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.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“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 501–600 of 1,220
Kim, C., Chung, H. J., Lee, H., & Huganir, R. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.211132798 · Cited by 364
Changes in reliability of synaptic function as a mechanism for plasticity
Stevens, C. F., & Wang, Y. (1994) · Nature · doi:10.1038/371704a0 · Cited by 364
Neuropharmacology of AMPA and kainate receptors
Bleakman, D., & Lodge, D. (1998) · Neuropharmacology · doi:10.1016/s0028-3908(98)00139-7 · Cited by 364
Cali, J. J., Zwaagstra, J. C., Mons, N., Cooper, D. M., & Krupinski, J. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)32700-x · Cited by 363
Koga, K., Descalzi, G., Chen, T., Ko, H., Lu, J., Li, S., Son, J., Kim, T., Kwak, C., Huganir, R. L., et al. (2014) · Neuron · doi:10.1016/j.neuron.2014.12.021 · Cited by 363
Self-citationJohn, R. A., Liu, F., Chien, N. A., Kulkarni, M. R., Zhu, C., Fu, Q., Basu, A., Liu, Z., & Mathews, N. (2018) · Advanced Materials · doi:10.1002/adma.201800220 · Cited by 364
Mansuy, I. M., Mayford, M. R., Jacob, B., Kandel, E. R., & Bach, M. E. (1998) · Cell · doi:10.1016/s0092-8674(00)80897-1 · Cited by 362
Calcium signaling in neurodegeneration
Marambaud, P., Dreses‐Werringloer, U., & Vingtdeux, V. (2009) · Molecular Neurodegeneration · doi:10.1186/1750-1326-4-20 · Cited by 363
Astrocyte signaling controls spike timing–dependent depression at neocortical synapses
Min, R., & Nevian, T. (2012) · Nature Neuroscience · doi:10.1038/nn.3075 · Cited by 361
The molecular and cellular biology of enhanced cognition
Lee, Y.-S., & Silva, A. J. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2572 · Cited by 361
Understanding LTP in Pain Pathways
Sandkühler, J. (2007) · Molecular Pain · doi:10.1186/1744-8069-3-9 · Cited by 361
Out of southern East Asia: the natural history of domestic dogs across the world
Wang, G., Zhai, W., Yang, H., Wang, L., Li, Z., Yan-hu, L., Fan, R., Yin, T., Zhu, C., Poyarkov, A. D., et al. (2015) · Cell Research · doi:10.1038/cr.2015.147 · Cited by 363
Osten, P., Srivastava, S., Inman, G. J., Vilim, F. S., Khatri, L., Lee, L. M., States, B. A., Einheber, S., Milner, T. A., Hanson, P. I., et al. (1998) · Neuron · doi:10.1016/s0896-6273(00)80518-8 · Cited by 358
Arancio, O., Kiebler, M., Lee, C. J., Lev-Ram, V., Tsien, R. Y., Kandel, E. R., & Hawkins, R. D. (1996) · Cell · doi:10.1016/s0092-8674(00)81797-3 · Cited by 357
Metaplasticity: A new vista across the field of synaptic plasticity
Abraham, W. C., & Tate, W. P. (1997) · Progress in Neurobiology · doi:10.1016/s0301-0082(97)00018-x · Cited by 356
Pang, P. T., & Lu, B. (2004) · Ageing Research Reviews · doi:10.1016/j.arr.2004.07.002 · Cited by 356
A mouse model for the learning and memory deficits associated with neurofibromatosis type I
Silva, A. J., Frankland, P. W., Marowitz, Z., Friedman, E., Lazlo, G., Cioffi, D., Jacks, T., & Bourtchuladze, R. (1997) · Nature Genetics · doi:10.1038/ng0397-281 · Cited by 356
Zhao, W.-Q., & Townsend, M. (2009) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2008.10.014 · Cited by 291
Natural patterns of activity and long-term synaptic plasticity
Paulsen, O. (2000) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00076-3 · Cited by 354
The neonatal ventral hippocampal lesion as a heuristic neurodevelopmental model of schizophrenia
Tseng, K. Y., Chambers, R. A., & Lipska, B. K. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.11.039 · Cited by 355
Wulfram Gerstner, B., Lehmann, M., Liakoni, V., Corneil, D., & Brea, J. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00053 · Cited by 354
Targeted deletion in astrocyte intermediate filament (Gfap) alters neuronal physiology.
