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
Flagged first, then by citations
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).
Cited by
Sorted by citations
Items 1,101–1,200 of 1,220
Rozov, A., Zilberter, Y., Wollmuth, L. P., & Burnashev, N. (1998) · The Journal of Physiology · doi:10.1111/j.1469-7793.1998.361bh.x · Cited by 114
Gut Metabolite TMAO Induces Synaptic Plasticity Deficits by Promoting Endoplasmic Reticulum Stress
Govindarajulu, M., Pinky, P. D., Steinke, I., Bloemer, J., Ramesh, S., Kariharan, T., Rella, R. T., Bhattacharya, S., Dhanasekaran, M., Suppiramaniam, V., et al. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.00138 · Cited by 113
A survey of multimodal deep generative models
Suzuki, M., & Matsuo, Y. (2022) · Advanced Robotics · doi:10.1080/01691864.2022.2035253 · Cited by 109
Engelhardt, J. V., Bocklisch, C., Tönges, L., Herb, A., Mishina, M., & Monyer, H. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00095 · Cited by 103
Long-term exercise is needed to enhance synaptic plasticity in the hippocampus
Patten, A. R., Sickmann, H., Hryciw, B. N., Kucharsky, T., Parton, R., Kernick, A., & Christie, B. R. (2013) · Learning & Memory · doi:10.1101/lm.030635.113 · Cited by 101
Nagy, V., Bozdagi, O., & Huntley, G. W. (2007) · Learning & Memory · doi:10.1101/lm.678307 · Cited by 107
Lapointe, V., Morin, F., Ratté, S., Croce, A., Conquet, F., & Lacaille, J. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2003.053603 · Cited by 103
Microglial large extracellular vesicles propagate early synaptic dysfunction in Alzheimer’s disease
Gabrielli, M., Prada, I., Joshi, P., Falcicchia, C., D’Arrigo, G., Rutigliano, G., Battocchio, E., Zenatelli, R., Tozzi, F., Radeghieri, A., et al. (2022) · Brain · doi:10.1093/brain/awac083 · Cited by 106
Chindemi, G., Abdellah, M., Amsalem, O., Benavides-Piccione, R., Delattre, V., Doron, M., Ecker, A., Jaquier, A. T., King, J., Kumbhar, P., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-30214-w · Cited by 102
Gulisano, W., Melone, M., Ripoli, C., Tropea, M. R., Li Puma, D. D., Giunta, S., Cocco, S., Marcotulli, D., Origlia, N., Palmeri, A., et al. (2019) · The Journal of Neuroscience · doi:10.1523/jneurosci.0163-19.2019 · Cited by 100
Wang, X. H., Li, L., Hölscher, C., Pan, Y. F., Chen, X. R., & Qi, J. S. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.08.028 · Cited by 99
Unique regulation of long term potentiation in the rat ventral hippocampus
Maggio, N., & Segal, M. (2007) · Hippocampus · doi:10.1002/hipo.20237 · Cited by 100
Investigations into the involvement of NMDA mechanisms in recognition memory
Warburton, E. C., Barker, G. R. I., & Brown, M. W. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.04.013 · Cited by 98
Locus Coeruleus and Dopamine-Dependent Memory Consolidation
Yamasaki, M., & Takeuchi, T. (2017) · Neural Plasticity · doi:10.1155/2017/8602690 · Cited by 91
Nicotine modulation of fear memories and anxiety: Implications for learning and anxiety disorders
Kutlu, M. G., & Gould, T. J. (2015) · Biochemical Pharmacology · doi:10.1016/j.bcp.2015.07.029 · Cited by 97
Brown, G. P., Blitzer, R. D., Connor, J. H., Wong, T., Shenolikar, S., Iyengar, R., & Landau, E. M. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-21-07880.2000 · Cited by 98
Uchino, S., Wada, H., Honda, S., Nakamura, Y., Ondo, Y., Uchiyama, T., Tsutsumi, M., Suzuki, E., Hirasawa, T., & Kohsaka, S. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03831.x · Cited by 95
Shang, Y., Wang, X., Shang, X., Zhang, H., Liu, Z., Yin, T., & Zhang, T. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.08.016 · Cited by 94
