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

Long-Term Depression Is Independent of GluN2 Subunit Composition

Wong, J. M., & Gray, J. A. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0394-18.2018 · Cited by 39

The Role of Neural Activity in Cortical Axon Branching

Uesaka, N., Ruthazer, E. S., & Yamamoto, N. (2006) · The Neuroscientist · doi:10.1177/1073858405281673 · Cited by 39

A Re-Examination of Hebbian-Covariance Rules and Spike Timing-Dependent Plasticity in Cat Visual Cortex in vivo

Frégnac, Y., Pananceau, M., René, A., Huguet, N., Marre, O., Levy, M. S., & Shulz, D. E. (2010) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2010.00147 · Cited by 36

Bidirectional regulation of synaptic plasticity in the basolateral amygdala induced by the D1‐like family of dopamine receptors and group II metabotropic glutamate receptors

Li, C., & Rainnie, D. G. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2014.277715 · Cited by 39

ALTERED BRAIN WAVE ACTIVITY IN PERSONS WITH CHRONIC SPINAL CORD INJURY

HERBERT, D., Tran, Y., Craig, A. R., Boord, P., Middleton, J. W., & Siddall, P. J. (2007) · International Journal of Neuroscience · doi:10.1080/00207450701242826 · Cited by 38

In VitroEye-Blink Classical Conditioning Is NMDA Receptor Dependent and Involves Redistribution of AMPA Receptor Subunit GluR4

Keifer, J. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-07-02434.2001 · Cited by 37

Early brain wiring: activity-dependent processes

Penn, A. A. (2001) · Schizophrenia Bulletin · doi:10.1093/oxfordjournals.schbul.a006880 · Cited by 37

Non-ionotropic signaling by the NMDA receptor: controversy and opportunity

Gray, J. A., Zito, K., & Hell, J. W. (2016) · F1000Research · doi:10.12688/f1000research.8366.1 · Cited by 37

Stimulus-dependent, reciprocal up- and downregulation of glutamic acid decarboxylase and Ca2+/calmodulin-dependent protein kinase II gene expression in rat cerebral cortex

Liang, F., Isackson, P. J., & Jones, E. G. (1996) · Experimental Brain Research · doi:10.1007/bf00228548 · Cited by 37

Group I metabotropic glutamate receptors enable two distinct forms of long‐term depression in the rat dentate gyrusin vivo

Naie, K., Tsanov, M., & Manahan‐Vaughan, D. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05583.x · Cited by 36

Ganglioside/calmodulin kinase ii signal inducing cdc42-mediated neuronal actin reorganization

Chen, N., Furuya, S., Doi, H., Hashimoto, Y., Kudo, Y., & Higashi, H. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00259-8 · Cited by 35

The reinforcing effects of chronic d ‐amphetamine and morphine are impaired in a line of memory‐deficient mice overexpressing calcineurin

Biała, G., Betancur, C., Mansuy, I. M., & Giros, B. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04132.x · Cited by 36

Transient translocation of conventional protein kinase C isoforms and persistent downregulation of atypical protein kinase Mζ in long-term depression

Hrabětová, S., & Sacktor, T. C. (2001) · Molecular Brain Research · doi:10.1016/s0169-328x(01)00185-1 · Cited by 36

Computational modeling of GABAA receptor-mediated paired-pulse inhibition in the dentate gyrus

Jedlička, P., Deller, T., & Schwarzacher, S. W. (2010) · Journal of Computational Neuroscience · doi:10.1007/s10827-010-0214-y · Cited by 40

Activation of a synapse weakening pathway by human Val66 but not Met66 pro-brain-derived neurotrophic factor (proBDNF)

Kailainathan, S., Piers, T. M., Yi, J. H., Choi, S., Fahey, M. S., Borger, E., Gunn‐Moore, F. J., O’Neill, L., Lever, M. B., Whitcomb, D. J., et al. (2015) · Pharmacological Research · doi:10.1016/j.phrs.2015.12.008 · Cited by 35

Role of Cofilin in Alzheimer’s Disease

Wang, Q., Yuan, W., Yang, X., Wang, Y., Li, Y., & Qiao, H. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.584898 · Cited by 35

Epilepsies and neuronal plasticity: for better or for worse?

