Long-Term Potentiation--A Decade of Progress?

A synaptic model of memory: long-term potentiation in the hippocampus

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

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Synaptic Activity and the Construction of Cortical Circuits

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Deficient Hippocampal Long-Term Potentiation in α-Calcium-Calmodulin Kinase II Mutant Mice

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Developmental mechanisms that generate precise patterns of neuronal connectivity

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Dendritic spine changes associated with hippocampal long-term synaptic plasticity

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

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Synaptic plasticity: LTP and LTD

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Inhibition of Postsynaptic PKC or CaMKII Blocks Induction But Not Expression of LTP

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

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Developmental Profile of the Changing Properties of NMDA Receptors at Cerebellar Mossy Fiber–Granule Cell Synapses

Cathala, L., Misra, C., & Cull-Candy, S. G. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-16-05899.2000 · Cited by 162

Targeting Fyn Kinase in Alzheimer’s Disease

Nygaard, H. B. (2018) · Biological Psychiatry · doi:10.1016/j.biopsych.2017.06.004 · Cited by 162

Brain Effects of TMS Delivered Over Prefrontal Cortex in Depressed Adults

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Antistress Effect of TRPV1 Channel on Synaptic Plasticity and Spatial Memory

Li, H.-B., Mao, R., Zhang, J., Yang, Y., Cao, J., & Xu, L. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.02.020 · Cited by 165

NMDA receptors inhibit synapse unsilencing during brain development

Adesnik, H., Li, G., During, M. J., Pleasure, S. J., & Nicoll, R. A. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0800946105 · Cited by 164

Clinically Significant Drug Interactions with Newer Antidepressants

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Retrograde Control of Synaptic Transmission by Postsynaptic CaMKII at the Drosophila Neuromuscular Junction

Haghighi, A. P., McCabe, B. D., Fetter, R. D., Palmer, J. E., Hom, S., & Goodman, C. S. (2003) · Neuron · doi:10.1016/s0896-6273(03)00427-6 · Cited by 160

CaMKII "Autonomy" Is Required for Initiating But Not for Maintaining Neuronal Long-Term Information Storage

Buard, I., Coultrap, S. J., Freund, R. K., Lee, Y.-S., Dell'Acqua, M. L., Silva, A. J., & Bayer, K. U. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1469-10.2010 · Cited by 160

Expression of Long-Term Plasticity at Individual Synapses in Hippocampus Is Graded, Bidirectional, and Mainly Presynaptic: Optical Quantal Analysis

Enoki, R., Hu, Y.-L., Hamilton, D. C., & Fine, A. (2009) · Neuron · doi:10.1016/j.neuron.2009.02.026 · Cited by 166

Unexpected Benefits of Intermittent Hypoxia: Enhanced Respiratory and Nonrespiratory Motor Function

Dale, E. A., Mabrouk, F. B., & Mitchell, G. S. (2014) · Physiology · doi:10.1152/physiol.00012.2013 · Cited by 166

AMPA and NMDA glutamate receptor trafficking: multiple roads for reaching and leaving the synapse

Groc, L., & Choquet, D. (2006) · Cell and Tissue Research · doi:10.1007/s00441-006-0254-9 · Cited by 170

Ras and Rap Signaling in Synaptic Plasticity and Mental Disorders

Stornetta, R. L., & Zhu, J. (2010) · The Neuroscientist · doi:10.1177/1073858410365562 · Cited by 161

Calmodulin-Dependent Kinase Kinase/Calmodulin Kinase I Activity Gates Extracellular-Regulated Kinase-Dependent Long-Term Potentiation

Schmitt, J., Guire, E. S., Saneyoshi, T., & Soderling, T. R. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4086-04.2005 · Cited by 162

Short-term and long-term plasticity at corticostriatal synapses: implications for learning and memory

Di Filippo, M., Picconi, B., Tantucci, M., Ghiglieri, V., Bagetta, V., Sgobio, C., Tozzi, A., Parnetti, L., & Calabresi, P. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.09.025 · Cited by 158