Le Grevès, M., Zhou, Q., Berg, M., Le Grevès, P., Fhölenhag, K., Meyerson, B., & Nyberg, F. (2006) · Experimental Brain Research · doi:10.1007/s00221-006-0438-2 · Cited by 92
Neurophysiology of Remembering
Buzsáki, G., McKenzie, S., & Davachi, L. (2022) · Annual Review of Psychology · doi:10.1146/annurev-psych-021721-110002 · Cited by 84
Martins, N. R. B., Angelica, A., Chakravarthy, K., Svidinenko, Y., Boehm, F. J., Opris, I., Lebedev, M. A., Swan, M., Garan, S. A., Rosenfeld, J. V., et al. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00112 · Cited by 91
A dynamic zone defines interneuron remodeling in the adult neocortex
Lee, W.-C. A., Chen, J. L., Huang, H., Leslie, J. H., Amitai, Y., So, P. T., & Nedivi, E. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0810149105 · Cited by 87
MHC class I modulates NMDA receptor function and AMPA receptor trafficking
Fourgeaud, L., Davenport, C. M., Tyler, C. M., Cheng, T. T., Spencer, M. B., & Boulanger, L. M. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0914064107 · Cited by 89
Physical activity and brain development
Gomes da Silva, S., & Arida, R. M. (2015) · Expert Review of Neurotherapeutics · doi:10.1586/14737175.2015.1077115 · Cited by 89
Determinants and mechanisms of attentional modulation of neural processing.
Schroeder, C. (2001) · Frontiers in bioscience · doi:10.2741/schroed · Cited by 87
Brain-specific repression of AMPKα1 alleviates pathophysiology in Alzheimer’s model mice
Zimmermann, H. R., Yang, W., Kasica, N. P., Zhou, X., Wang, X., Beckelman, B. C., Lee, J., Furdui, C. M., Keene, C. D., & Ma, T. (2020) · Journal of Clinical Investigation · doi:10.1172/jci133982 · Cited by 86
CA1 Long-Term Potentiation Is Diminished but Present in Hippocampal Slices from α-CaMKII Mutant Mice
Hinds, H. L., Tonegawa, S., & Malinow, R. (1998) · Learning & Memory · doi:10.1101/lm.5.4.344 · Cited by 86
Sambandan, S., Sauer, J.-F., Vida, I., & Bartos, M. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.2012-10.2010 · Cited by 82
Goshen, I., Avital, A., Kreisel, T., Licht, T., Segal, M., & Yirmiya, R. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.5352-08.2009 · Cited by 82
“Because synaptic plasticity was implicated in memory storage (Bliss and Collingridge, 1993; Eichenbaum, 1996), the restoration of the ability to express LTP in IL-1rKO mice may serve as a possible mechanism for the memory improvement observed in these mice after environmental enrichment.”
BackgroundArtificial Neural Networks Based on Memristive Devices: From Device to System
Huang, H.-M., Wang, Z., Wang, T., Xiao, Y., & Guo, X. (2020) · Advanced Intelligent Systems · doi:10.1002/aisy.202000149 · Cited by 82
Cognitive neuroscience perspective on memory: overview and summary
Sridhar, S., Khamaj, A., & Asthana, M. K. (2023) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2023.1217093 · Cited by 80
Le, X. T., Pham, H. T. N., Do, P. T., Fujiwara, H., Tanaka, K., Li, F., Van Nguyen, T., Nguyen, K. M., & Matsumoto, K. (2013) · Neurochemical Research · doi:10.1007/s11064-013-1129-6 · Cited by 79
Cooke, S. F., Wu, J., Plattner, F., Errington, M., Rowan, M., Peters, M., Hirano, A., Bradshaw, K. D., Anwyl, R., Bliss, T. V. P., et al. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.111559 · Cited by 77
Self-citationShang, Y., Wang, H., Mercaldo, V., Li, X., Chen, T., & Zhuo, M. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06314.x · Cited by 72
New Treatment Strategies of Depression: Based on Mechanisms Related to Neuroplasticity
Huang, Y.-J., Lane, H.-Y., & Lin, C.-H. (2017) · Neural Plasticity · doi:10.1155/2017/4605971 · Cited by 74
