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

Modulation of fear extinction processes using transcranial electrical stimulation

Abend, R., Jalon, I., Gurevitch, G., Sar-El, R., Shechner, T., Pine, D. S., Hendler, T., & Bar‐Haim, Y. (2016) · Translational Psychiatry · doi:10.1038/tp.2016.197 · Cited by 80

Impaired dendritic development and synaptic formation of postnatal-born dentate gyrus granular neurons in the absence of brain-derived neurotrophic factor signaling

Gao, X., Smith, G. M., & Chen, J. (2008) · Experimental Neurology · doi:10.1016/j.expneurol.2008.10.009 · Cited by 77

Inhibition of Upf2-Dependent Nonsense-Mediated Decay Leads to Behavioral and Neurophysiological Abnormalities by Activating the Immune Response

Johnson, J. L., Stoica, L., Liu, Y., Zhu, P., Bhattacharya, A., Buffington, S. A., Huq, R., Eissa, N. T., Larsson, O. S., Porse, B. T., et al. (2019) · Neuron · doi:10.1016/j.neuron.2019.08.027 · Cited by 80

Deletion of the n-terminus of murine map2 by gene targeting disrupts hippocampal ca1 neuron architecture and alters contextual memory

Khuchua, Z. A., Wozniak, D. F., Bardgett, M. E., Yue, Z., McDonald, M., Boero, J., Hartman, R. E., Sims, H. F., & Strauss, A. W. (2003) · Neuroscience · doi:10.1016/s0306-4522(03)00094-0 · Cited by 77

N-Methyl-d-aspartate-induced α-Amino-3-hydroxy-5-methyl-4-isoxazoleproprionic Acid (AMPA) Receptor Down-regulation Involves Interaction of the Carboxyl Terminus of GluR2/3 with Pick1

Iwakura, Y., Nagano, T., Kawamura, M., Horikawa, H., Ibaraki, K., Takei, N., & Nawa, H. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m103125200 · Cited by 75

A role for COX-2 and p38 mitogen activated protein kinase in long-term depression in the rat dentate gyrus in vitro

Murray, H. J., & O'Connor, J. J. (2003) · Neuropharmacology · doi:10.1016/s0028-3908(02)00375-1 · Cited by 74

Age-related alteration of PKC, a key enzyme in memory processes

Pascale, A., Govoni, S. M., & Battaini, F. (1998) · Molecular Neurobiology · doi:10.1007/bf02740602 · Cited by 72

Reactive oxygen species affect spinal cell type-specific synaptic plasticity in a model of neuropathic pain

Bittar, A., Jun, J., La, J., Wang, J., Leem, J. W., & Chung, J. M. (2017) · Pain · doi:10.1097/j.pain.0000000000001014 · Cited by 73

Transient and persistent increases in protein phosphatase activity during long-term depression in the adult hippocampus in vivo

Thiels, E., Norman, E. D., Barrionuevo, G., & Klann, E. (1998) · Neuroscience · doi:10.1016/s0306-4522(98)00135-3 · Cited by 72

Emerging memory devices for artificial synapses

Park, Y., Kim, M., & Lee, J. (2020) · Journal of Materials Chemistry C · doi:10.1039/d0tc01500h · Cited by 74

Interferon-α inhibits long-term potentiation and unmasks a long-term depression in the rat hippocampus

Mendoza-Fernández, V., Andrew, R. D., & Barajas‐López, C. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02877-8 · Cited by 72

Novel NMDA receptor modulators: an update

Santangelo, R., Acker, T. M., Zimmerman, S. S., Katzman, B. M., Strong, K. L., Traynelis, S. F., & Liotta, D. C. (2012) · Expert Opinion on Therapeutic Patents · doi:10.1517/13543776.2012.728587 · Cited by 72

Synaptic Correlates of Increased Cognitive Vulnerability with Aging: Peripheral Immune Challenge and Aging Interact to Disrupt Theta-Burst Late-Phase Long-Term Potentiation in Hippocampal Area CA1

Chapman, T. R., Barrientos, R. M., Ahrendsen, J. T., Maier, S. F., & Patterson, S. L. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.5172-09.2010 · Cited by 72

