Long-Term Potentiation--A Decade of Progress?

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

Long‐lasting potentiation of synaptic transmission in the dentate area of the unanaesthetized rabbit following stimulation of the perforant path

Bliss, T. V. P., & Gardner-Medwin, A. R. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010274 · Cited by 7,424

Synaptic Activity and the Construction of Cortical Circuits

Katz, L. C., & Shatz, C. J. (1996) · Science · doi:10.1126/science.274.5290.1133 · Cited by 3,048

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

Developmental mechanisms that generate precise patterns of neuronal connectivity

Goodman, C. S., & Shatz, C. J. (1993) · Cell · doi:10.1016/s0092-8674(05)80030-3 · Cited by 1,425

Dendritic spine changes associated with hippocampal long-term synaptic plasticity

Engert, F., & Bonhoeffer, T. (1999) · Nature · doi:10.1038/19978 · Cited by 1,412

Activation of postsynaptically silent synapses during pairing-induced LTP in CA1 region of hippocampal slice

Liao, D., Hessler, N. A., & Malinow, R. (1995) · Nature · doi:10.1038/375400a0 · Cited by 1,365

Synaptic plasticity: LTP and LTD

Bear, M. F., & Malenka, R. C. (1994) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(94)90101-5 · Cited by 1,355

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

Rapid Spine Delivery and Redistribution of AMPA Receptors After Synaptic NMDA Receptor Activation

Shi, S.-H., Hayashi, Y., Petralia, R. S., Zaman, S. H., Wenthold, R. J., Svoboda, K., & Malinow, R. (1999) · Science · doi:10.1126/science.284.5421.1811 · Cited by 1,276

Uncoupling the D1-N-Methyl-D-Aspartate (NMDA) Receptor Complex Promotes NMDA-Dependent Long-Term Potentiation and Working Memory

Nai, Q., Li, S., Wang, S., Liu, J., Lee, F. J. S., Frankland, P. W., & Liu, F. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.08.011 · Cited by 88

Chelators for investigating zinc metalloneurochemistry

Radford, R. J., & Lippard, S. J. (2013) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2013.01.009 · Cited by 91

Plasticity in Excitatory Amino Acid Receptor-Mediated Descending Pain Modulation after Inflammation

Guan, Y., Terayama, R., Dubner, R. A., & Ren, K. (2002) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.300.2.513 · Cited by 91

Neuromodulation of delay discounting, the reflection effect, and cigarette consumption

Sheffer, C. E., Mennemeier, M., Landes, R. D., Bickel, W. K., Brackman, S. L., Dornhoffer, J. L., Kimbrell, T. A., & Brown, G. J. (2013) · Journal of Substance Abuse Treatment · doi:10.1016/j.jsat.2013.01.012 · Cited by 96

Spike-Timing-Dependent Plasticity: The Relationship to Rate-Based Learning for Models with Weight Dynamics Determined by a Stable Fixed Point

Burkitt, A. N., Hamish Meffin, A., & Grayden, D. B. (2004) · Neural Computation · doi:10.1162/089976604773135041 · Cited by 91

Fetal iron deficiency induces chromatin remodeling at the Bdnf locus in adult rat hippocampus

Tran, P. V., Kennedy, B. C., Lien, Y., Simmons, R. A., & Georgieff, M. (2014) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00429.2014 · Cited by 90

Corticostriatal plasticity: life after the depression

Mahon, S., Deniau, J., & Charpier, S. (2004) · Trends in Neurosciences · doi:10.1016/j.tins.2004.06.010 · Cited by 90

A mechanism for learning with sleep spindles

Peyrache, A., & Seibt, J. (2020) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2019.0230 · Cited by 89

Methylphenidate facilitates learning-induced amygdala plasticity

Tye, K. M., Tye, L. D., Cone, J. J., Hekkelman, E. F., Janak, P. H., & Bonci, A. (2010) · Nature Neuroscience · doi:10.1038/nn.2506 · Cited by 89

The AMPA receptor-associated protein Shisa7 regulates hippocampal synaptic function and contextual memory

Schmitz, L. J. M., Klaassen, R. V., Ruiperez‐Alonso, M., Zamri, A. E., Stroeder, J., Rao‐Ruiz, P., Lodder, J. C., van der Loo, R. J., Mansvelder, H. D., Smit, A. B., et al. (2017) · eLife · doi:10.7554/elife.24192 · Cited by 88

