The DOI matches its Crossref record; 169 of the 169 references it cites were found in a registry or an index.
A synaptic model of memory: long-term potentiation in the hippocampus
Abstract
Long-term potentiation of synaptic transmission in the hippocampus is the primary experimental model for investigating the synaptic basis of learning and memory in vertebrates. The best understood form of long-term potentiation is induced by the activation of the N-methyl-D-aspartate receptor complex. This subtype of glutamate receptor endows long-term potentiation with Hebbian characteristics, and allows electrical events at the postsynaptic membrane to be transduced into chemical signals which, in turn, are thought to activate both pre- and postsynaptic mechanisms to generate a persistent increase in synaptic strength.
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In the citing paper
“Long-term potentiation (LTP) is a widely used paradigm for increasing synaptic efficacy, and its induction requires, in at least one of its forms, the activation of NMDARs (Bliss and Lømo, 1973; Bliss and Collingridge, 1993).”
From The essential role of hippocampal CA1 NMDA receptor-dependent synaptic plasticity in spatial memory. (1996) · cites this paper as Bliss and Collingridge, 1993
In the citing paper
“SW-Rs may conversely promote LTP and spike timedependent plasticity in hippocampal circuits (97,159,241,640,777).”
From About Sleep's Role in Memory (2013) · cites this paper as [97]
In the citing paper
“Spine enlargement and LTP require stronger stimulation compared with those for spine shrinkage and LTD.”
From State-dependent diffusion of actin-depolymerizing factor/cofilin underlies the enlargement and shrinkage of dendritic spines (2016) · cites this paper as [23]
In the citing paper
“For example, perforant path and the Schaffer collateral pathway LTP are both dependent on the activation of NMDA receptors (Bliss and Collingridge, 1993), whereas mossy fiber/CA3 LTP is not (Harris and Cotman, 1986;Z alutsky and Nicoll, 1990).”
From Type I Adenylyl Cyclase Mutant Mice Have Impaired Mossy Fiber Long-Term Potentiation (1998) · cites this paper as Bliss and Collingridge, 1993
In the citing paper
“Synapses are elements of the neural network that play a critical role in processing information in the brain, being involved in learning, long-term and short-term memory storage and deletion, and temporal information processing”
From Human Brain/Cloud Interface (2019) · cites this paper as Bliss and Collingridge, 1993
In the citing paper
“They play a crucial role in brain information processing (IBM, 2008) and are involved in learning and memory (Black et al., 1990; Bliss and Collingridge, 1993; Holtmaat and Svoboda, 2009; Liu et al., 2012), long-term and short-term memory storage and deletion (Kandel, 2001; Lee et al., 2008), and temporal information processing (Fuhrmann et al., 2002).”
From Human Brain/Cloud Interface (2019) · cites this paper as Bliss and Collingridge, 1993
In the citing paper
“a widely accepted cellular model for learning and memory (Bliss and Collingridge, 1993)”
From Wild-Type, but Not Mutant N296H, Human Tau Restores Aβ-Mediated Inhibition of LTP in Tau−/− mice (2017) · cites this paper as Bliss and Collingridge, 1993
