The DOI matches its Crossref record; 151 of the 151 references it cites were found in a registry or an index.
Subunit-Specific NMDA Receptor Trafficking to Synapses
Open accessAbstract
To elucidate mechanisms controlling the number and subunit composition of synaptic NMDA-Rs in hippocampal slice neurons, the NR1, NR2A, and NR2B subunits were optically and electrophysiologically tagged. The NR2 subunit directs delivery of receptors to synapses with different rules controlling NR2A and NR2B. Synaptic incorporation of NR2B-containing receptors is not limited by synaptic transmission nor enhanced by increased subunit expression. NR2A-containing receptors whose expression normally increases with age replace synaptic NR2B-containing receptors. Replacement is enhanced by increased NR2A expression and requires synaptic activity. Surprisingly, spontaneously released transmitter acting on synaptic NMDA-Rs is sufficient for replacement and reduces NMDA-R responses. Thus, as with AMPA-Rs, synaptic trafficking of NMDA-Rs is tightly regulated and has subunit-specific rules with functionally important consequences.
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
“The second approach utilizes mutations in the CTD of GluN2B that cannot bind CaMKII as replacement for the wt (CaMKII L1298A/R1300Q) (120, 121, 230) or either competing with overexpressed full-length constructs (GluN2B R1300S/Q1303D) (231) or competing by expressing just the wt GluN2B CTD (839–1482) (232). The results are highly variable as reviewed in Ref. 233, ranging from complete block of LTP”
From Synaptic memory and CaMKII (2023) · cites this paper as [231]
Citations
Cites
Hollmann, M., & Heinemann, S. F. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.000335 · Cited by 4,056
Glutamate receptor ion channels
Mayer, M. L. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.05.004 · Cited by 3,655
The Glutamate Receptor Ion Channels
Dingledine, R., Borges, K., Bowie, D., & Traynelis, S. F. (1999) · Pharmacological Reviews · doi:10.1016/s0031-6997(24)01394-2 · Cited by 3,554
Monyer, H., Burnashev, N., Laurie, D. J., Sakmann, B., & Seeburg, P. H. (1994) · Neuron · doi:10.1016/0896-6273(94)90210-0 · Cited by 3,535
Voltage-dependent block by Mg2+ of NMDA responses in spinal cord neurones
Mayer, M. L., Westbrook, G. L., & Guthrie, P. B. (1984) · Nature · doi:10.1038/309261a0 · Cited by 2,941
Heteromeric NMDA receptors: molecular and functional distinction of subtypes
Monyer, H., Sprengel, R., Schoepfer, R., Herb, A., Higuchi, M., Lomeli, H., Burnashev, N., Sakmann, B., & Seeburg, P. H. (1992) · Science · doi:10.1126/science.256.5060.1217 · Cited by 2,541
Quality control in the endoplasmic reticulum
Ellgaard, L., & Helenius, A. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1052 · Cited by 2,171
Domain Interaction Between NMDA Receptor Subunits and the Postsynaptic Density Protein PSD-95
Kornau, H., Schenker, L. T., Kennedy, M. B., & Seeburg, P. H. (1995) · Science · doi:10.1126/science.7569905 · Cited by 1,916
The molecular basis of CaMKII function in synaptic and behavioural memory
Lisman, J., Schulman, H., & Cline, H. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn753 · Cited by 1,860
Changing subunit composition of heteromeric NMDA receptors during development of rat cortex
Sheng, M., Cummings, J., Roldan, L. A., Jan, Y. N., & Jan, L. Y. (1994) · Nature · doi:10.1038/368144a0 · Cited by 1,377
Research works printed but not linked: 1
- Piccini, 2002, Critical PDZ interactions by GluR1 and GluR2 required at different subcellular sites, J. Neurosci., in press
Cited by
Sorted by citations
Items 101–200 of 516
Kumar, S. S., & Huguenard, J. R. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-31-10074.2003 · Cited by 142
Law, A. J., Weickert, C. S., Webster, M. J., Herman, M. M., Kleinman, J. E., & Harrison, P. J. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02850.x · Cited by 141
N-Methyl-D-aspartate Receptors: Subunit Assembly and Trafficking to the Synapse