Heterosynaptic Plasticity Determines the Set Point for Cortical Excitatory-Inhibitory Balance

Field, R. E., D’amour, J. A., Tremblay, R., Miehl, C., Rudy, B., Gjorgjieva, J., & Froemke, R. C. (2020) · Neuron · doi:10.1016/j.neuron.2020.03.002 · Cited by 91

GABAergic interneuronal loss and reduced inhibitory synaptic transmission in the hippocampal CA1 region after mild traumatic brain injury

Almeida-Suhett, C. P., Prager, E., Pidoplichko, V. I., Figueiredo, T. H., Marini, A., Li, Z., Eiden, L., & Braga, M. F. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.07.028 · Cited by 78

D-Serine differently modulates NMDA receptor function in rat CA1 hippocampal pyramidal cells and interneurons

Martina, M., Krasteniakov, N. V., & Bergeron, R. (2003) · The Journal of Physiology · doi:10.1111/j.1469-7793.2003.00411.x · Cited by 89

Mechanisms of Hippocampal Long-Term Depression Are Required for Memory Enhancement by Novelty Exploration

Dong, Z., Gong, B., Li, H., Bai, Y., Wu, X., Huang, Y. Y., He, W., Li, T., & Wang, Y. T. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0984-12.2012 · Cited by 89

Kainate-induced seizures alter protein composition and N-methyl-d-aspartate receptor function of rat forebrain postsynaptic densities

Wyneken, Ú., Smalla, K., Marengo, J., Soto, D., de la Cerda, A., Tischmeyer, W., Grimm, R., Boeckers, T. M., Wolf, G. L., Orrego, F., et al. (2001) · Neuroscience · doi:10.1016/s0306-4522(00)00469-3 · Cited by 88

Bidirectional Modification of Presynaptic Neuronal Excitability Accompanying Spike Timing-Dependent Synaptic Plasticity

Li, C., Lu, J., Wu, C.-P., Duan, S., & Poo, M. (2004) · Neuron · doi:10.1016/s0896-6273(03)00847-x · Cited by 89

Anatomical Parameters of tDCS to Modulate the Motor System after Stroke: A Review

Lefebvre, S., & Liew, S. (2017) · Frontiers in Neurology · doi:10.3389/fneur.2017.00029 · Cited by 95

Endocannabinoids restrict hippocampal long-term potentiation via CB1

Slanina, K. A., Roberto, M., & Schweitzer, P. (2005) · Neuropharmacology · doi:10.1016/j.neuropharm.2005.04.021 · Cited by 89

Rapid and reversible changes in dendrite morphology and synaptic efficacy following NMDA receptor activation: implication for a cellular defense against excitotoxicity

Ikegaya, Y., Kim, J.-A., Baba, M., Iwatsubo, T., Nishiyama, N., & Matsuki, N. (2001) · Journal of Cell Science · doi:10.1242/jcs.114.22.4083 · Cited by 88

Metabotropic and ionotropic glutamate receptors as neurobiological targets in anxiety and stress-related disorders: Focus on pharmacology and preclinical translational models

Harvey, B. H., & Shahid, M. (2011) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2011.06.014 · Cited by 90

Genetic dissection of the down syndrome critical region

Jiang, X., Liu, C., Yu, T., Zhang, L., Meng, K., Xing, Z., Belichenko, P. V., Kleschevnikov, A. M., Pao, A., Peresie, J., et al. (2015) · Human Molecular Genetics · doi:10.1093/hmg/ddv364 · Cited by 88

Investigation of protective effects of coenzyme Q10 on impaired synaptic plasticity in a male rat model of Alzheimer’s disease

Komaki, H., Faraji, N., Komaki‬, A., Shahidi, ‬., Etaee, F., Raoufi, S., & Mirzaei, F. (2019) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2019.01.025 · Cited by 91

Block of NMDA and non-NMDA receptor activation results in reduced background and evoked activity of central amygdala neurons in a model of arthritic pain

Li, W., & Neugebauer, V. (2004) · Pain · doi:10.1016/j.pain.2004.03.015 · Cited by 88

Spinal cord stimulation inhibits long-term potentiation of spinal wide dynamic range neurons