Syndecan-3-Deficient Mice Exhibit Enhanced LTP and Impaired Hippocampus-Dependent Memory

Kaksonen, M., Pavlov, I., Võikar, V., Lauri, S. E., Hienola, A., Riekki, R., Lakso, M., Taira, T., & Rauvala, H. (2002) · Molecular and Cellular Neuroscience · doi:10.1006/mcne.2002.1167 · Cited by 162

Inducible protein knockout reveals temporal requirement of CaMKII reactivation for memory consolidation in the brain

Wang, H., Shimizu, E., Tang, Y., Cho, M., Kyin, M., Zuo, W., Robinson, D. A., Alaimo, P. J., Zhang, C., Morimoto, H., et al. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0636870100 · Cited by 155

Phosphorylation of Munc18 by Protein Kinase C Regulates the Kinetics of Exocytosis

Barclay, J. W., Craig, T. J., Fisher, R. J., Ciufo, L. F., Evans, G. J., Morgan, A., & Burgoyne, R. D. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m211114200 · Cited by 160

Cocaine-induced potentiation of synaptic strength in dopamine neurons: Behavioral correlates in GluRA(–/–) mice

Dong, Y., Saal, D., Thomas, M., Faust, R., Bonci, A., Robinson, T., & Malenka, R. C. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401553101 · Cited by 158

Mushroom Body Output Neurons Encode Odor–Reward Associations

Strube-Bloss, M. F., Nawrot, M. P., & Menzel, R. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.2583-10.2011 · Cited by 157

Decreased NR1, NR2A, and SAP102 transcript expression in the hippocampus in bipolar disorder

McCullumsmith, R. E., Kristiansen, L. V., Beneyto, M., Scarr, E., Dean, B., & Meador‐Woodruff, J. H. (2006) · Brain Research · doi:10.1016/j.brainres.2006.09.011 · Cited by 156

Stop that! Inhibition, sensitization, and their neurovisceral concomitants

Thayer, J. F., & Friedman, B. H. (2002) · Scandinavian Journal of Psychology · doi:10.1111/1467-9450.00277 · Cited by 164

Mediation of Hippocampal Mossy Fiber Long-Term Potentiation by Presynaptic I h Channels

Mellor, J. R., Nicoll, R. A., & Schmitz, D. (2002) · Science · doi:10.1126/science.1064285 · Cited by 158

Glia as sculptors of synaptic plasticity

Sancho, L., Contreras, M., & Allen, N. J. (2020) · Neuroscience Research · doi:10.1016/j.neures.2020.11.005 · Cited by 160

P2X receptors and synaptic plasticity

Pankratov, Y. V., Lalo, U., Krishtal, O., & Verkhratsky, A. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.03.076 · Cited by 161

Cellular Plasticity Cascades: Genes-To-Behavior Pathways in Animal Models of Bipolar Disorder

Einat, H., & Manji, H. K. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.11.004 · Cited by 156

Long-Term Potentiation of Intrinsic Excitability in LV Visual Cortical Neurons

Cudmore, R. H., & Turrigiano, G. G. (2004) · Journal of Neurophysiology · doi:10.1152/jn.01059.2003 · Cited by 154

Donald O. Hebb's synapse and learning rule: a history and commentary

Cooper, S. J. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.09.009 · Cited by 166

Role for P2X Receptors in Long-Term Potentiation

Pankratov, Y. V., Lalo, U., & Krishtal, O. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-19-08363.2002 · Cited by 155

Postsynaptic signaling during plasticity of dendritic spines

Murakoshi, H., & Yasuda, R. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2011.12.002 · Cited by 158

Spinal NMDA receptor phosphorylation correlates with the presence of neuropathic signs following peripheral nerve injury in the rat