Ben‐Ari, Y. (2008) · Dialogues in Clinical Neuroscience · doi:10.31887/dcns.2008.10.1/ybenari · Cited by 35

Monitoring protein phosphatase 1 isoform levels as a marker for cellular stress

Camões, F., Henriques, A. G., Silva, O. A. B. D. C. E., & Silva, E. F. D. C. E. (2004) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2003.12.007 · Cited by 34

Distribution of choline acetyltransferase (ChAT) immunoreactivity in the brain of the adult trout and tract-tracing observations on the connections of the nuclei of the isthmus

Pérez, S. E., Y��ez, J., Marín, Ó., Anad�n, R., Gonz�lez, A., & Rodríguez‐Moldes, I. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20001218)428:3 · Cited by 96

Calcium Release From Internal Stores Is Required for the Generation of Spontaneous Hyperpolarizations in Dopaminergic Neurons of Neonatal Rats

Seutin, V., Mkahli, F., Massotte, L., & Dresse, A. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.1.192 · Cited by 34

Spatial features of calcium-regulated gene expression.

Finkbeiner, S., & Greenberg, M. (1997) · Bioessays · doi:10.1002/bies.950190803 · Cited by 39

Pattern and predictability in memory formation: From molecular mechanisms to clinical relevance

Philips, G. T., Kopec, A. M., & Carew, T. J. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.05.003 · Cited by 33

Shp2 in Forebrain Neurons Regulates Synaptic Plasticity, Locomotion, and Memory Formation in Mice

Kusakari, S., Saitow, F., Ago, Y., Shibasaki, K., Sato‐Hashimoto, M., Matsuzaki, Y., Kotani, T., Murata, Y., Hirai, H., Matsuda, T., et al. (2015) · Molecular and Cellular Biology · doi:10.1128/mcb.01339-14 · Cited by 33

Synaptic plasticity in area CA1 of rat hippocampal slices following intraventricular application of albumin

Salar, S., Lapilover, E., Müller, J., Hollnagel, J., Lippmann, K., Friedman, A., & Heinemann, U. (2016) · Neurobiology of Disease · doi:10.1016/j.nbd.2016.03.008 · Cited by 32

Elevated PSD-95 Blocks Ion-flux Independent LTD: A Potential New Role for PSD-95 in Synaptic Plasticity

Doré, K., & Malinow, R. (2020) · Neuroscience · doi:10.1016/j.neuroscience.2020.02.020 · Cited by 34

Effects of metabolic state on the regulation of melanocortin circuits

Lieu, L., Chau, D., Afrin, S., Dong, Y., Alhadeff, A. L., Betley, J. N., & Williams, K. W. (2020) · Physiology & Behavior · doi:10.1016/j.physbeh.2020.113039 · Cited by 35

Dentate granule cell layer collagen explant cultures: Spontaneous axonal growth and induction by brain-derived neurotrophic factor or basic fibroblast growth factor

Lowenstein, D. H., & Arsenault, L. (1996) · Neuroscience · doi:10.1016/0306-4522(96)00226-6 · Cited by 33

Developmental and Activity Dependent Regulation of Ionotropic Glutamate Receptors at Synapses

Molnár, E., & Isaac, J. T. R. (2002) · The Scientific World JOURNAL · doi:10.1100/tsw.2002.74 · Cited by 33

Modulation of long-term potentiation induction in the hippocampus by N-methyl-D-aspartate-mediated presynaptic inhibition.