Wallin, J., Fiskå, A., Tjølsen, A., Linderoth, B., & Hole, K. (2003) · Brain Research · doi:10.1016/s0006-8993(03)02530-7 · Cited by 88

The role of mammalian ionotropic receptors in synaptic plasticity: LTP, LTD and epilepsy

Kullmann, D. M., Asztély, F., & Walker, M. C. (2000) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000640 · Cited by 90

BAI1 regulates spatial learning and synaptic plasticity in the hippocampus

Zhu, D., Li, C., Swanson, A. M., Villalba, R. M., Guo, J., Zhang, Z., Matheny, S. L., Murakami, T., Stephenson, J. R., Daniel, S. M., et al. (2015) · Journal of Clinical Investigation · doi:10.1172/jci74603 · Cited by 89

Function of the hippocampus in memory formation: desperately seeking resolution

Riedel, G., & Micheau, J. (2001) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/s0278-5846(01)00153-1 · Cited by 91

Molecular mechanisms of neurotransmitter release

Fon, E. A., & Edwards, R. H. (2001) · Muscle & Nerve · doi:10.1002/mus.1044 · Cited by 89

Mechanism of SNARE protein binding and regulation of Cav2 channels by phosphorylation of the synaptic protein interaction site

Yokoyama, C. T., Myers, S. J., Fu, J., Mockus, S. M., Scheuer, T., & Catterall, W. A. (2004) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2004.08.019 · Cited by 87

Cellular and synaptic reorganization of arcuate NPY/AgRP and POMC neurons after exercise

He, Z., Gao, Y., Alhadeff, A. L., Castorena, C. M., Huang, Y., Lieu, L., Afrin, S., Sun, J. M., Betley, J. N., Guo, H., et al. (2018) · Molecular Metabolism · doi:10.1016/j.molmet.2018.08.011 · Cited by 84

Non-Associative Learning and Serotonin Induce Similar Bi-Directional Changes in Excitability of a Neuron Critical for Learning in the Medicinal Leech

Burrell, B. D., Sahley, C. L., & Muller, K. J. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-04-01401.2001 · Cited by 87

AMPA Receptors Unbound

Turrigiano, G. G. (2000) · Neuron · doi:10.1016/s0896-6273(00)81131-9 · Cited by 87

Dissecting the role of redox signaling in neuronal development

Bórquez, D. A., Urrutia, P. J., Wilson, C., van Zundert, B., Núñez, M. T., & González-Billault, C. E. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13581 · Cited by 86

Recent Advances on Neuromorphic Systems Using Phase-Change Materials

Wang, L., Lu, S.-R., & Wen, J. (2017) · Nanoscale Research Letters · doi:10.1186/s11671-017-2114-9 · Cited by 91

Neuroligin-1 Signaling Controls LTP and NMDA Receptors by Distinct Molecular Pathways

Wu, X., Morishita, W., Riley, A. M., Hale, W. D., Südhof, T. C., & Malenka, R. C. (2019) · Neuron · doi:10.1016/j.neuron.2019.02.013 · Cited by 89

Midbrain dopaminergic innervation of the hippocampus is sufficient to modulate formation of aversive memories

Tsetsenis, T., Badyna, J. K., Wilson, J., Zhang, X., Krizman, E. N., Subramaniyan, M., Yang, K., THOMAS, S. A., & Dani, J. A. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2111069118 · Cited by 84

Nobiletin, a citrus flavonoid with neurotrophic action, augments protein kinase A-mediated phosphorylation of the AMPA receptor subunit, GluR1, and the postsynaptic receptor response to glutamate in murine hippocampus

Matsuzaki, K., Miyazaki, K.-I., Sakai, S., Yawo, H., Nakata, N., Moriguchi, S., Fukunaga, K., Yokosuka, A., Sashida, Y., Mimaki, Y., et al. (2007) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2007.09.028 · Cited by 87

Synapse Geometry and Receptor Dynamics Modulate Synaptic Strength

Freche, D., Pannasch, U., Rouach, N., & Holcman, D. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025122 · Cited by 93

The neurobiology of opiate tolerance, dependence and sensitization: Mechanisms of NMDA receptor-dependent synaptic plasticity

Trujillo, K. A. (2002) · Neurotoxicity Research · doi:10.1080/10298420290023954 · Cited by 86