Klyubin, I., Nicoll, A. J., Khalili-Shirazi, A., Farmer, M., Canning, S., Mably, A., Linehan, J., Brown, A., Wakeling, M., Brandner, S., et al. (2014) · The Journal of Neuroscience · doi:10.1523/jneurosci.3526-13.2014 · Cited by 74
Ca2+ Dyshomeostasis Disrupts Neuronal and Synaptic Function in Alzheimer’s Disease
McDaid, J., Mustaly-Kalimi, S., & Stutzmann, G. E. (2020) · Cells · doi:10.3390/cells9122655 · Cited by 73
Muhia, M., Yee, B. K., Feldon, J., Markopoulos, F., & Knuesel, I. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07079.x · Cited by 71
Cholinergic systems and long-term potentiation in memory-impaired apolipoprotein E-deficient mice
Krzywkowski, P., Ghribi, O., Gagné, J., Chabot, C., Kar, S., Rochford, J., Massicotte, G., & Poirier, J. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00061-5 · Cited by 74
Removal of Synaptic Ca 2+ -Permeable AMPA Receptors during Sleep
Lanté, F., Toledo-Salas, J.-C., Ondrejcak, T., Rowan, M. J., & Ulrich, D. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.3210-10.2011 · Cited by 74
Yamada, T., Terashima, T., Okubo, T., Juneja, L. R., & Yokogoshi, H. (2005) · Nutritional Neuroscience · doi:10.1080/10284150500170799 · Cited by 72
Bell, M. E., Bourne, J. N., Chirillo, M. A., Mendenhall, J. M., Kuwajima, M., & Harris, K. M. (2014) · Journal of Comparative Neurology · doi:10.1002/cne.23646 · Cited by 72
Neuroinflammation in Alzheimer’s disease: Pleiotropic roles for cytokines and neuronal pentraxins
Swanson, A., Wolf, T., Sitzmann, A., & Willette, A. A. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.02.015 · Cited by 72
Role of amygdala oscillations in the consolidation of emotional memories
Pelletier, J. G., & Paré, D. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2003.08.019 · Cited by 71
Daw, M. I., Scott, H. L., & Isaac, J. T. R. (2007) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2007.01.001 · Cited by 70
Bayesian spiking neurons II: learning
Deneve, S. (2008) · Neural Computation · doi:10.1162/neco.2008.20.1.118 · Cited by 71
Molecular and cellular aspects of age-related cognitive decline and Alzheimer’s disease
Hullinger, R., & Puglielli, L. (2017) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.05.008 · Cited by 68
Murthy, V. N., Sejnowski, T. J., & Stevens, C. F. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.2.901 · Cited by 70
Bramham, C. R. (2007) · Progress in Brain Research · doi:10.1016/s0079-6123(07)63025-8 · Cited by 69
Chapman, C. A., Nuwer, J. L., & Jacob, T. C. (2022) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2022.911020 · Cited by 62
Dependence of hippocampal function on ERRγ-regulated mitochondrial metabolism
Pei, L., Mu, Y., Leblanc, M., Alaynick, W., Barish, G. D., Pankratz, M., Tseng, T. W., Kaufman, S., Liddle, C., Yu, R. T., et al. (2015) · Cell Metabolism · doi:10.1016/j.cmet.2015.03.004 · Cited by 65
Schmid, A. W., Lynch, M. A., & Herron, C. E. (2009) · Hippocampus · doi:10.1002/hipo.20542 · Cited by 64
Pandey, S. P., Singh, H. K., & Prasad, S. (2015) · PLOS ONE · doi:10.1371/journal.pone.0131862 · Cited by 64
Patten, A. R., Yau, S. Y., Fontaine, C. J., Meconi, A., Wortman, R. C., & Christie, B. R. (2015) · Brain Plasticity · doi:10.3233/bpl-150016 · Cited by 64
Burns, L. H., Everitt, B. J., & Robbins, T. W. (1994) · Behavioral and Neural Biology · doi:10.1016/s0163-1047(05)80007-x · Cited by 61
Horn, G., Nicol, A. U., & Brown, M. W. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.091094798 · Cited by 61
Steroid modulation of hippocampal plasticity: switching between cognitive and emotional memories
Maggio, N., & Segal, M. (2012) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2012.00012 · Cited by 60