Chronic Intermittent Low-Level Stimulation of Tragus Reduces Cardiac Autonomic Remodeling and Ventricular Arrhythmia Inducibility in a Post-Infarction Canine Model

Yu, L., Wang, S., Zhou, X., Wang, Z., Huang, B. S., Liao, K., Saren, G., Chen, M., Po, S. S., & Jiang, H. (2015) · JACC. Clinical electrophysiology · doi:10.1016/j.jacep.2015.11.006 · Cited by 72

Long-Term Depression Properties in a Simple System

Goda, Y., & Stevens, C. F. (1996) · Neuron · doi:10.1016/s0896-6273(00)80027-6 · Cited by 74

Rapid eye movement sleep deprivation decreases long-term potentiation stability and affects some glutamatergic signaling proteins during hippocampal development

Lopez, J., Roffwarg, H. P., Dreher, A., Bissette, G., Karolewicz, B., & Shaffery, J. P. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.01.072 · Cited by 71

Selective role for trkB neurotrophin receptors in rapid modulation of hippocampal synaptic transmission

Levine, E. S., Dreyfus, C. F., Black, I. B., & Plummer, M. R. (1996) · Molecular Brain Research · doi:10.1016/0169-328x(96)00025-3 · Cited by 71

Nuclear calcium: a key regulator of gene expression

Hardingham, G. E., & Bading, H. (1998) · BioMetals · doi:10.1023/a:1009257909785 · Cited by 69

Nutritional n-3 PUFA Deficiency Abolishes Endocannabinoid Gating of Hippocampal Long-Term Potentiation

Thomazeau, A., Bosch‐Bouju, C., Manzoni, O. J., & Layé, S. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw052 · Cited by 73

Asc-1 Transporter Regulation of Synaptic Activity via the Tonic Release of d-Serine in the Forebrain

Sason, H., Billard, J. M., Smith, G. P., Safory, H., Neame, S., Kaplan, E., Rosenberg, D., Zubedat, S., Foltyn, V. N., Christoffersen, C. T., et al. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv350 · Cited by 74

Protein kinase C in synaptic plasticity: Changes in the in situ phosphorylation state of identified pre- and postsynaptic substrates

Ramakers, G. M. J., Pasinelli, P., Hens, J. J. H., Gispen, W. H., & Graan, P. N. E. D. (1997) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/s0278-5846(97)00013-4 · Cited by 68

Metal‐Oxide Heterojunction Optoelectronic Synapse and Multilevel Memory Devices Enabled by Broad Spectral Photocarrier Modulation

Kim, J., Song, S., Lee, J., Nam, S., Kim, J., Hwang, D. K., Park, S. K., & Kim, Y. (2023) · Small · doi:10.1002/smll.202301186 · Cited by 69

Prenatal administration of morphine decreases CREBSerine‐133 phosphorylation and synaptic plasticity range mediated by glutamatergic transmission in the hippocampal CA1 area of cognitive‐deficient rat offspring

Yang, S. N., Huang, L., Wang, C., Chen, W.-F., Yang, C., Lin, S., Lai, M., Chen, S., & Tao, P. (2003) · Hippocampus · doi:10.1002/hipo.10137 · Cited by 68

Posttranslational Modifications and Receptor-Associated Proteins in AMPA Receptor Trafficking and Synaptic Plasticity

Jiang, J., Suppiramaniam, V. D., & Wooten, M. W. (2006) · Neurosignals · doi:10.1159/000105517 · Cited by 67

Long‐lasting effects of neonatal dexamethasone treatment on spatial learning and hippocampal synaptic plasticity. Involvement of the NMDA receptor complex

Kamphuis, P. J. G. H., Gardoni, F., Kamal, A., Croiset, G., Bakker, J. M., Cattabeni, F., Gispen, W. H., van Bel, F., Luca, M. D., & Wiegant, V. M. (2003) · The FASEB Journal · doi:10.1096/fj.02-0333fje · Cited by 66