Repetitive Hypoglycemia in Young Rats Impairs Hippocampal Long-Term Potentiation

Yamada, K. A., Rensing, N. R., Izumi, Y., de Erausquin, G. A., Gazit, V. A., Dorsey, D. A., & Herrera, D. G. (2003) · Pediatric Research · doi:10.1203/01.pdr.0000110523.07240.c1 · Cited by 86

Novel bioactive bromopyrrole alkaloids from the Mediterranean sponge Axinella verrucosa

Aiello, A., D’Esposito, M., Fattorusso, E., Menna, M., Müller, W. E. G., Perović‐Ottstadt, S., & Schröder, H. C. (2005) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2005.07.057 · Cited by 86

Constitutive cycling: A general mechanism to regulate cell surface proteins

Royle, S., & Murrell‐Lagnado, R. D. (2002) · BioEssays · doi:10.1002/bies.10200 · Cited by 86

Mechanisms and the Current State of Transcranial Magnetic Stimulation

George, M. S., Nahas, Z. H., Kozel, F. A., Li, X., Yamanaka, K., Mishory, A., & Bohning, D. E. (2003) · CNS Spectrums · doi:10.1017/s1092852900018976 · Cited by 86

Spatiotemporal specificity of synaptic plasticity: cellular rules and mechanisms

Bi, G. (2002) · Biological cybernetics · doi:10.1007/s00422-002-0349-7 · Cited by 102

Biophysical Model of AMPA Receptor Trafficking and Its Regulation during Long-Term Potentiation/Long-Term Depression

Earnshaw, B. A., & Bressloff, P. C. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3601-06.2006 · Cited by 86

Ribosomal S6 kinase 2 interacts with and phosphorylates PDZ domain-containing proteins and regulates AMPA receptor transmission

Thomas, G. M., Rumbaugh, G., Harrar, D. B., & Huganir, R. L. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0507476102 · Cited by 85

Morphine and Heroin Differentially Modulate In Vivo Hippocampal LTP in Opiate-Dependent Rat

Bao, G., Kang, L., Li, H., Li, Y., Pu, L., Xia, P., Ma, L., & Pei, G. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301308 · Cited by 85

Chronic Cocaine Enhances Corticotropin-Releasing Factor-Dependent Potentiation of Excitatory Transmission in Ventral Tegmental Area Dopamine Neurons

Hahn, J., Hopf, F. W., & Bonci, A. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4773-08.2009 · Cited by 83

Amygdala, Long-term Potentiation, and Fear Conditioning

Dityatev, A. E., & Bolshakov, V. Y. (2005) · The Neuroscientist · doi:10.1177/1073858404270857 · Cited by 85

System A Transporter SAT2 Mediates Replenishment of Dendritic Glutamate Pools Controlling Retrograde Signaling by Glutamate

Jenstad, M., Quazi, A. Z., Zilberter, M. Y., Haglerød, C., Berghuis, P., Saddique, N., Goiny, M., Buntup, D., Davanger, S., Haug, F. Š., et al. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhn151 · Cited by 86

Autoinactivation of Neuronal AMPA Receptors via Glutamate-Regulated TARP Interaction

Morimoto‐Tomita, M., Zhang, W., Straub, C., Cho, C.-H., Kim, K. S., Howe, J. R., & Tomita, S. (2009) · Neuron · doi:10.1016/j.neuron.2008.11.009 · Cited by 86

Serotonin facilitates long‐term depression induction in prefrontal cortex via p38 MAPK/Rab5‐mediated enhancement of AMPA receptor internalization

Zhong, P., Liu, W., Gu, Z., & Yan, Z. (2008) · The Journal of Physiology · doi:10.1113/jphysiol.2008.155143 · Cited by 83

Nicotine gates long‐term potentiation in the hippocampal CA1 region via the activation of α2* nicotinic ACh receptors

Nakauchi, S., Brennan, R. J., Boulter, J., & Sumikawa, K. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05513.x · Cited by 84

Spinal cord injury, dendritic spine remodeling, and spinal memory mechanisms

Tan, A. M., & Waxman, S. G. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.08.026 · Cited by 83

At Immature Mossy-Fiber–CA3 Synapses, Correlated Presynaptic and Postsynaptic Activity Persistently Enhances GABA Release and Network Excitability via BDNF and cAMP-Dependent PKA

