The DOI matches its Crossref record; 16 of the 16 references it cites were found in a registry or an index.
Intracellular injections of EGTA block induction of hippocampal long-term potentiation
Abstract
Hippocampal long-term potentiation (LTP) is a remarkably stable facilitation of synaptic responses resulting from very brief trains of high-frequency stimulation. Because of its persistence and modest induction conditions, LTP represents a promising candidate for a substrate of memory. Some progress has been made in localizing the changes responsible for the effect; for example, it has been shown that LTP is not accompanied by changes in the fibre volleys of the test afferents or by generalized alterations of the dendrites of their target cells. However, it is unknown whether the potentiation is due to pre- or postsynaptic changes and there is evidence in favour of each (for example, see refs 5, 6). We now report that intracellular injections of the calcium chelator EGTA block the development of LTP. These results strongly suggest that LTP is caused by a modification of the postsynaptic neurone and that its induction depends on the level of free calcium.
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
“loading postsynaptic cells with the Ca2+ chelator EGTA blocked LTP (176), suggesting that Ca2+ is necessary for LTP.”
From Synaptic memory and CaMKII (2023) · cites this paper as [176]
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
A calcium-activated hyperpolarization follows repetitive firing in hippocampal neurons
Hotson, J. R., & Prince, D. A. (1980) · Journal of Neurophysiology · doi:10.1152/jn.1980.43.2.409 · Cited by 569
Dunwiddie, T. V., & LYNCH, G. S. (1978) · The Journal of Physiology · doi:10.1113/jphysiol.1978.sp012239 · Cited by 479
Self-citationAlger, B. E., & Nicoll, R. A. (1980) · Science · doi:10.1126/science.7444438 · Cited by 421
Afterpotential generation in hippocampal pyramidal cells.
Wong, R. K. S., & Prince, D. A. (1981) · Journal of Neurophysiology · doi:10.1152/jn.1981.45.1.86 · Cited by 391
Long-term potentiation of the perforant path in vivo is associated with increased glutamate release
DOLPHIN, A. C., Errington, M. L., & Bliss, T. V. P. (1982) · Nature · doi:10.1038/297496a0 · Cited by 389
Andersen, P. N., Sundberg, S. H., Sveen, O., Swann, J. W., & Wigström, H. (1980) · The Journal of Physiology · doi:10.1113/jphysiol.1980.sp013256 · Cited by 366
Effects of EGTA on the Calcium-Activated Afterhyperpolarization in Hippocampal CA3 Pyramidal Cells
Schwartzkroin, P. A., & Stafstrom, C. E. (1980) · Science · doi:10.1126/science.6777871 · Cited by 275
Dunwiddie, T. V., & LYNCH, G. S. (1979) · Brain Research · doi:10.1016/0006-8993(79)90377-9 · Cited by 234
Self-citationMicromolar Calcium Stimulates Proteolysis and Glutamate Binding in Rat Brain Synaptic Membranes
Baudry, M., Bundman, M. C., Smith, E. K., & LYNCH, G. S. (1981) · Science · doi:10.1126/science.7015504 · Cited by 181
Self-citation
Flagged first, then by citations
Research works printed but not linked: 2
- Bliss, T. V. P. & Lomo, T. J. Physiol., Lond. 232, 331–356 (1973). · DOI · Paper page
- Lee, K., Oliver, M., Schottler, F. & Lynch, G. in Electrical Activity in Isolated Mammalian CNS Preparations (eds Kerkut, G. & Wheal, H. V.) 189–212 (Academic, New York, 1981).
Cited by
Sorted by citations
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
Malenka, R. C., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.012 · Cited by 3,968
Long-Term Potentiation--A Decade of Progress?
Malenka, R. C., & Nicoll, A. R. A. (1999) · Science · doi:10.1126/science.285.5435.1870 · Cited by 2,729
THE HEME OXYGENASE SYSTEM:A Regulator of Second Messenger Gases
Maines, M. D. (1997) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.37.1.517 · Cited by 2,489
Long-Term Potentiation and Memory
Lynch, M. A. (2004) · Physiological Reviews · doi:10.1152/physrev.00014.2003 · Cited by 2,074
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
The physiology of excitatory amino acids in the vertebrate central nervous system
Mayer, M. L., & Westbrook, G. L. (1987) · Progress in Neurobiology · doi:10.1016/0301-0082(87)90011-6 · Cited by 1,711
Hippocampal synaptic enhancement and information storage within a distributed memory system
McNaughton, B. L., & Morris, R. G. M. (1987) · Trends in Neurosciences · doi:10.1016/0166-2236(87)90011-7 · Cited by 1,304
A neuropsychological theory of multiple systems in category learning.