Post‐ischaemic long‐term synaptic potentiation in the striatum: a putative mechanism for cell type‐specific vulnerability

Calabresi, P., Saulle, E., Centonze, D., Pisani, A., Marfia, G. A., & Bernardi, G. (2002) · Brain · doi:10.1093/brain/awf073 · Cited by 66

The NMDA Receptor/Ion Channel Complex: A Drug Target for Modulating Synaptic Plasticity and Excitotoxicity

Albensi, B. C. (2007) · Current Pharmaceutical Design · doi:10.2174/138161207782341321 · Cited by 66

Aβ25–35-Induced Depression of Long-Term Potentiation in Area CA1 In Vivo and In Vitro Is Attenuated by Verapamil

Freir, D. B., Costello, D. A., & Herron, C. E. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00992.2002 · Cited by 66

Requirement for the RIIβ Isoform of PKA, But Not Calcium-Stimulated Adenylyl Cyclase, in Visual Cortical Plasticity

Fischer, Q. S., Beaver, C. J., Yang, Y., Rao, Y., Jakobsdóttir, K. B., Storm, D. R., McKnight, G. S., & Daw, N. W. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2409-04.2004 · Cited by 65

CREB and memory consolidation

Stevens, C. F. (1994) · Neuron · doi:10.1016/0896-6273(94)90244-5 · Cited by 65

Protein Phosphatase-Mediated Regulation of Protein Kinase C during Long-Term Depression in the Adult Hippocampus In Vivo

Thiels, E., Kanterewicz, B., Knapp, L., Barrionuevo, G., & Klann, E. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-19-07199.2000 · Cited by 67

Enhanced neuronal plasticity and elevated endogenous sAPPα levels in mice over‐expressing MMP9

Fragkouli, A., Papatheodoropoulos, C., Georgopoulos, S., Stamatakis, A., Stylianopoulou, F., Tsilibary, E. C., & Tzinia, A. K. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07637.x · Cited by 66

A Persistent Activity-Dependent Facilitation in Chromaffin Cells Is Caused by Ca2+Activation of Protein Kinase C

Smith, C. L. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-02-00589.1999 · Cited by 64

BNST GluN2D-Containing NMDA Receptors Influence Anxiety- and Depressive-like Behaviors and ModulateCell-Specific Excitatory/Inhibitory Synaptic Balance

Salimando, G. J., Hyun, M., Boyt, K. M., & Winder, D. G. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0270-20.2020 · Cited by 63

Surface protein phosphorylation by ecto-protein kinase is required for the maintenance of hippocampal long-term potentiation.

Chen, W., Wieraszko, A., Hogan, M. V., Yang, H. A., Kornecki, E., & Ehrlich, Y. H. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.16.8688 · Cited by 63

Suppression of Inhibitory Synaptic Potentiation by Presynaptic Activity through Postsynaptic GABAB Receptors in a Purkinje Neuron

Kawaguchi, S., & Hirano, T. (2000) · Neuron · doi:10.1016/s0896-6273(00)00041-6 · Cited by 64

Behaviour of NMDA and AMPA receptor‐mediated miniature EPSCs at rat cortical neuron synapses identified by calcium imaging

Umemiya, M., Senda, M., & Murphy, T. H. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.00113.x · Cited by 64

Impaired cognitive performance in neuronal nitric oxide synthase knockout mice is associated with hippocampal protein derangements

Kirchner, L., Weitzdoerfer, R., Hoeger, H., Url, A., Schmidt, P., Engelmann, M., Villar, S. R., Fountoulakis, M., Lübec, G., & Lubec, B. (2004) · Nitric Oxide · doi:10.1016/j.niox.2004.10.005 · Cited by 62

Protective effects of anthocyanins on the ectonucleotidase activity in the impairment of memory induced by scopolamine in adult rats

Gutierres, J. M., Carvalho, F. B., Schetinger, M. R. C., Rodrigues, M., Schmatz, R., Pimentel, V. C., Vieira, J. M., da Rosa, M. M., Marisco, P. C., Ribeiro, D. A., et al. (2012) · Life Sciences · doi:10.1016/j.lfs.2012.09.013 · Cited by 62