Sivakumaran, S., Mohajerani, M. H., & Cherubini, E. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5019-08.2009 · Cited by 84

GluA2-dependent AMPA receptor endocytosis and the decay of early and late long-term potentiation: possible mechanisms for forgetting of short- and long-term memories

Hardt, O. M., Nader, K., & Wang, Y.-T. (2013) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2013.0141 · Cited by 89

Enhancement of AMPA currents and GluR1 membrane expression through PKA‐coupled adenosine A2Areceptors

Dias, R. B., Ribeiro, J. A., & Sebastião, A. M. (2010) · Hippocampus · doi:10.1002/hipo.20894 · Cited by 84

Sensory Ecology of Predator-Induced Phenotypic Plasticity

Weiss, L. C. (2019) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00330 · Cited by 83

Novel Form of Long-Term Synaptic Depression in Rat Hippocampus Induced By Activation of α1 Adrenergic Receptors

Scheiderer, C. L., Dobrunz, L. E., & McMahon, L. L. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00420.2003 · Cited by 84

Interaction of the Tyrosine Kinase Pyk2 with the N-Methyl-d-aspartate Receptor Complex via the Src Homology 3 Domains of PSD-95 and SAP102

Seabold, G. K., Burette, A., Lim, I. A., Weinberg, R. J., & Hell, J. W. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m212825200 · Cited by 83

A Deconvolution-Based Method with High Sensitivity and Temporal Resolution for Detection of Spontaneous Synaptic Currents In Vitro and In Vivo

Pernía‐Andrade, A. J., Goswami, S. P., Stickler, Y., Fröbe, U., Schlögl, A., & Jónás, P. (2012) · Biophysical Journal · doi:10.1016/j.bpj.2012.08.039 · Cited by 83

Low frequency repetitive transcranial magnetic stimulation of the left dorsolateral prefrontal cortex transiently increases cue-induced craving for methamphetamine: A preliminary study

Li, X., Malcolm, R. J., Huebner, K., Hanlon, C. A., Taylor, J. J., Brady, K. T., George, M. S., & See, R. E. (2013) · Drug and Alcohol Dependence · doi:10.1016/j.drugalcdep.2013.08.012 · Cited by 85

Modulation of Synaptic Plasticity in the Cortex Needs to Understand All the Players

Meunier, C. N. J., Chameau, P. J. P., & Fossier, P. (2017) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2017.00002 · Cited by 86

Increased d-aspartate brain content rescues hippocampal age-related synaptic plasticity deterioration of mice

Errico, F., Nisticò, R., Napolitano, F., Mazzola, C., Astone, D., Pisapia, T., Giustizieri, M., D’Aniello, A., Mercuri, N. B., & Usiello, A. (2010) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2010.01.002 · Cited by 84

Neurosteroids in learning and memory processes

Vallée, M., Mayo, W., Koob, G. F., & Moal, M. L. (2001) · International review of neurobiology · doi:10.1016/s0074-7742(01)46066-1 · Cited by 87

Biophysical model of synaptic plasticity dynamics

Abarbanel, H. D. I., Gibb, L., Huerta, R., & Rabinovich, M. I. (2003) · Biological Cybernetics · doi:10.1007/s00422-003-0422-x · Cited by 81

Beyond Risk Factors: An Analytical Approach to Crime Prevention

Wikström, P. H., & Treiber, K. (2016) · Springer eBooks · doi:10.1007/978-3-319-44124-5_8 · Cited by 82

State-Dependent Partial Occlusion of Cortical LTP-Like Plasticity in Major Depression

Kühn, M., Mainberger, F., Feige, B., Maier, J. G., Mall, V., Jung, N. H., Reis, J., Klöppel, S., Normann, C., & Nissen, C. (2015) · Neuropsychopharmacology · doi:10.1038/npp.2015.310 · Cited by 86

Inhibition of nuclear factor κB is associated with neuroprotective effects of glycyrrhizic acid on glutamate-induced excitotoxicity in primary neurons

Cherng, J., Lin, H. J., Hung, M.-S., Lin, Y.-R., Chan, M., & Lin, J. (2006) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2006.06.080 · Cited by 84

Age-related effects of Ginkgo biloba extract on synaptic plasticity and excitability

Williams, B., Watanabe, C. M. H., Schultz, P. G., Rimbach, G. H., & Krucker, T. (2004) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2003.10.008 · Cited by 83