Ashby, F. G., Alfonso-Reese, L. A., Turken, A. U., & Waldron, E. M. (1998) · Psychological Review · doi:10.1037/0033-295x.105.3.442 · Cited by 1,216
Plasticity in the human central nervous system
Cooke, S. F. (2006) · Brain · doi:10.1093/brain/awl082 · Cited by 1,260
NMDA receptors - their role in long-term potentiation
Collingridge, G. L., & Bliss, T. (1987) · Trends in Neurosciences · doi:10.1016/0166-2236(87)90175-5 · Cited by 1,178
A Requirement for the Intercellular Messenger Nitric Oxide in Long-Term Potentiation
Schuman, E. M., & Madison, D. V. (1991) · Science · doi:10.1126/science.1720572 · Cited by 1,135
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
The Biochemistry of Memory: A New and Specific Hypothesis
LYNCH, G. S., & Baudry, M. (1984) · Science · doi:10.1126/science.6144182 · Cited by 1,041
Self-citationCalcium regulation of neuronal gene expression
West, A. E., Chen, W., Dalva, M. B., Dolmetsch, R. E., Kornhauser, J. M., Shaywitz, A. J., Takasu, M. A., Xu, T., & Greenberg, M. E. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.191352298 · Cited by 1,047
An essential role for postsynaptic calmodulin and protein kinase activity in long-term potentiation
Malenka, R. C., Kauer, J. A., Perkel, D. J., Mauk, M. D., Kelly, P. T., Nicoll, R. A., & Waxham, M. N. (1989) · Nature · doi:10.1038/340554a0 · Cited by 1,025
AMPARs and Synaptic Plasticity: The Last 25 Years
Huganir, R. L., & Nicoll, R. A. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.025 · Cited by 968
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
NMDA-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
The molecular biology of memory: cAMP, PKA, CRE, CREB-1, CREB-2, and CPEB
Kandel, E. R. (2012) · Molecular Brain · doi:10.1186/1756-6606-5-14 · Cited by 931
Jones, M. W., Errington, M. L., French, P. J., Fine, A., Bliss, T., Garel, S., Charnay, P., Bozon, B., Laroche, S., & Davis, S. (2001) · Nature Neuroscience · doi:10.1038/85138 · Cited by 925
Requirement of a Critical Period of Transcription for Induction of a Late Phase of LTP
Nguyen, P. V., Abel, T., & Kandel, E. R. (1994) · Science · doi:10.1126/science.8066450 · Cited by 888
A mechanism for the Hebb and the anti-Hebb processes underlying learning and memory.
Lisman, J. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.23.9574 · Cited by 1,127
Larson, J., Wong, D., & Lynch, G. (1986) · Brain Research · doi:10.1016/0006-8993(86)90579-2 · Cited by 1,037
Self-citationA Brief History of Long-Term Potentiation
Nicoll, R. A. (2017) · Neuron · doi:10.1016/j.neuron.2016.12.015 · Cited by 841
Postsynaptic Calcium Is Sufficient for Potentiation of Hippocampal Synaptic Transmission
Malenka, R. C., Kauer, J. A., Zucker, R. S., & Nicoll, R. A. (1988) · Science · doi:10.1126/science.2845577 · Cited by 829
Artola, A., & Singer, W. (1993) · Trends in Neurosciences · doi:10.1016/0166-2236(93)90081-v · Cited by 799
Malinow, R., & Tsien, R. W. (1990) · Nature · doi:10.1038/346177a0 · Cited by 797
Long-term potentiation and functional synapse induction in developing hippocampus
Durand, G. M., Kovalchuk, Y., & Konnerth, A. (1996) · Nature · doi:10.1038/381071a0 · Cited by 789
Nitric 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
The Life Cycle of Ca2+ Ions in Dendritic Spines
Sabatini, B. L., Oertner, T. G., & Svoboda, K. (2002) · Neuron · doi:10.1016/s0896-6273(02)00573-1 · Cited by 745
Impact of aging on hippocampal function: plasticity, network dynamics, and cognition
Rosenzweig, E. S., & Barnes, C. A. (2003) · Progress in Neurobiology · doi:10.1016/s0301-0082(02)00126-0 · Cited by 755
Dendritic Excitability and Synaptic Plasticity
Sjöström, P. J., Rancz, E. A., Roth, A., & Häusser, M. (2008) · Physiological Reviews · doi:10.1152/physrev.00016.2007 · Cited by 740
Physiology and Pathophysiology of the Calcium Store in the Endoplasmic Reticulum of Neurons
Verkhratsky, A. (2004) · Physiological Reviews · doi:10.1152/physrev.00004.2004 · Cited by 718
Two components of long-term potentiation induced by different patterns of afferent activation