Kato, K., Li, S.-T., & Zorumski, C. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00080-9 · Cited by 33

Activation of group I metabotropic glutamate receptors induces long-term depression at sensory synapses in superficial spinal dorsal horn

Chen, J., Heinke, B., & Sandkühler, J. (2000) · Neuropharmacology · doi:10.1016/s0028-3908(00)00084-8 · Cited by 33

TREM2 and Microglia Contribute to the Synaptic Plasticity: from Physiology to Pathology

Yu, C.-J., Wang, M., Ruiyang, L., Wei, T., Yang, H.-C., Yin, Y., Mi, Y., Qin, Q., & Tang, Y. (2022) · Molecular Neurobiology · doi:10.1007/s12035-022-03100-1 · Cited by 34

Cyclic AMP and Afferent Activity Govern Bidirectional Synaptic Plasticity in Striatopallidal Neurons

Augustin, S. M., Beeler, J. A., McGehee, D. S., & Zhuang, X. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.3906-13.2014 · Cited by 34

Functional Diversity of Actin Cytoskeleton in Neurons and its Regulation by Tropomyosin

Schevzov, G., Curthoys, N. M., Gunning, P. W., & Fath, T. (2012) · International review of cytology · doi:10.1016/b978-0-12-394309-5.00002-x · Cited by 34

Capture of activity-induced ultrastructural changes at synapses by high-pressure freezing of brain tissue

Studer, D., Zhao, S., Chai, X., Jonas, P., Graber, W., Nestel, S., & Frotscher, M. (2014) · Nature Protocols · doi:10.1038/nprot.2014.099 · Cited by 31

Hebb's concept of synaptic plasticity and neuronal cell assemblies.

Spatz, H. (1996) · Behavioural Brain Research · doi:10.1016/0166-4328(95)00221-9 · Cited by 34

Dissecting the Effect of Aging on the Neural Substrates of Memory: Deterioration, Preservation or Functional Reorganization?

Della‐Maggiore, V., Grady, C. L., & McIntosh, A. R. (2002) · Reviews in the Neurosciences · doi:10.1515/revneuro.2002.13.2.167 · Cited by 31

Low-frequency stimulation induces long-term depression and slow onset long-term potentiation at perforant path-dentate gyrus synapses in vivo

Gonzalez, J., Morales, I. S., Villarreal, D. M., & Derrick, B. E. (2013) · Journal of Neurophysiology · doi:10.1152/jn.00941.2012 · Cited by 32

Involvement of calmodulin-dependent protein kinases-I and -IV in long-term potentiation.

Tokuda, M., Ahmed, B. Y., Lu, Y.-F., Matsui, H., Miyamoto, O., Yamaguchi, F., Konishi, R., & Hatase, O. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00189-3 · Cited by 28

Differential association of postsynaptic signaling protein complexes in striatum and hippocampus

Baucum, A. J., Brown, A. M., & Colbran, R. J. (2012) · Journal of Neurochemistry · doi:10.1111/jnc.12101 · Cited by 29

Ionotropic and Metabotropic Glutamate Receptor Agonist‐Induced [Ca2+]i Increase in Isolated Rat Supraoptic Neurons

Hattori, Y., Shibuya, I., Tanaka, K., Kabashima, N., Ueta, Y., & Yamashita, H. (1998) · Journal of Neuroendocrinology · doi:10.1046/j.1365-2826.1998.00219.x · Cited by 30

Chapter 9 Mechanisms involved in development of retinotectal connections: Roles of Eph receptor tyrosine kinases, NMDA receptors and nitric oxide

Ernst, A. F., Jurney, W. M., & McLoon, S. C. (1998) · Progress in brain research · doi:10.1016/s0079-6123(08)63204-5 · Cited by 30

The influence of steady magnetic fields on the mouse hippocampal evoked potentials in vitro

Trabulsi, R., Pawlowski, B., & Wieraszko, A. (1996) · Brain Research · doi:10.1016/0006-8993(96)00508-2 · Cited by 30

Decreased expression of the alpha subunit of Ca2+/ calmodulin-dependent protein kinase type II mRNA in the adult rat CNS following recurrent limbic seizures.

