The DOI matches its Crossref record; 86 of the 86 references it cites were found in a registry or an index.
Regulation of NMDA receptor Ca2+ signalling and synaptic plasticity
Open accessAbstract
NMDARs (N-methyl-D-aspartate receptors) are critical for synaptic function throughout the CNS (central nervous system). NMDAR-mediated Ca2+ influx is implicated in neuronal differentiation, neuronal migration, synaptogenesis, structural remodelling, long-lasting forms of synaptic plasticity and higher cognitive functions. NMDAR-mediated Ca2+ signalling in dendritic spines is not static, but can be remodelled in a cell- and synapse-specific manner by NMDAR subunit composition, protein kinases and neuronal activity during development and in response to sensory experience. Recent evidence indicates that Ca2+ permeability of neuronal NMDARs, NMDAR-mediated Ca2+ signalling in spines and induction of NMDAR-dependent LTP (long-term potentiation) at hippocampal Schaffer collateral–CA1 synapses are under control of the cAMP/PKA (protein kinase A) signalling cascade. Thus, by enhancing Ca2+ influx through NMDARs in spines, PKA can regulate the induction of LTP. An emerging concept is that activity-dependent regulation of NMDAR-mediated Ca2+ signalling by PKA and by extracellular signals that modulate cAMP or protein phosphatases at synaptic sites provides a dynamic and potentially powerful mechanism for bi-directional regulation of synaptic efficacy and remodelling.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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
“CaMKII is vital in controlling NMDA receptor activity (Incontro et al., 2018), which also acts as a calcium channel (Lau et al., 2009).”
From APOE3 Christchurch modulates β-catenin/Wnt signaling in iPS cell-derived cerebral organoids from Alzheimer’s cases (2024) · cites this paper as Lau et al., 2009
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Malenka, R. C., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.012 · Cited by 3,968
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
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
PDZ domain proteins of synapses
Kim, E., & Sheng, M. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1517 · Cited by 1,630
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
Morphological Changes in Dendritic Spines Associated with Long-Term Synaptic Plasticity
Yuste, R., & Bonhoeffer, T. (2001) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.24.1.1071 · Cited by 1,269
Probabilistic decision making by slow reverberation in cortical circuits
Wang, X.-J. (2002) · Neuron · doi:10.1016/s0896-6273(02)01092-9 · Cited by 1,242
NMDA receptor trafficking in synaptic plasticity and neuropsychiatric disorders
Lau, C. G., & Zukin, R. S. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2153 · Cited by 1,159 · cited 6×
“Synaptic NMDARs are localized to PSDs (postsynaptic densities), where they are structurally organized (and spatially restricted) in a large macromolecular signalling complex comprising scaffolding and adaptor proteins, which physically link the receptors to kinases and phosphoprotein phosphatases and other downstream…”
InfluentialSelf-citationAKAP signalling complexes: focal points in space and time
Wong, W., & Scott, J. D. (2004) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1527 · Cited by 1,073
Receptor trafficking and synaptic plasticity
Collingridge, G. L., Isaac, J. T. R., & Wang, Y. T. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1556 · Cited by 1,046
Activity level controls postsynaptic composition and signaling via the ubiquitin-proteasome system
Ehlers, M. D. (2003) · Nature Neuroscience · doi:10.1038/nn1013 · Cited by 977
Dentritic spines : structure, dynamics and regulation
Hering, H., & Sheng, M. (2001) · Nature Reviews Neuroscience · doi:10.1038/35104061 · Cited by 961
Balancing Structure and Function at Hippocampal Dendritic Spines
Bourne, J. N., & Harris, K. M. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.060407.125646 · Cited by 916
