
Amidfar, M., Woelfer, M., Réus, G. Z., Quevedo, J., Walter, M., & Kim, Y. (2019) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2019.109668 · Cited by 95
Kuszczyk, M. A., Sanchez, S., Pankiewicz, J., Kim, J., Duszczyk, M., Guridi, M., Asuni, A. A., Sullivan, P. M., Holtzman, D. M., & Sadowski, M. J. (2013) · The American Journal of Pathology · doi:10.1016/j.ajpath.2013.01.034 · Cited by 89
“org causing impairment of the ubiquitin-proteasome system,(9)which also controls the fate of NMDARs undergoing endocytic vesicular trafficking.(50) ApoE-promoted buildup of Ab oligomers along the endosomal/lysosomal pathway may therefore affect intracellular trafficking and sorting of synaptic proteins and may indicat…”
BackgroundWang, G., Gilbert, J. P., & Man, H. (2012) · Neural Plasticity · doi:10.1155/2012/825364 · Cited by 91
Kastning, K., Kukhtina, V., Kittler, J. T., Chen, G., Pechstein, A., Enders, S., Lee, S. H., Sheng, M., Yan, Z., & Haucke, V. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611170104 · Cited by 88
Todd, G., Flavel, S. C., & Ridding, M. C. (2009) · Experimental Brain Research · doi:10.1007/s00221-009-1791-8 · Cited by 86
Neuronal protein trafficking associated with Alzheimer disease
Tang, B. L. (2009) · Cell Adhesion & Migration · doi:10.4161/cam.3.1.7254 · Cited by 85
Glutamatergic mechanisms for speed control and network operation in the rodent locomotor CPG
Talpalar, A. E. (2010) · Frontiers in Neural Circuits · doi:10.3389/fncir.2010.00019 · Cited by 82
Soares, C., Lee, K. F. H., Nassrallah, W., & Béïque, J.-C. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.1873-13.2013 · Cited by 80
Erickson, J. D., De Gois, S., Varoqui, H., Schafer, M. K.-H., & Weihe, E. (2006) · Neurochemistry International · doi:10.1016/j.neuint.2005.12.029 · Cited by 89
The Effects of General Anesthetics on Synaptic Transmission
Hao, X., Ou, M., Zhang, D., Zhao, W., Yang, Y., Liu, J., Yang, H., Zhu, T., Li, Y., & Zhou, C. (2020) · Current Neuropharmacology · doi:10.2174/1570159x18666200227125854 · Cited by 81
G protein-coupled receptors control NMDARs and metaplasticity in the hippocampus
MacDonald, J. F., Jackson, M. F., & Beazely, M. A. (2006) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2006.12.006 · Cited by 79
Chen, N., Chen, X., & Wang, J. (2008) · Journal of Cell Science · doi:10.1242/jcs.022368 · Cited by 73
Palatable Hyper-Caloric Foods Impact on Neuronal Plasticity
Morin, J., Rodríguez-Durán, L. F., Guzmán-Ramos, K. R., Perez‐Cruz, C., Ferreira, G., Díaz-Cintra, S. Y., & Pacheco‐López, G. (2017) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2017.00019 · Cited by 83
Metadata
- Authors
- Pérez-Otaño, I., & Ehlers, M. D.
- Affiliations
- Duke Medical Center (US)
- Corresponding author
- Ehlers, Michael D.
- ORCID
- Ehlers, Michael D.
- Venue
- Trends in Neurosciences
- Publisher
- Elsevier BV
- Published
- 2005-05
- Volume
- 28
- Issue
- 5
- Pages
- 229-238
- ISSN
- 0166-2236 (ISSN-L)
- OpenAlex
- W2020939800
- Cited by
- 356
- References
- 116
- Citations by year
- 2025: 3 · 2024: 3 · 2023: 4 · 2022: 4 · 2021: 11 · 2020: 11 · 2019: 16 · 2018: 7 · 2017: 12 · 2016: 10 · 2015: 13 · 2014: 14 · 2013: 25 · 2012: 22
- FWCI
- 3.53
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Trends in Neurosciences (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Alliance for Research on Schizophrenia and Depression
- National Institute of Mental Health (R01MH064748, MH 64748)
- National Institute of Neurological Disorders and Stroke (NS 39402, R01NS039402, NS 32742)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Keywords
- homeostatic plasticity, NMDA receptor trafficking, synaptic scaling, metaplasticity, Hebbian plasticity, long-term potentiation, long-term depression, AMPA receptor trafficking, glutamatergic synapses, activity-dependent synaptic plasticity
- MeSH terms
- Animals, Homeostasis, Humans, Neuronal Plasticity, Receptors, N-Methyl-D-Aspartate, Protein Transport
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review