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

Dysregulated Src upregulation of NMDA receptor activity: a common link in chronic pain and schizophrenia

Salter, M. W., & Pitcher, G. M. (2011) · FEBS Journal · doi:10.1111/j.1742-4658.2011.08390.x · Cited by 77

Enhanced synaptic plasticity in mice with phosphomimetic mutation of the GluA1 AMPA receptor

Makino, Y., Johnson, R. C., Yu, Y., Takamiya, K., & Huganir, R. L. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1105261108 · Cited by 77

Functional improvement and neuroplastic effects of anodal transcranial direct current stimulation (tDCS) delivered 1day vs. 1week after cerebral ischemia in rats

Yoon, K. J., Oh, B., & Kim, D. Y. (2012) · Brain Research · doi:10.1016/j.brainres.2012.02.062 · Cited by 83

Review Article : Molecular and Cellular Mechanisms Underlying the Cognitive Deficits Associated With Neurofibromatosis 1

Costa, R. M., & Silva, A. J. (2002) · Journal of Child Neurology · doi:10.1177/088307380201700813 · Cited by 79

Calcium stores and synaptic plasticity

Fitzjohn, S. M., & Collingridge, G. L. (2002) · Cell Calcium · doi:10.1016/s0143416002001999 · Cited by 77

Leucine-Rich Repeat Transmembrane Proteins Are Essential for Maintenance of Long-Term Potentiation

Soler-Llavina, G. J., Arstikaitis, P., Morishita, W., Ahmad, M., Südhof, T. C., & Malenka, R. C. (2013) · Neuron · doi:10.1016/j.neuron.2013.06.007 · Cited by 79

Stress Enables Synaptic Depression in CA1 Synapses by Acute and Chronic Morphine: Possible Mechanisms for Corticosterone on Opiate Addiction

Yang, Y., Zheng, X., Wang, Y., Cao, J., Dong, Z., Cai, J., Sui, N., & Xu, L. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.5544-03.2004 · Cited by 77

Intracellular trafficking of AMPA receptors in synaptic plasticity

Man, H., Ju, W., Ahmadian, G., & Wang, Y. T. (2000) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000637 · Cited by 79

Erratum to “Cellular mechanisms underlying acquired epilepsy: The calcium hypothesis of the induction and maintenance of epilepsy” [Pharmacol. Ther. 105(3) (2005) 229–266]

DeLorenzo, R. J., Sun, D. A., & Deshpande, L. S. (2005) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2004.10.015 · Cited by 77

Exocytic trafficking is required for nicotine-induced up-regulation of α4β2 nicotinic acetylcholine receptors

Darsow, T., Booker, T. K., Piña-Crespo, J. C., & Heinemann, S. F. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m501157200 · Cited by 76

NMDA receptor-dependent long-term potentiation in the telencephalon of the zebrafish

Nam, R.-H., Kim, W., & Lee, C. (2004) · Neuroscience Letters · doi:10.1016/j.neulet.2004.08.037 · Cited by 76

L‐Type Voltage‐Gated Calcium Channels Are Involved in the in Vivo and in Vitro Expression of Fear Conditioning

Shinnick‐Gallagher, P., McKERNAN, M. G., Xie, J., & Zinebi, F. (2003) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2003.tb07078.x · Cited by 79

Quercetin improves cognitive deficits in rats with chronic cerebral ischemia and inhibits voltage‐dependent sodium channels in hippocampal CA1 pyramidal neurons

Yao, Y., Han, D. D., Zhang, T., & Yang, Z. R. (2009) · Phytotherapy Research · doi:10.1002/ptr.2902 · Cited by 76

The Basolateral Amygdala Is Critical for the Acquisition and Extinction of Associations between a Neutral Stimulus and a Learned Danger Signal But Not between Two Neutral Stimuli

Parkes, S. L., & Westbrook, R. F. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.2949-10.2010 · Cited by 87

Chemical Quenched Flow Kinetic Studies Indicate an Intraholoenzyme Autophosphorylation Mechanism for Ca2+/Calmodulin-dependent Protein Kinase II

Bradshaw, J. M., Hudmon, A., & Schulman, H. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m202154200 · Cited by 78

Dynamics and pathology of dendritic spines

Halpain, S., Spencer, K., & Graber, S. (2005) · Progress in Brain Research · doi:10.1016/s0079-6123(04)47003-4 · Cited by 88