Murray, K. D., Gall, C. M., Benson, D., Jones, E., & Isackson, P. (1995) · Brain Research. Molecular Brain Research · doi:10.1016/0169-328x(95)00080-c · Cited by 30

Properties of Conditioned Abducens Nerve Responses in a Highly Reduced In Vitro Brain Stem Preparation From the Turtle

Anderson, C. W., & Keifer, J. (1999) · Journal of Neurophysiology · doi:10.1152/jn.1999.81.3.1242 · Cited by 30

PRESENCE D’UNE PRÉDISPOSITION : PREMIER ÉPISODE D’UNE SÉRIE DE HUIT ÉPISODES SUR LE CERVEAU

Fahim, C. (2022) · Cortica · doi:10.26034/cortica.2022.3344 · Cited by 29

Role of N-Methyl-D-aspartate Receptors in Antidepressant-Like Effects of σ1 Receptor Agonist 1-(3,4-Dimethoxyphenethyl)-4-(3-phenylpropyl)piperazine Dihydrochloride (SA-4503) in Olfactory Bulbectomized Rats

Wang, D., Noda, Y., Tsunekawa, H., Zhou, Y., Miyazaki, M., Senzaki, K., Nitta, A., & Nabeshima, T. (2007) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.107.124685 · Cited by 29

Kinetic simulation of signal transduction system in hippocampal long-term potentiation with dynamic modeling of protein phosphatase 2A

Kikuchi, S., Fujimoto, K., Kitagawa, N., Fuchikawa, T., Abe, M., Oka, K., Takei, K., & Tomita, M. (2003) · Neural Networks · doi:10.1016/j.neunet.2003.09.002 · Cited by 29

Role of PDE9 in Cognition

Dorner‐Ciossek, C., Kroker, K. S., & Rosenbrock, H. (2017) · Advances in neurobiology · doi:10.1007/978-3-319-58811-7_9 · Cited by 29

Serine/threonine kinases as molecular targets of antidepressants: implications for pharmacological treatment and pathophysiology of affective disorders

Popoli, M. (2001) · Pharmacology & Therapeutics · doi:10.1016/s0163-7258(00)00108-x · Cited by 29

Effects of the Ca2+ antagonist nimodipine on functional deficits in the peripheral and central nervous system of streptozotocin-diabetic rats

Biessels, G. J., ter Laak-Poort, M., Kamal, A., & Gispen, W. H. (2005) · Brain Research · doi:10.1016/j.brainres.2004.12.025 · Cited by 29

Calcineurin in the adult rat hippocampus: different distribution in CA1 and CA3 subfields

Morioka, M., Nagahiro, S., Fukunaga, K., Miyamoto, E., & Ushio, Y. (1997) · Neuroscience · doi:10.1016/s0306-4522(96)00626-4 · Cited by 30

Modulation of gene expression following long-term synaptic depression in the striatum

Napolitano, M., Marfia, G. A., Vacca, A., Centonze, D., Bellavia, D., Marcotullio, L. D., Frati, L., Bernardi, G., Gulino, A., & Calabresi, P. (1999) · Molecular Brain Research · doi:10.1016/s0169-328x(99)00213-2 · Cited by 29

AMPA receptor phosphorylation is selectively regulated by constitutive phospholipase A2and 5-lipoxygenase activities

Ménard, C., Valastro, B., Martel, M., Chartier, É., Marineau, A., Baudry, M., & Massicotte, G. (2005) · Hippocampus · doi:10.1002/hipo.20061 · Cited by 29

Impaired learning and memory generated by hyperthyroidism is rescued by restoration of AMPA and NMDA receptors function

Zhu, W., Wu, F., Li, J., Meng, L., Zhang, W., Zhang, H., Cha, S., Zhang, J., & Guo, G. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105807 · Cited by 29

Sleep deprivation impairs learning and memory by decreasing protein O ‐GlcNAcylation in the brain of adult zebrafish

Lee, Y., Park, J. W., Kim, S., Nam, K., Lee, W., Cho, H., & Han, I. (2019) · The FASEB Journal · doi:10.1096/fj.201901399rr · Cited by 28

Neural Plasticity and the Development of Sex Differences

Juraska, J. M. (1998) · Annual Review of Sex Research · doi:10.1080/10532528.1998.10559925 · Cited by 27

The inositol 1,4,5-trisphosphate receptor of cerebellum. Mn2+ permeability and regulation by cytosolic Mn2+.