Prybylowski, K., & Wenthold, R. J. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.r300029200 · Cited by 137
Yin, X., Takei, Y., Kido, M. A., & Hirokawa, N. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.049 · Cited by 136
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
New developments on the role of NMDA receptors in Alzheimer's disease
Malinow, R. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.09.001 · Cited by 132
Self-citationBrenner, G. J., Ji, R., Shaffer, S., & Woolf, C. J. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03506.x · Cited by 132
Kaufman, A. M., Milnerwood, A. J., Sepers, M. D., Coquinco, A., She, K., Wang, L., Lee, H., Craig, A. M., Cynader, M. S., & Raymond, L. A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.4129-11.2012 · Cited by 135
Alvarez, V. A., Ridenour, D. A., & Sabatini, B. L. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.0956-07.2007 · Cited by 132
Sinagra, M., Verrier, D., Frankova, D., Korwek, K. M., Blahos, J., Weeber, E. J., Manzoni, O. J., & Chavis, P. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.1757-05.2005 · Cited by 128
Decker, J. M., Krüger, L., Sydow, A., Dennissen, F. J. A., Šišková, Z., Mandelkow�, E., & Mandelkow, E. (2016) · EMBO Reports · doi:10.15252/embr.201541439 · Cited by 130
Nicoll, R. A., & Schulman, H. (2023) · Physiological Reviews · doi:10.1152/physrev.00034.2022 · Cited by 126
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
Synaptic GluN2A-Containing NMDA Receptors: From Physiology to Pathological Synaptic Plasticity
Franchini, L., Carrano, N., Luca, M. D., & Gardoni, F. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21041538 · Cited by 127
Li, L., Stefan, M. I., & Novère, N. G. L. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043810 · Cited by 124
Endocytosis and Degradative Sorting of NMDA Receptors by Conserved Membrane-Proximal Signals
Scott, D. B., Michailidis, I. E., Mu, Y., Logothetis, D. E., & Ehlers, M. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.0780-04.2004 · Cited by 130
AMPA signalling in nascent glutamatergic synapses: there and not there!
Groc, L., Gustafsson, B., & Hanse, E. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.01.005 · Cited by 125
Báez, M. V., Cercato, M. C., & Jerusalinsky, D. A. (2018) · Neural Plasticity · doi:10.1155/2018/5093048 · Cited by 125
PSD-95 stabilizes NMDA receptors by inducing the degradation of STEP 61
Won, S., Incontro, S., Nicoll, R. A., & Roche, K. W. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1609702113 · Cited by 125
Zhao, X., Rosenke, R., Kronemann, D., Brim, B. C., Das, S. R., Dunah, A. W., & Magnusson, K. R. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.05.018 · Cited by 120
Agonist binding to the NMDA receptor drives movement of its cytoplasmic domain without ion flow
Doré, K., Aow, J., & Malinow, R. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1520023112 · Cited by 109
Self-citationCarpenter‐Hyland, E. P., & Chandler, L. J. (2007) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2007.01.016 · Cited by 110
Pérez‐Otaño, I., & Ehlers, M. (2004) · Neurosignals · doi:10.1159/000077524 · Cited by 118
Postsynaptic silent synapses: evidence and mechanisms
Isaac, J. T. R. (2003) · Neuropharmacology · doi:10.1016/s0028-3908(03)00229-6 · Cited by 113
Co-agonists differentially tune GluN2B-NMDA receptor trafficking at hippocampal synapses
Ferreira, J. S., Papouin, T., Ladépêche, L., Yao, A., Langlais, V. C., Bouchet, D., Dulong, J., Mothet, J.-P., Sacchi, S., Pollegioni, L., et al. (2017) · eLife · doi:10.7554/elife.25492 · Cited by 110
Role of NR2B-type NMDA receptors in selective neurodegeneration in Huntington disease
Li, L. (2003) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2003.04.003 · Cited by 110
Chen, W. S., & Bear, M. F. (2006) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.07.003 · Cited by 108
Chen, C., Hardy, M., Zhang, J., LaHoste, G. J., & Bazan, N. G. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.12.021 · Cited by 110
