Long-Term Potentiation--A Decade of Progress?

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

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

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Dendritic spine changes associated with hippocampal long-term synaptic plasticity

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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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Inhibitory and Excitatory Spike-Timing-Dependent Plasticity in the Auditory Cortex

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Multiple sclerosis and cognition: synaptic failure and network dysfunction

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Opposing roles of synaptic and extrasynaptic NMDA receptors in neuronal calcium signalling and BDNF gene regulation

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Dopamine Mediates Context-Dependent Modulation of Sensory Plasticity in C. elegans

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Reconsolidation and the dynamic nature of memory

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Localized Synaptic Potentiation by BDNF Requires Local Protein Synthesis in the Developing Axon

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Structure and Regulation of Calcium/Calmodulin-Dependent Protein Kinases

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Tyrosine phosphatase STEP is a tonic brake on induction of long-term potentiation

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Linking Hebb's coincidence-detection to memory formation

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Modulation of LTP at rat hippocampal CA3-CA1 synapses by direct current stimulation

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New perspectives in glutamate and anxiety

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Understanding Synapses: Past, Present, and Future

Südhof, T. C., & Malenka, R. C. (2008) · Neuron · doi:10.1016/j.neuron.2008.10.011 · Cited by 207

Environmental enrichment reverses cognitive and molecular deficits induced by developmental lead exposure

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Genome-wide gene expression profiles of the developing mouse hippocampus

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Molecular and systems mechanisms of memory consolidation and storage

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Transcranial magnetic stimulation, synaptic plasticity and network oscillations

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Reduction in Size of Perforated Postsynaptic Densities in Hippocampal Axospinous Synapses and Age-Related Spatial Learning Impairments

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Temporal Sequence Learning, Prediction, and Control: A Review of Different Models and Their Relation to Biological Mechanisms

Wörgötter, F., & Porr, B. (2005) · Neural Computation · doi:10.1162/0899766053011555 · Cited by 203

A hebbian form of long-term potentiation dependent on mGluR1a in hippocampal inhibitory interneurons

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Cognitive disruption and altered hippocampus synaptic function in Reelin haploinsufficient mice

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Fyn kinase inhibition as a novel therapy for Alzheimer’s disease

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Metabotropic Glutamate Receptor Ligands as Potential Therapeutics for Addiction

Olive, M. F. (2009) · Current Drug Abuse Reviews · doi:10.2174/1874473710902010083 · Cited by 207

Expression mechanisms underlying long-term potentiation: a postsynaptic view

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The Stability of a Stochastic CaMKII Switch: Dependence on the Number of Enzyme Molecules and Protein Turnover

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Making memories stick: cell-adhesion molecules in synaptic plasticity

Benson, D. L. (2000) · Trends in Cell Biology · doi:10.1016/s0962-8924(00)01838-9 · Cited by 199

Regulation of NMDA receptors by the tyrosine kinase Fyn

Trepanier, C. H., Jackson, M. F., & MacDonald, J. F. (2011) · FEBS Journal · doi:10.1111/j.1742-4658.2011.08391.x · Cited by 195

Long-Lasting Potentiation of GABAergic Synapses in Dopamine Neurons after a Single In Vivo Ethanol Exposure

Melis, M., Camarini, R., Ungless, M. A., & Bonci, A. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-06-02074.2002 · Cited by 196

Abnormal Long-Lasting Synaptic Plasticity and Cognition in Mice Lacking the Mental Retardation GenePak3

Meng, J., Meng, Y., Hanna, A., Janus, C., & Jia, Z. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0028-05.2005 · Cited by 202

Synaptic Localization of Nitric Oxide Synthase and Soluble Guanylyl Cyclase in the Hippocampus

Burette, A., Zabel, U., Weinberg, R. J., Schmidt, H. H. H. W., & Valtschanoff, J. G. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-20-08961.2002 · Cited by 198

AMPA Receptor Trafficking and the Control of Synaptic Transmission

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Challenges in Developing Novel Treatments for Childhood Disorders: Lessons from Research on Anxiety

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Mitochondria, Synaptic Plasticity, And Schizophrenia

Ben‐Shachar, D., & Laifenfeld, D. (2004) · International review of neurobiology · doi:10.1016/s0074-7742(04)59011-6 · Cited by 191

Hebbian plasticity requires compensatory processes on multiple timescales

Zenke, F., & Wulfram Gerstner, B. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0259 · Cited by 206

Long-term potentiation decay and memory loss are mediated by AMPAR endocytosis

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Tissue plasminogen activator in central nervous system physiology and pathology

Melchor, J. P., & Strickland, S. (2005) · Thrombosis and Haemostasis · doi:10.1160/th04-12-0838 · Cited by 193

Chronic treatment of old rats with donepezil or galantamine: effects on memory, hippocampal plasticity and nicotinic receptors

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The role of the endoplasmic reticulum Ca2+ store in the plasticity of central neurons

Bardo, S. J., Cavazzini, M., & Emptage, N. J. (2006) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2005.12.008 · Cited by 188

Postsynaptic Density Protein-95 Regulates NMDA Channel Gating and Surface Expression

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Ischemic Insults Direct Glutamate Receptor Subunit 2-Lacking AMPA Receptors to Synaptic Sites

Liu, B., Liao, M., Mielke, J. G., Ning, K., Chen, Y., Li, L., El-Hayek, Y. H., Gomez, E., Zukin, R. S., Fehlings, M. G., et al. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0567-06.2006 · Cited by 192

mGluR5 and NMDA Receptors Drive the Experience- and Activity-Dependent NMDA Receptor NR2B to NR2A Subunit Switch

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Increased Threshold for Spike-Timing-Dependent Plasticity Is Caused by Unreliable Calcium Signaling in Mice Lacking Fragile X Gene Fmr1

Meredith, R. M., Holmgren, C. D., Weidum, M., Burnashev, N., & Mansvelder, H. D. (2007) · Neuron · doi:10.1016/j.neuron.2007.04.028 · Cited by 190

Towards artificial neurons and synapses: a materials point of view

Jeong, D. S., Kim, I., Ziegler, M., & Kohlstedt, H. (2012) · RSC Advances · doi:10.1039/c2ra22507g · Cited by 191

Behavioural pharmacology and its contribution to the molecular basis of memory consolidation

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Neuropsychology of Learning and Memory in Teleost Fish

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The importance of being subtle: small changes in calcium homeostasis control cognitive decline in normal aging

Toescu, E. C., & Verkhratsky, A. (2007) · Aging Cell · doi:10.1111/j.1474-9726.2007.00296.x · Cited by 184

Homeostatic plasticity and STDP: keeping a neuron's cool in a fluctuating world

Watt, A. J. (2010) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2010.00005 · Cited by 195

AMPA receptors regulate transcription of the plasticity-related immediate-early gene Arc

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Silent synapses in the developing hippocampus: Lack of functional AMPA receptors or low probability of glutamate release?

Gasparini, S., Saviane, C., Voronin, L. L., & Cherubini, E. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.170032297 · Cited by 188

Coordinated PKA and PKC phosphorylation suppresses RXR-mediated ER retention and regulates the surface delivery of NMDA receptors

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Modulation of Presynaptic Plasticity and Learning by the H-ras/Extracellular Signal-Regulated Kinase/Synapsin I Signaling Pathway

Kushner, S. A., Elgersma, Y., Murphy, G. G., Jaarsma, D., van Woerden, G. M., Hojjati, M. R., Cui, Y., LeBoutillier, J. C., Marrone, D. F., Choi, E. S., et al. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2836-05.2005 · Cited by 193

Amygdalar Inactivation Blocks Stress-Induced Impairments in Hippocampal Long-Term Potentiation and Spatial Memory

Kim, J. J., Koo, J. W., Lee, H. J., & Han, J.-S. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.4623-04.2005 · Cited by 184

Plasticity of NMDA receptor NR2B subunit in memory and chronic pain

Zhuo, M. (2009) · Molecular Brain · doi:10.1186/1756-6606-2-4 · Cited by 185

GABA-mediated giant depolarizing potentials as coincidence detectors for enhancing synaptic efficacy in the developing hippocampus

Kasyanov, A. M., Safiulina, V. F., Voronin, L. L., & Cherubini, E. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0305974101 · Cited by 181

Extent of Dorsolateral Prefrontal Cortex Plasticity and Its Association With Working Memory in Patients With Alzheimer Disease

Kumar, S., Zomorrodi, R., Ghazala, Z., Goodman, M. S., Blumberger, D. M., Cheam, A., Fischer, C. E., Daskalakis, Z. J., Mulsant, B. H., Pollock, B. G., et al. (2017) · JAMA Psychiatry · doi:10.1001/jamapsychiatry.2017.3292 · Cited by 188

Evidence for glutamate, in addition to acetylcholine and GABA, neurotransmitter synthesis in basal forebrain neurons projecting to the entorhinal cortex

Manns, I. D., Mainville, L., & Jones, B. E. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00302-5 · Cited by 186

Modulation of neurotransmitter release by the second messenger-activated protein kinases: Implications for presynaptic plasticity