Citations
Cites
Bliss, T. V. P., & Gardner-Medwin, A. R. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010274 · Cited by 7,424
Self-citationGarthwaite, J., Charles, S. L., & Chess‐Williams, R. (1988) · Nature · doi:10.1038/336385a0 · Cited by 2,540
Collingridge, G. L., Kehl, S. J., & McLennan, H. (1983) · The Journal of Physiology · doi:10.1113/jphysiol.1983.sp014478 · Cited by 2,413
Self-citationNitric oxide, a novel neuronal messenger
Bredt, D. S., & Snyder, S. H. (1992) · Neuron · doi:10.1016/0896-6273(92)90104-l · Cited by 1,852
MacDermott, A. B., Mayer, M. L., Westbrook, G. L., Smith, S. J., & Barker, J. L. (1986) · Nature · doi:10.1038/321519a0 · Cited by 1,835
RNA editing in brain controls a determinant of ion flow in glutamate-gated channels
Sommer, B., Köhler, M., Sprengel, R., & Seeburg, P. H. (1991) · Cell · doi:10.1016/0092-8674(91)90568-j · Cited by 1,517
Deficient Hippocampal Long-Term Potentiation in α-Calcium-Calmodulin Kinase II Mutant Mice
Silva, A. J., Stevens, C. F., Tonegawa, S., & Wang, Y. (1992) · Science · doi:10.1126/science.1378648 · Cited by 1,472
Inhibition of Postsynaptic PKC or CaMKII Blocks Induction But Not Expression of LTP
Malinow, R., Schulman, H., & Tsien, R. W. (1989) · Science · doi:10.1126/science.2549638 · Cited by 1,325
Flip and Flop: A Cell-Specific Functional Switch in Glutamate-Operated Channels of the CNS
Sommer, B., KEINÄNEN, K. P., Verdoorn, T. A., Wisden, W., Burnashev, N., Herb, A., Köhler, M. G., Takagi, T., Sakmann, B. J., & Seeburg, P. H. (1990) · Science · doi:10.1126/science.1699275 · Cited by 1,272
The Neurobiology of Learning and Memory
Thompson, R. F. (1986) · Science · doi:10.1126/science.3738519 · Cited by 1,164
Research works printed but not linked: 6
- Hebb, D. O. The Organization of Behaviour (Wiley, New York, 1949).
- Konorski, J. Conditioned Reflexes and Neuron Organisation (Cambridge Univ. Press, Cambridge, 1948).
- Bliss, T. V. P. & Lømo, T. J. Physiol., Lond. 232, 331–356 (1973). · DOI · Paper page
- Collingridge, G. L. et al. Int. Acad. Biomed. Drug Res. 2, 41–49 (1991).
- Voronin, L. L., Kuhnt, U. & Gusev, A. G. Expl Brain Res. 89, 288–299 (1992).
- Fazeli, M. S., Corbet, J., Dunn, M, J., Dolphin, A. C. & Bliss, T. V. P. J. Neurosci. 13(4) (in the press).
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Peterchev, A. V., Rosa, M. A., Deng, Z.-D., Prudic, J., & Lisanby, S. H. (2010) · The Journal of ECT · doi:10.1097/yct.0b013e3181e48165 · Cited by 213
Reconsolidation and the dynamic nature of memory
Nader, K. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a021782 · Cited by 221
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Sacktor, T. C. (2008) · Progress in Brain Research · doi:10.1016/s0079-6123(07)00002-7 · Cited by 208
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QIU, S., KORWEK, K., PRATTDAVIS, A., PETERS, M., BERGMAN, M., & WEEBER, E. (2006) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2005.11.001 · Cited by 202
Tong, L., Thornton, P. L., Balazs, R., & Cotman, C. W. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m010450200 · Cited by 206
Is high extracellular glutamate the key to excitotoxicity in traumatic brain injury?
Obrenovitch, T. P., & Urenjak, J. (1997) · Journal of Neurotrauma · doi:10.1089/neu.1997.14.677 · Cited by 205
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Mody, M., Cao, Y., Cui, Z., Tay, K.-Y., Shyong, A., Shimizu, E., Pham, K., Schultz, P., Welsh, D., & Tsien, J. Z. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.141244998 · Cited by 205
Scharf, M. T., Woo, N. H., Lattal, K. M., Young, J. Z., Nguyen, P. V., & Abel, T. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.87.6.2770 · Cited by 204
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Huerta, P. T., & Volpe, B. T. (2009) · Journal of NeuroEngineering and Rehabilitation · doi:10.1186/1743-0003-6-7 · Cited by 204
Deidda, G., Bozarth, I. F., & Cancedda, L. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00119 · Cited by 192
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HARVEY, J., SOLOVYOVA, N., & IRVING, A. (2006) · Progress in Lipid Research · doi:10.1016/j.plipres.2006.03.001 · Cited by 202
Stewart, M. G., Davies, H. A., Sandi, C., Kraev, I. V., Rogachevsky, V. V., Peddie, C. J., Rodriguez, J. J., Cordero, M. I., Donohue, H. S., Gabbott, P. L. A., et al. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2004.10.031 · Cited by 197
Miller, P., Zhabotinsky, A. M., Lisman, J. E., & Wang, X.-J. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030107 · Cited by 199
Chapter 6 Regulation of hippocampus-dependent memory by cyclic AMP-dependent protein kinase
Abel, T., & Nguyen, P. V. (2008) · Progress in Brain Research · doi:10.1016/s0079-6123(07)00006-4 · Cited by 198
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Nishiyama, J., & Yasuda, R. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.043 · Cited by 199
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Finnie, P. S. B., & Nader, K. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2012.03.008 · Cited by 189
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Krugers, H. J., Hoogenraad, C. C., & Groc, L. (2010) · Nature Reviews Neuroscience · doi:10.1038/nrn2913 · Cited by 197
α‐Synuclein produces a long‐lasting increase in neurotransmitter release
Liu, S., Ninan, I., Antonova, I., Battaglia, F., Trinchese, F., Narasanna, A., Kolodilov, N., Dauer, W., Hawkins, R. D., & Arancio, O. (2004) · The EMBO Journal · doi:10.1038/sj.emboj.7600451 · Cited by 198
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Yang, H., & Chen, C. (2008) · Current Pharmaceutical Design · doi:10.2174/138161208784480144 · Cited by 195
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Wu, D., Bacaj, T., Morishita, W., Goswami, D., Arendt, K. L., Xu, W., Chen, L., Malenka, R. C., & Südhof, T. C. (2017) · Nature · doi:10.1038/nature21720 · Cited by 195
The absence of a major Ca 2+ signaling pathway in GABAergic neurons of the hippocampus
Sík, A., Hájos, N., Gulácsi, A., Mody, I., & Freund, T. F. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.6.3245 · Cited by 186
Duchon, A., & Herault, Y. (2016) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2016.00104 · Cited by 181
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Conner, J. M., Franks, K. M., Titterness, A. K., Russell, K., Merrill, D. A., Christie, B. R., Sejnowski, T. J., & Tuszynski, M. H. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.2594-09.2009 · Cited by 189
Citron binds to PSD-95 at glutamatergic synapses on inhibitory neurons in the hippocampus
Zhang, W., Vazquez, L., Apperson, M., & Kennedy, M. B. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-01-00096.1999 · Cited by 190
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Cho, Y. H., Giese, K. P., Tanila, H., Silva, A. J., & Eichenbaum, H. (1998) · Science · doi:10.1126/science.279.5352.867 · Cited by 189
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Villacres, E. C., Wong, S. T., Chavkin, C., & Storm, D. R. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-09-03186.1998 · Cited by 187
“AC1 mutant mice exhibit normal perforant pathway LTP The perforant pathway, from the pyramidal cells in the entorhinal area to the granule cells of the dentate gyrus, exhibits NMDAdependent LTP (Bliss and Collingridge, 1993).”
BackgroundMaccaferri, G., & McBain, C. J. (1995) · Neuron · doi:10.1016/0896-6273(95)90071-3 · Cited by 182
Bozdagi, O., Nagy, V., Kwei, K. T., & Huntley, G. W. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00202.2007 · Cited by 182
Suri, S., Heise, V., Trachtenberg, A. J., & Mackay, C. E. (2013) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2013.10.010 · Cited by 183
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Kapczinski, F., Frey, B. N., Kauer-Sant’Anna, M., & Grassi-Oliveira, R. (2008) · Expert Review of Neurotherapeutics · doi:10.1586/14737175.8.7.1101 · Cited by 181
A large pool of releasable vesicles in a cortical glutamatergic synapse
Hallermann, S., Pawlu, C., Jonas, P., & Heckmann, M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1432836100 · Cited by 181
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Tarpey, P., Parnau, J., Blow, M., Woffendin, H., Bignell, G., Cox, C., Cox, J., Davies, H., Edkins, S., Holden, S., et al. (2004) · The American Journal of Human Genetics · doi:10.1086/422703 · Cited by 176
Swanson-Park, J. L., Coussens, C. M., Mason-Parker, S. E., Raymond, C. R., Hargreaves, E. L., Dragunow, M., Cohen, A. S., & Abraham, W. C. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00010-x · Cited by 175
Moult, P. R., Gladding, C. M., Sanderson, T. M., Fitzjohn, S. M., Bashir, Z. I., Molnar, E., & Collingridge, G. L. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.4322-05.2006 · Cited by 172
Self-citationAkashi, K., Kakizaki, T., Kamiya, H., Fukaya, M., Yamasaki, M., Abe, M., Natsume, R., Watanabe, M., & Sakimura, K. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5531-08.2009 · Cited by 163
Wyszynski, M., Kharazia, V., Shanghvi, R., Rao, A., Beggs, A. H., Craig, A. M., Weinberg, R., & Sheng, M. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-04-01383.1998 · Cited by 168
Selective activation of microglia facilitates synaptic strength
Clark, A. K., Gruber-Schoffnegger, D., Drdla-Schutting, R., Gerhold, K. J., Malcangio, M., & Sandkühler, J. (2015) · The Journal of Neuroscience · doi:10.1523/jneurosci.2061-14.2015 · Cited by 171
PTP and LTP at a hippocampal mossy fiber-interneuron synapse
Alle, H., Jonas, P., & Geiger, J. R. P. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.251610898 · Cited by 158
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Richards, D. A., Mateos, J. M., Hugel, S., de Paola, V., Caroni, P., Gähwiler, B. H., & McKinney, R. A. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501881102 · Cited by 161
Lu, J.-T., Li, C.-Y., Zhao, J.-P., Poo, M.-M., & Zhang, X.-H. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.2513-07.2007 · Cited by 163
Lamsa, K., Heeroma, J. H., & Kullmann, D. M. (2005) · Nature Neuroscience · doi:10.1038/nn1486 · Cited by 158
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Hermann, D. M., & Zechariah, A. (2009) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2009.100 · Cited by 162
Sleep recalibrates homeostatic and associative synaptic plasticity in the human cortex
Kuhn, M., Wolf, E., Maier, J. G., Mainberger, F., Feige, B., Schmid, H., Bürklin, J., Maywald, S., Mall, V., Jung, N. H., et al. (2016) · Nature Communications · doi:10.1038/ncomms12455 · Cited by 152
Jorgenson, L. A., Sun, M., O'Connor, M., & Georgieff, M. K. (2005) · Hippocampus · doi:10.1002/hipo.20128 · Cited by 162
Leptin: a potential cognitive enhancer?
Harvey, J., Shanley, L. J., O'Malley, D., & Irving, A. J. (2005) · Biochemical Society Transactions · doi:10.1042/bst0331029 · Cited by 162
Huntley, G., Vickers, J., Janssen, W., Brose, N., Heinemann, S., & Morrison, J. (1994) · The Journal of Neuroscience · doi:10.1523/jneurosci.14-06-03603.1994 · Cited by 161
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
Neurogranin enhances synaptic strength through its interaction with calmodulin
Zhong, L., Cherry, T., Bies, C. E., Florence, M. A., & Gerges, N. Z. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.236 · Cited by 158
Huang, C. S., Shi, S.-H., Ule, J., Ruggiu, M., Barker, L. A., Darnell, R. B., Jan, Y. N., & Jan, L. Y. (2005) · Cell · doi:10.1016/j.cell.2005.07.033 · Cited by 157
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Rosenblum, K., Futter, M., Voss, K., Erent, M., Skehel, P. A., French, P., Obosi, L., Jones, M. W., & Bliss, T. V. P. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-13-05432.2002 · Cited by 155
Self-citationLong-Term Depression in Hippocampal Interneurons: Joint Requirement for Pre- and Postsynaptic Events
Laezza, F., Doherty, J. J., & Dingledine, R. (1999) · Science · doi:10.1126/science.285.5432.1411 · Cited by 157
Wibrand, K., Messaoudi, E., Håvik, B., Steenslid, V., Løvlie, R., Steen, V. M., & Bramham, C. R. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.04687.x · Cited by 153
Kandola, A., Hendrikse, J., Lucassen, P. J., & Yücel, M. (2016) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2016.00373 · Cited by 155
“LTP is one model of synaptic plasticity that refers to the strengthening of synaptic connections between neurons (Bliss and Collingridge, 1993).”
Seidenbecher, T., Reymann, K. G., & Balschun, D. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.4.1494 · Cited by 154
Bodhinathan, K., Kumar, A., & Foster, T. C. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5485-09.2010 · Cited by 153
“Introduction The NMDA receptor (NMDAR) is a major source of Ca 2 influx into the postsynaptic neuron during the induction of LTP at hippocampal CA3–CA1 synapses (Bliss and Collingridge, 1993).”
BackgroundCui, M., Yang, Y., Yang, J., Zhang, J., Han, H., Ma, W., Li, H., Mao, R., Xu, L., Hao, W., et al. (2006) · Neuroscience Letters · doi:10.1016/j.neulet.2006.05.048 · Cited by 153
Molecular Mechanisms of Early and Late LTP
Baltaci, S. B., Mogulkoc, R., & Baltaci, A. K. (2019) · Neurochemical Research · doi:10.1007/s11064-018-2695-4 · Cited by 152
Sharma, M. K., Jalewa, J., & Hölscher, C. (2014) · Journal of Neurochemistry · doi:10.1111/jnc.12469 · Cited by 151
Denis, I., Potier, B., Vancassel, S., Heberden, C., & Lavialle, M. (2013) · Ageing Research Reviews · doi:10.1016/j.arr.2013.01.007 · Cited by 150
DCC expression by neurons regulates synaptic plasticity in the adult brain
Horn, K. E., Glasgow, S. D., Gobert, D., Bull, S.-J., Luk, T., Girgis, J., Tremblay, M.-E., McEachern, D., Bouchard, J.-F., Haber, M., et al. (2013) · Cell Reports · doi:10.1016/j.celrep.2012.12.005 · Cited by 147
Manahan‐Vaughan, D., von Haebler, D., Winter, C., Juckel, G., & Heinemann, U. (2008) · Hippocampus · doi:10.1002/hipo.20367 · Cited by 149
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Humeau, Y., Herry, C., Kemp, N., Shaban, H., Fourcaudot, E., Bissière, S., & Lüthi, A. (2005) · Neuron · doi:10.1016/j.neuron.2004.12.019 · Cited by 148
Yamagata, Y., Kobayashi, S., Umeda, T., Inoue, A., Sakagami, H., Fukaya, M., Watanabe, M., Hatanaka, N., Totsuka, M., Yagi, T., et al. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0707-09.2009 · Cited by 146
Dalton, G. L., Wu, D. C., Wang, Y. T., Floresco, S. B., & Phillips, A. G. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.09.001 · Cited by 144
Mechanisms Underlying the Rules for Associative Plasticity at Adult Human Neocortical Synapses
Verhoog, M. B., Goriounova, N. A., Obermayer, J., Stroeder, J., Hjorth, J. J. J., Testa-Silva, G., Baayen, J. C., de Kock, C. P. J., Meredith, R. M., & Mansvelder, H. D. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.3158-13.2013 · Cited by 127
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Farovik, A., Dupont, L. M., & Eichenbaum, H. (2010) · Learning & Memory · doi:10.1101/lm.1616209 · Cited by 140
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Lanté, F., Meunier, J., Guiramand, J., Maurice, T., Cavalier, M., de Jesus Ferreira, M.-C., Aimar, R., Cohen-Solal, C., Vignes, M., & Barbanel, G. (2007) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2007.01.027 · Cited by 140
Frey, S., & Frey, J. U. (2008) · Progress in brain research · doi:10.1016/s0079-6123(07)00007-6 · Cited by 139
