Synaptic plasticity in the hippocampus: LTP and LTD

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

The Medial Temporal Lobe Memory System

Squire, L. R., & Zola-Morgan, S. (1991) · Science · doi:10.1126/science.1896849 · Cited by 3,282

Dynamics of the Hippocampal Ensemble Code for Space

Wilson, M. A., & McNaughton, B. L. (1993) · Science · doi:10.1126/science.8351520 · Cited by 2,350

Mechanisms underlying induction of homosynaptic long-term depression in area CA1 of the hippocampus

Mulkey, R. M., & Malenka, R. C. (1992) · Neuron · doi:10.1016/0896-6273(92)90248-c · Cited by 1,113

Involvement of a calcineurin/ inhibitor-1 phosphatase cascade in hippocampal long-term depression

Mulkey, R. M., Endo, S., Shenolikar, S., & Malenka, R. C. (1994) · Nature · doi:10.1038/369486a0 · Cited by 1,083

NMDA-receptor-dependent synaptic plasticity: multiple forms and mechanisms

Malenka, R. C., & Nicoll, R. A. (1993) · Trends in Neurosciences · doi:10.1016/0166-2236(93)90197-t · Cited by 904

Nitric Oxide and Synaptic Function

Schuman, E. M., & Madison, D. V. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.001101 · Cited by 774

Induction of LTP in the hippocampus needs synaptic activation of glutamate metabotropic receptors

Bashir, Z. I., Bortolotto, Z. A., Davies, C. H., Berretta, N., Irving, A. J., Seal, A., Henley, J. M., Jane, D. E., Watkins, J. C., & Collingridge, G. L. (1993) · Nature · doi:10.1038/363347a0 · Cited by 733

An Essential Role for Protein Phosphatases in Hippocampal Long-Term Depression

Mulkey, R. M., Herron, C. E., & Malenka, R. C. (1993) · Science · doi:10.1126/science.8394601 · Cited by 699

Arachidonic acid induces a long-term activity-dependent enhancement of synaptic transmission in the hippocampus

Williams, J. H., Errington, M., Lynch, M., & Bliss, T. (1989) · Nature · doi:10.1038/341739a0 · Cited by 630

Effects of changes in glucose concentration on synaptic plasticity in hippocampal slices

Kamal, A., Spoelstra, K., Biessels, G. J., Urban, I. J. A., & Gispen, W. H. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01215-9 · Cited by 20

Decreased calcineurin and increased phosphothreonine‐DARPP‐32 in the striatum of rats behaviorally sensitized to methamphetamine

Lin, X., Hashimoto, T., Kitamura, N., Murakami, N., Shirakawa, O., & Maeda, K. (2002) · Synapse · doi:10.1002/syn.10071 · Cited by 20

Detection of gene expression in single neurons by patch-clamp and single-cell reverse transcriptase polymerase chain reaction.

Chiang, L. W. (1998) · Journal of Chromatography A · doi:10.1016/s0021-9673(98)00156-3 · Cited by 19

Synaptic Plasticity and Respiratory Control

Poon, C. (2007) · Springer eBooks · doi:10.1007/978-0-585-34964-0_6 · Cited by 20

Plasticity of Synaptic Transmission in Human Stem Cell-Derived Neural Networks

Dong, Y., Xiong, M., Chen, Y., Tao, Y., Li, X., Bhattacharyya, A., & Zhang, S.-C. (2020) · iScience · doi:10.1016/j.isci.2020.100829 · Cited by 19

Age-related Loss of miR-124 Causes Cognitive Deficits via Derepressing RyR3 Expression

Liu, K., Yin, Y., Le, Y., Ouyang, W., Pan, A., Huang, J., Xie, Z., Zhu, Q., & Tong, J. (2022) · Aging and Disease · doi:10.14336/ad.2022.0204 · Cited by 19

Modulation of hippocampal long-term potentiation by slow increases in ethanol concentration