Inducing Homeostatic-Like Plasticity in Human Motor Cortex Through Converging Corticocortical Inputs

Pötter‐Nerger, M., Fischer, S., Mastroeni, C., Groppa, S., Deuschl, G., Volkmann, J., Quartarone, A., Münchau, A. M., & Siebner, H. R. (2009) · Journal of Neurophysiology · doi:10.1152/jn.91046.2008 · Cited by 61

Neurotoxic effects of perfluoroalkyl acids: Neurobehavioral deficit and its molecular mechanism

Wang, Y., Wang, L., Chang, W., Zhang, Y., Zhang, Y., & Liu, W. (2019) · Toxicology Letters · doi:10.1016/j.toxlet.2019.01.012 · Cited by 65

BH‐protocadherin‐c, a member of the cadherin superfamily, interacts with protein phosphatase 1 alpha through its intracellular domain

Yoshida, K., Watanabe, M., Kato, H., Dutta, A., & Sugano, S. (1999) · FEBS Letters · doi:10.1016/s0014-5793(99)01309-5 · Cited by 60

Chronic ΔFosB expression and increased AP-1 transcription factor binding are associated with the long term plasticity changes in epilepsy

Morris, T., Jafari, N., & DeLorenzo, R. J. (2000) · Molecular Brain Research · doi:10.1016/s0169-328x(00)00112-1 · Cited by 58

Regulation of Intracellular Calcium Release Channel Function by Arachidonic Acid and Leukotriene B4

Striggow, F., & Ehrlich, B. E. (1997) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1997.7152 · Cited by 60

Control of Action Potential-Induced Ca2+Signaling in the Soma of Hippocampal Neurons by Ca2+Release from Intracellular Stores

Jacobs, J. M., & Meyer, T. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-11-04129.1997 · Cited by 60

Evaluation of brain pharmacokinetics of (+)MK-801 in relation to behaviour

Wegener, N., Nagel, J., Gross, R., Chambon, C., Greco, S., Pietraszek, M., Gravius, A., & Danysz, W. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.08.012 · Cited by 59

BDNF potentiates spontaneous Ca2+ oscillations in cultured hippocampal neurons

Sakai, N., Yamada, M., Numakawa, T., Ogura, A., & Hatanaka, H. (1997) · Brain Research · doi:10.1016/s0006-8993(97)01052-4 · Cited by 58

Bidirectional synaptic plasticity as a consequence of interdependent Ca2+‐controlled phosphorylation and dephosphorylation pathways

d’Alcantara, P., Schiffmann, S. N., & Swillens, S. (2003) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2003.02693.x · Cited by 59

Regulation of neuronal plasticity in the central nervous system by phosphorylation and dephosphorylation

Tokuda, M., & Hatase, O. (1998) · Molecular Neurobiology · doi:10.1007/bf02802028 · Cited by 59

Rubinstein-Taybi Syndrome and Epigenetic Alterations

Korzus, E. (2017) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-53889-1_3 · Cited by 61

Chapter 12 Modulation of LTP induction by NMDA receptor activation and nitric oxide release

Zorumski, C. F., & Izumi, Y. (1998) · Progress in brain research · doi:10.1016/s0079-6123(08)63207-0 · Cited by 57

Pharmacological reversal of behavioral and cellular indices of cocaine sensitization in the rat

Li, Y., White, F. J., & Wolf, M. E. (2000) · Psychopharmacology · doi:10.1007/s002130000454 · Cited by 57

Emulating synaptic plasticity and resistive switching characteristics through amorphous Ta2O5 embedded layer for neuromorphic computing

Ismail, M., Abbas, H., Sokolov, A. S., Mahata, C., Choi, C., & Kim, S. (2021) · Ceramics International · doi:10.1016/j.ceramint.2021.07.257 · Cited by 56

Prenatal corticosteroid exposure affects hippocampal plasticity and reduces lifespan

Noorlander, C. W., Visser, G. H. A., Ramakers, G. M. J., Nikkels, P. G. J., & Graan, P. N. E. D. (2007) · Developmental Neurobiology · doi:10.1002/dneu.20583 · Cited by 56

Tetrahydroxystilbene glucoside, a plant-derived cognitive enhancer, promotes hippocampal synaptic plasticity

Wang, T., Yang, Y., Wu, P., Wang, W., Hu, Z., Long, L., Xie, N., Fu, H. Q., Wang, F., & Chen, J. (2010) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2010.10.002 · Cited by 55

Effects of perfluorooctane sulfonate and its alternatives on long-term potentiation in the hippocampus CA1 region of adult rats in vivo

Zhang, Q., Liu, W., Niu, Q. L., Wang, Y., Zhao, H., Zhang, H., Song, J., Tsuda, S., & Saito, N. (2016) · Toxicology Research · doi:10.1039/c5tx00184f · Cited by 55

When Pain Hurts: Nociceptive Stimulation Induces a State of Maladaptive Plasticity and Impairs Recovery after Spinal Cord Injury

Grau, J. W., Huang, Y.-J., Turtle, J. D., Strain, M. M., Miranda, R. C., Garraway, S. M., & Hook, M. A. (2016) · Journal of Neurotrauma · doi:10.1089/neu.2016.4626 · Cited by 59

Age‐dependent alterations of long‐term synaptic plasticity in thyroid‐deficient rats

Vara, H., Muñoz‐Cuevas, J., & Colino, A. (2003) · Hippocampus · doi:10.1002/hipo.10132 · Cited by 55

Molecular cloning and characterization of neural activity‐related RING finger protein (NARF): a new member of the RBCC family is a candidate for the partner of myosin V

Ohkawa, N., Kokura, K., Matsuura, T., Obinata, T., Konishi, Y., & Tamura, T. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00373.x · Cited by 55

Phosphorylation and Dephosphorylation in the Proline‐Rich C‐Terminal Domain of Microtubule‐Associated Protein 2

Sánchez, C., Tompa, P., Szücs, K., Friedrich, P., & Ávila, J. (1996) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1996.00765.x · Cited by 55

Enhanced long-term depression and impaired reversal learning in phosphodiesterase 4B-knockout (PDE4B−/−) mice

Rutten, K., Wallace, T. L., Works, M. G., Prickaerts, J., Blokland, A., Novak, T. J., Santarelli, L., & Misner, D. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.03.020 · Cited by 54

REVIEW ■ : LTP and LTD: Dynamic and Interactive Processes of Synaptic Plasticity

Malenka, R. (1995) · The Neuroscientist · doi:10.1177/107385849500100106 · Cited by 61

Kindling: Separate vs. Shared Mechanisms in Affective Disorders and Epilepsy

Weiss, S. R. B., & Post, R. M. (1998) · Neuropsychobiology · doi:10.1159/000026533 · Cited by 54

Glycogen synthase kinase 3β in the basolateral amygdala is critical for the reconsolidation of cocaine reward memory

Wu, P., Xue, Y.-X., Ding, Z., Xue, L., Xu, C., & Lü, L. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07277.x · Cited by 53

Spatial cognition and sexually dimorphic synaptic plasticity balance impairment in rats with chronic prenatal ethanol exposure

An, L., & Zhang, T. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.09.017 · Cited by 53

Differentiation of Glycine Antagonist Sites ofN-Methyl-d-aspartate Receptor Subtypes

Honer, M., Benke, D., Laube, B., Kuhse, J., Heckendorn, R., Allgeier, H., Angst, C., Monyer, H., Seeburg, P. H., Betz, H., et al. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.18.11158 · Cited by 53

Stimulation of M3 Muscarinic Receptors Induces Phosphorylation of the Cdc42 Effector Activated Cdc42Hs-associated Kinase-1 via a Fyn Tyrosine Kinase Signaling Pathway

Linseman, D. A., Heidenreich, K. A., & Fisher, S. K. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m006812200 · Cited by 52

Chapter 27. Plasticity of excitatory synaptic transmission in the spinal cord dorsal horn

Randić, M. (1996) · Progress in brain research · doi:10.1016/s0079-6123(08)61104-8 · Cited by 52