AMPAR trafficking in synapse maturation and plasticity

Bassani, S., Folci, A., Zapata, J., & Passafaro, M. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1309-1 · Cited by 86

Regulation of NMDA Receptor Activity by F-Actin and Myosin Light Chain Kinase

Lei, S., Czerwinska, E., Czerwinski, W., Walsh, M. P., & MacDonald, J. F. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-21-08464.2001 · Cited by 85

Cellular and network properties in the functioning of the nervous system: from central pattern generators to cognition

Arshavsky, Y. I. (2003) · Brain Research Reviews · doi:10.1016/s0165-0173(02)00249-7 · Cited by 84

Optical Quantal Analysis Indicates That Long-Term Potentiation at Single Hippocampal Mossy Fiber Synapses Is Expressed through Increased Release Probability, Recruitment of New Release Sites, and Activation of Silent Synapses

Reid, C. A., Dixon, D. B., Takahashi, M., Bliss, T., & Fine, A. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3567-03.2004 · Cited by 82

Synaptic transmission changes in the pyramidal cells of the hippocampus in streptozotocin-induced diabetes mellitus in rats

Kamal, A., Biessels, G. J., Gispen, W. H., & Ramakers, G. M. J. (2006) · Brain Research · doi:10.1016/j.brainres.2005.12.070 · Cited by 81

On the cause of mental retardation in Down syndrome: extrapolation from full and segmental trisomy 16 mouse models

Galdzicki, Z., Siarey, R. J., Pearce, R., Stoll, J., & Rapoport, S. I. (2001) · Brain Research Reviews · doi:10.1016/s0926-6410(00)00074-4 · Cited by 84

Recurrently connected silicon neurons with active dendrites for one-shot learning

Arthur, J. V., & Boahen, K. A. (2005) · International Joint Conference on Neural Networks (IJCNN) · doi:10.1109/ijcnn.2004.1380858 · Cited by 80

Density‐dependent changes of the pore properties of the P2X2 receptor channel

Fujiwara, Y., & Kubo, Y. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.064568 · Cited by 81

Altered Mitochondrial Dynamics in Motor Neuron Disease: An Emerging Perspective

Kodavati, M. M., Wang, H., & Hegde, M. L. (2020) · Cells · doi:10.3390/cells9041065 · Cited by 87

The Group I Metabotropic Glutamate Receptor Agonist (S)-3,5-Dihydroxyphenylglycine Induces a Novel Form of Depotentiation in the CA1 Region of the Hippocampus

Zho, W.-M., You, J.-L., Huang, C., & Hsu, K. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-20-08838.2002 · Cited by 81

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

Neurochemical mechanisms for memory processing during sleep: basic findings in humans and neuropsychiatric implications

Feld, G. B., & Jan Born, A. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0490-9 · Cited by 84

Novel Approach to the Role of NMDA Receptors in Traumatic Brain Injury

Shohami, E., & Biegon, A. R. (2014) · CNS & Neurological Disorders - Drug Targets · doi:10.2174/18715273113126660196 · Cited by 80

Remodelling by early-life stress of NMDA receptor-dependent synaptic plasticity in a gene–environment rat model of depression

Ryan, B. K., Musazzi, L., Mallei, A., Tardito, D., Gruber, S. H. M., Khoury, A. E., Anwyl, R., Racagni, G., Mathé, A. A., Rowan, M. J., et al. (2008) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145708009607 · Cited by 81

A comparison of molecular alterations in environmental and genetic rat models of ADHD: A pilot study

DasBanerjee, T., Middleton, F. A., Berger, D. F., Lombardo, J. P., Sagvolden, T., & Faraone, S. V. (2008) · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · doi:10.1002/ajmg.b.30877 · Cited by 81

Physiological Dissociation in Hippocampal Subregions in Response to Amygdala Stimulation

Vouimba, R., & Richter‐Levin, G. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhi058 · Cited by 80

Synaptic Plasticity and NO-cGMP-PKG Signaling Regulate Pre- and Postsynaptic Alterations at Rat Lateral Amygdala Synapses Following Fear Conditioning

Ota, K. T., Monsey, M. S., Wu, M. S., & Schafe, G. E. (2010) · PLoS ONE · doi:10.1371/journal.pone.0011236 · Cited by 79

Synaptically Driven Calcium Transients via Nicotinic Receptors on Somatic Spines

Shoop, R. D., Chang, K. T., Ellisman, M. H., & Berg, D. K. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-03-00771.2001 · Cited by 80

TNFα-induced AMPA-receptor trafficking in CNS neurons; relevance to excitotoxicity?