Tokuda, K., Zorumski, C. F., & Izumi, Y. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.01.037 · Cited by 19

Recovery from Retinal Lesions: Molecular Plasticity Mechanisms in Visual Cortex Far beyond the Deprived Zone

Hu, T., den Bergh, G. V., Thorrez, L., Heylen, K., Eysel, U. T., & Arckens, L. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhr079 · Cited by 19

Calcium-Independent Inhibitory G-Protein Signaling Induces Persistent Presynaptic Muting of Hippocampal Synapses

Crawford, D. C., Chang, C. Y., Hyrc, K. L., & Mennerick, S. J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.4960-10.2011 · Cited by 20

Functional relationship between age‐related immunodeficiency and learning deterioration

Zhang, Y., Moriguchi, T., Saitō, H., & Nishiyama, N. (1998) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1998.00393.x · Cited by 19

A Nitric Oxide-Independent and β-Adrenergic Receptor-Sensitive Form of Metaplasticity Limits θ-Frequency Stimulation-Induced LTP in the Hippocampal CA1 RegionPreprint

Moody, T. D., Carlisle, H. J., & O’Dell, T. J. (1999) · Learning & Memory · doi:10.1101/lm.6.6.619 · Cited by 19

Steroid Modulation of the Nicotinic Acetylcholine Receptor

Buisson, B., & Bertrand, D. (1999) · Humana Press eBooks · doi:10.1007/978-1-59259-693-5_12 · Cited by 17

Expression and subcellular localization of multifunctional calmodulin-dependent protein kinases-I, -II and -IV are altered in rat hippocampal CA1 neurons after induction of long-term potentiation.

Ahmed, B. Y., Yamaguchi, F., Tsumura, T., Gotoh, T., Sugimoto, K., Tai, Y., Konishi, R., Kobayashi, R., & Tokuda, M. (2000) · Neuroscience Letters · doi:10.1016/s0304-3940(00)01347-1 · Cited by 15

Fading memories in aging and neurodegeneration: Is p75 neurotrophin receptor a culprit?

Wong, L., Wang, Z., Ang, S. R. X., & Sajikumar, S. (2022) · Ageing Research Reviews · doi:10.1016/j.arr.2022.101567 · Cited by 19

Self‐Rectifying Short‐Term Memory Phenomena Through Integration of TiOx Oxygen Reservoir and Al 2 O 3 Barrier Layers for Neuromorphic System

Ji, H., Kim, S., & Kim, S. (2024) · Advanced Materials Technologies · doi:10.1002/admt.202400895 · Cited by 17

Retinotopic map plasticity in adult cat visual cortex is accompanied by changes in ca2+/calmodulin-dependent protein kinase ii α autophosphorylation

den Bergh, G. V., Eysel, U. T., Vandenbussche, E., Vandesande, F., & Arckens, L. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00291-4 · Cited by 17

Interaction between Hippocampal .GAMMA.-Aminobutyric AcidA and N-Methyl-D-aspartate Receptors in the Retention of Spatial Working Memory in Rats

Saito, S., Okada, A., Ouwa, T., Kato, A., Akagi, M., & Kamei, C. (2010) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.33.439 · Cited by 17

Nanoparticulate TiO2‐mediated inhibition of the Wnt signaling pathway causes dendritic development disorder in cultured rat hippocampal neurons

Hong, F., Ze, Y., Zhou, Y., Hong, J., Yu, X., Sheng, L., & Wang, L. (2017) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.36073 · Cited by 17

Stimulation of gene expression of NeuroD-related factor in the mouse brain following pentylenetetrazol-induced seizures

Konishi, Y., Matsuura, T., Mikoshiba, K., & Tamura, T. (2001) · Molecular Brain Research · doi:10.1016/s0169-328x(01)00308-4 · Cited by 17

Covariance Learning of Correlated Patterns in Competitive Networks

Minai, A. A. (1997) · Neural Computation · doi:10.1162/neco.1997.9.3.667 · Cited by 17