McCall, M. A., Gregg, R. G., Behringer, R. R., Brenner, M., Delaney, C. L., Galbreath, E. J., Zhang, C. L., Pearce, R. A., Chiu, S. Y., & Messing, A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.13.6361 · Cited by 353
O’Donnell, J., Zeppenfeld, D., McConnell, E., Pena, S., & Nedergaard, M. (2012) · Neurochemical Research · doi:10.1007/s11064-012-0818-x · Cited by 399
Man, H.-Y., Wang, Q., Lu, W.-Y., Ju, W., Ahmadian, G., Liu, L., D'Souza, S., Wong, T. P., Taghibiglou, C., Lu, J., et al. (2003) · Neuron · doi:10.1016/s0896-6273(03)00228-9 · Cited by 307
Evidence for presynaptic N-methyl-D-aspartate autoreceptors in the spinal cord dorsal horn.
Liu, H., Wang, H., Sheng, M., Jan, L. Y., Jan, Y. N., & Basbaum, A. I. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.18.8383 · Cited by 352
Lisman, J., Cooper, K., Sehgal, M., & Silva, A. J. (2018) · Nature Neuroscience · doi:10.1038/s41593-018-0076-6 · Cited by 351
What happened? Alcohol, memory blackouts, and the brain.
White, A. M. (2003) · Europe PMC (PubMed Central) · Cited by 351
Neuromodulation of Na+ channels: An unexpected form of cellular platicity
Cantrell, A. R., & Catterall, W. A. (2001) · Nature reviews. Neuroscience · doi:10.1038/35077553 · Cited by 351
Conservation of total synaptic weight through balanced synaptic depression and potentiation
Royer, S., & Paré, D. (2003) · Nature · doi:10.1038/nature01530 · Cited by 351
Miller, K. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-01-00409.1994 · Cited by 351
Khairova, R. A., Machado-Vieira, R., Du, J., & Manji, H. K. (2009) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145709009924 · Cited by 350
Rodrigues, S. M., Schafe, G. E., & LeDoux, J. E. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-17-06889.2001 · Cited by 350
Neural Mechanisms Underlying Anxiety–Chronic Pain Interactions
Zhuo, M. (2016) · Trends in Neurosciences · doi:10.1016/j.tins.2016.01.006 · Cited by 350
The nitric oxide-cyclic GMP signalling pathway in rat brain
Southam, E., & Garthwaite, J. (1993) · Neuropharmacology · doi:10.1016/0028-3908(93)90021-t · Cited by 350
The role of 5-HT1A receptors in learning and memory
Ögren, S. O., Eriksson, T. M., Elvander-Tottie, E., D’Addario, C., Ekstrom, J. C., Svenningsson, P., Meister, B., Kehr, J., & Stiedl, O. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.02.023 · Cited by 348
Koester, H. J., & Sakmann, B. J. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.16.9596 · Cited by 348
Spatial memory dissociations in mice lacking GluR1
Reisel, D., Bannerman, D. M., Schmitt, W. B., Deacon, R. M. J., Flint, J., Borchardt, T., Seeburg, P. H., & Rawlins, J. N. P. (2002) · Nature Neuroscience · doi:10.1038/nn910 · Cited by 346
Li, S., Wang, C., Wang, M., Murakami, Y., & Matsumoto, K. (2006) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2006.01.004 · Cited by 346
Liang, W. S., Dunckley, T. L., Beach, T. G., Grover, A., Mastroeni, D., Walker, D. G., Caselli, R. J., Kukull, W. A., McKeel, D. W., Morris, J. C., et al. (2006) · Physiological Genomics · doi:10.1152/physiolgenomics.00208.2006 · Cited by 346
Heath, P. R., & Shaw, P. J. (2002) · Muscle & Nerve · doi:10.1002/mus.10186 · Cited by 345
A model of hippocampal memory encoding and retrieval: GABAergic control of synaptic plasticity
Paulsen, O., & Moser, E. I. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01205-8 · Cited by 345
Palmer, M. J., Irving, A. J., Seabrook, G. R., Jane, D. E., & Collingridge, G. L. (1997) · Neuropharmacology · doi:10.1016/s0028-3908(97)00181-0 · Cited by 345
Self-citationAKAP Mediated Signal Transduction
