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Synaptic plasticity in the hippocampus: LTP and LTD
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“Long-term potentiation and long-term depression (LTP/LTD) can be elicited by activating N-methyl-D-aspartate (NMDA)-type glutamate receptors, typically by the coincident activity of pre-and postsynaptic neurons.”
From NMDA receptor-dependent long-term potentiation and long-term depression (LTP/LTD). (2012) · cites this paper as Malenka 1994
In the citing paper
“LTP and LTD are induced by specific patterns of activity (Malenka 1994).”
From NMDA receptor-dependent long-term potentiation and long-term depression (LTP/LTD). (2012) · cites this paper as Malenka 1994
In the citing paper
“Indeed, it is now fairly well accepted that modest activation of NMDARs leading to modest increases in postsynaptic calcium are optimal for triggering LTD, whereas much stronger activation of NMDARs leading to much larger increases in postsynaptic calcium are required to trigger LTP (Malenka 1994).”
From NMDA receptor-dependent long-term potentiation and long-term depression (LTP/LTD). (2012) · cites this paper as Malenka 1994
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Cites
A synaptic model of memory: long-term potentiation in the hippocampus
Bliss, T. V. P., & Collingridge, G. L. (1993) · Nature · doi:10.1038/361031a0 · Cited by 11,566
The Medial Temporal Lobe Memory System
Squire, L. R., & Zola-Morgan, S. (1991) · Science · doi:10.1126/science.1896849 · Cited by 3,282
Dynamics of the Hippocampal Ensemble Code for Space
Wilson, M. A., & McNaughton, B. L. (1993) · Science · doi:10.1126/science.8351520 · Cited by 2,350
Mechanisms underlying induction of homosynaptic long-term depression in area CA1 of the hippocampus
Mulkey, R. M., & Malenka, R. C. (1992) · Neuron · doi:10.1016/0896-6273(92)90248-c · Cited by 1,113
Self-citationInvolvement of a calcineurin/ inhibitor-1 phosphatase cascade in hippocampal long-term depression
Mulkey, R. M., Endo, S., Shenolikar, S., & Malenka, R. C. (1994) · Nature · doi:10.1038/369486a0 · Cited by 1,083
Self-citationNMDA-receptor-dependent synaptic plasticity: multiple forms and mechanisms
Malenka, R. C., & Nicoll, R. A. (1993) · Trends in Neurosciences · doi:10.1016/0166-2236(93)90197-t · Cited by 904
Self-citationNitric Oxide and Synaptic Function
Schuman, E. M., & Madison, D. V. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.001101 · Cited by 774
Induction of LTP in the hippocampus needs synaptic activation of glutamate metabotropic receptors
Bashir, Z. I., Bortolotto, Z. A., Davies, C. H., Berretta, N., Irving, A. J., Seal, A., Henley, J. M., Jane, D. E., Watkins, J. C., & Collingridge, G. L. (1993) · Nature · doi:10.1038/363347a0 · Cited by 733
An Essential Role for Protein Phosphatases in Hippocampal Long-Term Depression
Mulkey, R. M., Herron, C. E., & Malenka, R. C. (1993) · Science · doi:10.1126/science.8394601 · Cited by 699
Self-citationWilliams, J. H., Errington, M., Lynch, M., & Bliss, T. (1989) · Nature · doi:10.1038/341739a0 · Cited by 630
Research works printed but not linked: 6
- Dudek, 1992, 89, 4363
- Klann, 1993, 90, 8337
- Lisman, 1989, 86, 9574
- O'Dell, 1991, 88, 11285
- Sacktor, 1993, 90, 8342
- Schwartz, 1993, 90, 8310
Cited by