Dysplasticity, metaplasticity, and schizophrenia: Implications for risk, illness, and novel interventions

Keshavan, M. S., Mehta, U. M., Padmanabhan, J. L., & Shah, J. L. (2015) · Development and Psychopathology · doi:10.1017/s095457941500019x · Cited by 79

Treatment-resistant depression: molecular mechanisms and management

Kajumba, M. M., Kakooza‐Mwesige, A., Nakasujja, N., Attix, D. K., & Canli, T. (2024) · Molecular Biomedicine · doi:10.1186/s43556-024-00205-y · Cited by 93

Differential induction of bidirectional long‐term changes in neurotransmitter release by frequency‐coded patterns at the cerebellar input

D’Errico, A., Prestori, F., & D'Angelo, E. U. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.177162 · Cited by 75

Synapse development: still looking for the forest, still lost in the trees

Garner, C. C., Waites, C. L., & Ziv, N. E. (2006) · Cell and Tissue Research · doi:10.1007/s00441-006-0278-1 · Cited by 78

Prominence of Direct Entorhinal–CA1 Pathway Activation in Sensorimotor and Cognitive Tasks Revealed by 2-DG Functional Mapping in Nonhuman Primate

Sybirska, E. H., Davachi, L., & Goldman‐Rakic, P. S. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-15-05827.2000 · Cited by 75

Temporal modulation of spike-timing-dependent plasticity

Froemke, R. C. (2010) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2010.00019 · Cited by 76

Impairment in Short-Term but Enhanced Long-Term Synaptic Potentiation and ERK Activation in Adult Hippocampal Area CA1 Following Developmental Thyroid Hormone Insufficiency*

Sui, L., Anderson, W. L., & Gilbert, M. E. (2005) · Toxicological Sciences · doi:10.1093/toxsci/kfi095 · Cited by 75

AMPA receptor ligands: Synthetic and pharmacological studies of polyamines and polyamine toxins

Strømgaard, K., & Mellor, I. R. (2004) · Medicinal Research Reviews · doi:10.1002/med.20004 · Cited by 76

The impact of neuroinflammation on neuronal integrity

Tastan, B., & Heneka, M. T. (2024) · Immunological Reviews · doi:10.1111/imr.13419 · Cited by 81

The actin cytoskeleton in memory formation

Lamprecht, R. (2014) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2014.02.001 · Cited by 76

Role of AMPA receptor trafficking in NMDA receptor‐dependent synaptic plasticity in the rat lateral amygdala

Yu, S. Y., Wu, D., Liu, L., Ge, Y., & Wang, Y. T. (2008) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2008.05461.x · Cited by 75

Decreased calcium/calmodulin‐dependent protein kinase II and protein kinase C activities mediate impairment of hippocampal long‐term potentiation in the olfactory bulbectomized mice

Moriguchi, S., Han, F., Nakagawasai, O., Tadano, T., & Fukunaga, K. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03710.x · Cited by 74

Calcium, Reactive Oxygen Species, and Synaptic Plasticity

Hidalgo, C., & Arias‐Cavieres, A. (2016) · Physiology · doi:10.1152/physiol.00038.2015 · Cited by 75

Cellular neuroplasticity mechanisms mediating pain persistence.

Salter, M. W. (2004) · PubMed · Cited by 74

Learning and Memory

Byrne, J. H., LaBar, K. S., LeDoux, J. E., Schafe, G. E., & Thompson, R. F. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-397179-1.00020-8 · Cited by 74

Molecular Network and Chromosomal Clustering of Genes Involved in Synaptic Plasticity in the Hippocampus

Park, C. S., Gong, R., Stuart, J. M., & Tang, S.-J. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m605876200 · Cited by 72

Molecular Changes in Glutamatergic Synapses Induced by Pb2+: Association with Deficits of LTP and Spatial Learning

Nihei, M. K., & Guilarte, T. R. (2001) · NeuroToxicology · doi:10.1016/s0161-813x(01)00035-3 · Cited by 75

Enhancement of Long-Term Potentiation by a Potent Nitric Oxide-Guanylyl Cyclase Activator, 3-(5-Hydroxymethyl-2-furyl)-1-benzyl-indazole

Chien, W., Liang, K., Teng, C., Kuo, S., Lee, F., & Fu, W. (2003) · Molecular Pharmacology · doi:10.1124/mol.63.6.1322 · Cited by 74