PKA phosphorylation of AMPA receptor subunits controls synaptic trafficking underlying plasticity
Esteban, J. A., Shi, S.-H., Wilson, C., Nuriya, M., Huganir, R. L., & Malinow, R. (2003) · Nature Neuroscience · doi:10.1038/nn997 · Cited by 894
Micromolar concentrations of Zn2+ antagonize NMDA and GABA responses of hippocampal neurons
Westbrook, G. L., & Mayer, M. L. (1987) · Nature · doi:10.1038/328640a0 · Cited by 852
Role of Distinct NMDA Receptor Subtypes at Central Synapses
Cull-Candy, S. G., & Leszkiewicz, D. N. (2004) · Science s STKE · doi:10.1126/stke.2552004re16 · Cited by 796
Signal-Processing Machines at the Postsynaptic Density
Kennedy, M. B. (2000) · Science · doi:10.1126/science.290.5492.750 · Cited by 788
Developmental changes in distribution of NMDA receptor channel subunit mRNAs
Watanabe, M., Inoue, Y., Sakimura, K., & Mishina, M. (1992) · Neuroreport · doi:10.1097/00001756-199212000-00027 · Cited by 721
Activity-Dependent Decrease in NMDA Receptor Responses During Development of the Visual Cortex
Carmignoto, G., & Vicini, S. (1992) · Science · doi:10.1126/science.1279803 · Cited by 721
Regulatory mechanisms of AMPA receptors in synaptic plasticity
Derkach, V. A., Oh, M. C., Guire, E. S., & Soderling, T. R. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2055 · Cited by 708
Activity-Dependent Modulation of Synaptic AMPA Receptor Accumulation
O’Brien, R. J., Kamboj, S., Ehlers, M. D., Rosen, K. R., Fischbach, G. D., & Huganir, R. L. (1998) · Neuron · doi:10.1016/s0896-6273(00)80624-8 · Cited by 688
NR2A Subunit Expression Shortens NMDA Receptor Synaptic Currents in Developing Neocortex
Flint, A. C., Maisch, U. S., Weishaupt, J. H., Kriegstein, A. R., & Monyer, H. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-07-02469.1997 · Cited by 623
Rapid, experience-dependent expression of synaptic NMDA receptors in visual cortex in vivo
Quinlan, E. M., Philpot, B. D., Huganir, R. L., & Bear, M. F. (1999) · Nature Neuroscience · doi:10.1038/7263 · Cited by 579
Ca2+-permeable AMPA receptors in synaptic plasticity and neuronal death
Liu, S. J., & Zukin, R. S. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.01.006 · Cited by 530
Self-citationTingley, W. G., Ehlers, M., Kameyama, K., Doherty, C., Ptak, J., Riley, C. T., & Huganir, R. L. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.8.5157 · Cited by 507
Assembly of New Individual Excitatory Synapses
Friedman, H., Bresler, T., Garner, C. C., & Ziv, N. E. (2000) · Neuron · doi:10.1016/s0896-6273(00)00009-x · Cited by 499
Kutsuwada, T., Sakimura, K., Manabe, T., Takayama, C., Katakura, N., Kushiya, E., Natsume, R., Watanabe, M., Inoue, Y., Yagi, T., et al. (1996) · Neuron · doi:10.1016/s0896-6273(00)80051-3 · Cited by 498
Regulation of NMDA Receptors by an Associated Phosphatase-Kinase Signaling Complex
Westphal, R. S., Tavalin, S. J., Lin, J., Alto, N. M., Fraser, I. D. C., Langeberg, L. K., Sheng, M., & Scott, J. D. (1999) · Science · doi:10.1126/science.285.5424.93 · Cited by 495
Activity Regulates the Synaptic Localization of the NMDA Receptor in Hippocampal Neurons
Rao, A., & Craig, A. M. (1997) · Neuron · doi:10.1016/s0896-6273(00)80962-9 · Cited by 492
Hestrin, S., Nicoll, R. A., Perkel, D. J., & Sah, P. (1990) · The Journal of Physiology · doi:10.1113/jphysiol.1990.sp017980 · Cited by 491
Targeted disruption of NMDA receptor 1 gene abolishes NMDA response and results in neonatal death
Forrest, D., Yuzaki, M., Soares, H. D., Ng, L., Luk, D. C., Sheng, M., Stewart, C. L., Morgan, J. I., Connor, J. A., & Curran, T. (1994) · Neuron · doi:10.1016/0896-6273(94)90350-6 · Cited by 491
Postsynaptic organisation and regulation of excitatory synapses
Scannevin, R. H., & Huganir, R. L. (2000) · Nature reviews. Neuroscience · doi:10.1038/35039075 · Cited by 472
Targeting of PKA to Glutamate Receptors through a MAGUK-AKAP Complex
Colledge, M., Dean, R. A., Scott, G. K., Langeberg, L. K., Huganir, R. L., & Scott, J. D. (2000) · Neuron · doi:10.1016/s0896-6273(00)00013-1 · Cited by 467