Increased Presynaptic Protein Kinase C Activity and Glutamate Release in Rats with a Prenatally Induced Hippocampal Lesion

Luca, M. D., Caputi, A., Cattabeni, F., Graan, P. N. E. D., Gispen, W. H., Raiteri, M., Fassio, A., Schmid, G., & Bonanno, G. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01624.x · Cited by 17

Identification and neuron specific expression of the S182/presenilin I protein in human and rodent brains

Elder, G. A., Tezapsidis, N., Carter, J. E., Shioi, J., Bouras, C., Li, H. ‐., Johnston, J. M., Efthimiopoulos, S., Friedrich, V. L., & Robakis, N. K. R. K. (1996) · Journal of Neuroscience Research · doi:10.1002/(sici)1097-4547(19960801)45:3 · Cited by 91

Artificial Synapse Emulated by Indium Tin Oxide/SiN/TaN Resistive Switching Device for Neuromorphic System

Ju, D., Kim, S., & Kim, S. (2023) · Nanomaterials · doi:10.3390/nano13172477 · Cited by 16

Synapses tagged, memories kept: synaptic tagging and capture hypothesis in brain health and disease

Ibrahim, M. Z. B., Wang, Z., & Sajikumar, S. (2024) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2023.0237 · Cited by 16

Increased ratio of calcineurin immunoreactive neurons in the caudate nucleus of patients with schizophrenia

Wada, A., Kunii, Y., Ikemoto, K., Yang, Q., Hino, M., Matsumoto, J., & Niwa, S. (2012) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2012.01.005 · Cited by 16

Long-term depression is differentially expressed in distinct lamina of hippocampal CA1 dendrites

Ramachandran, B., Ahmed, S., & Dean, C. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00023 · Cited by 16

Astrocyte and Neuronal Panx1 Support Long-Term Reference Memory in Mice

Obot, P., Subah, G., Schonwald, A., Pan, J. G., Velı́šek, L., Velı́šková, J., Stanton, P. K., & Scemes, E. (2023) · ASN NEURO · doi:10.1177/17590914231184712 · Cited by 16

Characterization of signaling function and expression of HLA class I molecules in medulloblastoma

Smith, C., Santi, M., Rushing, E. J., Cornelison, R., MacDonald, T. J., & Vukmanović, S. (2010) · Journal of Neuro-Oncology · doi:10.1007/s11060-010-0378-3 · Cited by 15

Changes in the excitability of primary hippocampal neurons following exposure to 3.0 GHz radiofrequency electromagnetic fields

Echchgadda, I., Cantu, J. C., Tolstykh, G. P., Butterworth, J. W., Payne, J. A., & Ibey, B. L. (2022) · Scientific Reports · doi:10.1038/s41598-022-06914-0 · Cited by 15

SYNTHESIS AND IN VITRO AND IN VIVO EVALUATION OF [11C]METHYL-BIII277CL FOR IMAGING THE PCP-BINDING SITE OF THE NMDA RECEPTOR BY PET

Kokic, M., Honer, M., Kessler, L. J., Grauert, M., Schubiger, P. A., & Ametamey, S. M. (2002) · Journal of Receptors and Signal Transduction · doi:10.1081/rrs-120014591 · Cited by 15

Microtubule-associated protein 2 phosphorylation is decreased in the human epileptic temporal lobe cortex

Sánchez, C., Arellano, J. I., Rodrı́guez-Sánchez, P., Ávila, J., DeFelipe, J., & Díez-Guerra, F. J. (2001) · Neuroscience · doi:10.1016/s0306-4522(01)00338-4 · Cited by 14

Inhibition of mGluR1 and IP3Rs impairs long-term memory formation in young chicks

Baker, K., Edwards, T. M., & Rickard, N. S. (2008) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2008.04.004 · Cited by 15

Dynamic NMDAR-mediated properties of place cells during the object place memory task

Faust, T. (2013) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2013.00202 · Cited by 13