Grover, L. M., & Teyler, T. J. (1990) · Nature · doi:10.1038/347477a0 · Cited by 708
Deisseroth, K., Bito, H., & Tsien, R. W. (1996) · Neuron · doi:10.1016/s0896-6273(00)80026-4 · Cited by 698
Structure, Function, and Pharmacology of Glutamate Receptor Ion Channels
Hansen, K. B., Wollmuth, L. P., Bowie, D., Furukawa, H., Menniti, F. S., Sobolevsky, A. I., Swanson, G. T., Swanger, S. A., Greger, I. H., Nakagawa, T., et al. (2021) · Pharmacological Reviews · doi:10.1124/pharmrev.120.000131 · Cited by 686
Lee, H.-K., Kameyama, K., Huganir, R. L., & Bear, M. F. (1998) · Neuron · doi:10.1016/s0896-6273(00)80632-7 · Cited by 668
Gally, J. A., Montague, P. R., Reeke, G. N., & Edelman, G. M. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.9.3547 · Cited by 645
Regulation of NMDA receptor subunit expression and its implications for LTD, LTP, and metaplasticity
Yashiro, K., & Philpot, B. D. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.07.046 · Cited by 649
Potentiation of synaptic transmission in the hippocampus by phorbol esters
Malenka, R. C., Madison, D. V., & Nicoll, R. A. (1986) · Nature · doi:10.1038/321175a0 · Cited by 633
Yuste, R., & Katz, L. C. (1991) · Neuron · doi:10.1016/0896-6273(91)90243-s · Cited by 591
Hebbian synapses in hippocampus.
Kelso, S. R., Ganong, A. H., & Brown, T. H. (1986) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.83.14.5326 · Cited by 555
Self-citationThe current excitement in long term potentiation
Nicoll, R. A., Kauer, J. A., & Malenka, R. C. (1988) · Neuron · doi:10.1016/0896-6273(88)90193-6 · Cited by 535
The Role of NMDA Receptors in Alzheimer’s Disease
Liu, J., Chang, L., Song, Y., Li, H., & Wu, Y. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00043 · Cited by 535
A Physiological Basis for a Theory of Synapse Modification
Bear, M. F., Cooper, L. N., & Ebner, F. F. (1987) · Science · doi:10.1126/science.3037696 · Cited by 528
Mayford, M., Wang, J., Kandel, E., & O'Dell, T. (1995) · Cell · doi:10.1016/0092-8674(95)90009-8 · Cited by 552
The CaM kinase II hypothesis for the storage of synaptic memory.
Lisman, J. (1994) · Trends in Neurosciences · doi:10.1016/0166-2236(94)90014-0 · Cited by 526
Mayford, M., Siegelbaum, S. A., & Kandel, E. R. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005751 · Cited by 500
A persistent postsynaptic modification mediates long-term potentiation in the hippocampus
Kauer, J. A., Malenka, R. C., & Nicoll, R. A. (1988) · Neuron · doi:10.1016/0896-6273(88)90148-1 · Cited by 497
Bear, M., Kleinschmidt, A., Gu, Q., & Singer, W. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-03-00909.1990 · Cited by 488
Activity-Dependent Changes in the Intrinsic Properties of Cultured Neurons
Turrigiano, G. G., Abbott, L. F., & Marder, E. E. (1994) · Science · doi:10.1126/science.8178157 · Cited by 484
Neurotrophins and Time: Different Roles for TrkB Signaling in Hippocampal Long-Term Potentiation
Kang, H., Welcher, A. A., Shelton, D., & Schuman, E. M. (1997) · Neuron · doi:10.1016/s0896-6273(00)80378-5 · Cited by 481
Dendritic spines as individual neuronal compartments for synaptic Ca2+ responses
Müller, W. S., & Connor, J. A. (1991) · Nature · doi:10.1038/354073a0 · Cited by 479
Induction of synaptic potentiation in hippocampus by patterned stimulation involves two events
Larson, J., & Lynch, G. (1986) · Science · doi:10.1126/science.3704635 · Cited by 597
Self-citationMyosin Vb mobilizes recycling endosomes and AMPA receptors for postsynaptic plasticity
Wang, Z., Edwards, J. G., Riley, N., Provance, D. W., Karcher, R., Li, X.-D., Davison, I. G., Ikebe, M., Mercer, J. A., Kauer, J. A., et al. (2008) · Cell · doi:10.1016/j.cell.2008.09.057 · Cited by 470
Cheng, B., & Mattson, M. P. (1991) · Neuron · doi:10.1016/0896-6273(91)90347-3 · Cited by 460
Inescapable versus escapable shock modulates long-term potentiation in the rat hippocampus
Shors, T. J., Seib, T. B., Levine, S., & Thompson, R. F. (1989) · Science · doi:10.1126/science.2704997 · Cited by 458
Spine Ca2+Signaling in Spike-Timing-Dependent Plasticity