How the Shape of Pre- and Postsynaptic Signals Can Influence STDP: A Biophysical Model

Saudargienė, A., Porr, B., & Wörgötter, F. (2004) · Neural Computation · doi:10.1162/089976604772744929 · Cited by 72

Differential Regulation of Metabotropic Glutamate Receptor- and AMPA Receptor-Mediated Dendritic Ca2+Signals by Presynaptic and Postsynaptic Activity in Hippocampal Interneurons

Topolnik, L., Congar, P., & Lacaille, J.-C. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.4388-04.2005 · Cited by 73

Non-invasive transcranial brain modulation for neurological disorders treatment: A narrative review

Mosilhy, E. A., Alshial, E. E., Eltaras, M. M., Rahman, M. M. A., Helmy, H. I., Elazoul, A. H., Hamdy, O., & Mohammed, H. S. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.120869 · Cited by 77

Ferroelectric artificial synapses for high-performance neuromorphic computing: Status, prospects, and challenges

Zhao, L., Fang, H., Wang, J., Nie, F., Li, R., Wang, Y., & Zheng, L. (2024) · Applied Physics Letters · doi:10.1063/5.0165029 · Cited by 76

Schizophrenia as a Disorder of Neuroplasticity

McCullumsmith, R. E., Clinton, S. M., & Meador‐Woodruff, J. H. (2004) · International review of neurobiology · doi:10.1016/s0074-7742(04)59002-5 · Cited by 73

Hippocampal synaptic plasticity in mice devoid of cellular prion protein

Maglio, L. E., Pérez, M. F., Martins, V. R., Brentani, H., & Ramírez, O. A. (2004) · Molecular Brain Research · doi:10.1016/j.molbrainres.2004.08.004 · Cited by 73

The Potential of Caffeine for Functional Modification from Cortical Synapses to Neuron Networks in the Brain

Yoshimura, H. (2005) · Current Neuropharmacology · doi:10.2174/157015905774322543 · Cited by 73

Alterations in the emotional and memory behavioral phenotypes of transient receptor potential vanilloid type 1-deficient mice are mediated by changes in expression of 5-HT1A, GABAA, and NMDA receptors

You, I., Jung, Y., Kim, M., Kwon, S., Hong, S., Lee, S., & Jang, C. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.10.013 · Cited by 73

Neuroinflammatory challenges compromise neuronal function in the aging brain: Postoperative cognitive delirium and Alzheimer’s disease

Cortese, G. P., & Bürger, C. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.08.027 · Cited by 77

Protein kinases regulate the phosphorylation of the GluR1 subunit of AMPA receptors of spinal cord in rats following noxious stimulation

Fang, L., Wu, J., Lin, Q., & Willis, W. D. (2003) · Molecular Brain Research · doi:10.1016/j.molbrainres.2003.08.002 · Cited by 73

Selective Presynaptic Propagation of Long-Term Potentiation in Defined Neural Networks

Tao, H. W., Zhang, L. I., Bi, G., & Poo, M. (2000) · Journal of Neuroscience · doi:10.1523/jneurosci.20-09-03233.2000 · Cited by 73

Kainate Receptor-Dependent Short-Term Plasticity of Presynaptic Ca2+Influx at the Hippocampal Mossy Fiber Synapses

Kamiya, H., Ozawa, S., & Manabe, T. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-21-09237.2002 · Cited by 77

Fragile X mental retardation protein is required for chemically‐induced long‐term potentiation of the hippocampus in adult mice

Shang, Y., Wang, H., Mercaldo, V., Li, X., Chen, T., & Zhuo, M. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06314.x · Cited by 72

Enhancement of learning behaviour by a potent nitric oxide‐guanylate cyclase activator YC‐1

Chien, W., Liang, K., Teng, C., Kuo, S., Lee, F., & Fu, W. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.03993.x · Cited by 72

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

Synaptic plasticity during recovery from permanent occlusion of the middle cerebral artery

Centonze, D., Rossi, S., Tortiglione, A., Picconi, B., Prosperetti, C., Chiara, V. D., Bernardi, G., & Calabresi, P. (2007) · Neurobiology of Disease · doi:10.1016/j.nbd.2007.03.012 · Cited by 73

Dendritic mitoflash as a putative signal for stabilizing long-term synaptic plasticity

Fu, Z.-X., Tan, X., Fang, H., Lau, P.-M., