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

Mechanism of TrkB-Mediated Hippocampal Long-Term Potentiation

Minichiello, L., Calella, A. M., Medina, D. L., Bonhoeffer, T., Klein, R., & Korte, M. (2002) · Neuron · doi:10.1016/s0896-6273(02)00942-x · Cited by 506

β Phorbol Ester- and Diacylglycerol-Induced Augmentation of Transmitter Release Is Mediated by Munc13s and Not by PKCs

Rhee, J.-S., Betz, A., Pyott, S., Reim, K., Varoqueaux, F., Augustin, I., Hesse, D., Südhof, T. C., Takahashi, M., Rosenmund, C., et al. (2002) · Cell · doi:10.1016/s0092-8674(01)00635-3 · Cited by 500

Control of Dorsal Raphe Serotonergic Neurons by the Medial Prefrontal Cortex: Involvement of Serotonin-1A, GABAA, and Glutamate Receptors

Celada, P., Puig, M. V., Casanovas, J. M., Guillazo, G., & Artigas, F. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-24-09917.2001 · Cited by 497

Glutamate transporters: confining runaway excitation by shaping synaptic transmission

Tzingounis, A. V., & Wadiche, J. I. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2274 · Cited by 496

Plasticity-induced growth of dendritic spines by exocytic trafficking from recycling endosomes

Park, M., Salgado, J. M., Ostroff, L., Helton, T. D., Robinson, C. G., Harris, K. M., & Ehlers, M. D. (2006) · Neuron · doi:10.1016/j.neuron.2006.09.040 · Cited by 493

Molecular mechanisms underlying emotional learning and memory in the lateral amygdala

Rodrigues, S. M., Schafe, G. E., & LeDoux, J. E. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.014 · Cited by 491

Glutamatergic substrates of drug addiction and alcoholism

Gass, J. T., & Olive, M. F. (2007) · Biochemical Pharmacology · doi:10.1016/j.bcp.2007.06.039 · Cited by 502

Synchronous Gamma activity: a review and contribution to an integrative neuroscience model of schizophrenia

Lee, K.-H., Williams, L. M., Breakspear, M. J., & Gordon, E. (2003) · Brain Research Reviews · doi:10.1016/s0165-0173(02)00220-5 · Cited by 483

Untitled work

Lisman (2001) · doi:10.1016/s0896-6273(01)00364-6 · Cited by 480

Mechanisms of late-onset cognitive decline after early-life stress

Brunson, K. L., Kramár, E., Lin, B., Chen, Y., Colgin, L. L., Yanagihara, T. K., Lynch, G., & Baram, T. Z. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.2281-05.2005 · Cited by 479

Myosin 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

Targeting of PKA to Glutamate Receptors through a MAGUK-AKAP Complex

Colledge, M., Dean, R. A., Scott, G. K., Langeberg, L. K., Huganir, R. L., & Scott, J. D. (2000) · Neuron · doi:10.1016/s0896-6273(00)00013-1 · Cited by 467

Involvement of the CA3–CA1 Synapse in the Acquisition of Associative Learning in Behaving Mice

Gruart, A., Muñoz, M.-D., & Delgado-Garcia, J. M. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.2834-05.2006 · Cited by 474

Dopamine and serotonin: influences on male sexual behavior

Hull, E. M., Muschamp, J. W., & Sato, S. (2004) · Physiology & Behavior · doi:10.1016/j.physbeh.2004.08.018 · Cited by 465

Postsynaptic organisation and regulation of excitatory synapses

Scannevin, R. H., & Huganir, R. L. (2000) · Nature reviews. Neuroscience · doi:10.1038/35039075 · Cited by 472

Hippocampal long-term potentiation suppressed by increased inhibition in the Ts65Dn mouse, a genetic model of Down syndrome

Kleschevnikov, A. M., Belichenko, P. V., Villar, A. J., Epstein, C. J., Malenka, R. C., & Mobley, W. C. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.1766-04.2004 · Cited by 459

Plasticity of Cortical Excitatory-Inhibitory Balance

Froemke, R. C. (2015) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-071714-034002 · Cited by 458

Ageing and diabetes: implications for brain function

Biessels, G. J., van der Heide, L. P., Kamal, A., Bleys, R. L. A. W., & Gispen, W. H. (2002) · European Journal of Pharmacology · doi:10.1016/s0014-2999(02)01486-3 · Cited by 458