Temporal dynamics of NMDA receptor-induced changes in spine morphology and AMPA receptor recruitment to spines

Lin, H., Huganir, R. L., & Liao, D. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.02.086 · Cited by 53

Long-term potentiation and long-term depression are induced through pharmacologically distinct NMDA receptors

Hrabětová, S., & Sacktor, T. C. (1997) · Neuroscience Letters · doi:10.1016/s0304-3940(97)00252-8 · Cited by 50

Neurogranin, Encoded by the Schizophrenia Risk Gene NRGN, Bidirectionally Modulates Synaptic Plasticity via Calmodulin-Dependent Regulation of the Neuronal Phosphoproteome

Hwang, H., Szucs, M. J., Ding, L. J., Allen, A., Ren, X., Haensgen, H., Gao, F., Rhim, H., Andrade, A., Pan, J. Q., et al. (2021) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.07.014 · Cited by 49

Dual modulation of excitatory synaptic transmission by agonists at group I metabotropic glutamate receptors in the rat spinal dorsal horn

Zhong, J., Gerber, G., Kojić, L., & Randić, M. (2000) · Brain Research · doi:10.1016/s0006-8993(00)03066-3 · Cited by 49

Acupuncture as a multifunctional neuroprotective therapy ameliorates cognitive impairment in a rat model of vascular dementia: A quantitative iTRAQ proteomics study

Yang, J., Wang, X., Zhang, M., Xiao, L., Zhu, W. X., Ji, C., & Liu, C. (2018) · CNS Neuroscience & Therapeutics · doi:10.1111/cns.13063 · Cited by 48

Transspinal stimulation increases motoneuron output of multiple segments in human spinal cord injury

Murray, L. M., & Knikou, M. (2019) · PLoS ONE · doi:10.1371/journal.pone.0213696 · Cited by 48

A Review of Glutamate Receptors I: Current Understanding of Their Biology

Rousseaux, C. G. (2008) · Journal of Toxicologic Pathology · doi:10.1293/tox.21.25 · Cited by 48

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Bhattacharyya, S. (2016) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2016.03.003 · Cited by 53

Ceramide-induced sustained depression of synaptic currents mediated by ionotropic glutamate receptors in the hippocampus: an essential role of postsynaptic protein phosphatases

Yang, S.-N. (2000) · Neuroscience · doi:10.1016/s0306-4522(99)00582-5 · Cited by 45

Electrophysiological profile of avian hippocampal unit activity: A basis for regional subdivisions

Siegel, J. J., Nitz, D. A., & Bingman, V. P. (2002) · The Journal of Comparative Neurology · doi:10.1002/cne.10167 · Cited by 46

NMDA-Dependent Modulation of Hippocampal Kainate Receptors by Calcineurin and Ca2+/Calmodulin-Dependent Protein Kinase

Ghetti, A., & Heinemann, S. F. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-08-02766.2000 · Cited by 46

A role for histone deacetylases in the cellular and behavioral mechanisms underlying learning and memoryPreprint

Mahgoub, M., & Monteggia, L. M. (2014) · Learning & Memory · doi:10.1101/lm.036012.114 · Cited by 45

Repetitive febrile seizures in rat pups cause long-lasting deficits in synaptic plasticity and NR2A tyrosine phosphorylation

Chang, Y., Kuo, Y., Huang, A., & Huang, C. (2005) · Neurobiology of Disease · doi:10.1016/j.nbd.2004.12.012 · Cited by 45

Modification of glutamate receptors by phospholipase A2: its role in adaptive neural plasticity

Massicotte, G. (2000) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000639 · Cited by 46

Book Review: Na+ Signals at Central Synapses

Rose, C. R. (2002) · The Neuroscientist · doi:10.1177/1073858402238512 · Cited by 45

The magnitude of hippocampal long term depression depends on the synaptic location of activated NR2-containing N-methyl-d-aspartate receptors

Kollen, M., Dutar, P., & Jouvenceau, A. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.04.045 · Cited by 44