A biopolymer transistor: Electrical amplification by microtubules
Priel, A., Ramos, A. J., Tuszynski, J. A., & Cantiello, H. F. (2006) · Biophysical Journal · doi:10.1529/biophysj.105.078915 · Cited by 138
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Maccaferri, G., & McBain, C. J. (1996) · The Journal of Neuroscience · doi:10.1523/jneurosci.16-17-05334.1996 · Cited by 133
Nitric oxide S -nitrosylates serine racemase, mediating feedback inhibition of d -serine formation
Mustafa, A. K., Kumar, M., Selvakumar, B., Ho, G. P. H., Ehmsen, J. T., Barrow, R. K., Amzel, L. M., & Snyder, S. H. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611620104 · Cited by 136
Comparison of computational models of familiarity discrimination in the perirhinal cortex
Bogacz, R., & Brown, M. W. (2003) · Hippocampus · doi:10.1002/hipo.10093 · Cited by 134
Dysfunctional neural plasticity in patients with schizophrenia
Daskalakis, Z. J., Christensen, B. K., Fitzgerald, P. B., & Chen, R. (2008) · Archives of General Psychiatry · doi:10.1001/archpsyc.65.4.378 · Cited by 130
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Malinow, R. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.09.001 · Cited by 132
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Choi, Y.-B., Chen, H.-S. V., & Lipton, S. A. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-02-00392.2001 · Cited by 132
Hebbian spike-driven synaptic plasticity for learning patterns of mean firing rates
Fusi, S. (2002) · Biological Cybernetics · doi:10.1007/s00422-002-0356-8 · Cited by 131
MicroRNA Expression and Regulation in Human, Chimpanzee, and Macaque Brains
Hu, H. Y., Guo, S., Xi, J., Yan, Z., Fu, N., Zhang, X., Menzel, C., Liang, H., Yang, H., Zhao, M., et al. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002327 · Cited by 130
Coogan, A. N., O'Neill, L. A. J., & O'Connor, J. J. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00100-1 · Cited by 129
The N-methyl-d-aspartate receptor, synaptic plasticity, and depressive disorder
Petrie, R. X. A., Reid, I. C., & Stewart, C. A. (2000) · Pharmacology & Therapeutics · doi:10.1016/s0163-7258(00)00063-2 · Cited by 129
Shiroma, P. R., Albott, C. S., Johns, B., Thuras, P., Wels, J., & Lim, K. O. (2014) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145714001011 · Cited by 126
Yang, J., Hou, C., Ma, N., Liu, J., Zhang, Y., Zhou, J., Xu, L., & Li, L. (2007) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2006.09.001 · Cited by 127
Alkondon, M., Pereira, E. F. R., Barbosa, C. T. F., & Albuquerque, E. X. (1997) · The Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)37139-3 · Cited by 127
Huang, C.-C., Liang, Y.-C., & Hsu, K.-S. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-22-09728.1999 · Cited by 127
Is Persistent Activity of Calcium/Calmodulin-Dependent Kinase Required for the Maintenance of LTP?