Nevian, T., & Sakmann, B. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.1749-06.2006 · Cited by 458
Sacktor, T. C., Osten, P., Valsamis, H. A., Jiang, X., Naik, M. U., & Sublette, M. E. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.18.8342 · Cited by 450
Ca2+ Signaling Requirements for Long-Term Depression in the Hippocampus
Cummings, J., Mulkey, R. M., Nicoll, R. A., & Malenka, R. C. (1996) · Neuron · doi:10.1016/s0896-6273(00)80102-6 · Cited by 465
Tonic Activation of NMDA Receptors by Ambient Glutamate Enhances Excitability of Neurons
Sah, P., Hestrin, S., & Nicoll, R. A. (1989) · Science · doi:10.1126/science.2573153 · Cited by 443
Malgaroli, A., & Tsien, R. (1992) · Nature · doi:10.1038/357134a0 · Cited by 385
Long-Term Synaptic Potentiation
Brown, T. H., Chapman, P. F., Kairiss, E. W., & Keenan, C. L. (1988) · Science · doi:10.1126/science.2903551 · Cited by 418
Huang, Y.-Y., Li, X.-C., & Kandel, E. R. (1994) · Cell · doi:10.1016/0092-8674(94)90401-4 · Cited by 490
Frequency-dependent involvement of NMDA receptors in the hippocampus: a novel synaptic mechanism
Herron, C. E., Lester, R. A. J., Coan, E. J., & Collingridge, G. L. (1986) · Nature · doi:10.1038/322265a0 · Cited by 418
Egger, V., Feldmeyer, D., & Sakmann, B. J. (1999) · Nature Neuroscience · doi:10.1038/16026 · Cited by 411
Colbran, R. J., Schworer, C. M., Hashimoto, Y., Fong, Y. L., Rich, D. P., Smith, M. K., & Soderling, T. R. (1989) · Biochemical Journal · doi:10.1042/bj2580313 · Cited by 406
Glutamate: its role in learning, memory, and the aging brain
McEntee, W. J., & Crook, T. H. (1993) · Psychopharmacology · doi:10.1007/bf02253527 · Cited by 414
Physiological mechanisms underlying long-term potentiation
Gustafsson, B., & Wigström, H. (1988) · Trends in Neurosciences · doi:10.1016/0166-2236(88)90142-7 · Cited by 398
The BCM theory of synapse modification at 30: interaction of theory with experiment
Cooper, L. N., & Bear, M. F. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3353 · Cited by 395
The spread of Na+ spikes determines the pattern of dendritic Ca2+ entry into hippocampal neurons
Jaffe, D. B., Johnston, D., Lasser‐Ross, N., Lisman, J. E., Miyakawa, H., & Ross, W. N. (1992) · Nature · doi:10.1038/357244a0 · Cited by 396
Calcium-Mediated Reduction of Ionic Currents: A Biophysical Memory Trace
Alkon, D. L. (1984) · Science · doi:10.1126/science.6093258 · Cited by 393
Calcium and the aging nervous system
Gibson, G. E., & Peterson, C. (1987) · Neurobiology of Aging · doi:10.1016/0197-4580(87)90072-8 · Cited by 387
Learning to Modulate Transmitter Release: Themes and Variations in Synaptic Plasticity
Hawkins, R. D., Kandel, E. R., & Siegelbaum, S. A. (1993) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.16.030193.003205 · Cited by 385
From form to function: calcium compartmentalization in dendritic spines
Yuste, R., Majewska, A. K., & Holthoff, K. (2000) · Nature Neuroscience · doi:10.1038/76609 · Cited by 378
The comparative psychology of intelligence
Macphail, E. M. (1987) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00054984 · Cited by 372
Glioma synapses recruit mechanisms of adaptive plasticity
Taylor, K. R., Barron, T., Hui, A., Spitzer, A., Yalçın, B., Ivec, A. E., Geraghty, A. C., Hartmann, G. G., Arzt, M., Gillespie, S. M., et al. (2023) · Nature · doi:10.1038/s41586-023-06678-1 · Cited by 378
Calcium signaling in neurodegeneration
Marambaud, P., Dreses‐Werringloer, U., & Vingtdeux, V. (2009) · Molecular Neurodegeneration · doi:10.1186/1750-1326-4-20 · Cited by 363
Siman, R. G., Noszek, J. C., & Kegerise, C. (1989) · Journal of Neuroscience · doi:10.1523/jneurosci.09-05-01579.1989 · Cited by 352
Ca2+ signaling in dendritic spines
Sabatini, B. L., Maravall, M., & Svoboda, K. (2001) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00218-x · Cited by 359
Locally Distributed Synaptic Potentiation in the Hippocampus
Schuman, E. M., & Madison, D. V. (1994) · Science · doi:10.1126/science.8290963 · Cited by 352
Protein kinase C modulation of NMDA currents: an important link for LTP induction.
Ben-Ari, Y., Aniksztejn, L., & Bregestovski, P. (1992) · Trends in Neurosciences · doi:10.1016/0166-2236(92)90049-e · Cited by 348
A Spatial-Temporal Model of Cell Activation
Alkon, D. L., & Rasmussen, H. (1988) · Science · doi:10.1126/science.2830669 · Cited by 342
NMDA application potentiates synaptic transmission in the hippocampus
Kauer, J. A., Malenka, R. C., & Nicoll, R. A. (1988) · Nature · doi:10.1038/334250a0 · Cited by 423
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
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
Long-term potentiation and long-term depression: a clinical perspective
Bliss, T. V. P., & Cooke, S. F. (2011) · Clinics · doi:10.1590/s1807-59322011001300002 · Cited by 333
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 and long-term depression in the neocortex.
Tsumoto, T. (1992) · Progress in neurobiology · doi:10.1016/0301-0082(92)90011-3 · Cited by 283
Calcium regulation of gene expression in neuronal cells
Ghosh, A., Ginty, D. D., Bading, H., & Greenberg, M. E. (1994) · Journal of Neurobiology · doi:10.1002/neu.480250309 · Cited by 326
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
Malinow, R., & Miller, J. P. (1986) · Nature · doi:10.1038/320529a0 · Cited by 323
Long-term potentiation: What's learning got to do with it?
Shors, T. J., & Matzel, L. D. (1997) · Behavioral and Brain Sciences · doi:10.1017/s0140525x97001593 · Cited by 320
Molecular machines integrate coincident synaptic signals
Bourne, H. R., & Nicoll, R. A. (1993) · Cell · doi:10.1016/s0092-8674(05)80029-7 · Cited by 311
Beckhauser, T. F., Francis-Oliveira, J., & De Pasquale, R. (2016) · Journal of Experimental Neuroscience · doi:10.4137/jen.s39887 · Cited by 301
Arancio, O., Kandel, E. R., & Hawkins, R. D. (1995) · Nature · doi:10.1038/376074a0 · Cited by 301
Stable depression of potentiated synaptic responses in the hippocampus with 1–5 Hz stimulation
Staubli, U. V., & LYNCH, G. S. (1990) · Brain Research · doi:10.1016/0006-8993(90)91096-y · Cited by 308
Self-citationSignaling from cAMP/PKA to MAPK and Synaptic Plasticity
Waltereit, R., & Weller, M. (2003) · Molecular Neurobiology · doi:10.1385/mn:27:1:99 · Cited by 303
Sustained Dendritic Gradients of Ca 2+ Induced by Excitatory Amino Acids in CA1 Hippocampal Neurons
Connor, J. A., Wadman, W. J., Hockberger, P. E., & Wong, R. K. S. (1988) · Science · doi:10.1126/science.2452481 · Cited by 299
Metadata
- Authors
- Lynch, G., Larson, J., Kelso, S., Barrionuevo, G., & Schottler, F.
- Affiliations
- University of California, Irvine (US)
- ORCID
- Lynch, Gary
- Venue
- Nature
- Published
- 1983-10
- Volume
- 305
- Issue
- 5936
- Pages
- 719-721
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2031739172
- Cited by
- 1,116
- References
- 16
- Citations by year
- 2026: 6 · 2025: 9 · 2024: 11 · 2023: 7 · 2022: 10 · 2021: 9 · 2020: 9 · 2019: 25 · 2018: 18 · 2017: 14 · 2016: 16 · 2015: 19 · 2014: 17 · 2013: 19 · 2012: 28
- FWCI
- 6.65
- 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, EGTA, calcium chelation, intracellular injection, free calcium, synaptic plasticity, memory substrate, high-frequency stimulation
- MeSH terms
- Animals, Calcium, Egtazic Acid, Electric Stimulation, Ethylene Glycols, Evoked Potentials, Hippocampus, Membrane Potentials, Time Factors, Rats
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