A history of spike-timing-dependent plasticity

Markram, H. (2011) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2011.00004 · Cited by 454

Different molecular cascades in different sites of the brain control memory consolidation

Izquierdo, I., Bevilaqua, L. R., Rossato, J. I., Bonini, J. S., Medina, J. H., & Cammarota, M. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.07.005 · Cited by 467

Synaptic activity at calcium-permeable AMPA receptors induces a switch in receptor subtype

Liu, S. J., & Cull-Candy, S. G. (2000) · Nature · doi:10.1038/35013064 · Cited by 452

A Calcium-Dependent Feedback Mechanism Participates in Shaping Single NMDA Miniature EPSCs

Umemiya, M., Chen, N., Raymond, L. A., & Murphy, T. H. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-01-00001.2001 · Cited by 449

Role of ampa receptor endocytosis in synaptic plasticity

Carroll, R. C., Beattie, E. C., von Zastrow, M., & Malenka, R. C. (2001) · Nature Reviews Neuroscience · doi:10.1038/35072500 · Cited by 448

A Cooperative Switch Determines the Sign of Synaptic Plasticity in Distal Dendrites of Neocortical Pyramidal Neurons

Sjöström, P. J., & Häusser, M. (2006) · Neuron · doi:10.1016/j.neuron.2006.06.017 · Cited by 433

Developmental Remodeling of the Retinogeniculate Synapse

Chen, C., & Regehr, W. G. (2000) · Neuron · doi:10.1016/s0896-6273(00)00166-5 · Cited by 439

NMDA Receptors and L-Type Voltage-Gated Calcium Channels Contribute to Long-Term Potentiation and Different Components of Fear Memory Formation in the Lateral Amygdala

Bauer, E. P., Schafe, G. E., & LeDoux, J. E. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-12-05239.2002 · Cited by 438

The Neuropharmacological Basis for the Use of Memantine in the Treatment of Alzheimer's Disease

Rogawski, M. A., & Wenk, G. L. (2003) · CNS Drug Reviews · doi:10.1111/j.1527-3458.2003.tb00254.x · Cited by 449

Gut microbiome-wide association study of depressive symptoms

Radjabzadeh, D., Bosch, J. A., Uitterlinden, A. G., Zwinderman, A. H., Ikram, M. A., van Meurs, J. B. J., Luik, A. I., Nieuwdorp, M., Lok, A., van Duijn, C. M., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-34502-3 · Cited by 464

High-Resolution Proteomics Unravel Architecture and Molecular Diversity of Native AMPA Receptor Complexes

Schwenk, J., Harmel, N., Brechet, A., Zolles, G., Berkefeld, H., Müller, C. S., Bildl, W., Baehrens, D., Hüber, B., Kulik, A., et al. (2012) · Neuron · doi:10.1016/j.neuron.2012.03.034 · Cited by 433

Reactive oxygen species and synaptic plasticity in the aging hippocampus

Serrano, F., & Klann, E. (2004) · Ageing Research Reviews · doi:10.1016/j.arr.2004.05.002 · Cited by 426

Protein kinase C modulates NMDA receptor trafficking and gating

Lan, J.-Y., Skeberdis, V. A., Jover, T., Grooms, S. Y., Lin, Y., Araneda, R. C., Zheng, X., Bennett, M. V. L., & Zukin, R. S. (2001) · Nature Neuroscience · doi:10.1038/86028 · Cited by 421

Neuromodulated Spike-Timing-Dependent Plasticity, and Theory of Three-Factor Learning Rules

Frémaux, N., & Wulfram Gerstner, B. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00085 · Cited by 449

Timing and Location of Nicotinic Activity Enhances or Depresses Hippocampal Synaptic Plasticity

Ji, D., Lape, R., & Dani, J. A. (2001) · Neuron · doi:10.1016/s0896-6273(01)00332-4 · Cited by 419

Protein kinase Mζ is necessary and sufficient for LTP maintenance

Ling, D. S. F., Benardo, L. S., Serrano, P. A., Blace, N., Kelly, M. T., Crary, J. F., & Sacktor, T. C. (2002) · Nature Neuroscience · doi:10.1038/nn829 · Cited by 419