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Items 101–200 of 653
Moechars, D., Lorent, K., De Strooper, B., Dewachter, I., & Van Leuven, F. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00468.x · Cited by 201
Neuroadaptive processes in GABAergic and glutamatergic systems in benzodiazepine dependence
Allison, C., & Pratt, J. A. (2003) · Pharmacology & Therapeutics · doi:10.1016/s0163-7258(03)00029-9 · Cited by 160
Neuronal Oscillations Enhance Stimulus Discrimination by Ensuring Action Potential Precision
Schaefer, A. T., Angelo, K., Spors, H., & Margrie, T. W. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040163 · Cited by 169
NCAM-antibodies modulate induction of long-term potentiation in rat hippocampal CA1
Rønn, L. C. B., Bock, E., Linnemann, D., & Jahnsen, H. (1995) · Brain Research · doi:10.1016/0006-8993(95)00147-i · Cited by 156
Negative Regulation and Gain Control of Sensory Neurons by the C. elegans Calcineurin TAX-6
Kuhara, A., Inada, H., Katsura, I., & Mori, I. (2002) · Neuron · doi:10.1016/s0896-6273(02)00607-4 · Cited by 153
Hrabětová, S., & Sacktor, T. C. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-17-05324.1996 · Cited by 156
Joshi, I., & Wang, L. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2001.013506 · Cited by 151
Mereu, M., Bonci, A., Newman, A. H., & Tanda, G. (2013) · Psychopharmacology · doi:10.1007/s00213-013-3232-4 · Cited by 151
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
Phosphorylation of the Kv2.1 K+ Channel Alters Voltage-Dependent Activation
Murakoshi, H., Shi, G., Scannevin, R. H., & Trimmer, J. S. (1997) · Molecular Pharmacology · doi:10.1124/mol.52.5.821 · Cited by 147
Martins‐de‐Souza, D., Gattaz, W. F., Schmitt, A., Rewerts, C., Marangoni, S., Novello, J. C., Maccarrone, G., Turck, C. W., & Dias‐Neto, E. (2008) · Journal of Neural Transmission · doi:10.1007/s00702-008-0156-y · Cited by 146
Long-term modifications of synaptic efficacy in the human inferior and middle temporal cortex.
Chen, W. R., Lee, S., Kato, K., Spencer, D. D., Shepherd, G. M., & Williamson, A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.15.8011 · Cited by 146
Zilberter, Y., Kaiser, K. M. M., & Sakmann, B. J. (1999) · Neuron · doi:10.1016/s0896-6273(00)81044-2 · Cited by 140
Long-Term Potentiation in Distinct Subtypes of Hippocampal Nonpyramidal Neurons
Maccaferri, G., & McBain, C. J. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-17-05334.1996 · Cited by 133
Synaptotagmin 7 functions as a Ca2+-sensor for synaptic vesicle replenishment
Liu, H., Bai, H., Hui, E., Lu, Y., Evans, C. S., Wang, Z., Kwon, S. E., & Chapman, E. R. (2014) · eLife · doi:10.7554/elife.01524 · Cited by 137
Yu, L., Scherlag, B. J., LI, S., Sheng, X., Lu, Z., Nakagawa, H., Zhang, Y., Jackman, W. M., Lazzara, R., Jiang, H., et al. (2010) · Journal of Cardiovascular Electrophysiology · doi:10.1111/j.1540-8167.2010.01908.x · Cited by 135
Clinical effects of COX?2 inhibitors on cognition in schizophrenia
M�ller, N., Riedel, M. J., Schwarz, M., & Engel, R. R. (2004) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-004-0548-4 · Cited by 135
Cho, Y. H., Friedman, E., & Silva, A. J. (1998) · Behavioural Brain Research · doi:10.1016/s0166-4328(98)00054-0 · Cited by 140
Protein kinases: which one is the memory molecule?
Micheau, J. (1999) · Cellular and Molecular Life Sciences · doi:10.1007/s000180050312 · Cited by 136
Hrabětová, S., Serrano, P. A., Blace, N., Tse, H., Skifter, D. A., Jane, D. E., Monaghan, D. T., & Sacktor, T. C. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-12-j0002.2000 · Cited by 134
Long‐term plasticity in the hippocampus: maintaining within and ‘tagging’ between synapses
Bin Ibrahim, M. Z., Benoy, A., & Sajikumar, S. (2022) · The FEBS Journal · doi:10.1111/febs.16065 · Cited by 137
Siciliano, J. C., Toutant, M., Derkinderen, P., Sasaki, T., & Girault, J. (1996) · Journal of Biological Chemistry · doi:10.1074/jbc.271.46.28942 · Cited by 131
Bidirectional Changes in Spatial Dendritic Integration Accompanying Long-Term Synaptic Modifications
Wang, Z., Xu, N.-L., Wu, C.-P., Duan, S., & Poo, M. (2003) · Neuron · doi:10.1016/s0896-6273(02)01189-3 · Cited by 131
The application of transcranial magnetic stimulation in psychiatry and neurosciences research
Fitzgerald, P. B., Brown, T. L., & Daskalakis, Z. J. (2002) · Acta Psychiatrica Scandinavica · doi:10.1034/j.1600-0447.2002.1r179.x · Cited by 128
Role of Ca2+‐stimulated adenylyl cyclases in LTP and memory formation
Poser, S., & Storm, D. R. (2001) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(00)00094-0 · Cited by 128
Velasco, M., Velasco, F., & Velasco, A. L. (2001) · Journal of Clinical Neurophysiology · doi:10.1097/00004691-200111000-00001 · Cited by 127
β-Amyloid-induced Dynamin 1 Depletion in Hippocampal Neurons
Kelly, B. L., Vassar, R. J., & Ferreira, A. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m503259200 · Cited by 129
Potential role of calcineurin for brain ischemia and traumatic injury
Morioka, M., Hamada, J., Ushio, Y., & Miyamoto, E. (1999) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00073-2 · Cited by 127
Broeder, S., Nackaerts, E., Heremans, E., Vervoort, G., Meesen, R., Verheyden, G., & Nieuwboer, A. (2015) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2015.08.010 · Cited by 133
Ouimet, C. C., Silva, E. F. D. C. E., & Greengard, P. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.8.3396 · Cited by 125
Steinman, M. Q., Gao, V., & Alberini, C. M. (2016) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2016.00010 · Cited by 128
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Rousseaux, C. G., & Greene, S. F. (2015) · Journal of Receptors and Signal Transduction · doi:10.3109/10799893.2015.1015737 · Cited by 123
Klann, E., & Thiels, E. (1999) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/s0278-5846(99)00002-0 · Cited by 120
Zhuang, P., Toro, C., Grafman, J. H., Manganotti, P., Leocani, L., & Hallett, M. (1997) · Electroencephalography and Clinical Neurophysiology · doi:10.1016/s0013-4694(96)96030-7 · Cited by 121
Rutten, K., Misner, D., Works, M. G., Blokland, A., Novak, T. J., Santarelli, L., & Wallace, T. L. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06349.x · Cited by 114
When Are Class I Metabotropic Glutamate Receptors Necessary for Long-Term Potentiation?
Wilsch, V. W., Behnisch, T., Jäger, T., Reymann, K. G., & Balschun, D. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-16-06071.1998 · Cited by 117
Parent, A., Linden, D. J., Sisodia, S. S., & Borchelt, D. (1999) · Neurobiology of Disease · doi:10.1006/nbdi.1998.0207 · Cited by 116
Li, H., Weiss, S. R. B., Chuang, D., Post, R. M., & Rogawski, M. A. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-05-01662.1998 · Cited by 114
Postsynaptic Mechanisms for Bidirectional Control of MAP2 Phosphorylation by Glutamate Receptors
Quinlan, E. M., & Halpain, S. (1996) · Neuron · doi:10.1016/s0896-6273(00)80053-7 · Cited by 135