Ultenius, C., Linderoth, B., Meyerson, B. A., & Wallin, J. (2006) · Neuroscience Letters · doi:10.1016/j.neulet.2006.01.018 · Cited by 154

Loss of AKAP150 perturbs distinct neuronal processes in mice

Tunquist, B. J., Hoshi, N., Guire, E. S., Zhang, F., Müllendorff, K., Langeberg, L. K., Raber, J., & Scott, J. D. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0805922105 · Cited by 158

PDZ Protein Interactions Regulating Glutamate Receptor Function and Plasticity

Tomita, S., Nicoll, R. A., & Bredt, D. S. (2001) · The Journal of Cell Biology · doi:10.1083/jcb.153.5.f19 · Cited by 154

Synaptic plasticity in the ischaemic brain

Calabresi, P., Centonze, D., Pisani, A., Cupini, L. M., & Bernardi, G. (2003) · The Lancet Neurology · doi:10.1016/s1474-4422(03)00532-5 · Cited by 154

Molecular Mechanisms of Early and Late LTP

Baltaci, S. B., Mogulkoc, R., & Baltaci, A. K. (2019) · Neurochemical Research · doi:10.1007/s11064-018-2695-4 · Cited by 152

Comprehensive Mapping of Post-Translational Modifications on Synaptic, Nuclear, and Histone Proteins in the Adult Mouse Brain

Tweedie‐Cullen, R. Y., Reck, J. M., & Mansuy, I. M. (2009) · Journal of Proteome Research · doi:10.1021/pr9003739 · Cited by 151

Characterization of the Mechanism Underlying the Reversal of Long Term Potentiation by Low Frequency Stimulation at Hippocampal CA1 Synapses

Huang, C., Liang, Y., & Hsu, K. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m106388200 · Cited by 152

Bidirectional Synaptic Plasticity Correlated With the Magnitude of Dendritic Calcium Transients Above a Threshold

Cormier, R. J., Greenwood, A. C., & Connor, J. A. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.85.1.399 · Cited by 152

Chronic Caffeine Treatment Prevents Sleep Deprivation-Induced Impairment of Cognitive Function and Synaptic Plasticity

Alhaider, I. A., Aleisa, A. M., Tran, T. T., Alzoubi, K. H., & Alkadhi, K. A. (2010) · SLEEP · doi:10.1093/sleep/33.4.437 · Cited by 151

Mechanisms underlying the inability to induce area CA1 LTP in the mouse after traumatic brain injury

Schwarzbach, E., Bonislawski, D. P., Xiong, G., & Cohen, A. S. (2006) · Hippocampus · doi:10.1002/hipo.20183 · Cited by 156

Mitochondrial potassium channels and uncoupling proteins in synaptic plasticity and neuronal cell death

Mattson, M. P., & Liu, D. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(03)00627-2 · Cited by 151

Amyloid β Prevents Activation of Calcium/Calmodulin-Dependent Protein Kinase II and AMPA Receptor Phosphorylation During Hippocampal Long-Term Potentiation

Zhao, D., Watson, J. B., & Xie, C.-W. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00485.2004 · Cited by 152

Microelectrode array recordings of cultured hippocampal networks reveal a simple model for transcription and protein synthesis‐dependent plasticity

Arnold, F. J. L., Hofmann, F., Bengtson, C. P., Wittmann, M., Vanhoutte, P., & Bading, H. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.077446 · Cited by 148

Simvastatin enhances learning and memory independent of amyloid load in mice

Li, L., Cao, D., Kim, H., Lester, R. A. J., & Fukuchi, K. (2006) · Annals of Neurology · doi:10.1002/ana.21053 · Cited by 156

Effects of dendritic morphology on CA3 pyramidal cell electrophysiology: a simulation study

Krichmar, J. L., Nasuto, S. J., Scorcioni, R., Washington, S. D., & Ascoli, G. A. (2002) · Brain Research · doi:10.1016/s0006-8993(02)02488-5 · Cited by 154