Leenders, A. G. M., & SHENG, Z. (2004) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2004.10.012 · Cited by 181

The antidepressant tianeptine persistently modulates glutamate receptor currents of the hippocampal CA3 commissural associational synapse in chronically stressed rats

Kole, M. H. P., Swan, L., & Fuchs, E. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.02136.x · Cited by 181

Regulation of synaptic transmission and plasticity by neuronal nicotinic acetylcholine receptors

McKay, B. E., Placzek, A. N., & Dani, J. A. (2007) · Biochemical Pharmacology · doi:10.1016/j.bcp.2007.07.001 · Cited by 181

Ethanol Induces Long-Term Facilitation of NR2B-NMDA Receptor Activity in the Dorsal Striatum: Implications for Alcohol Drinking Behavior

Wang, J., Carnicella, S., Phamluong, K., Jeanblanc, J., Ronesi, J. A., Chaudhri, N., Janak, P. H., Lovinger, D. M., & Dorit Ron, A. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4749-06.2007 · Cited by 183

EPAC Null Mutation Impairs Learning and Social Interactions via Aberrant Regulation of miR-124 and Zif268 Translation

Yang, Y., Shu, X., Liu, D., Shang, Y., Wu, Y., Pei, L., Xu, X., Tian, Q., Zhang, J., Qian, K., et al. (2012) · Neuron · doi:10.1016/j.neuron.2012.02.003 · Cited by 183

The Role of Mitochondrial Porins and the Permeability Transition Pore in Learning and Synaptic Plasticity

Weeber, E. J., Levy, M., Sampson, M. J., Anflous, K., Armstrong, D. L., Brown, S. E., Sweatt, J. D., & Craigen, W. J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m201649200 · Cited by 179

Intracellular Domains of NMDA Receptor Subtypes Are Determinants for Long-Term Potentiation Induction

Köhr, G., Jensen, V., Koester, H. J., Mihaljević, A. L., Utvik, J. K., Kvello, A., Ottersen, O. P., Seeburg, P. H., Sprengel, R., & Hvalby, Ø. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-34-10791.2003 · Cited by 183

The BDNF Val66Met polymorphism impairs NMDA receptor-dependent synaptic plasticity in the hippocampus

Ninan, I., Bath, K. G., Dagar, K., Perez-Castro, R., Plummer, M. R., Lee, F. S., & Chao, M. V. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1405-10.2010 · Cited by 180

Hebbian and neuromodulatory mechanisms interact to trigger associative memory formation

Johansen, J. P., Díaz-Mataix, L., Hamanaka, H., Ozawa, T., Ycu, E. A., Koivumaa, J., Kumar, A., Hou, M., Deisseroth, K. A., Boyden, E. S., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1421304111 · Cited by 179

Neto1 Is a Novel CUB-Domain NMDA Receptor–Interacting Protein Required for Synaptic Plasticity and Learning

Ng, D., Pitcher, G. M., Szilard, R. K., Sertie, A. L., Kanisek, M., Clapcote, S. J., Lipina, T. V., Kalia, L. V., Joo, D. T., McKerlie, C., et al. (2009) · PLoS Biology · doi:10.1371/journal.pbio.1000041 · Cited by 185

Age-related shift in LTD is dependent on neuronal adenosine A2A receptors interplay with mGluR5 and NMDA receptors

Temido‐Ferreira, M., Ferreira, D. G., Batalha, V. L., Marques-Morgado, I., Coelho, J. E., Pereira, P., Gomes, R., Pinto, A., Carvalho, S., Canas, P. M., et al. (2018) · Molecular Psychiatry · doi:10.1038/s41380-018-0110-9 · Cited by 194

Activity-Dependent Long-Term Potentiation of Intrinsic Excitability in Hippocampal CA1 Pyramidal Neurons

Xu, J., Kang, N., Jiang, L., Nedergaard, M., & Kang, J. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.4217-04.2005 · Cited by 178

Spatial long-term memory is related to mossy fiber synaptogenesis

Ramı́rez-Amaya, V., Balderas, I., Sandoval, J., Escobar, M. L., & Bermúdez-Rattoni, F. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-18-07340.2001 · Cited by 177

Dynamic Gain Control of Dopamine Delivery in Freely Moving Animals

Montague, P. R., McClure, S. M., Baldwin, P. R., Phillips, P. E. M., Budygin, E. A., Stuber, G. D., Kilpatrick, M., & Wightman, R. M. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4279-03.2004 · Cited by 174