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Weitzdoerfer, R., Hoeger, H., Engidawork, E., Engelmann, M., Singewald, N., Lübec, G., & Lubec, B. (2004) · Nitric Oxide · doi:10.1016/j.niox.2004.03.007 · Cited by 114
Hyde, L. W., Gard, A. M., Tomlinson, R. C., Burt, S. A., Mitchell, C. M., & Monk, C. S. (2020) · American Psychologist · doi:10.1037/amp0000741 · Cited by 128
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Velasco, M., Velasco, F., Velasco, A. L., Jiménez, F., Brito, F., & Márquez, I. (2000) · Archives of Medical Research · doi:10.1016/s0188-4409(00)00085-0 · Cited by 113
Siddik, A., Haldar, P. K., Paul, T., Das, U., Barman, A. R., Roy, A., & Sarkar, P. K. (2021) · Nanoscale · doi:10.1039/d0nr08214g · Cited by 114
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Li, H., Chen, A., Xing, G., Wei, M.-L., & Rogawski, M. A. (2001) · Nature Neuroscience · doi:10.1038/88432 · Cited by 111
Zajaczkowski, W., Frankiewicz, T., Parsons, C. G., & Danysz, W. (1997) · Neuropharmacology · doi:10.1016/s0028-3908(97)00070-1 · Cited by 112
Rac1 Induces the Clustering of AMPA Receptors during Spinogenesis
Wiens, K. M., Lin, H., & Liao, D. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.1947-05.2005 · Cited by 111
Kumar‐Singh, S., Dewachter, I., Moechars, D., Lübke, U., Jonghe, C. D., Ceuterick, C., Checler, F., Naidu, A., Cordell, B., Cras, P. P., et al. (2000) · Neurobiology of Disease · doi:10.1006/nbdi.1999.0272 · Cited by 106
Focal photolysis of caged glutamate produces long-term depression of hippocampal glutamate receptors
Kandler, K., Katz, L. C., & Kauer, J. A. (1998) · Nature Neuroscience · doi:10.1038/368 · Cited by 111
Chabot, C., Massicotte, G., Milot, M., Trudeau, F., & Gagné, J. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00648-3 · Cited by 108
Page, L. R., & Parries, S. C. (2000) · The Journal of Comparative Neurology · doi:10.1002/(sici)1096-9861(20000320)418:4 · Cited by 84
Protein phosphorylation in neuronal plasticity and gene expression
Schulman, H. (1995) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(95)80051-4 · Cited by 105
MacMillan, L. B., Bass, M. A., Cheng, N., Howard, E. F., Tamura, M., Strack, S., Wadzinski, B. E., & Colbran, R. J. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.50.35845 · Cited by 105
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Lewicki, M. S. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-18-05854.1996 · Cited by 104
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Herry, C., Vouimba, R., & Garcia, R. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.82.5.2827 · Cited by 104
An alternative to the LTP orthodoxy: a plasticity-pathology continuum model
McEachern, J. C., & Shaw, C. (1996) · Brain Research Reviews · doi:10.1016/0165-0173(96)00006-9 · Cited by 106
Applications of TMS to Therapy in Psychiatry
Lisanby, S. H., Kinnunen, L. H., & Crupain, M. J. (2002) · Journal of Clinical Neurophysiology · doi:10.1097/00004691-200208000-00007 · Cited by 102
Sandler, V. M., & Barbara, J. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-11-04325.1999 · Cited by 102
Kunkler, P. E., & Kraig, R. P. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-09-03416.1998 · Cited by 98
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
The role of glial cells in synaptic function
Bacci, A., Verderio, C., Pravettoni, E., & Matteoli, M. (1999) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.1999.0393 · Cited by 101
Kawaguchi, S., & Hirano, T. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-10-03969.2002 · Cited by 99
Multiple behavioral anomalies in GluR2 mutant mice exhibiting enhanced LTP
Gerlai, R. T., Henderson, J. T., Roder, J., & Jia, Z. (1998) · Behavioural Brain Research · doi:10.1016/s0166-4328(98)00002-3 · Cited by 100
Exercising our brains: how physical activity impacts synaptic plasticity in the dentate gyrus.