Li, L., Murphy, T. H., Hayden, M. R., & Raymond, L. A. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00308.2004 · Cited by 106
Developmental loss of miniature N -methyl- d -aspartate receptor currents in NR2A knockout mice
Townsend, M., Yoshii, A., Mishina, M., & Constantine‐Paton, M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0335786100 · Cited by 107
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
Silent synapses in selectively activated nucleus accumbens neurons following cocaine sensitization
Koya, E., Cruz, F. C., Ator, R., Golden, S. A., Hoffman, A. F., Lupica, C. R., & Hope, B. T. (2012) · Nature Neuroscience · doi:10.1038/nn.3232 · Cited by 112
Synaptic homeostasis and input selectivity follow from a calcium-dependent plasticity model
Yeung, L. C., Shouval, H. Z., Blais, B. S., & Cooper, L. N. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0405555101 · Cited by 106
Conformational signaling required for synaptic plasticity by the NMDA receptor complex
Aow, J., Doré, K., & Malinow, R. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1520029112 · Cited by 97
Self-citationWang, F., Chen, H., Steketee, J. D., & Sharp, B. M. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301033 · Cited by 97
Calcium flux-independent NMDA receptor activity is required for Aβ oligomer-induced synaptic loss
Birnbaum, J. H., Bali, J., Rajendran, L., Nitsch, R. M., & Tackenberg, C. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.160 · Cited by 101
Glutamate receptor dynamics and protein interaction: Lessons from the NMDA receptor
Bard, L., & Groc, L. (2011) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2011.05.009 · Cited by 93
Jung, S., Kim, J., & Hoffman, D. A. (2008) · Neuron · doi:10.1016/j.neuron.2008.08.029 · Cited by 94
Jung, S., Kim, J., Kwon, O. B., Jung, J. H., An, K., Jeong, A. Y., Lee, C. J., Choi, Y., Bailey, C. H., Kandel, E. R., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1001084107 · Cited by 97
Dysbindin regulates hippocampal LTP by controlling NMDA receptor surface expression
Tang, T. T.-T., Yang, F., Chen, B.-S., Lü, Y., Ji, Y., Roche, K. W., & Lu, B. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910499106 · Cited by 95
A critical role for VEGF and VEGFR2 in NMDA receptor synaptic function and fear-related behavior
Rossi, P. D., Harde, E., Dupuis, J. P., Martin, L., Chounlamountri, N., Bardin, M., Watrin, C., Benetollo, C., Pernet‐Gallay, K., Luhmann, H. J., et al. (2016) · Molecular Psychiatry · doi:10.1038/mp.2015.195 · Cited by 101
Fan, J., Gladding, C. M., Wang, L., Zhang, L. Y. J., Kaufman, A. M., Milnerwood, A. J., & Raymond, L. A. (2011) · Neurobiology of Disease · doi:10.1016/j.nbd.2011.12.019 · Cited by 94
Dumas, T. C. (2005) · Hippocampus · doi:10.1002/hipo.20077 · Cited by 94
Novel glutamatergic agents for major depressive disorder and bipolar disorder
Machado-Vieira, R., Ibrahim, L., Henter, I. D., & Zarate, C. A. (2012) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2011.09.010 · Cited by 92
Liu, Q., Chen, B., Yankova, M. P., Morest, D. K., Maryon, E. B., Hand, A. R., Nonet, M. L., & Wang, Z. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1730-05.2005 · Cited by 92
Brittain, J. M., Chen, L., Wilson, S. M., Brustovetsky, T., Gao, X., Ashpole, N. M., Molosh, A. I., You, H., Hudmon, A., Shekhar, A., et al. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.255455 · Cited by 89
Subcellular segregation of distinct heteromeric NMDA glutamate receptors in the striatum
Dunah, A. W., & Standaert, D. G. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.01744.x · Cited by 89
Lesiak, A., Zhu, M., Chen, H., Appleyard, S. M., Impey, S., Lein, P. J., & Wayman, G. A. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.2884-13.2014 · Cited by 88
“Organotypic hippocampal slices from P5 Sprague–Dawley rats (Charles River Laboratories) were cultured for 3 d, as described previously (Barria and Malinow, 2002).”