Postmortem brain calcineurin protein levels in schizophrenia patients are not different from controls

Kozlovsky, N., Scarr, E., Dean, B., & Agam, G. (2006) · Schizophrenia Research · doi:10.1016/j.schres.2005.12.843 · Cited by 15

Different Routes of Ca2+ Influx in NMDA‐Mediated Generation of Nitric Oxide and Arachidonic Acid

Rodrı́guez-Álvarez, J., Lafon‐Cazal, M., Blanco, I., & Bockaert, J. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01437.x · Cited by 15

The Role of GABA in Memory Processes

Gasbarri, A., & Pompili, A. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-408139-0.00003-1 · Cited by 14

Neuronal plasticity: implications in epilepsy progression and management

Hamed, S. A. (2007) · Drug Development Research · doi:10.1002/ddr.20217 · Cited by 14

Inactivation of ATRX in forebrain excitatory neurons affects hippocampal synaptic plasticity

Gugustea, R., Tamming, R. J., Martin‐Kenny, N., Bérubé, N. G., & Leung, L.-W. S. (2019) · Hippocampus · doi:10.1002/hipo.23174 · Cited by 14

Nitric oxide synthase expression in the central nervous system of Sepia officinalis: an in situ hybridization study

Cristo, C. D., Fiore, G., Scheinker, V., Enikolopov, G., d’Ischia, M., Palumbo, A., & Cosmo, A. D. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05765.x · Cited by 14

Integrative Proteomics: Functional and Molecular Characterization of a Particular Glutamate-Related Neuregulin Isoform

Schillo, S., Pejović, V., Hunzinger, C., Hansen, T., Poznanović, S., Kriegsmann, J., Schmidt, W., & Schrattenholz, A. S. (2005) · Journal of Proteome Research · doi:10.1021/pr050012p · Cited by 13

Probabilistic Synaptic Transmission in the Associative Net

Graham, B. P., & Willshaw, D. J. (1999) · Neural Computation · doi:10.1162/089976699300016845 · Cited by 14

α2-Adrenergic receptor activation promotes long-term potentiation at excitatory synapses in the mouse accessory olfactory bulbPreprint

Huang, G.-Z., Taniguchi, M., Zhou, Y., Zhang, J.-J., Okutani, F., Murata, Y., Yamaguchi, M., & Kaba, H. (2018) · Learning & Memory · doi:10.1101/lm.046391.117 · Cited by 14

Species-specific differences in synaptic transmission and plasticity

Beed, P. S., Ray, S., Velasquez, L. M., Stumpf, A., Parthier, D., Swaminathan, A., Nitzan, N., Breustedt, J., Las, L., Brecht, M., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-73547-6 · Cited by 13

Recent Advances in Halide Perovskite-Based Nonvolatile Resistive Random-Access Memory

Siddik, A., Sarkar, P. K., & Haldar, P. K. (2021) · Journal of Electronic Materials · doi:10.1007/s11664-021-09328-2 · Cited by 15

Preconditioning effects of tumor necrosis factor-α and glutamate on calcium dynamics in rat organotypic hippocampal cultures

Watters, O., Pickering, M., & O'Connor, J. J. (2011) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2011.01.008 · Cited by 13

Extracellular carbohydrate-signal triggering camp-dependent protein kinase-dependent neuronal actin-reorganization

Chen, N., Furuya, S., Shinoda, Y., Yumoto, M., Ohtake, A., Sato, K., Doi, H., Hashimoto, Y., Kudo, Y., & Higashi, H. (2003) · Neuroscience · doi:10.1016/j.neuroscience.2003.08.042 · Cited by 13

Hebbian Covariance Learning

Young, D. L., & Poon, C. (1998) · Advances in experimental medicine and biology · doi:10.1007/978-1-4757-9077-1_14 · Cited by 13

Non‐ionotropic NMDAR signalling activates Panx1 to induce P2X4R‐dependent long‐term depression in the hippocampus