Optical Quantal Analysis Reveals a Presynaptic Component of LTP at Hippocampal Schaffer-Associational Synapses

Emptage, N. J., Reid, C. A., Fine, A., & Bliss, T. (2003) · Neuron · doi:10.1016/s0896-6273(03)00325-8 · Cited by 150

Mice lacking 5‐HT7 receptors show specific impairments in contextual learning

Roberts, A. J., Krucker, T., Levy, C. L., Slanina, K. A., Sutcliffe, J. G., & Hedlund, P. B. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03288.x · Cited by 151

Effects of serotonin in the hippocampus: how SSRIs and multimodal antidepressants might regulate pyramidal cell function

Dale, E., Pehrson, A. L., Jeyarajah, T., Li, Y., Leiser, S. C., Smagin, G. N., Olsen, C. K., & Sánchez, C. (2015) · CNS Spectrums · doi:10.1017/s1092852915000425 · Cited by 156

Activity-driven postsynaptic translocation of CaMKII

Merrill, M. A., Chen, Y., Strack, S., & Hell, J. W. (2005) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2005.10.003 · Cited by 155

CaMKII in cerebral ischemia

Coultrap, S. J., Vest, R. S., Ashpole, N. M., Hudmon, A., & Bayer, K. U. (2011) · Acta Pharmacologica Sinica · doi:10.1038/aps.2011.68 · Cited by 148

Excitatory interneurons dominate sensory processing in the spinal substantia gelatinosa of rat

Santos, S. F. A., Rebelo, S., Derkach, V. A., & Safronov, B. V. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2006.126912 · Cited by 148

Potentiation of Hippocampal Synaptic Transmission by Superoxide Requires the Oxidative Activation of Protein Kinase C

Knapp, L. T., & Klann, E. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-03-00674.2002 · Cited by 148

Presynaptic Remodeling Contributes to Activity-Dependent Synaptogenesis

Nikonenko, I., Jourdain, P., & Müller, D. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-24-08498.2003 · Cited by 149

A mammalian nervous-system-specific plasma membrane proteasome complex that modulates neuronal function

Ramachandran, K. V., & Margolis, S. S. (2017) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.3389 · Cited by 151

Cocaine Enhances NMDA Receptor-Mediated Currents in Ventral Tegmental Area Cells via Dopamine D5Receptor-Dependent Redistribution of NMDA Receptors

Schilström, B., Yaka, R., Argilli, E., Suvarna, N. U., Schumann, J., Chen, B. T., Carman, M., Singh, V., Mailliard, W. S., Dorit Ron, A., et al. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5179-05.2006 · Cited by 147

NOS2Gene Deficiency Protects from Sepsis-Induced Long-Term Cognitive Deficits

Weberpals, M., Hermes, M., Hermann, S., Kummer, M. P., Terwel, D., Semmler, A., Berger, M., Schäfers, M. A., & Heneka, M. T. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3238-09.2009 · Cited by 146

Amyloid β-Induced Impairments in Hippocampal Synaptic Plasticity Are Rescued by Decreasing Mitochondrial Superoxide

Ma, T., Hoeffer, C. A., Wong, H., Massaad, C. A., Zhou, P., Iadecola, C., Murphy, M. P., Pautler, R. G., & Klann, E. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.6566-10.2011 · Cited by 147

Carnitine palmitoyltransferase 1C: From cognition to cancer

Casals, N., Zammit, V. A., Herrero, L., Fadó, R., Rodríguez‐Rodríguez, R., & Serra, D. (2015) · Progress in Lipid Research · doi:10.1016/j.plipres.2015.11.004 · Cited by 149

Plasticity and repair in the post-ischemic brain

Filippo, M. D., Tozzi, A., Costa, C., Belcastro, V., Tantucci, M., Picconi, B., & Calabresi, P. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.01.012 · Cited by 151