Striggow, F., & Ehrlich, B. E. (1996) · The Journal of General Physiology · doi:10.1085/jgp.108.2.115 · Cited by 27

Synaptic modification in neural circuits: A timely action

Berninger, B., & Bi, G. (2002) · BioEssays · doi:10.1002/bies.10060 · Cited by 27

Roles of Inhibitory Interneurons in the Cerebellar Cortex

Hirano, T., WATANABE, D., Kawaguchi, S., Pastan, I. H., & Nakanishi, S. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb07583.x · Cited by 26

Platelet activating factor (PAF) in memory formation: role as a retrograde messenger in long-term potentiation

Kornecki, E., Wieraszko, A., Chan, J., & Ehrlich, Y. H. (1996) · Journal of Lipid Mediators and Cell Signalling · doi:10.1016/0929-7855(96)01517-9 · Cited by 26

Low-Level Baroreceptor Stimulation Suppresses Atrial Fibrillation by Inhibiting Ganglionated Plexus Activity

Liao, K., Yu, L., Zhou, X., Saren, G., Wang, S., Wang, Z., Huang, B. S., Yang, K., & Jiang, H. (2015) · Canadian Journal of Cardiology · doi:10.1016/j.cjca.2015.01.007 · Cited by 25

A Hyperactive Form of unc-13 Enhances Ca2+ Sensitivity and Synaptic Vesicle Release Probability in C. elegans

Li, L., Liu, H., Hall, Q., Wang, W., Yu, Y., Kaplan, J. M., & Hu, Z. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.08.018 · Cited by 24

Characterization of NMDA induced depression in rat hippocampus: involvement of AMPA and NMDA receptors

Li, R., Dozmorov, M. G., Hellberg, F., Tian, Y., Jilderos, B., & Wigström, H. (2004) · Neuroscience Letters · doi:10.1016/j.neulet.2003.11.004 · Cited by 25

Neuronal activity and the establishment of normal and epileptic circuits during brain development

Swann, J. W., Smith, K. L., & Lee, C. L. (2001) · International review of neurobiology · doi:10.1016/s0074-7742(01)45007-0 · Cited by 25

EPO induces changes in synaptic transmission and plasticity in the dentate gyrus of rats

Almaguer‐Melian, W., Mercerón‐Martínez, D., Delgado‐Ocaña, S., Fuentes, N. P., Ledón, N., & Bergado, J. A. (2016) · Synapse · doi:10.1002/syn.21895 · Cited by 23

Regulation of Calcineurin, a Calcium/Calmodulin-dependent Protein Phosphatase, in C. elegans

Bandyopadhyay, J., Lee, J., & Bandyopadhyay, A. (2004) · Molecules and Cells · doi:10.1016/s1016-8478(23)13075-5 · Cited by 24

Estrogen and Environmental Enrichment Differentially Affect Neurogenesis, Dendritic Spine Immunolabeling and Synaptogenesis in the Hippocampus of Young and Reproductively Senescent Female Rats

Sager, T. M., Kashon, M. L., & Krajnak, K. (2017) · Neuroendocrinology · doi:10.1159/000479699 · Cited by 24

In vivo visualization of hippocampal cells and dynamics of Ca2+ concentration during anoxia: feasibility of a fiber-optic plate microscope system for in vivo experiments

Hirano, M., Yamashita, Y., & Miyakawa, A. (1996) · Brain Research · doi:10.1016/0006-8993(96)00487-8 · Cited by 24

NMDA-glutamate receptors regulate phosphorylation of dendritic cytoskeletal proteins in the hippocampus.

Sánchez, C., Ulloa, L., Montoro, R. J., López-Barneo, J., & Ávila, J. (1997) · Brain Research · doi:10.1016/s0006-8993(97)00563-5 · Cited by 27

A new twist in an old story: The role for crosstalk of neuronal and trophic activity

Knipper, M., & Rylett, R. J. (1997) · Neurochemistry International · doi:10.1016/s0197-0186(97)00009-0 · Cited by 24

Roles of Endomembrane Alkali Cation/Proton Exchangers in Synaptic Function and Neurodevelopmental Disorders

Gao, A. Y. L., Filippis, E. L.-D., Orlowski, J., & McKinney, R. A. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.892196 · Cited by 26