Alternatively spliced isoforms of the NMDARI receptor subunit
Zukin, R. S., & Bennett, M. V. L. (1995) · Trends in Neurosciences · doi:10.1016/0166-2236(95)93920-s · Cited by 464
Self-citationDevelopmental switch in the expression of NMDA receptors occurs in vivo and in vitro
Williams, K. L., Russell, S. L., Shen, Y. M., & Molinoff, P. B. (1993) · Neuron · doi:10.1016/0896-6273(93)90317-k · Cited by 461
Gating of CaMKII by cAMP-Regulated Protein Phosphatase Activity During LTP
Blitzer, R. D., Connor, J. H., Brown, G. P., Wong, T., Shenolikar, S., Iyengar, R., & Landau, E. M. (1998) · Science · doi:10.1126/science.280.5371.1940 · Cited by 445
Philpot, B. D., Sekhar, A. K., Shouval, H., & Bear, M. (2001) · Neuron · doi:10.1016/s0896-6273(01)00187-8 · Cited by 440
Postnatal synaptic potentiation: delivery of GluR4-containing AMPA receptors by spontaneous activity
Zhu, J. J., Esteban, J. A., Hayashi, Y., & Malinow, R. (2000) · Nature Neuroscience · doi:10.1038/80614 · Cited by 437
Kirkwood, A., Lee, H., & Bear, M. F. (1995) · Nature · doi:10.1038/375328a0 · Cited by 430
Emptage, N. J., Bliss, T., & Fine, A. (1999) · Neuron · doi:10.1016/s0896-6273(00)80683-2 · Cited by 429
Genetically lean mice result from targeted disruption of the RIIβ subunit of protein kinase A
Cummings, D. E., Brandon, E. P., Planas, J. V., Motamed, K., Idzerda, R. L., & McKnight, G. S. (1996) · Nature · doi:10.1038/382622a0 · Cited by 420
Spine-Neck Geometry Determines NMDA Receptor-Dependent Ca2+ Signaling in Dendrites
Noguchi, J., Matsuzaki, M., Ellis-Davies, G. C. R., & Kasai, H. (2005) · Neuron · doi:10.1016/j.neuron.2005.03.015 · Cited by 419
Regulation of morphological postsynaptic silent synapses in developing hippocampal neurons
Liao, D., Zhang, X., O’Brien, R., Ehlers, M., & Huganir, R. L. (1999) · Nature Neuroscience · doi:10.1038/4540 · Cited by 396
Rebola, N., Lujan, R., Cunha, R. A., & Mulle, C. (2008) · Neuron · doi:10.1016/j.neuron.2007.11.023 · Cited by 376
Wenthold, R. J., Prybylowski, K., Standley, S., Sans, N., & Petralia, R. S. (2003) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.43.100901.135803 · Cited by 374
LTP leads to rapid surface expression of NMDA but not AMPA receptors in adult rat CA1
Grosshans, D. R., Clayton, D. A., Coultrap, S. J., & Browning, M. D. (2001) · Nature Neuroscience · doi:10.1038/nn779 · Cited by 362
Ca2+ signaling in dendritic spines
Sabatini, B. L., Maravall, M., & Svoboda, K. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00218-x · Cited by 359
Homeostatic plasticity and NMDA receptor trafficking
Pérez-Otaño, I., & Ehlers, M. D. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.03.004 · Cited by 356
Snyder, G. L., Fienberg, A. A., Huganir, R. L., & Greengard, P. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-24-10297.1998 · Cited by 336
Protein kinase A regulates calcium permeability of NMDA receptors
Skeberdis, V. A., Chevaleyre, V., Lau, C. G., Goldberg, J. H., Pettit, D. L., Suadicani, S. O., Lin, Y., Bennett, M. V. L., Yuste, R., Castillo, P. E., et al. (2006) · Nature Neuroscience · doi:10.1038/nn1664 · Cited by 332
Self-citationA developmental switch in the signaling cascades for LTP induction
Yasuda, H., Barth, A. L., Stellwagen, D., & Malenka, R. C. (2003) · Nature Neuroscience · doi:10.1038/nn985 · Cited by 325
Man, H.-Y., Sekine-Aizawa, Y., & Huganir, R. L. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611698104 · Cited by 311
NMDA-receptor trafficking and targeting: implications for synaptic transmission and plasticity
Carroll, R. C., & Zukin, R. S. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)02272-5 · Cited by 303
Self-citationNMDA Receptor Subunit-Dependent [Ca2+] Signaling in Individual Hippocampal Dendritic Spines
Sobczyk, A., Scheuß, V., & Svoboda, K. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1221-05.2005 · Cited by 294
Fractional contribution of calcium to the cation current through glutamate receptor channels