Smaller hippocampal volume as a vulnerability factor for the persistence of post-traumatic stress disorder

van Rooij, S. J. H., Kennis, M., Sjouwerman, R., van den Heuvel, M. P., Kahn, R. S., & Geuze, E. (2015) · Psychological Medicine · doi:10.1017/s0033291715000707 · Cited by 145

Near-future CO2 levels impair the olfactory system of a marine fish

Porteus, C. S., Hubbard, P. C., Webster, T. M. U., van Aerle, R., Canário, A. V. M., Santos, E. M., & Wilson, R. W. (2018) · Nature Climate Change · doi:10.1038/s41558-018-0224-8 · Cited by 139

An emerging molecular and cellular framework for memory processing by the hippocampus

Wittenberg, G. M. (2002) · Trends in Neurosciences · doi:10.1016/s0166-2236(02)02231-2 · Cited by 148

Moving visual stimuli rapidly induce direction sensitivity of developing tectal neurons

Engert, F., Tao, H. W., Zhang, L. I., & Poo, M. (2002) · Nature · doi:10.1038/nature00988 · Cited by 146

NMDA GluN2A and GluN2B receptors play separate roles in the induction of LTP and LTD in the amygdala and in the acquisition and extinction of conditioned fear

Dalton, G. L., Wu, D. C., Wang, Y. T., Floresco, S. B., & Phillips, A. G. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.09.001 · Cited by 144

Melatonin ameliorates cognitive impairment induced by sleep deprivation in rats: Role of oxidative stress, BDNF and CaMKII

Zhang, L., Zhang, H., Liang, X., Zhang, H., Zhang, T., & Liu, F. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.07.051 · Cited by 144

LTP Regulates Burst Initiation and Frequency at Mossy Fiber–Granule Cell Synapses of Rat Cerebellum: Experimental Observations and Theoretical Predictions

Nieus, T. R., Sola, E., Mapelli, J., Saftenku, E. É., Rossi, P., & D'Angelo, E. U. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00696.2005 · Cited by 143

Dopamine D1and NMDA Receptors Mediate Potentiation of Basolateral Amygdala-Evoked Firing of Nucleus Accumbens Neurons

Floresco, S., Blaha, C. D., Yang, C. R., & Phillips, A. G. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-16-06370.2001 · Cited by 142

Phosphodiesterase 1B Knock-Out Mice Exhibit Exaggerated Locomotor Hyperactivity and DARPP-32 Phosphorylation in Response to Dopamine Agonists and Display Impaired Spatial Learning

Reed, T. M., Repaske, D. R., Snyder, G. L., Greengard, P., & Vorhees, C. V. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-12-05188.2002 · Cited by 141

High Frequency of Mosaicism among Patients with Neurofibromatosis Type 1 (NF1) with Microdeletions Caused by Somatic Recombination of the JJAZ1 Gene

Kehrer‐Sawatzki, H., Kluwe, L., Sandig, C., Kohn, M., Wimmer, K., Krammer, U., Peyrl, A., Jenne, D. E., Hansmann, I., & Mautner, V. (2004) · The American Journal of Human Genetics · doi:10.1086/423624 · Cited by 141

Modulation of synaptic plasticity by stress and antidepressants

Popoli, M., Gennarelli, M., & Racagni, G. (2002) · Bipolar Disorders · doi:10.1034/j.1399-5618.2002.01159.x · Cited by 142

NMDA receptor activation limits the number of synaptic connections during hippocampal development

Lüthi, A., Schwyzer, L., Mateos, J. M., Gähwiler, B. H., & McKinney, R. A. (2001) · Nature Neuroscience · doi:10.1038/nn744 · Cited by 139

Immunohistochemical localization of the P2Y1 purinergic receptor in neurons and glial cells of the central nervous system

Morán‐Jiménez, M., & Matute, C. (2000) · Molecular Brain Research · doi:10.1016/s0169-328x(00)00067-x · Cited by 138

Retrograde signaling at central synapses

Tao, H. W., & Poo, M. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.191351698 · Cited by 140