An NMDA receptor ER retention signal regulated by phosphorylation and alternative splicing

Scott, D. B., Blanpied, T. A., Swanson, G. T., Zhang, C., & Ehlers, M. D. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-09-03063.2001 · Cited by 418

Dopamine Receptor Activation Is Required for Corticostriatal Spike-Timing-Dependent Plasticity

Pawlak, V., & Kerr, J. N. D. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.4402-07.2008 · Cited by 430

Sleep transforms the cerebral trace of declarative memories

Gais, S., Albouy, G., Boly, M., Dang-Vu, T. T., Darsaud, A., Desseilles, M., Rauchs, G., Schabus, M., Sterpenich, V., Vandewalle, G., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705454104 · Cited by 412

Abnormal Glutamate Receptor Expression in the Medial Temporal Lobe in Schizophrenia and Mood Disorders

Beneyto, M., Kristiansen, L. V., Oni-Orisan, A., McCullumsmith, R. E., & Meador-Woodruff, J. H. (2007) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301312 · Cited by 408

The Role of Brain-Derived Neurotrophic Factor Receptors in the Mature Hippocampus: Modulation of Long-Term Potentiation through a Presynaptic Mechanism involving TrkB

Xu, B., Gottschalk, W., Chow, A., Wilson, R. I., Schnell, E., Zang, K., Wang, D., Nicoll, R. A., Lu, B., & Reichardt, L. F. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-18-06888.2000 · Cited by 404

Stimulation in Hippocampal Region CA1 in Behaving Rats Yields Long-Term Potentiation when Delivered to the Peak of Theta and Long-Term Depression when Delivered to the Trough

Hyman, J. M., Wyble, B., Goyal, V., Rossi, C. A., & Hasselmo, M. E. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-37-11725.2003 · Cited by 404

Invited Review: Neuroplasticity in respiratory motor control

Mitchell, G. S., & Johnson, S. M. (2003) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00523.2002 · Cited by 394

Autism, oxytocin and interoception

Quattrocki, E., & Friston, K. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.09.012 · Cited by 393

Auxiliary Subunits Assist AMPA-Type Glutamate Receptors

Nicoll, R. A., Tomita, S., & Bredt, D. S. (2006) · Science · doi:10.1126/science.1123339 · Cited by 390

Lead neurotoxicity: From exposure to molecular effects

Toscano, C. D., & Guilarte, T. R. (2005) · Brain Research Reviews · doi:10.1016/j.brainresrev.2005.02.004 · Cited by 389

The Impact of Studying Brain Plasticity

Mateos‐Aparicio, P., & Moreno, A. R. (2019) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2019.00066 · Cited by 465

Nicotine addiction and comorbidity with alcohol abuse and mental illness

Dani, J. A., & Harris, R. A. (2005) · Nature Neuroscience · doi:10.1038/nn1580 · Cited by 382

Obesity and Hypertriglyceridemia Produce Cognitive Impairment

Farr, S. A., Yamada, K. A., Butterfield, D. A., Abdul, H. M., Xu, L., Miller, N. E., Banks, W. A., & Morley, J. E. (2008) · Endocrinology · doi:10.1210/en.2007-1722 · Cited by 382

Is Heterosynaptic modulation essential for stabilizing hebbian plasiticity and memory

Bailey, C. H., Giustetto, M., Huang, Y.-Y., Hawkins, R. D., & Kandel, E. R. (2000) · Nature Reviews Neuroscience · doi:10.1038/35036191 · Cited by 382

Regulation of Neuregulin Signaling by PSD-95 Interacting with ErbB4 at CNS Synapses

Huang, Y. Z., Won, S., Ali, D. W., Wang, Q., Tanowitz, M., Du, Q., Pelkey, K. A., Yang, D. J., Xiong, W., Salter, M. W., et al. (2000) · Neuron · doi:10.1016/s0896-6273(00)81176-9 · Cited by 381

Identification of PSD-95 as a Regulator of Dopamine-Mediated Synaptic and Behavioral Plasticity

Yao, W., Gainetdinov, R. R., Arbuckle, M. I., Sotnikova, T. D., Cyr, M., Beaulieu, J., Torres, G. E., Grant, S. G. N., & Caron, M. G. (2004) · Neuron · doi:10.1016/s0896-6273(04)00048-0 · Cited by 390