Schneggenburger, R., Zhou, Z., Konnerth, A., & Neher, E. (1993) · Neuron · doi:10.1016/0896-6273(93)90277-x · Cited by 281
Leonard, A. S., & Hell, J. W. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.18.12107 · Cited by 279
β-Adrenergic Regulation of Synaptic NMDA Receptors by cAMP-Dependent Protein Kinase
Raman, I. M., Tong, G., & Jahr, C. E. (1996) · Neuron · doi:10.1016/s0896-6273(00)80059-8 · Cited by 278
NMDA Receptor-Mediated Subthreshold Ca2+Signals in Spines of Hippocampal Neurons
Kovalchuk, Y., Eilers, J., Lisman, J. E., & Konnerth, A. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-05-01791.2000 · Cited by 270
Huang, Y.-Y., Kandel, E. R., Varshavsky, L., Brandont, E. P., Qi, M., Idzerda, R. L., Stanley McKnight, G., & Bourtchouladz, R. (1995) · Cell · doi:10.1016/0092-8674(95)90146-9 · Cited by 267
Activity-Dependent mRNA Splicing Controls ER Export and Synaptic Delivery of NMDA Receptors
Mu, Y., Otsuka, T., Horton, A. C., Scott, D. B., & Ehlers, M. (2003) · Neuron · doi:10.1016/s0896-6273(03)00676-7 · Cited by 246
Schiller, J., Schiller, Y., & Clapham, D. E. (1998) · Nature Neuroscience · doi:10.1038/363 · Cited by 237
Akaaboune, M., Culican, S. M., Turney, S., & Lichtman, J. (1999) · Science · doi:10.1126/science.286.5439.503 · Cited by 228
Brandon, E. P., Zhuo, M., Huang, Y. Y., Qi, M., Gerhold, K. A., Burton, K. A., Kandel, E. R., McKnight, G. S., & Idzerda, R. L. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.19.8851 · Cited by 216
Obligatory Role of NR2A for Metaplasticity in Visual Cortex
Philpot, B. D., Cho, K. K. A., & Bear, M. F. (2007) · Neuron · doi:10.1016/j.neuron.2007.01.027 · Cited by 207
Regulation of NMDA receptors in cultured hippocampal neurons by protein phosphatases 1 and 2A
Wang, L., Orser, B. A., Brautigan, D. L., & MacDonald, J. F. (1994) · Nature · doi:10.1038/369230a0 · Cited by 204
A proportional but slower NMDA potentiation follows AMPA potentiation in LTP
Watt, A. J., Sjöström, P. J., Häusser, M., Nelson, S. B., & Turrigiano, G. G. (2004) · Nature Neuroscience · doi:10.1038/nn1220 · Cited by 178
Age‐dependent requirement of AKAP150‐anchored PKA and GluR2‐lacking AMPA receptors in LTP
Lü, Y., Allen, M., Halt, A. R., Weisenhaus, M., Dallapiazza, R. F., Hall, D. D., Usachev, Y. M., McKnight, G. S., & Hell, J. W. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601884 · Cited by 170
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
Blank, T., Nijholt, I. M., Teichert, U., Kügler, H., Behrsing, H. P., Fienberg, A. A., Greengard, P., & Spiess, J. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.26.14859 · Cited by 138
Oliveria, S. F., Gomez, L. L., & Dell'Acqua, M. L. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200209127 · Cited by 129
Subcellular Dynamics of Type II PKA in Neurons
Zhong, H., Sia, G.-M., Sato, T., Gray, N. W., Mao, T., Khuchua, Z. A., Huganir, R. L., & Svoboda, K. (2009) · Neuron · doi:10.1016/j.neuron.2009.03.013 · Cited by 126
Inhibition of the cAMP Pathway Decreases Early Long-Term Potentiation at CA1 Hippocampal Synapses
Otmakhova, N. A., Otmakhov, N., Mortenson, L. H., & Lisman, J. E. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-12-04446.2000 · Cited by 124
Garaschuk, O., Schneggenburger, R., Schirra, C., Tempia, F., & Konnerth, A. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021255 · Cited by 122
Hensch, T. K., Gordon, J. A., Brandon, E. P., McKnight, G. S., Idzerda, R. L., & Stryker, M. P. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-06-02108.1998 · Cited by 117
Activity-Dependent Plasticity of the NMDA-Receptor Fractional Ca2+ Current
Sobczyk, A., & Svoboda, K. (2007) · Neuron · doi:10.1016/j.neuron.2006.11.016 · Cited by 111
Enhancement of the response in spinal dorsal horn neurons by cAMP-dependent protein kinase
Cerne, R., Rusin, K. I., & Randić, M. (1993) · Neuroscience Letters · doi:10.1016/0304-3940(93)90275-p · Cited by 110
Cyclic AMP-dependent protein kinase mediates ocular dominance shifts in cat visual cortex