Total Recall--the Memory of Addiction

Nestler, E. J. (2001) · Science · doi:10.1126/science.1063024 · Cited by 177

Molecular dissection of hippocampal theta-burst pairing potentiation

Hoffman, D. A., Sprengel, R., & Sakmann, B. J. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.092157999 · Cited by 177

Roles of the hippocampal formation in pain information processing

Liu, M., & Chen, J. (2009) · Neuroscience Bulletin · doi:10.1007/s12264-009-0905-4 · Cited by 178

Two cis-acting elements in the 3′ untranslated region of α-CaMKII regulate its dendritic targeting

Mori, Y., Imaizumi, K., Katayama, T., Yoneda, T., & Tohyama, M. (2000) · Nature Neuroscience · doi:10.1038/80591 · Cited by 178

The contribution of pharmacology to research on the mechanisms of memory formation

McGaugh, J. L., & Izquierdo, I. (2000) · Trends in Pharmacological Sciences · doi:10.1016/s0165-6147(00)01473-5 · Cited by 178

Alzheimer Amyloid β-Peptide Inhibits the Late Phase of Long-Term Potentiation through Calcineurin-Dependent Mechanisms in the Hippocampal Dentate Gyrus

Chen, Q.-S., Wei, W., Shimahara, T., & Xie, C.-W. (2002) · Neurobiology of Learning and Memory · doi:10.1006/nlme.2001.4034 · Cited by 176

Long‐term potentiation of human visual evoked responses

Teyler, T. J., Hamm, J. P., Clapp, W. C., Johnson, B. W., Corballis, M. C., & Kirk, I. J. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04007.x · Cited by 170

An experimental test of the role of postsynaptic calcium levels in determining synaptic strength using perirhinal cortex of rat

Cho, K., Aggleton, J. P., Brown, M. W., & Bashir, Z. I. (2001) · The Journal of Physiology · doi:10.1111/j.1469-7793.2001.0459f.x · Cited by 170

An Essential Role for PICK1 in NMDA Receptor-Dependent Bidirectional Synaptic Plasticity

Terashima, A., Pelkey, K. A., Rah, J., Suh, Y. H., Roche, K. W., Collingridge, G. L., McBain, C. J., & Isaac, J. T. R. (2008) · Neuron · doi:10.1016/j.neuron.2008.01.028 · Cited by 179

The impact of diabetes on cognition: What can be learned from rodent models?

Biessels, G. J., & Gispen, W. H. (2005) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2005.08.015 · Cited by 172

Three-dimensional Reconstructions of Calcium/Calmodulin-dependent (CaM) Kinase IIα and Truncated CaM Kinase IIα Reveal a Unique Organization for Its Structural Core and Functional Domains

Kolodziej, S. J., Hudmon, A., Waxham, M. N., & Stoops, J. K. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.19.14354 · Cited by 170

Aromatase Inhibition Abolishes LTP Generation in Female But Not in Male Mice

Vierk, R., Glassmeier, G., Zhou, L., Brandt, N., Fester, L., Dudzinski, D., Wilkars, W., Bender, R. A., Lewerenz, M., Gloger, S., et al. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5319-11.2012 · Cited by 177

Pair Recordings Reveal All-Silent Synaptic Connections and the Postsynaptic Expression of Long-Term Potentiation

Montgomery, J. M., Pavlidis, P., & Madison, D. V. (2001) · Neuron · doi:10.1016/s0896-6273(01)00244-6 · Cited by 174

Long-term potentiation of exogenous glutamate responses at single dendritic spines

Bagal, A. A., Kao, J. P. Y., Tang, C.-M., & Thompson, S. M. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0501956102 · Cited by 169

Sleep Deprivation Impairs Long-Term Potentiation in Rat Hippocampal Slices

Campbell, I. G., Guinan, M. J., & Horowitz, J. M. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.88.2.1073 · Cited by 169

Neuroligin-2 Deletion Selectively Decreases Inhibitory Synaptic Transmission Originating from Fast-Spiking but Not from Somatostatin-Positive Interneurons

Gibson, J. R., Huber, K. M., & Südhof, T. C. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2457-09.2009 · Cited by 174

A Synthetic Neural Cell Adhesion Molecule Mimetic Peptide Promotes Synaptogenesis, Enhances Presynaptic Function, and Facilitates Memory Consolidation

Cambon, K., Hansen, S. M., Venero, C., Herrero, A. I., Skibo, G. G., Berezin, V., Bock, E., & Sandi, C. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.0436-04.2004 · Cited by 172

Bistability in the Ca2+/Calmodulin-Dependent Protein Kinase-Phosphatase System

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Glutamatergic modulation of hyperactivity in mice lacking the dopamine transporter

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