Dynamic actin filaments are required for stable long-term potentiation (LTP) in area CA1 of the hippocampus

Krucker, T., Siggins, G. R., & Halpain, S. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.100139797 · Cited by 374

Increasing Numbers of Synaptic Puncta during Late-Phase LTP

Bozdagi, O., Shan, W., Tanaka, H., Benson, D. L., & Huntley, G. W. (2000) · Neuron · doi:10.1016/s0896-6273(00)00100-8 · Cited by 384

Heart rate variability and its relation to prefrontal cognitive function: The effects of training and detraining

Hansen, A. L., Johnsen, B. H., Sollers, J. J., Stenvik, K., & Thayer, J. F. (2004) · European Journal of Applied Physiology · doi:10.1007/s00421-004-1208-0 · Cited by 354

Cocaine but Not Natural Reward Self-Administration nor Passive Cocaine Infusion Produces Persistent LTP in the VTA

Chen, B. T., Bowers, M. S., Martín, M., Hopf, F. W., Guillory, A. M., Carelli, R. M., Chou, J., & Bonci, A. (2008) · Neuron · doi:10.1016/j.neuron.2008.05.024 · Cited by 350

Synapse-specific regulation of AMPA receptor function by PSD-95.

Béïque, J.-C., Lin, D.-T., Kang, M.-G., Aizawa, H., Takamiya, K., & Huganir, R. L. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0608492103 · Cited by 398

Intra-Amygdala Blockade of the NR2B Subunit of the NMDA Receptor Disrupts the Acquisition But Not the Expression of Fear Conditioning

Rodrigues, S. M., Schafe, G. E., & LeDoux, J. E. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-17-06889.2001 · Cited by 350

RNA Editing at Arg607 Controls AMPA Receptor Exit from the Endoplasmic Reticulum

Greger, I. H., Khatri, L., & Ziff, E. B. (2002) · Neuron · doi:10.1016/s0896-6273(02)00693-1 · Cited by 350

Making synaptic plasticity and memory last: mechanisms of translational regulationPreprint

Richter, J. D., & Klann, E. (2009) · Genes & Development · doi:10.1101/gad.1735809 · Cited by 350

Anisotropic Black Phosphorus Synaptic Device for Neuromorphic Applications

Tian, H., Guo, Q., Xie, Y., Zhao, H., Cheng, L., Cha, J. J., Xia, F., & Wang, H. (2016) · Advanced Materials · doi:10.1002/adma.201600166 · Cited by 346

The role of 5-HT1A receptors in learning and memory

Ögren, S. O., Eriksson, T. M., Elvander-Tottie, E., D’Addario, C., Ekstrom, J. C., Svenningsson, P., Meister, B., Kehr, J., & Stiedl, O. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.02.023 · Cited by 348

Activation of PI3-Kinase Is Required for AMPA Receptor Insertion during LTP of mEPSCs in Cultured Hippocampal Neurons

Man, H.-Y., Wang, Q., Lu, W.-Y., Ju, W., Ahmadian, G., Liu, L., D'Souza, S., Wong, T. P., Taghibiglou, C., Lu, J., et al. (2003) · Neuron · doi:10.1016/s0896-6273(03)00228-9 · Cited by 307

Gene expression profiles in anatomically and functionally distinct regions of the normal aged human brain

Liang, W. S., Dunckley, T. L., Beach, T. G., Grover, A., Mastroeni, D., Walker, D. G., Caselli, R. J., Kukull, W. A., McKeel, D. W., Morris, J. C., et al. (2006) · Physiological Genomics · doi:10.1152/physiolgenomics.00208.2006 · Cited by 346

Postsynaptic Density-95 Mimics and Occludes Hippocampal Long-Term Potentiation and Enhances Long-Term Depression

Stein, V., House, D. R. C., Bredt, D. S., & Nicoll, R. A. (2003) · The Journal of Neuroscience · doi:10.1523/jneurosci.23-13-05503.2003 · Cited by 341

Protein palmitoylation: a regulator of neuronal development and function

El-Husseini, A., & Bredt, D. S. (2002) · Nature reviews. Neuroscience · doi:10.1038/nrn940 · Cited by 341

Three exercise paradigms differentially improve sensory recovery after spinal cord contusion in rats