Acute rosmarinic acid treatment enhances long-term potentiation, BDNF and GluR-2 protein expression, and cell survival rate against scopolamine challenge in rat organotypic hippocampal slice cultures

Hwang, E., Kim, H.-B., Choi, G.-Y., Lee, S., Lee, S.-O., Kim, S. S., & Park, J. H. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.04.153 · Cited by 23

Molecular Mechanisms of Cannabis Signaling in the Brain

Ronan, P. J., Wongngamnit, N., & Beresford, T. P. (2015) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2015.10.002 · Cited by 25

Patch clamp-assisted single neuron lipidomics

Merrill, C. B., Basit, A., Armirotti, A., Jia, Y., Gall, C. M., LYNCH, G. S., & Piomelli, D. (2017) · Scientific Reports · doi:10.1038/s41598-017-05607-3 · Cited by 23

Influence of visual experience on developmental shift from long‐term depression to long‐term potentiation in the rat medial vestibular nuclei

Grassi, S., Dieni, C. V., Frondaroli, A., & Pettorossi, V. E. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.069658 · Cited by 23

Bidirectional Effects of Fentanyl on Dendritic Spines and AMPA Receptors Depend Upon the Internalization of Mu Opioid Receptors

Lin, H., Higgins, P. J., Loh, H. H., Law, P., & Liao, D. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2009.34 · Cited by 23

In vitro classical conditioning of the turtle eyeblink reflex: approaching cellular mechanisms of acquisition

Keifer, J. (2003) · The Cerebellum · doi:10.1080/14734220309428 · Cited by 23

Theta bursts in the olfactory nerve paired with β-adrenoceptor activation induce calcium elevation in mitral cells: A mechanism for odor preference learning in the neonate ratPreprint

Yuan, Q. (2009) · Learning & Memory · doi:10.1101/lm.1569309 · Cited by 23

Important Roles of Ring Finger Protein 112 in Embryonic Vascular Development and Brain Functions

Tsou, J., Yang, Y.-C., Pao, P., Lin, H., Huang, N., Lin, S.-T., Hsu, K., Yeh, C.-M., Lee, K., Kuo, C.-J., et al. (2016) · Molecular Neurobiology · doi:10.1007/s12035-016-9812-7 · Cited by 24

Metaplasticity within the spinal cord: Evidence brain-derived neurotrophic factor (BDNF), tumor necrosis factor (TNF), and alterations in GABA function (ionic plasticity) modulate pain and the capacity to learn

Grau, J. W., & Huang, Y.-J. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.04.007 · Cited by 22

Evolution of Cartesian Genetic Programs for Development of Learning Neural Architecture

Khan, G. M., Miller, J. F., & Halliday, D. M. (2011) · Evolutionary Computation · doi:10.1162/evco_a_00043 · Cited by 23

Cognitive deficits and Alzheimer-like neuropathological impairments during adolescence in a rat model of type 2 diabetes mellitus

Li, W., Jin, L., Li, Y.-P., Feng, Q., Ren, L., Wang, F., & Bo, G.-J. (2018) · Neural Regeneration Research · doi:10.4103/1673-5374.239448 · Cited by 22

The influence of developmental periods of sodium valproate exposure on synaptic plasticity in the CA1 region of rat hippocampus

Zhang, M., Yu, K., Xiao, C., & Ruan, D. (2003) · Neuroscience Letters · doi:10.1016/j.neulet.2003.08.010 · Cited by 22

Long-term potentiation protects rat hippocampal slices from the effects of acute hypoxia

Youssef, F. F., Addae, J. I., McRae‐Degueurce, A., & Stone, T. W. (2001) · Brain Research · doi:10.1016/s0006-8993(01)02594-x · Cited by 22

Synaptic plasticity in hippocampal interneurons? A commentary

McBain, C. J., & Maccaferri, G. (1997) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y97-034 · Cited by 23

Plasticity in adult sensory cortex: a review

Das, A. (1997) · Network Computation in Neural Systems · doi:10.1088/0954-898x/8/2/001 · Cited by 22