The Developing Brain and Neural Plasticity: Implications for Normality, Psychopathology,and Resilience

Cicchetti, D., & Curtis, W. J. (2015) · Wiley eBooks · doi:10.1002/9780470939390.ch1 · Cited by 142

Hippocampal Long-Term Potentiation Is Supported by Presynaptic and Postsynaptic Tyrosine Receptor Kinase B-Mediated Phospholipase Cγ Signaling

Gärtner, A., Polnau, D. G., Staiger, V., Sciarretta, C., Minichiello, L., Thoenen, H., Bonhoeffer, T., & Körte, M. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3792-05.2006 · Cited by 138

Presynaptic long-term plasticity

Yang, Y., & Calakos, N. (2013) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2013.00008 · Cited by 146

Alcohol-related amnesia and dementia: Animal models have revealed the contributions of different etiological factors on neuropathology, neurochemical dysfunction and cognitive impairment

Vetreno, R. P., Hall, J. M., & Savage, L. M. (2011) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2011.01.003 · Cited by 136

Insulin-like growth factor-1 in CNS and cerebrovascular aging

Sonntag, W. E., Deák, F., Ashpole, N. M., Tóth, P., Csiszár, A., Freeman, W. M., & Ungvari, Z. I. (2013) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2013.00027 · Cited by 139

Interaction of Calcineurin and Type-A GABA Receptor γ2Subunits Produces Long-Term Depression at CA1 Inhibitory Synapses

Wang, J., Liu, S., Haditsch, U., Tu, W., Cochrane, K., Ahmadian, G., Tran, L., Paw, J., Wang, Y., Mansuy, I. M., et al. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-03-00826.2003 · Cited by 134

Revisiting the Function of PSA-NCAM in the Nervous System

Cremer, H., & Durbec, P. (2001) · Molecular Neurobiology · doi:10.1385/mn:24:1-3:053 · Cited by 140

Regulation of Calcium/Calmodulin-dependent Protein Kinase II Docking toN-Methyl-d-aspartate Receptors by Calcium/Calmodulin and α-Actinin

Leonard, A. S., Bayer, K. U., Merrill, M. A., Lim, I. A., Shea, M. A., Schulman, H., & Hell, J. W. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m205164200 · Cited by 139

Episodic memory and cortico–hippocampal interactions

Shastri, L. (2002) · Trends in Cognitive Sciences · doi:10.1016/s1364-6613(02)01868-5 · Cited by 136

Surface trafficking of N-methyl-d-aspartate receptors: Physiological and pathological perspectives

Groc, L., Bard, L., & Choquet, D. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.05.029 · Cited by 135

Self-administration enhances excitatory synaptic transmission in the bed nucleus of the stria terminalis

Dumont, É. C., Mark, G. P., Mader, S. L., & Williams, J. T. (2005) · Nature Neuroscience · doi:10.1038/nn1414 · Cited by 136

CaMKII

Shonesy, B. C., Jalan‐Sakrikar, N., Cavener, V. S., & Colbran, R. J. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-420170-5.00003-9 · Cited by 140

Enhancement of presynaptic neuronal excitability by correlated presynaptic and postsynaptic spiking

Ganguly, K., Kiss, L., & Poo, M. (2000) · Nature Neuroscience · doi:10.1038/79838 · Cited by 136

Increased neurotransmitter release during long‐term potentiation at mossy fibre–granule cell synapses in rat cerebellum

Sola, E., Prestori, F., Rossi, P., Taglietti, V., & D'Angelo, E. U. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2003.060285 · Cited by 135

Time Domains of the Hypoxic Ventilatory Response and Their Molecular Basis

Pamenter, M. E., & Powell, F. L. (2016) · Comprehensive physiology · doi:10.1002/cphy.c150026 · Cited by 169

The Role of RNA Editing of Kainate Receptors in Synaptic Plasticity and Seizures

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