Hutchinson, K. J. (2004) · Brain · doi:10.1093/brain/awh160 · Cited by 341

Learning in spiking neural networks by reinforcement of stochastic synaptic transmission

Seung, H. S. (2003) · Neuron · doi:10.1016/s0896-6273(03)00761-x · Cited by 340

Regulation of late-phase LTP and long-term memory in normal and aging hippocampus: role of secreted proteins tPA and BDNF

Pang, P. T., & Lu, B. (2004) · Ageing Research Reviews · doi:10.1016/j.arr.2004.07.002 · Cited by 356

Presynaptic Ca2+-Activated K+Channels in Glutamatergic Hippocampal Terminals and Their Role in Spike Repolarization and Regulation of Transmitter Release

Hu, H., Shao, L.-R., Chavoshy, S., Gu, N., Trieb, M., Behrens, R., Laake, P., Pongs, O., Knaus, H., Ottersen, O. P., et al. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-24-09585.2001 · Cited by 340

Molecular aspects of glutamate dysregulation: implications for schizophrenia and its treatment

Konradi, C., & Heckers, S. (2003) · Pharmacology & Therapeutics · doi:10.1016/s0163-7258(02)00328-5 · Cited by 336

Presynaptic Regulation of Quantal Size by the Vesicular Glutamate Transporter VGLUT1

Wilson, N. R., Kang, J., Hueske, E. V., Leung, T., Varoqui, H., Murnick, J. G., Erickson, J. D., & Liu, G. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.3003-04.2005 · Cited by 335

Malleability of Spike-Timing-Dependent Plasticity at the CA3–CA1 Synapse

Wittenberg, G. M., & Wang, S. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5388-05.2006 · Cited by 334

Supramolecular Assemblies and Localized Regulation of Voltage-Gated Ion Channels

Dai, S., Hall, D. D., & Hell, J. W. (2009) · Physiological Reviews · doi:10.1152/physrev.00029.2007 · Cited by 339

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

Efficacy and Time Course of Theta Burst Stimulation in Healthy Humans

Wischnewski, M., & Schutter, D. J. L. G. (2015) · Brain stimulation · doi:10.1016/j.brs.2015.03.004 · Cited by 350

Selective Regulation of Neurite Extension and Synapse Formation by the β but not the α Isoform of CaMKII

Fink, C. C., Bayer, K.-U., Myers, J. W., Ferrell, J. E., Schulman, H., & Meyer, T. (2003) · Neuron · doi:10.1016/s0896-6273(03)00428-8 · Cited by 328

Long-term potentiation in the amygdala: A cellular mechanism of fear learning and memory

Sigurdsson, T., Doyère, V., Cain, C. K., & LeDoux, J. E. (2006) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.06.022 · Cited by 333

Transcranial magnetic stimulation and synaptic plasticity: Experimental framework and human models

Thickbroom, G. W. (2007) · Experimental Brain Research · doi:10.1007/s00221-007-0991-3 · Cited by 326

Synaptic Plasticity and AMPA Receptor Trafficking

Malenka, R. C. (2003) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1300.001 · Cited by 333

Foundation and Practice of Neurofeedback for the Treatment of Epilepsy

Sterman, M. B., & Egner, T. (2006) · Applied Psychophysiology and Biofeedback · doi:10.1007/s10484-006-9002-x · Cited by 336

Structure, Function, and Pharmacology of NMDA Receptor Channels

Vyklický, V., Kořı́nek, M., Smejkalová, T., Balík, A., Krausová, B. H., Kaniaková, M., Lichnerová, K., Černý, J., Krůšek, J., Dittert, I., et al. (2014) · Physiological Research · doi:10.33549/physiolres.932678 · Cited by 338

A developmental switch in the signaling cascades for LTP induction

Yasuda, H., Barth, A. L., Stellwagen, D., & Malenka, R. C. (2003) · Nature Neuroscience · doi:10.1038/nn985 · Cited by 325

Fear Conditioning Occludes LTP-Induced Presynaptic Enhancement of Synaptic Transmission in the Cortical Pathway to the Lateral Amygdala

Tsvetkov, E., Carlezon, W. A., Benes, F. M., Kandel, E. R., & Bolshakov, V. Y. (2002) · Neuron · doi:10.1016/s0896-6273(02)00645-1 · Cited by 321