Nielsen, A. C., Anderson, C. L., Ens, C., Boyce, A. K. J., & Thompson, R. J. (2024) · The Journal of Physiology · doi:10.1113/jp285193 · Cited by 12

Different effects of low frequency stimulation to infralimbic prefrontal cortex on extinction of aversive memories

Shehadi, K., & Maroun, M. (2012) · Brain Research · doi:10.1016/j.brainres.2012.10.026 · Cited by 16

PPAR-δ Activation Ameliorates Diabetes-Induced Cognitive Dysfunction by Modulating Integrin-linked Kinase and AMPA Receptor Function

Abdel‐Rahman, E. A., Bhattacharya, S., Buabeid, M. A., Majrashi, M., Bloemer, J., Tao, Y., Dhanasekaran, M., Escobar, M. E., Amin, R., & Suppiramaniam, V. D. (2019) · Journal of the American College of Nutrition · doi:10.1080/07315724.2019.1598307 · Cited by 12

A SPICE Model of Phase Change Memory for Neuromorphic Circuits

Chen, X., Hu, H., Huang, X., Cai, W., Liu, M., Lam, C. H., Lin, X., Zhang, L., & Chan, M. (2020) · IEEE Access · doi:10.1109/access.2020.2995907 · Cited by 12

The Molecular Mechanisms Underlying Synaptic Transmission

Ashery, U., Bielopolski, N., Lavi, A., Barak, B., Michaeli, L., Ben‐Simon, Y., Sheinin, A., Bar-On, D., Shapira, Z., & Gottfried, I. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-418675-0.00002-x · Cited by 13

Methods of detection of the transcription factor NF-κB in rat hippocampal slices

Butler, M. P., Moynagh, P. N., & O'Connor, J. J. (2002) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(02)00171-1 · Cited by 12

Seizure-mediated neuronal activation induces DREAM gene expression in the mouse brain

Matsuura, T., Konishi, Y., Aoki, T., Naranjo, J. R., Mikoshiba, K., & Tamura, T. (2002) · Molecular Brain Research · doi:10.1016/s0169-328x(02)00562-4 · Cited by 12

Orexin receptors mediate long-term depression of excitatory synaptic transmission in the spinal cord dorsal horn

Park, K. B., & Weon, H. (2017) · Neuroscience Letters · doi:10.1016/j.neulet.2017.08.068 · Cited by 12

Differential downregulation of protein kinase C isoforms in spreading depression

Osten, P., Hrabětová, S., & Sacktor, T. C. (1996) · Neuroscience Letters · doi:10.1016/s0304-3940(96)13280-8 · Cited by 12

Putative pathological mechanisms of late-life depression and Alzheimer’s disease

Hasan, S. M. N., Clarke, C., Strand, T., & Bambico, F. R. (2023) · Brain Research · doi:10.1016/j.brainres.2023.148423 · Cited by 13

Ca2+/calmodulin-dependent protein kinase II and protein kinase C activities mediate extracellular glucose-regulated hippocampal synaptic efficacy

Moriguchi, S., Oomura, Y., Shioda, N., Han, F., Hori, N., Aou, S., & Fukunaga, K. (2010) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2010.08.010 · Cited by 11

The Kappa Opioid Receptor System in Temporal Lobe Epilepsy

Zangrandi, L., & Schwarzer, C. (2021) · Handbook of experimental pharmacology · doi:10.1007/164_2021_444 · Cited by 11

Prenatal Exposures to LTP-Patterned Magnetic Fields: Quantitative Effects on Specific Limbic Structures and Acquisition of Contextually Conditioned Fear

Whissell, P. D., Tsang, E. W., Mulligan, B. P., & Persinger, M. A. (2009) · International Journal of Neuroscience · doi:10.1080/00207450802480283 · Cited by 11

Differential induction of long term synaptic plasticity in inhibitory synapses of the hippocampus

Mendoza, E., Galarraga, E., Tapia, D., Laville, A., Hernández, E., & Bargas, J. (2006) · Synapse · doi:10.1002/syn.20331 · Cited by 11