Leonoudakis, D., Braithwaite, S. P., Beattie, M. S., & Beattie, E. C. (2004) · Neuron Glia Biology · doi:10.1017/s1740925x05000608 · Cited by 78

Novel modulatory mechanisms revealed by the sustained application of nicotine in the guinea‐pig hippocampus in vitro

Mann, E. O., & Greenfield, S. A. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.045492 · Cited by 79

Multiple, Developmentally Regulated Expression Mechanisms of Long-Term Potentiation at CA1 Synapses

Palmer, M. J., Isaac, J. T. R., & Collingridge, G. L. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.0170-04.2004 · Cited by 79

Endocannabinoids and food consumption: comparisons with benzodiazepine and opioid palatability-dependent appetite

Cooper, S. J. (2004) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2004.07.009 · Cited by 78

DendritesPreprint

Jan, Y. N., & Jan, L. Y. (2001) · Genes & Development · doi:10.1101/gad.916501 · Cited by 82

Channel-mediated astrocytic glutamate modulates hippocampal synaptic plasticity by activating postsynaptic NMDA receptors

Park, H., Han, K.-S., Seo, J., Lee, J., Dravid, S. M., Woo, J., Chun, H., Cho, S., Bae, J. Y., An, H., et al. (2015) · Molecular Brain · doi:10.1186/s13041-015-0097-y · Cited by 79

Dendritic signals from rat hippocampal CA1 pyramidal neurons during coincident pre‐ and post‐synaptic activity: a combined voltage‐ and calcium‐imaging study

Canepari, M., Djurisic, M. R., & Zečević, D. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2006.125005 · Cited by 78

Chronic intermittent ethanol exposure enhances NMDA-receptor-mediated synaptic responses and NMDA receptor expression in hippocampal CA1 region

Nelson, T. E., Ur, C. L., & Gruol, D. L. (2005) · Brain Research · doi:10.1016/j.brainres.2005.04.041 · Cited by 78

Increased hippocampal glycine uptake and cognitive dysfunction after peripheral nerve injury

Kodama, D., Ono, H., & Tanabe, M. (2011) · Pain · doi:10.1016/j.pain.2010.12.029 · Cited by 78

IRS-2 Deficiency Impairs NMDA Receptor-Dependent Long-term Potentiation

Martín, E. D., Sánchez‐Pérez, A. M., Trejo, J. L., Martin-Aldana, J. A., Cano‐Jaimez, M., Pons, S., Umanzor, C. A., Menes, L., White, M. F., & Burks, D. J. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr216 · Cited by 80

A CalDAG-GEFI/Rap1/B-Raf Cassette Couples M1Muscarinic Acetylcholine Receptors to the Activation of ERK1/2

Guo, F.-F., Kumahara, E., & Saffen, D. W. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m101277200 · Cited by 78

Acute EPA-induced learning and memory impairment in mice is prevented by DHA

Liu, J.-H., Wang, Q., You, Q.-L., Li, Z.-L., Hu, N.-Y., Wang, Y., Jin, Z.-L., Li, S.-J., Li, X.-W., Yang, J.-M., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-19255-1 · Cited by 77

Long-Term PotentiationÑA Decade of Progress?

Malenka, R. C., & Nicoll, R. A. (2015)

S CIENCE ’ S C OMPASS ● REVIEW REVIEW: NEUROSCIENCE Long-Term Potentiation—A Decade of Progress?

Malenka, R. C., & Nicoll, R. A. (2010)

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

Long-Term Potentiation

Ioannou, A., & Anastassiou‐Hadjicharalambous, X. (2018) · Springer eBooks · doi:10.1007/978-3-319-16999-6_1033-1 · Cited by 1

Long-term potentiation in the hippocampus: discovery, mechanisms and function

Bliss, T., Collingridge, G. L., Morris, R., & Reymann, K. G. (2018) · e-Neuroforum · doi:10.1515/nf-2017-a059 · Cited by 122