Michel, J. J. C., & Scott, J. D. (2002) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.42.083101.135801 · Cited by 345
Kutlu, M. G., & Gould, T. J. (2016) · Learning & Memory · doi:10.1101/lm.042192.116 · Cited by 345
Anisotropic Black Phosphorus Synaptic Device for Neuromorphic Applications
Tian, H., Guo, Q., Xie, Y., Zhao, H., Cheng, L., Cha, J. J., Xia, F., & Wang, H. (2016) · Advanced Materials · doi:10.1002/adma.201600166 · Cited by 346
Wan, C., Cai, P., Wang, M., Qian, Y., Huang, W., & Chen, X. (2019) · Advanced Materials · doi:10.1002/adma.201902434 · Cited by 347
Endogenous amyloid‐β is necessary for hippocampal synaptic plasticity and memory
Puzzo, D., Privitera, L., Fa', M., Staniszewski, A., Hashimoto, G., Aziz, F., Sakurai, M., Ribe, E. M., Troy, C. M., Mercken, M., et al. (2011) · Annals of Neurology · doi:10.1002/ana.22313 · Cited by 278
Long-term depression: multiple forms and implications for brain function
Massey, P. V., & Bashir, Z. I. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.02.005 · Cited by 342
Glutamate receptors: brain function and signal transduction
Nakanishi, S., Nakajima, Y., Masu, M., Ueda, Y., Nakahara, K., Watanabe, D., Yamaguchi, S., Kawabata, S., & Okada, M. (1998) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00033-7 · Cited by 342
Nalbantoglu, J. N., Santiago, G. T., Lahsaïni, A., Poirier, J., Goncalves, O., Verge, G. M., Momoli, F., Welner, S. A., Massicotte, G., Julien, J., et al. (1997) · Nature · doi:10.1038/387500a0 · Cited by 342
Altered synaptic plasticity and memory formation in nitric oxide synthase inhibitor-treated rats.
Böhme, G. A., Bon, C. L. M., Lemaire, M., Reibaud, M., Piot, O., Stutzmann, J. M., Doble, A., & Blanchard, J. C. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.19.9191 · Cited by 341
Long-term synaptic plasticity in hippocampal interneurons
Kullmann, D. M., & Lamsa, K. P. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2207 · Cited by 340
Diamond, D. M., Fleshner, M., Ingersoll, N., & Rose, G. M. (1996) · Behavioral Neuroscience · doi:10.1037//0735-7044.110.4.661 · Cited by 340
Different forms of synaptic plasticity in somatosensory and motor areas of the neocortex
Castro‐Alamancos, M. A., Donoghue, J. P., & Connors, B. W. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-07-05324.1995 · Cited by 341
Luo, Z., Xia, X., Yang, M., Wilson, N. R., Gruverman, A. L., & Alexe, M. (2019) · ACS Nano · doi:10.1021/acsnano.9b07687 · Cited by 339
Neuroinflammation in the normal aging hippocampus
Barrientos, R. M., Kitt, M. M., Watkins, L. R., & Maier, S. F. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.03.007 · Cited by 338
Supramolecular Assemblies and Localized Regulation of Voltage-Gated Ion Channels
Dai, S., Hall, D. D., & Hell, J. W. (2009) · Physiological Reviews · doi:10.1152/physrev.00029.2007 · Cited by 339
Dendrodendritic Inhibition in the Olfactory Bulb Is Driven by NMDA Receptors
Schoppa, N. E., Kinzie, J. M., Sahara, Y., Segerson, T. P., & Westbrook, G. L. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-17-06790.1998 · Cited by 338
Targeting NMDA receptors in stroke: new hope in neuroprotection
Wu, Q. J., & Tymianski, M. (2018) · Molecular Brain · doi:10.1186/s13041-018-0357-8 · Cited by 338
NEURAL MECHANISMS OF MAMMALIAN OLFACTORY LEARNING
Brennan, P., & Keverne, E. B. (1997) · Progress in Neurobiology · doi:10.1016/s0301-0082(96)00069-x · Cited by 337
Wind‐up and the NMDA receptor complex from a clinical perspective
Eide, P. K. (2000) · European Journal of Pain · doi:10.1053/eujp.1999.0154 · Cited by 337
Hippocampal long-term depression: master or minion in declarative memory processes?