Identification of a biphasic signaling pathway involved in ischemic resistance of the hippocampal dentate gyrus

Blanquet, P., Mariani, J., & Fournier, B. (2006) · Experimental Neurology · doi:10.1016/j.expneurol.2006.06.016 · Cited by 11

Modeling and Training Radial Basis Functions with Integrate-and-Fire Neurons

Hudson, R. E., Marvel, J. A., & Newman, W. S. (2010) · International Conference on Machine Learning and Applications · doi:10.1109/icmla.2010.39 · Cited by 11

Biochemistry and Pharmacology of Calmodulin-Regulated Phosphatase Calcineurin

Perrino, B. A., & Soderling, T. R. (1998) · Elsevier eBooks · doi:10.1016/b978-0-08-092636-0.50008-6 · Cited by 12

Kindling and Quenching: Conceptual Links to rTMS

Weiss, S. R. B., Li, X., Heynen, T., Noguera, E. C., Huan⁃ting, L. I., & Post, R. M. (1997) · CNS Spectrums · doi:10.1017/s1092852900004442 · Cited by 11

Transgenic Mouse Models: New Tools for Psychiatric Research

Holsboer, F. (1997) · The Neuroscientist · doi:10.1177/107385849700300514 · Cited by 11

Presenilins regulate synaptic plasticity in the perforant pathways of the hippocampus

Lee, S. H., Bolshakov, V. Y., & Shen, J. (2023) · Molecular Brain · doi:10.1186/s13041-023-01009-x · Cited by 10

Dentate granule cells encode auditory decisions after reinforcement learning in rats

Shen, J., Yao, P., Ge, S., & Xiong, Q. (2021) · Scientific Reports · doi:10.1038/s41598-021-93721-8 · Cited by 9

Benzyl alcohol inhibits N-methyl-d-aspartate receptor-mediated neurotoxicity and calcium accumulation in cultured rat cortical neurons

Takadera, T., & Ohyashiki, T. (2008) · Journal of Biomedical Science · doi:10.1007/s11373-008-9276-5 · Cited by 9

Transcranial Current Stimulation as a Tool of Neuromodulation of Cognitive Functions in Parkinson’s Disease

Brak, I. V., Filimonova, E., Zakhariya, O., Khasanov, R., & Stepanyan, I. V. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.781488 · Cited by 13

Symmetric and Asymmetric Synapses Driving Neurodegenerative Disorders

Romaus‐Sanjurjo, D., Custodia, A., Aramburu-Núñez, M., Posado-Fernández, A., Vázquez‐Vázquez, L., Camino-Castiñeiras, J., Leira, Y., Peleteiro, J. M. P., Aldrey, J. M., Ouro, A., et al. (2021) · Symmetry · doi:10.3390/sym13122333 · Cited by 8

Long-term depression with a flash

Malenka, R., & Nicoll, R. (1998) · Nature Neuroscience · doi:10.1038/333 · Cited by 10

Effects of lactate/pyruvate on synaptic plasticity in the hippocampal dentate gyrus

Yang, B., Sakurai, T., Takata, T., & Yokono, K. (2003) · Neuroscience Research · doi:10.1016/s0168-0102(03)00096-8 · Cited by 9

Epileptic Activity Prevents Synapse Formation of Hippocampal Mossy Fibers via L-Type Calcium Channel Activation In Vitro

Ikegaya, Y., Yoshida, M., Saito, H., & Nishiyama, N. (1997) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)36378-5 · Cited by 9

A neuromagnetic view of hippocampal memory functions

Sandyk, R. (1998) · International Journal of Neuroscience · doi:10.3109/00207459808986430 · Cited by 9

Signal transduction in neuropathic pain, with special emphasis on the analgesic role of opioids - Part I: The basic science of phenotype expression in normal and regenerating nerves

McCormack, K. (1999) · Pain Reviews · doi:10.1191/096813099676046619 · Cited by 9