A Neuronal-specific Mammalian Homolog of theDrosophilaRetinal Degeneration B Gene with Expression Restricted to the Retina and Dentate Gyrus

Lu, C., Vihtelic, T. S., Hyde, D. R., & Li, T. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-17-07317.1999 · Cited by 44

Long-Term Potentiation of Synaptic Transmission in the Avian Hippocampus

Margrie, T. W., Rostas, J. A. P., & Sah, P. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-04-01207.1998 · Cited by 44

The metabolism hypothesis of Alzheimer’s disease: from the concept of central insulin resistance and associated consequences to insulin therapy

Morgen, K., & Frölich, L. (2015) · Journal of Neural Transmission · doi:10.1007/s00702-015-1377-5 · Cited by 43

Induction of long-term potentiation and long-term depression is cell-type specific in the spinal cord

Kim, H. Y., Jun, J., Wang, J., Bittar, A., Chung, K., & Chung, J. M. (2015) · Pain · doi:10.1097/01.j.pain.0000460354.09622.ec · Cited by 43

Topographic maps: Developing roles of synaptic plasticity

Cline, H. T. (1998) · Current Biology · doi:10.1016/s0960-9822(07)00525-8 · Cited by 43

Timing in the absence of supraspinal input I: Variable, but not fixed, spaced stimulation of the sciatic nerve undermines spinally-mediated instrumental learning

Baumbauer, K. M., Hoy, K. C., Huie, J. R., Hughes, A. J., Woller, S. A., Puga, D. A., Setlow, B., & Grau, J. W. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.07.003 · Cited by 43

The effect of gamma-linolenic acid–alpha-lipoic acid on functional deficits in the peripheral and central nervous system of streptozotocin-diabetic rats

Biessels, G. J., Smale, S., Duis, S., Kamal, A., & Gispen, W. H. (2001) · Journal of the Neurological Sciences · doi:10.1016/s0022-510x(00)00456-1 · Cited by 43

Low-Frequency Stimulation Depresses the Primate Anterior-Cingulate-Cortex and Prevents Spontaneous Recovery of Aversive Memories

Klavir, O., Genud-Gabai, R., & Paz, R. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.6481-11.2012 · Cited by 43

Cooperation between cholinergic and glutamatergic receptors are essential to induce BDNF‐dependent long‐lasting memory storage

Navakkode, S., & Körte, M. (2011) · Hippocampus · doi:10.1002/hipo.20902 · Cited by 41

Implications of Kindling And Quenching For the Possible Frequency Dependence Of rTMS

Post, R. M., Kimbrell, T. A., Frye, M., George, M. S., McCann, U., Little, J. T., Dunn, R. T., Li, H., & Weiss, S. R. B. (1997) · CNS Spectrums · doi:10.1017/s1092852900004508 · Cited by 42

Repetitive spinal electromagnetic stimulation opens a window of synaptic plasticity in damaged spinal cord: role of NMDA receptors

Hunanyan, A. S., Petrosyan, H. A., Alessi, V., & Arvanian, V. L. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00015.2012 · Cited by 43

Emergence of order in visual system development

Shatz, C. J. (1996) · Journal of Physiology-Paris · doi:10.1016/s0928-4257(97)81413-1 · Cited by 41

Calcium‐dependent mechanisms involved in presynaptic long‐term depression at the hippocampal mossy fibre–CA3 synapse

Kobayashi, K., Manabe, T., & Takahashi, T. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00578.x · Cited by 44

Contributions of extracellular-signal regulated kinase 1/2 activity to the memory trace

Ramos, S. O., Feld, M., & Fustiñana, M. S. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.988790 · Cited by 43

S-Palmitoylation of Synaptic Proteins in Neuronal Plasticity in Normal and Pathological Brains

Buszka, A., Pytyś, A., Colvin, D., Włodarczyk, J., & Wójtowicz, T. (2023) · Cells · doi:10.3390/cells12030387 · Cited by 44

Properties of LTD and LTP of retinocollicular synaptic transmission in the developing rat superior colliculus

Lo, F., & Mize, R. R. (2002) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2002.01979.x · Cited by 40

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