Christie, B. R., Eadie, B. D., Kannangara, T. S., Robillard, J. M., Shin, J., & Titterness, A. K. (2008) · NeuroMolecular Medicine · doi:10.1007/s12017-008-8033-2 · Cited by 99
Baldwin, A. E., Sadeghian, K., Holahan, M. R., & Kelley, A. E. (2002) · Neurobiology of Learning and Memory · doi:10.1006/nlme.2000.4002 · Cited by 99
Long-Term Potentiation Is Increased in the CA1 Area of the Hippocampus of APPswe/ind CRND8 Mice
Jolas, T. (2002) · Neurobiology of Disease · doi:10.1006/nbdi.2002.0557 · Cited by 100
Cao, Z., Yang, X., Zhang, H., Wang, H., Huang, W., Xu, F., Zhuang, C., Wang, X., & Li, Y. (2016) · Chemosphere · doi:10.1016/j.chemosphere.2016.02.092 · Cited by 98
Dynamic Synapses in the Cortex
Zador, A. M., & Dobrunz, L. E. (1997) · Neuron · doi:10.1016/s0896-6273(00)80341-4 · Cited by 97
Murai, K., Misner, D., & Ranscht, B. (2002) · Current Biology · doi:10.1016/s0960-9822(02)00680-2 · Cited by 98
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Lu, Y., Sun, X.-D., Hou, F., Bi, L., Yin, D., Liu, F., Chen, Y., Bean, J. C., Jiao, H.-F., Liu, X., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.09.029 · Cited by 98
Complexity of calcium signaling in synaptic spines
Franks, K. M., & B, T. J. S. A. (2002) · BioEssays · doi:10.1002/bies.10193 · Cited by 98
Sancheti, H., Akopian, G. K., Yin, F., Brinton, R. D., Walsh, J. P., & Cadenas, E. (2013) · PLoS ONE · doi:10.1371/journal.pone.0069830 · Cited by 98
Guan, P.-P., Cao, L., & Wang, P. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22115900 · Cited by 99
Aging modulates nitric oxide synthesis and cGMP levels in hippocampus and cerebellum
Chalimoniuk, M., & Strosznajder, J. B. (1998) · Molecular and Chemical Neuropathology · doi:10.1007/bf02815117 · Cited by 94
Nitric Oxide Synthase Inhibitors as Antidepressants
Wegener, G., & Volke, V. (2010) · Pharmaceuticals · doi:10.3390/ph3010273 · Cited by 94
Gozariu, M., Bragard, D., Willer, J. C., & Bars, D. L. (1997) · Journal of Neurophysiology · doi:10.1152/jn.1997.78.6.3165 · Cited by 94
Intact spatial learning and memory in transgenic mice with reduced BDNF
Montkowski, A., & Holsboer, F. (1997) · Neuroreport · doi:10.1097/00001756-199702100-00040 · Cited by 93
Aou, S., Li, X.-L., Li, A.-J., Oomura, Y., Shiraishi, T., Sasaki, K., Imamura, T., & Wayner, M. J. (2003) · Neuroscience · doi:10.1016/s0306-4522(02)00745-5 · Cited by 91
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
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Fukunaga, K., Müller, D., Ohmitsu, M., Bakó, É., DePaoli-Roach, A. A., & Miyamoto, E. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.740807.x · Cited by 90
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Silva, A. J., Giese, K.-P., Fedorov, N. B., Frankland, P. W., & Kogan, J. H. (1998) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1998.3837 · Cited by 92
Wang, D., Noda, Y., Tsunekawa, H., Zhou, Y., Miyazaki, M., Senzaki, K., & Nabeshima, T. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.01.003 · Cited by 89
The involvement of astrocytes in early‐life adversity induced programming of the brain
Abbink, M. R., van Deijk, A. F., Heine, V. M., Verheijen, M. H. G., & Kőrösi, A. (2019) · Glia · doi:10.1002/glia.23625 · Cited by 95
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Centonze, D., Gubellini, P., Bernardi, G., & Calabresi, P. (1999) · Brain Research Reviews · doi:10.1016/s0165-0173(99)00018-1 · Cited by 89
Ismail, M., Abbas, H., Choi, C., & Kim, S. (2020) · Applied Surface Science · doi:10.1016/j.apsusc.2020.147107 · Cited by 89
Cellular and synaptic reorganization of arcuate NPY/AgRP and POMC neurons after exercise
He, Z., Gao, Y., Alhadeff, A. L., Castorena, C. M., Huang, Y., Lieu, L., Afrin, S., Sun, J. M., Betley, J. N., Guo, H., et al. (2018) · Molecular Metabolism · doi:10.1016/j.molmet.2018.08.011 · Cited by 84
Post, R. M., Denicoff, K. D., Frye, M. A., Dunn, R. T., Leverich, G. S., Osuch, E. A., & Speer, A. (1998) · Neuropsychobiology · doi:10.1159/000026532 · Cited by 87
RIC, a calmodulin‐binding Ras‐like GTPase.