Research Methodology and Statistics

Weiss, D. S., & Delucchi, K. (2015) · doi:10.1002/9781118753378.ch131 · Cited by 9

Quenching

Weiss, S. R. B., Li, X., Noguera, E. C., Heynen, T., Li, H., Rosen, J. B., & Post, R. M. (1998) · Advances in behavioral biology · doi:10.1007/978-1-4615-5375-5_9 · Cited by 9

Pseudo-transistors for emerging neuromorphic electronics

Fu, J., Wang, J., He, X., Ming, J., Wang, L., Wang, Y., Shao, H., Zheng, C., Xie, L., & Ling, H. (2023) · Science and Technology of Advanced Materials · doi:10.1080/14686996.2023.2180286 · Cited by 8

Sleep and Appetitive Conditioned Memory

Tripathi, S., Tripathi, S., Anjali, & Jha, S. K. (2019) · Springer eBooks · doi:10.1007/978-981-13-2814-5_9 · Cited by 8

A potential mechanism for first-person internal sensation of memory provides evidence for the relationship between learning and LTP induction

Vadakkan, K. I. (2018) · Behavioural Brain Research · doi:10.1016/j.bbr.2018.11.038 · Cited by 9

Multi-scale modeling of the circadian modulation of learning and memory

Sisobhan, S., & Sriram, K. (2019) · PLoS ONE · doi:10.1371/journal.pone.0219915 · Cited by 9

Cerebral Damage after Stroke: The Role of Neuroplasticity as Key for Recovery

Muhammad, M., & Hassan, T. M. (2021) · IntechOpen eBooks · doi:10.5772/intechopen.95512 · Cited by 8

Effects of Diethylstilbestrol on Mouse Hippocampal Evoked Potentials in Vitro

Martín, S. S., Gutiérrez, M., Menéndez, L., Hidalgo, A., & Baamonde, A. (1999) · Cellular and Molecular Neurobiology · doi:10.1023/a:1006996805017 · Cited by 8

Brain Plasticity and Remodeling of AMPA Receptor Properties by Calcium-Dependent Enzymes

Massicotte, G., & Baudry, M. (2004) · Springer eBooks · doi:10.1007/978-0-306-48573-2_12 · Cited by 8

Targeted Disruption of the Protein Kinase A System in Mice

McKnight, G. S., Idzerda, R. L., Kandel, E. R., Brandon, E. P., Zhuo, M., Qi, M., Bourtchouladze, R., Huang, Y.-Y., Burton, K. A., Skålhegg, B. S., et al. (1996) · Springer eBooks · doi:10.1007/978-3-662-03230-5_6 · Cited by 8

Prospects and challenges in NMDAR signaling in spinal cord injury recovery and neural circuit remodeling

Gong, H., Xu, X. P., Talifu, Z., Zhang, C.-J., Sun, Y., Yue, Z.-M., Rao, J., Du, L., & Du, X. (2025) · Regenerative Therapy · doi:10.1016/j.reth.2025.03.008 · Cited by 7

Trans-cinnamaldehyde ameliorates neuroinflammation-mediated synaptic plasticity and memory impairment by blocking TLR4/MyD88/MAPKs pathway in global cerebral ischemia

Liu, X., Lu, Z., He, G., Gao, W., Hu, K., Pan, J., Zhao, Y., Wang, X., Yang, G., & Xu, Y. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111456 · Cited by 7

A pilot study to examine the association between COX-2 rs5275 polymorphism and the response to repetitive transcranial stimulation in schizophrenia

Wang, P., Guan, X., Su, X., Wu, F., & Xiu, M. (2023) · Schizophrenia · doi:10.1038/s41537-023-00386-5 · Cited by 8

The Role of Vesicle Release and Synaptic Transmission in Depression

Zhang, C., Zhu, L., Shi, H., & Zhu, L. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.10.001 · Cited by 7