Kemp, A., & Manahan-Vaughan, D. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.01.002 · Cited by 336
Can molecules explain long-term potentiation?
Sanes, J. R., & Lichtman, J. W. (1999) · Nature Neuroscience · doi:10.1038/10154 · Cited by 336
Meningeal γδ T cell-derived IL-17 controls synaptic plasticity and short-term memory
Ribeiro, M., Brigas, H. C., Temido-Ferreira, M., Pousinha, P. A., Regen, T., Santa, C., Coelho, J. E., Marques-Morgado, I., Valente, C. A., Omenetti, S., et al. (2019) · Science Immunology · doi:10.1126/sciimmunol.aay5199 · Cited by 335
Formation of Regulatory Patterns During Signal Propagation in a Mammalian Cellular Network
Ma’ayan, A., Jenkins, S. L., Neves, S. R., Hasseldine, A., Grace, E. A., Dubin‐Thaler, B. J., Eungdamrong, N. J., Weng, G., Ram, P. T., Rice, J. J., et al. (2005) · Science · doi:10.1126/science.1108876 · Cited by 335
Lazzaro, V. D., Profice, P., Ranieri, F., Capone, F., Dileone, M., Oliviero, A., & Pilato, F. (2011) · Brain stimulation · doi:10.1016/j.brs.2011.07.008 · Cited by 335
Malleability of Spike-Timing-Dependent Plasticity at the CA3–CA1 Synapse
Wittenberg, G. M., & Wang, S. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5388-05.2006 · Cited by 334
Regulation of hippocampal synaptic plasticity by cyclic AMP-dependent protein kinases
Nguyen, P., & Woo, N. H. (2003) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2003.12.003 · Cited by 333
Long-term potentiation in the amygdala: A cellular mechanism of fear learning and memory
Sigurdsson, T., Doyère, V., Cain, C. K., & LeDoux, J. E. (2006) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.06.022 · Cited by 333
Unpacking the cognitive map: The parallel map theory of hippocampal function.
Jacobs, L. F., & Schenk, F. (2003) · Psychological Review · doi:10.1037/0033-295x.110.2.285 · Cited by 334
The Persistence and Transience of Memory
Richards, B. A., & Frankland, P. W. (2017) · Neuron · doi:10.1016/j.neuron.2017.04.037 · Cited by 338
An Essential Role for Retinoid Receptors RARβ and RXRγ In Long-Term Potentiation and Depression
Chiang, M.-Y., Misner, D., Kempermann, G., Schikorski, T., Giguère, V., Sucov, H. M., Gage, F. H., Stevens, C. F., & Evans, R. M. (1998) · Neuron · doi:10.1016/s0896-6273(00)80654-6 · Cited by 332
Raymond, L. A., André, V. M., Cepeda, C., Gladding, C. M., Milnerwood, A. J., & Levine, M. S. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.08.052 · Cited by 336
Kainate receptors are involved in synaptic plasticity
Bortolotto, Z. A., Clarke, V. R. J., Delany, C. M., Parry, M., Smolders, I. J., Vignes, M., Ho, K. H., Miu, P., Brinton, B. T., Fantaske, R. P., et al. (1999) · Nature · doi:10.1038/46290 · Cited by 332
Self-citationReymann, K. G., & Frey, J. U. (2007) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.07.026 · Cited by 331
Src activation in the induction of long-term potentiation in CA1 hippocampal neurons.