MethodKristiansen, L. V., Patel, S. A., Haroutunian, V. H., & Meador‐Woodruff, J. H. (2010) · Synapse · doi:10.1002/syn.20754 · Cited by 87
Leptin Induces Hippocampal Synaptogenesis via CREB-Regulated MicroRNA-132 Suppression of p250GAP
Dhar, M., Zhu, M., Impey, S., Lambert, T. J., Bland, T., Karatsoreos, I. N., Nakazawa, T., Appleyard, S. M., & Wayman, G. A. (2014) · Molecular Endocrinology · doi:10.1210/me.2013-1332 · Cited by 84
The Emergence of NMDA Receptor Metabotropic Function: Insights from Imaging
Doré, K., Aow, J., & Malinow, R. (2016) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2016.00020 · Cited by 83
Self-citationAndres, A. L., Regev, L., Phi, L., Seese, R. R., Chen, Y., Gall, C. M., & Baram, T. Z. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1445-13.2013 · Cited by 79
A family of photoswitchable NMDA receptors
Berlin, S., Szobota, S., Reiner, A., Carroll, E. C., Kienzler, M. A., Guyon, A., Xiao, T., Trauner, D. H., & Isacoff, E. Y. (2016) · eLife · doi:10.7554/elife.12040 · Cited by 87
McQuail, J. A., Beas, B. S., Kelly, K. B., Simpson, K. L., Frazier, C. J., Setlow, B., & Bizon, J. L. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.2332-16.2016 · Cited by 80
Nong, Y., Huang, Y., & Salter, M. W. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.05.001 · Cited by 79
SAP102 Mediates Synaptic Clearance of NMDA Receptors
Chen, B.-S., Gray, J. A., Sanz-Clemente, A., Wei, Z., Thomas, E. V., Nicoll, R. A., & Roche, K. W. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.09.024 · Cited by 81
Ethanol Alters Trafficking and Functional N-Methyl-D-aspartate Receptor NR2 Subunit Ratio via H-Ras
Suvarna, N. U., Borgland, S. L., Wang, J., Phamluong, K., Auberson, Y. P., Bonci, A., & Dorit Ron, A. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m504120200 · Cited by 83
Gascón, S., Deogracias, R., Sobrado, M., Roda, J. M., Renart, J., Rodríguez‐Peña, A., & Díaz‐Guerra, M. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m504108200 · Cited by 78
A Wnt/Calcium Signaling Cascade Regulates Neuronal Excitability and Trafficking of NMDARs
McQuate, A. L., Latorre-Esteves, E. S., & Barría, A. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.09.023 · Cited by 78
Li, B., Otsu, Y., Murphy, T. H., & Raymond, L. A. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-35-11244.2003 · Cited by 78
Counotte, D. S., Smit, A. B., Pattij, T., & Spijker, S. (2011) · Developmental Cognitive Neuroscience · doi:10.1016/j.dcn.2011.05.010 · Cited by 77
Guilarte, T. R., & McGlothan, J. L. (2003) · Molecular Brain Research · doi:10.1016/s0169-328x(03)00083-4 · Cited by 77
Ehsanifar, M., Montazeri, Z., Taheri, M. A., Rafati, M., Behjati, M., & Karimian, M. (2021) · Neurochemistry International · doi:10.1016/j.neuint.2021.104989 · Cited by 77
Holehonnur, R., Phensy, A. J., Kim, L. J., Milivojevic, M., Vuong, D., Daison, D. K., Alex, S., Tiner, M., Jones, L. E., Kroener, S., et al. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.1743-16.2016 · Cited by 74
Yan, J.-Z., Xu, Z., Ren, S., Hu, B., Yao, W., Wang, S.-H., Liu, S., & Lü, W. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.192708 · Cited by 75
NMDA-Receptor Activation but Not Ion Flux Is Required for Amyloid-Beta Induced Synaptic Depression
Tamburri, A., Dudilot, A., Licea, S., Bourgeois, C., & Boehm, J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0065350 · Cited by 75
Molecular mechanisms of synaptic remodeling in alcoholism
Kyzar, E. J., & Pandey, S. C. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.01.051 · Cited by 75
Hormonal regulation of hippocampal dendritic morphology and synaptic plasticity