Wes, P. D., Yu, M. C., & Montell, C. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00971.x · Cited by 86
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Tan, H. L., Chiu, S., Zhu, Q., & Huganir, R. L. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2014827117 · Cited by 83
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Cossenza, M., Socodato, R., Portugal, C. C., Domith, I., Gladulich, L., da Encarnação, T. G., Calaza, K. D. C., Mendonça, H. R., Campello‐Costa, P., & Paes‐de‐Carvalho, R. (2014) · Vitamins and hormones · doi:10.1016/b978-0-12-800254-4.00005-2 · Cited by 87
Hardt, O. M., Nader, K., & Wang, Y.-T. (2013) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0141 · Cited by 89
Komai, S., Matsuyama, T., Matsumoto, K., Kato, K., Kobayashi, M., Imamura, K., Yoshida, S., Ugawa, S., & Shiosaka, S. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00035.x · Cited by 84
Nitric oxide synthases: catalytic function and progress towards selective inhibition
Mayer, B., & Andrew, P. (1998) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/pl00005233 · Cited by 84
Jun, K., Choi, G., Yang, S., Choi, K. Y., Kim, H., Chan, G. C. ‐., Storm, D. R., Albert, C., Mayr, G. W., Lee, C.-J., et al. (1998) · Learning & Memory · doi:10.1101/lm.5.4.317 · 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
Isoflurane Reduces N-Methyl-D-Aspartate Toxicity In Vivo in the Rat Cerebral Cortex
Harada, H., Kelly, P. J., Cole, D. J., Drummond, J. C., & Patel, P. M. (1999) · Anesthesia & Analgesia · doi:10.1097/00000539-199912000-00022 · Cited by 82
Moriguchi, S., Yabuki, Y., & Fukunaga, K. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07608.x · Cited by 78
Manschot, S., Biessels, G. J., Cameron, N. E., Cotter, M. A., Kamal, A., Kappelle, L. J., & Gispen, W. H. (2003) · Brain Research · doi:10.1016/s0006-8993(02)04211-7 · Cited by 80
Is the mTOR‐signalling cascade disrupted in Schizophrenia?
Gururajan, A., & van den Buuse, M. (2013) · Journal of Neurochemistry · doi:10.1111/jnc.12622 · Cited by 81
Takadera, T., Matsuda, I., & Ohyashiki, T. (1999) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1999.0730548.x · Cited by 81
Metadata
- Authors
- Malenka, R. C.
- Affiliations
- University of California, San Francisco (US)
- Corresponding author
- Malenka, Robert C.
- ORCID
- Malenka, Robert C.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 1994-08
- Volume
- 78
- Issue
- 4
- Pages
- 535-538
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2070094949
- Cited by
- 655
- References
- 26
- Citations by year
- 2026: 8 · 2025: 5 · 2024: 13 · 2023: 15 · 2022: 15 · 2021: 14 · 2020: 22 · 2019: 19 · 2018: 19 · 2017: 13 · 2016: 18 · 2015: 19 · 2014: 18 · 2013: 17 · 2012: 15
- FWCI
- 3.35
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- long-term potentiation, long-term depression, synaptic plasticity, hippocampus, NMDA receptor, calcium buffering, calcium-dependent protein kinase, CaMKII, CaMKI, CaMKIV
- MeSH terms
- Animals, Hippocampus, Humans, Memory, Models, Neurological, Neuronal Plasticity, Signal Transduction, Long-Term Potentiation
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