Beaver, C. J., Ji, Q., Fischer, Q. S., & Daw, N. W. (2001) · Nature Neuroscience · doi:10.1038/83985 · Cited by 85
Schneggenburger, R. (1996) · Biophysical Journal · doi:10.1016/s0006-3495(96)79782-5 · Cited by 78
Fischer, Q. S., Beaver, C. J., Yang, Y., Rao, Y., Jakobsdóttir, K. B., Storm, D. R., McKnight, G. S., & Daw, N. W. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2409-04.2004 · Cited by 65
Barrel Map Development Relies on Protein Kinase A Regulatory Subunit IIβ-Mediated cAMP Signaling
Inan, M., Lu, H., Albright, M. J., She, W.-C., & Crair, M. C. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3745-05.2006 · Cited by 60
Nie, T., McDonough, C. B., Huang, T. T., Nguyen, P., & Abel, T. G. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1602-07.2007 · Cited by 46
Recombinant lonotropic Glutamate Receptors: Functional Distinctions Imparted by Different Subunits
Burnashev, N. (1993) · Cellular Physiology and Biochemistry · doi:10.1159/000154696 · Cited by 38
Roles of Protein Kinase A and Protein Kinase G in Synaptic Plasticity in the Visual Cortex
Liu, S. (2003) · Cerebral Cortex · doi:10.1093/cercor/13.8.864 · Cited by 28
Yang, Y., Takeuchi, K., Rodenas-Ruano, A., Takayasu, Y., Bennett, M. V. L., & Zukin, R. S. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.08.013 · Cited by 23
Self-citation
Cited by
Sorted by citations
The Role of NMDA Receptors in Alzheimer’s Disease
Liu, J., Chang, L., Song, Y., Li, H., & Wu, Y. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00043 · Cited by 535
Oxidative Stress and Neurodegenerative Disorders
Li, J., Wuliji, O., Li, W., Jiang, Z.-G., & Ghanbari, H. (2013) · International Journal of Molecular Sciences · doi:10.3390/ijms141224438 · Cited by 520
Kamat, P. K., Kalani, A., Rai, S., Swarnkar, S., Tota, S., Nath, C., & Tyagi, N. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-9053-6 · Cited by 511
Dysfunction of NMDA receptors in Alzheimer’s disease
Zhang, Y., Li, P., Feng, J., & Wu, M. (2016) · Neurological Sciences · doi:10.1007/s10072-016-2546-5 · Cited by 282
“NMDARs are the primary channel that mediates Ca 2 ? signals in hippocampal neurons and contribute to the expression of long-term potentiation (LTP) and long-term depression (LTD) and for synaptic plasticity [8].”
BackgroundThe decade of the dendritic nmda spike
Antic, S. D., Zhou, W., Moore, A. R., Short, S. M., & Ikonomu, K. D. (2010) · Journal of Neuroscience Research · doi:10.1002/jnr.22444 · Cited by 222
Metadata
- Authors
- Lau, C. G., Takeuchi, K., Rodenas-Ruano, A., Takayasu, Y., Murphy, J., Bennett, M. V. L., & Zukin, R. S.
- Affiliations
- Albert Einstein College of Medicine (US)
- Corresponding author
- Zukin, R. Suzanne
- Venue
- Biochemical Society Transactions
- Publisher
- Portland Press Ltd.
- Published
- 2009-11-19
- Volume
- 37
- Issue
- 6
- Pages
- 1369-1374
- ISSN
- 0300-5127 (ISSN-L)
- 1470-8752
- PMC
- PMC3501105
- OpenAlex
- W2022873534
- Cited by
- 138
- References
- 86
- Citations by year
- 2026: 13 · 2025: 14 · 2024: 11 · 2023: 11 · 2022: 15 · 2021: 13 · 2020: 9 · 2019: 9 · 2018: 3 · 2017: 7 · 2016: 4 · 2015: 3 · 2014: 7 · 2013: 4 · 2012: 5
- FWCI
- 2.07
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Biochemical Society Transactions (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute of Neurological Disorders and Stroke (NS-20752, R01NS020752)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Health Sciences › Medicine › Pharmacology (medical) › Treatment of Major Depression
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Keywords
- NMDA receptor, calcium signaling, synaptic plasticity, long-term potentiation, dendritic spines, cAMP/PKA signaling, protein kinase A, NMDA receptor subunit composition, calcium permeability, protein phosphatase, synaptic remodeling
- MeSH terms
- Animals, Calcium, Isoenzymes, Neuronal Plasticity, Receptors, N-Methyl-D-Aspartate, Long-Term Potentiation, Cyclic AMP-Dependent Protein Kinases, Calcium Signaling, Dendritic Spines
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