Moult, P. R., & Harvey, J. (2008) · Cell Adhesion & Migration · doi:10.4161/cam.2.4.6354 · Cited by 72
GluN3A: An NMDA Receptor Subunit with Exquisite Properties and Functions
Kehoe, L. A., Bernardinelli, Y., & Müller, D. (2013) · Neural Plasticity · doi:10.1155/2013/145387 · Cited by 75
The Thorny Side of Addiction: Adaptive Plasticity and Dendritic Spines
Mulholland, P. J., & Chandler, L. J. (2007) · The Scientific World JOURNAL · doi:10.1100/tsw.2007.247 · Cited by 69
Experience-dependent changes in NMDA receptor composition at mature central synapses
Kopp, C., Longordo, F., & Lüthi, A. (2007) · Neuropharmacology · doi:10.1016/j.neuropharm.2007.03.014 · Cited by 71
Mitochondrial ROS control neuronal excitability and cell fate in frontotemporal dementia
Esteras, N., Kopach, O., Maiolino, M., Lariccia, V., Amoroso, S., Qamar, S., Wray, S., Rusakov, D. A., Jaganjac, M., & Abramov, A. Y. (2021) · Alzheimer s & Dementia · doi:10.1002/alz.12394 · Cited by 70
NMDA receptor subunit composition determines the polarity of leptin-induced synaptic plasticity
Moult, P. R., & Harvey, J. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.06.021 · Cited by 67
MicroRNAs in Neuronal Communication
Higa, G. S. V., de Sousa, É., Walter, L. T., Kinjo, É. R., Resende, R. R., & Kihara, A. H. (2014) · Molecular Neurobiology · doi:10.1007/s12035-013-8603-7 · Cited by 68
Huang, Y., Shi, X., Xu, H., Yang, H., Tian, C., Chen, S., & Chen, X. (2010) · Neurochemical Research · doi:10.1007/s11064-010-0152-0 · Cited by 71
Ehsanifar, M., Jafari, A. J., Nikzad, H., Salami, M., Atlasi, M. A., Mohammadi, H., & Tameh, A. A. (2019) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2019.03.090 · Cited by 68
Alsabban, A. H., Morikawa, M., Tanaka, Y., Takei, Y., & Hirokawa, N. (2019) · The EMBO Journal · doi:10.15252/embj.2018101090 · Cited by 66
The Role of the PDZ Protein GIPC in Regulating NMDA Receptor Trafficking
Yi, Z., Petralia, R. S., Fu, Z., Swanwick, C. C., Wang, Y., Prybylowski, K., Sans, N., Vicini, S., & Wenthold, R. J. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3252-07.2007 · Cited by 66
Kamphuis, P. J. G. H., Gardoni, F., Kamal, A., Croiset, G., Bakker, J. M., Cattabeni, F., Gispen, W. H., van Bel, F., Luca, M. D., & Wiegant, V. M. (2003) · The FASEB Journal · doi:10.1096/fj.02-0333fje · Cited by 66
Sachana, M., Rolaki, A., & Bal‐Price, A. (2018) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2018.02.024 · Cited by 67
Aoki, C. J., Kojima, N., Sabaliauskas, N. A., Shah, L. N., Ahmed, T. H., Oakford, J., Ahmed, T., Yamazaki, H., Hanamura, K., & Shirao, T. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22137 · Cited by 66
Receptor-ligand interactions for optimized endocytosis in targeted therapies
Sung, Y., Choi, Y., Kim, E. S., Ryu, J. H., & Kwon, I. C. (2025) · Journal of Controlled Release · doi:10.1016/j.jconrel.2025.01.060 · Cited by 64
Clinton, S. M., Haroutunian, V. H., & Meador‐Woodruff, J. H. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03954.x · Cited by 64
Williams, J. M., Guévremont, D., Mason‐Parker, S. E., Luxmanan, C., Tate, W. P., & Abraham, W. C. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2348-07.2007 · Cited by 69
Yang, X., Gong, R., Qin, L., Bao, Y., Fu, Y., Gao, S., Yang, H., Ni, J. D., Yuan, T., & Lü, W. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111217 · Cited by 68
Pian, J. P., Criado, J. R., Milner, R., & Ehlers, C. L. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.06.065 · Cited by 62
Selective impairment of GABAergic synaptic transmission in the flurothyl model of neonatal seizures