Differences in multiple forms of short‐term plasticity between excitatory and inhibitory hippocampal neurons in culture

Kaplan, M. P., Wilcox, K. S., & Dichter, M. A. (2003) · Synapse · doi:10.1002/syn.10244 · Cited by 21

Activities of calcineurin and phosphatase 2A in the hippocampus after transient forebrain ischemia

Morioka, M., Fukunaga, K., Hasegawa, S., Okamura, A., Korematsu, K., Kai, Y., Hamada, J.-I., Nagahiro, S., Miyamoto, E., & Ushio, Y. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01349-9 · Cited by 21

Research Methodology and Statistics

Weiss, D. S. (2008) · doi:10.1002/9780470515167.ch128 · Cited by 21

Platelet-activating factor and group I metabotropic glutamate receptors interact for full development and maintenance of long-term potentiation in the rat medial vestibular nuclei

Grassi, S., Francescangeli, E., Goracci, G., & Pettorossi, V. E. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00284-5 · Cited by 21

Acute and prophylactic effects of anticonvulsants in bipolar depression

Post, R. M., Speer, A. M., Obrocea, G. V., & Leverich, G. S. (2002) · Clinical Neuroscience Research · doi:10.1016/s1566-2772(02)00047-6 · Cited by 20

Lithium, but not valproate, induces the serine/threonine phosphatase activity of protein phosphatase 2A in the rat brain, without affecting its expression

Tsuji, S., Morinobu, S., Tanaka, K., Kawano, K.-I., & Yamawaki, S. (2003) · Journal of Neural Transmission · doi:10.1007/s00702-002-0798-0 · Cited by 20

Cortical glucose metabolism correlates negatively with delta‐slowing and spike‐frequency in epilepsy associated with tuberous sclerosis

Nishida, M., Asano, E., Juhász, C., Muzik, O., Sood, S., & Chugani, H. T. (2007) · Human Brain Mapping · doi:10.1002/hbm.20461 · Cited by 20

Calcium control of triphasic hippocampal STDP

Bush, D., & Jin, Y. (2012) · Journal of Computational Neuroscience · doi:10.1007/s10827-012-0397-5 · Cited by 20

Fructose 1,6-Bisphosphatase 2 Plays a Crucial Role in the Induction and Maintenance of Long-Term Potentiation

Duda, P., Wójtowicz, T., Janczara, J., Krowarsch, D., Czyrek, A. A., Gizak, A., & Rakus, D. (2020) · Cells · doi:10.3390/cells9061375 · Cited by 20

Short-Term Extremely Low-Frequency Electromagnetic Field Inhibits Synaptic Plasticity of Schaffer Collateral-CA1 Synapses in Rat Hippocampus via the Ca2+/Calcineurin Pathway

Xia, P., Zheng, Y., Dong, L., & Tian, C. (2021) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.1c00500 · Cited by 20

Long-term depression in rat CA1-subicular synapses depends on the G-protein coupled mACh receptors

Li, H., Zhang, J., Xiong, W., Xu, T., Cao, J., & Xu, L. (2005) · Neuroscience Research · doi:10.1016/j.neures.2005.04.002 · Cited by 20

Ganglioside/protein kinase signals triggering cytoskeletal actin reorganization

Higashi, H., & Chen, N. H. (2003) · Glycoconjugate Journal · doi:10.1023/b:glyc.0000016742.88750.1a · Cited by 20

Immunohistochemical evidence for impaired nitric oxide signaling of the locus coeruleus in bipolar disorder.

Bielau, H., Brisch, R., Bernard-Mittelstaedt, J., Dobrowolny, H., Gos, T., Baumann, B., Mawrin, C., Bernstein, H., Bogerts, B., & Steiner, J. (2012) · Brain Research · doi:10.1016/j.brainres.2012.04.022 · Cited by 17

Potentiation of N-methyl-d-aspartate currents by isoproterenol in the acutely dissociated rat amygdalar neurons

Huang, C., Lin, C.-H., & Gean, P. (1998) · Neuroscience Letters · doi:10.1016/s0304-3940(98)00571-0 · Cited by 20

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