Noguchi, J., Hayama, T., Watanabe, S., Ucar, H., Yagishita, S., Takahashi, N., & Kasai, H. (2016) · Scientific Reports · doi:10.1038/srep32897 · Cited by 60
The Non-Benzodiazepine Hypnotic Zolpidem Impairs Sleep-Dependent Cortical Plasticity
(2008) · Sleep · doi:10.5665/sleep/31.10.1381 · Cited by 60
Miller, B. H., & Gore, A. C. (2002) · Endocrinology · doi:10.1210/en.2002-220346 · Cited by 59
Pelkey, K. A., & McBain, C. J. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2007.148635 · Cited by 58
Diniz, C. R. A. F., Casarotto, P. C., Resstel, L., & Joca, S. R. L. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.04.001 · Cited by 58
Green tea extract enhances parieto-frontal connectivity during working memory processing
Schmidt, A., Hammann, F., Wölnerhanssen, B., Meyer-Gerspach, A. C., Drewe, J., Beglinger, C., & Borgwardt, S. (2014) · Psychopharmacology · doi:10.1007/s00213-014-3526-1 · Cited by 57
Kindler, S., Rehbein, M., Classen, B., Richter, D., & Böckers, T. M. (2004) · Molecular Brain Research · doi:10.1016/j.molbrainres.2004.03.014 · Cited by 56
Nishida, M., Hirai, N., Miwakeichi, F., Maehara, T., Kawai, K., Shimizu, H., & Uchida, S. (2004) · Neuroscience Research · doi:10.1016/j.neures.2004.08.004 · Cited by 54
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Chen, L., Huang, Z., Du, Y., Fu, M., Han, H., Wang, Y., & Dong, Z. (2017) · Journal of Alzheimer's Disease · doi:10.3233/jad-170337 · Cited by 54
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Callaghan, B. L., Li, S., & Richardson, R. (2014) · Trends in Neurosciences · doi:10.1016/j.tins.2013.10.007 · Cited by 51
Skosnik, P. D., Sloshower, J., Safi-Aghdam, H., Pathania, S., Syed, S., Pittman, B., & D’Souza, D. C. (2023) · Journal of Psychopharmacology · doi:10.1177/02698811231179800 · Cited by 51
Plasticity in the Hippocampus, Neurogenesis and Drugs of Abuse
Avchalumov, Y., & Mandyam, C. D. (2021) · Brain Sciences · doi:10.3390/brainsci11030404 · Cited by 49
Nelson, P. A., Sage, J. R., Wood, S. C., Davenport, C. M., Anagnostaras, S. G., & Boulanger, L. M. (2013) · Learning & Memory · doi:10.1101/lm.031351.113 · Cited by 49
Cognitive Remediation in Schizophrenia
Kaneko, Y., & Keshavan, M. (2012) · Clinical Psychopharmacology and Neuroscience · doi:10.9758/cpn.2012.10.3.125 · Cited by 51
Das, R. K., Tamman, A., Nikolova, V., Freeman, T. P., Bisby, J. A., Lazzarino, A. I., & Kamboj, S. K. (2016) · Psychological Medicine · doi:10.1017/s003329171600026x · Cited by 49
Burns, A. M., Farinelli-Scharly, M., Hugues-Ascery, S., Sanchez-Mut, J. V., Santoni, G., & Gräff, J. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2116797119 · Cited by 49
Saraf, M. K., Anand, A., & Prabhakar, S. (2010) · Neurochemical Research · doi:10.1007/s11064-009-0051-4 · Cited by 48
Giannopoulos, P. F., Chu, J., Sperow, M., Li, J.-G., Yu, W. H., Kirby, L. G., Abood, M., & Praticò, D. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2015.01.015 · Cited by 48
RetractedVoltage-Controlled Plasticity at GluR2-Deficient Synapses Onto Hippocampal Interneurons
Laezza, F., & Dingledine, R. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00425.2004 · Cited by 47
Neurodevelopment in Down syndrome: Concordance in humans and models
Klein, J. A., & Haydar, T. F. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.941855 · Cited by 47
“…in size in DS are the structures that are responsible for executive function (frontal lobe, parietal lobe, and cerebellum) (Nowrangi et al., 2014) and memory – specifically declarative memory (hippocampus) (Scoville and Milner, 1957; Squire and Zolamorgan, 1991; Bliss and Collingridge, 1993).”