Chen, H.-X., Otmakhov, N., Strack, S., Colbran, R. J., & Lisman, J. E. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.4.1368 · Cited by 126
Milnerwood, A. J., & Raymond, L. A. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.142448 · Cited by 126
Lien, C., Martina, M., Schultz, J. H., Ehmke, H., & Jonas, P. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2001.013066 · Cited by 124
Wang, H., Pineda, V. V., Chan, G. C. K., Wong, S. T., Muglia, L. J., & Storm, D. R. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-30-09710.2003 · Cited by 120
Hanson, J. E., La, H., Plise, E., Chen, Y.-H., Ding, X., Hanania, T., Sabath, E. V., Alexandrov, V., Brunner, D., Leahy, E., et al. (2013) · PLoS ONE · doi:10.1371/journal.pone.0069964 · Cited by 121
Yaka, R., Salomon, S., Matzner, H., & Weinstock, M. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.01.018 · Cited by 120
The role of the basal ganglia in category learning
Ashby, F. G., & Ennis, J. M. (2006) · Psychology of Learning and Motivation · doi:10.1016/s0079-7421(06)46001-1 · Cited by 120
Attention influences the excitability of cortical motor areas in healthy humans
Conte, A., Gilio, F., Iezzi, E., Frasca, V., Inghilleri, M., & Berardelli, A. (2007) · Experimental Brain Research · doi:10.1007/s00221-007-0975-3 · Cited by 118
Decreased glutamate + glutamine in Alzheimer’s disease detected in vivo with 1 H-MRS at 0.5 T
Antuono, P. G., Jones, J. L., Wang, Y., & Li, S.-J. (2001) · Neurology · doi:10.1212/wnl.56.6.737 · Cited by 119
Neto1 Is an Auxiliary Subunit of Native Synaptic Kainate Receptors
Tang, M., Pelkey, K. A., Ng, D., Ivakine, E., McBain, C. J., Salter, M. W., & McInnes, R. R. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6617-10.2011 · Cited by 112
Glutamatergic synapses onto hippocampal interneurons: precision timing without lasting plasticity
McBain, C. J., Freund, T. F., & Mody, I. (1999) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01347-2 · Cited by 113
The Brain-Enriched MicroRNA miR-9-3p Regulates Synaptic Plasticity and Memory
Sim, S.-E., Lim, C.-S., Kim, J.-I., Seo, D., Chun, H., Yu, N.-K., Lee, J., Kang, S. J., Ko, H.-G., Choi, J.-H., et al. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.0630-16.2016 · Cited by 116
Mazarakis, N. K., Cybulska-Klosowicz, A., Grote, H., Pang, T., Van Dellen, A., Kossut, M., Blakemore, C., & Hannan, A. J. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.4320-04.2005 · Cited by 115
Shaffery, J. P., Sinton, C. M., Bissette, G., Roffwarg, H. P., & Marks, G. A. (2002) · Neuroscience · doi:10.1016/s0306-4522(01)00589-9 · Cited by 114
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Vivar, C., & van Praag, H. (2017) · Physiology · doi:10.1152/physiol.00017.2017 · Cited by 114
REM sleep deprivation inhibits LTP in vivo in area CA1 of rat hippocampus
Kim, E. Y., Mahmoud, G. S., & Grover, L. M. (2005) · Neuroscience Letters · doi:10.1016/j.neulet.2005.06.057 · Cited by 114
Metadata
- Authors
- Bliss, T. V. P., & Collingridge, G. L.
- Affiliations
- National Institute for Medical Research (GB)
- ORCID
- Collingridge, G. L.
- Venue
- Nature
- Published
- 1993-01
- Volume
- 361
- Issue
- 6407
- Pages
- 31-39
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2049511526
- Cited by
- 11,566
- References
- 169
- Citations by year
- 2026: 154 · 2025: 254 · 2024: 254 · 2023: 299 · 2022: 252 · 2021: 321 · 2020: 308 · 2019: 312 · 2018: 347 · 2017: 361 · 2016: 354 · 2015: 377 · 2014: 390 · 2013: 384 · 2012: 371
- FWCI
- 34.50
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (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, hippocampus, synaptic plasticity, memory, learning, NMDA receptor, glutamate receptors, Hebbian learning, synaptic transmission, postsynaptic mechanisms
- MeSH terms
- Animals, Calcium, Electrophysiology, Evoked Potentials, Hippocampus, Memory, Models, Neurological, Synapses, Signal Transduction, Receptors, N-Methyl-D-Aspartate
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