Timing and plasticity in the cerebellum: focus on the granular layer

D'Angelo, E. U., & Zeeuw, C. I. D. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2008.09.007 · Cited by 324

The Receptor Tyrosine Kinase EphB2 Regulates NMDA-Dependent Synaptic Function

Henderson, J. T., Georgiou, J., Jia, Z., Robertson, J. V., Elowe, S., Roder, J., & Pawson, T. J. (2001) · Neuron · doi:10.1016/s0896-6273(01)00553-0 · Cited by 320

Hippocampal theta rhythm: A tag for short‐term memory

Vertes, R. P. (2005) · Hippocampus · doi:10.1002/hipo.20118 · Cited by 319

PDZ Proteins Interacting with C-Terminal GluR2/3 Are Involved in a PKC-Dependent Regulation of AMPA Receptors at Hippocampal Synapses

Daw, M. I., Chittajallu, R., Bortolotto, Z. A., Dev, K. K., Duprat, F., Henley, J. M., Collingridge, G. L., & Isaac, J. T. R. (2000) · Neuron · doi:10.1016/s0896-6273(00)00160-4 · Cited by 323

Cholesterol 24-Hydroxylase: an enzyme of cholesterol turnover in the brain

Russell, D. W., Halford, R. W., Ramirez, D. M. O., Shah, R., & Kotti, T. (2009) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.78.072407.103859 · Cited by 317

Patch-clamp recording from mossy fiber terminals in hippocampal slices

Bischofberger, J., Engel, D., Li, L., Geiger, J. R., & Jónás, P. (2006) · Nature Protocols · doi:10.1038/nprot.2006.312 · Cited by 311

Phospholipase Cβ Serves as a Coincidence Detector through Its Ca2+ Dependency for Triggering Retrograde Endocannabinoid Signal

Hashimotodani, Y., Ohno‐Shosaku, T., Tsubokawa, H., Ogata, H., Emoto, K., Maejima, T., Araishi, K., Shin, H., & Kano, M. (2005) · Neuron · doi:10.1016/j.neuron.2005.01.004 · Cited by 317

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Krystal, J. H., Petrakis, I. L., Mason, G. F., Trevisan, L. A., & D’Souza, D. C. (2003) · Pharmacology & Therapeutics · doi:10.1016/s0163-7258(03)00054-8 · Cited by 318

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Heynen, A. J., Yoon, B.-J., Liu, C.-H., Chung, H. J., Huganir, R. L., & Bear, M. F. (2003) · Nature Neuroscience · doi:10.1038/nn1100 · Cited by 310

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Dingemans, M. M. L., van den Berg, M., & Westerink, R. H. S. (2011) · Environmental Health Perspectives · doi:10.1289/ehp.1003035 · Cited by 316

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Horn, G. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1324 · Cited by 308

Functional Electrical Stimulation and rehabilitation—an hypothesis

Rushton, D. N. (2002) · Medical Engineering & Physics · doi:10.1016/s1350-4533(02)00040-1 · Cited by 308

Exposure to hypoxia produces long-lasting sympathetic activation in humans

Xie, A., Skatrud, J. B., Puleo, D. S., & Morgan, B. J. (2001) · Journal of Applied Physiology · doi:10.1152/jappl.2001.91.4.1555 · Cited by 306

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Goto, Y., Yang, C. R., & Otani, S. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.08.026 · Cited by 316

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Pozueta, J., Lefort, R., & Shelanski, M. L. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.05.050 · Cited by 319

Insulin promotes rapid delivery of N -methyl- d - aspartate receptors to the cell surface by exocytosis

Skeberdis, V. A., Lan, J.-Y., Zheng, X., Zukin, R. S., & Bennett, M. V. L. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.051634698 · Cited by 303

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Stuber, G. D., Klanker, M., de Ridder, B., Bowers, M. S., Joosten, R. N. J. M. A., Feenstra, M. G. P., & Bonci, A. (2008) · Science · doi:10.1126/science.1160873 · Cited by 319

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Valtschanoff, J. G., & Weinberg, R. J. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-04-01211.2001 · Cited by 301

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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)

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Bliss, T. V. P., & Collingridge, G. L. (1993) · Nature · doi:10.1038/361031a0 · Cited by 11,566

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

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