BackgroundPharmacological enhancement of memory or cognition in normal subjects
Lynch, G. (2014) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2014.00090 · Cited by 46
Kasica, N. P., Zhou, X., Yang, Q., Wang, X., Yang, W., Zimmermann, H. R., Holland, C. E., Koscielniak, E., Wu, H., Cox, A. O., et al. (2022) · Journal of Neurochemistry · doi:10.1111/jnc.15562 · Cited by 34
Uysal, N. (2015) · Medical Science Monitor · doi:10.12659/msm.893159 · Cited by 44
Drinking after water deprivation prolongs “unsaturated” LTP in the dentate gyrus of rats
Seidenbecher, T., Balschun, D., & Reymann, K. G. (1995) · Physiology & Behavior · doi:10.1016/0031-9384(94)00352-6 · Cited by 44
Freitas da Rocha, A., Pereira, A., & Bezerra Coutinho, F. A. (2001) · Progress in Neurobiology · doi:10.1016/s0301-0082(00)00069-1 · Cited by 41
audinat, E., Lambolez, B., & Rossier, J. (1996) · Neurochemistry International · doi:10.1016/0197-0186(95)00075-5 · Cited by 41
Learned stressor resistance requires extracellular signal-regulated kinase in the prefrontal cortex
Christianson, J. P., Flyer-Adams, J. G., Drugan, R. C., Amat, J., Daut, R. A., Foilb, A. R., Watkins, L. R., & Maier, S. F. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00348 · Cited by 39
The contribution of ion channels in input-output plasticity
Debanne, D., & Russier, M. (2019) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2019.107095 · Cited by 38
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Hamilton, K., & Harvey, J. (2021) · Pharmaceuticals · doi:10.3390/ph14010052 · Cited by 36
Ingram, R., Kang, H., Lightman, S., Jane, D. E., Bortolotto, Z. A., Collingridge, G. L., Lodge, D., & Volianskis, A. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.06.008 · Cited by 36
Self-citationSynaptic PDZ domain-mediated protein interactions are disrupted by inhalational anesthetics
Fang, M., Tao, Y.-X., He, F., Zhang, M., Levine, C. F., Mao, P., Tao, F., Chou, C.-L., Sadegh-Nasseri, S., & Johns, R. A. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m303520200 · Cited by 34
Watanabe, Y., Murakami, T., Kawashima, M., Hasegawa-Baba, Y., Mizukami, S., Imatanaka, N., Akahori, Y., Yoshida, T., & Shibutani, M. (2017) · Neurotoxicity Research · doi:10.1007/s12640-016-9660-2 · Cited by 34
Kanzari, A., Bourcier-Lucas, C., Freyssin, A., Abrous, D. N., Haddjeri, N., & Lucas, G. (2018) · Molecular Psychiatry · doi:10.1038/mp.2017.94 · Cited by 33
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Mehta, M., Ahmed, Z., Fernando, S. S., Cano‐Sanchez, P., Adayev, T., Ziemnicka, D., Wieraszko, A., & Banerjee, P. (2007) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2007.04448.x · Cited by 30
Sáez-Orellana, F., Leroy, T., Ribeiro, F., Kreis, A., Leroy, K., Lalloyer, F., Baugé, E., Staels, B., Duyckaerts, C., Brion, J.-P., et al. (2021) · JCI Insight · doi:10.1172/jci.insight.150099 · Cited by 29
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Jing, H., Hao, Y., Bi, Q., Zhang, J., & Yang, P. (2015) · Neuroscience Research · doi:10.1016/j.neures.2014.10.015 · Cited by 28
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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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