A model of bi-directional interactions between complementary learning systems for memory consolidation of sequential experiences

Howard, M. D., Skorheim, S. W., & Pilly, P. K. (2022) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2022.972235 · Cited by 10

Control of Neural Information Transmission by Synaptic Dynamics

Cartling, B. G. (2002) · Journal of Theoretical Biology · doi:10.1006/jtbi.2001.2462 · Cited by 7

Attenuated Glial K + Clearance Contributes to Long-Term Synaptic Potentiation Via Depolarizing GABA in Dorsal Horn Neurons of Rat Spinal Cord

Lee, J., Favorov, O. V., Tommerdahl, M., Lee, C. J., & Whitsel, B. L. (2014) · Experimental Neurobiology · doi:10.5607/en.2014.23.1.53 · Cited by 7

Exploring Cortical Plasticity and Oscillatory Brain Dynamics via Transcranial Magnetic Stimulation and Resting-State Electroencephalogram

Noh, N. A. (2016) · Malaysian Journal of Medical Sciences · doi:10.21315/mjms2016.23.4.2 · Cited by 7

Prandial Increases of Leptin and Orexin in the Brain Modulate Spatial Learning and Memory

Oomura, Y., Aou, S., Fukunaga, K., Moriguchi, S., & Sasaki, K. (2011) · Neuroscience and Behavioral Physiology · doi:10.1007/s11055-011-9405-x · Cited by 7

Inhibition of transmitter release and long-term depression in the avian hippocampus

Margrie, T. W., Rostas, J. A. P., & Sah, P. (2000) · Neuroscience Letters · doi:10.1016/s0304-3940(00)00992-7 · Cited by 7

Influence of restraint stress on the expression and the serine/threonine phosphatase activity of calcineurin in the rat brain

Takahashi, J., Tanaka, K., Morinobu, S., Fujimaki, K., Li, S., Katō, K., Ohkawa, M., Yamawaki, S., & Kato, N. (2001) · Synapse · doi:10.1002/syn.1034 · Cited by 7

[3H]CGP 61594, the first photoaffinity ligand for the glycine site of NMDA receptors

Benke, D., Honer, M., Heckendorn, R., Pozza, M. F., Allgeier, H., Angst, C., & Möhler, H. (1999) · Neuropharmacology · doi:10.1016/s0028-3908(98)00191-9 · Cited by 7

Temporal-Specific Sex and Injury-Dependent Changes on Neurogranin-Associated Synaptic Signaling After Controlled Cortical Impact in Rats

Svirsky, S. E., Henchir, J. J., Li, Y., Carlson, S. W., & Dixon, C. E. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04043-5 · Cited by 7

Simulation of neural functions based on organic semiconductor/MXene synaptic transistors

Qiu, H., Lan, S., Lin, Q., Zhu, H., Liao, W., & Yang, L. (2024) · Organic Electronics · doi:10.1016/j.orgel.2024.107090 · Cited by 6

Hippocampal Synaptic Enhancement as a Basis for Learning and Memory:A Selected Review of Current Evidence from Behaving Animals

Barnes, C. A., Erickson, C. A., Davis, S., & McNaughton, B. L. (1995) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195082944.003.0016 · Cited by 11

Long-term potentiation: What's learning got to do with it?

Shors, T. J., & Matzel, L. D. (1997) · Behavioral and Brain Sciences · doi:10.1017/s0140525x97001593 · Cited by 320

Pretraining and the Function of Hippocampal Long-Term Potentiation

Moser, M., & Moser, E. I. (2000) · Neuron · doi:10.1016/s0896-6273(00)81192-7 · Cited by 17

Physiological significance of long-term potentiation.

Esposito, E., & Pulvirenti, L. (1992) · PubMed · Cited by 4

Hippocampal synaptic enhancement and information storage within a distributed memory system

McNaughton, B. L., & Morris, R. G. M. (1987) · Trends in Neurosciences · doi:10.1016/0166-2236(87)90011-7 · Cited by 1,304