Isaeva, E., Isaev, D. S., Khazipov, R., & Holmes, G. L. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04693.x · Cited by 60
Albani, S. H., McHail, D. G., & Dumas, T. C. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.04.009 · Cited by 63
Changes in the expression of the NR2B subunit during aging in macaque monkeys
Bai, L., Hof, P. R., Standaert, D. G., Xing, Y., Nelson, S. E., Young, A. B., & Magnusson, K. R. (2003) · Neurobiology of Aging · doi:10.1016/s0197-4580(03)00091-5 · Cited by 59
Control of Intracellular Calcium Signaling as a Neuroprotective Strategy
Duncan, R. S., Goad, D. L., Grillo, M. A., Kaja, S., Payne, A. J., & Koulen, P. (2010) · Molecules · doi:10.3390/molecules15031168 · Cited by 59
Yin, X., Xue, F., Takei, Y., & Hirokawa, N. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0718-12.2012 · Cited by 59
Role of GPCR signaling and calcium dysregulation in Alzheimer's disease
Sushma, & Mondal, A. C. (2019) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2019.103414 · Cited by 56
Janssen, W. G. M., Vissavajjhala, P., Andrews, G., Moran, T. M., Hof, P. R., & Morrison, J. H. (2004) · Experimental Neurology · doi:10.1016/j.expneurol.2004.08.020 · Cited by 61
Oray, S., Majewska, A. K., & Sur, M. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhj019 · Cited by 61
Lipid dynamics at dendritic spines
Dotti, C. G., Esteban, J. A., & Ledesma, M. D. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00076 · Cited by 57
Hruska, M., Cain, R. E., & Dalva, M. B. (2022) · Nature Communications · doi:10.1038/s41467-022-28504-4 · Cited by 58
Habas, A., Kharebava, G., Szatmari, E. M., & Hetman, M. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03543.x · Cited by 57
Yamazaki, Y., Jia, Y., Niu, R., & Sumikawa, K. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04714.x · Cited by 57
NMDA Receptors and Brain Development
Ewald, R. C., & Cline, H. T. (2008) · Frontiers in neuroscience · doi:10.1201/9781420044157.ch1 · Cited by 59
Procedures for Culturing and Genetically Manipulating Murine Hippocampal Postnatal Neurons
Moutin, E., Hemonnot-Girard, A.-L., Seube, V., Linck, N., Rassendren, F., Perroy, J., & Compan, V. (2020) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2020.00019 · Cited by 60
Metadata
- Authors
- Barria, A., & Malinow, R.
- Affiliations
- Cold Spring Harbor Laboratory (US)
- Corresponding author
- Malinow, Roberto
- ORCID
- Malinow, Roberto
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2002-07
- Volume
- 35
- Issue
- 2
- Pages
- 345-353
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2030377743
- Cited by
- 515
- References
- 151
- Citations by year
- 2026: 5 · 2025: 14 · 2024: 16 · 2023: 12 · 2022: 14 · 2021: 14 · 2020: 17 · 2019: 22 · 2018: 12 · 2017: 15 · 2016: 26 · 2015: 27 · 2014: 28 · 2013: 23 · 2012: 23
- FWCI
- 10.46
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 4034 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
- Keywords
- NMDA receptor, receptor trafficking, NR2A, NR2B, NR1, subunit composition, hippocampal neurons, spontaneous neurotransmission, receptor subunit expression, synaptic plasticity
- MeSH terms
- Animals, Animals, Newborn, Cell Compartmentation, Cells, Cultured, Dendrites, Dose-Response Relationship, Drug, Hippocampus, Indicators and Reagents, Luminescent Proteins, Membrane Potentials, Mutation, Synaptic Transmission, Organ Culture Techniques, Recombinant Fusion Proteins, Synapses, Receptors, N-Methyl-D-Aspartate, Pyramidal Cells, Excitatory Amino Acid Antagonists, Protein Transport, Sodium Channel Blockers, Green Fluorescent Proteins
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