Lu, Y. M., Roder, J., Davidow, J., & Salter, M. (1998) · Science · doi:10.1126/science.279.5355.1363 · Cited by 356
Hippocampal ripples and memory consolidation
Girardeau, G., & Zugaro, M. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.02.005 · Cited by 330
Sandkühler, J., Chen, J.-G., Cheng, G., & Randić, M. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-16-06483.1997 · Cited by 323
NMDA receptor-dependent excitotoxicity: the role of intracellular Ca2+ release
Módy, I. (1995) · Trends in Pharmacological Sciences · doi:10.1016/s0165-6147(00)89070-7 · Cited by 330
Age-Dependent Impairment of Cognitive and Synaptic Function in the htau Mouse Model of Tau Pathology
Polydoro, M., Acker, C. M., Duff, K., Castillo, P. E., & Davies, P. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.1065-09.2009 · Cited by 329
Mayford, M. R., Baranes, D., Podsypanina, K., & Kandel, E. R. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.23.13250 · Cited by 329
Short-term synaptic plasticity is altered in mice lacking synapsin I
Rosahl, T. (1993) · Cell · doi:10.1016/0092-8674(93)90487-b · Cited by 328
Okamoto, K.-I., Narayanan, R., Lee, S. H., Murata, K., & Hayashi, Y. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0701656104 · Cited by 328
Smith, D., Stevens, M. E., Sudanagunta, S. P., Bronson, R. T., Makhinson, M., Watabe, A. M., O’Dell, T. J., Fung, J., Weier, H. G., Cheng, J., et al. (1997) · Nature Genetics · doi:10.1038/ng0597-28 · Cited by 328
Zhang, K., Förster, R., He, W., Liao, X., Li, J., Yang, C., Qin, H., Wang, M., Ding, R., Li, R., et al. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00949-8 · Cited by 328
Clinical relevance of the neurotrophins and their receptors
Allen, S. J., & Dawbarn, D. (2006) · Clinical Science · doi:10.1042/cs20050161 · Cited by 327
Chung, H. J., Huang, Y., Lau, L., & Huganir, R. L. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.0546-04.2004 · Cited by 327
GABAA receptor subunits in the rat hippocampus I: Immunocytochemical distribution of 13 subunits
Sperk, G., Schwarzer, C., Tsunashima, K., Fuchs, K., & Sieghart, W. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00146-2 · Cited by 327
Epigenetic codes in cognition and behaviour
Gräff, J., & Mansuy, I. M. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.01.021 · Cited by 328
Geinisman, Y., deToledo‐Morrell, L., Morrell, F., & Heller, R. E. (1995) · Progress in Neurobiology · doi:10.1016/0301-0082(94)00047-l · Cited by 327
Postsynaptic CAMP pathway gates early LTP in hippocampal CA1 region
Blitzer, R. D., Wong, T., Nouranifar, R., Iyengar, R., & Landau, E. M. (1995) · Neuron · doi:10.1016/0896-6273(95)90018-7 · Cited by 326
Extrasynaptic glutamate spillover in the hippocampus: evidence and implications
Kullmann, D. M., & Asztély, F. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01150-8 · Cited by 326
Cognitive Memory: Cellular and Network Machineries and Their Top-Down Control
Miyashita, Y. (2004) · Science · doi:10.1126/science.1101864 · Cited by 326
All-or-none potentiation at CA3-CA1 synapses
Petersen, C. C. H., Malenka, R. C., Nicoll, R. A., & Hopfield, J. J. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.8.4732 · Cited by 325
Veh, R. W., Lichtinghagen, R., Sewing, S., Wunder, F., Grumbach, I. M., & Pongs, O. (1995) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1995.tb00641.x · Cited by 324
The Cognitive Neuroscience of Memory: An Introduction
Eichenbaum, H. (2002) · doi:10.1093/acprof:oso/9780195141740.001.0001 · Cited by 323
Early synaptic pathophysiology in neurodegeneration: insights from Huntington's disease
Milnerwood, A. J., & Raymond, L. A. (2010) · Trends in Neurosciences · doi:10.1016/j.tins.2010.08.002 · Cited by 323
A revised model of short-term memory and long-term learning of verbal sequences
Burgess, N., & Hitch, G. J. (2006) · Journal of Memory and Language · doi:10.1016/j.jml.2006.08.005 · Cited by 323
Daw, M. I., Chittajallu, R., Bortolotto, Z. A., Dev, K. K., Duprat, F., Henley, J. M., Collingridge, G. L., & Isaac, J. T. R. (2000) · Neuron · doi:10.1016/s0896-6273(00)00160-4 · Cited by 323
Self-citationTsvetkov, E., Carlezon, W. A., Benes, F. M., Kandel, E. R., & Bolshakov, V. Y. (2002) · Neuron · doi:10.1016/s0896-6273(02)00645-1 · Cited by 321
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
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
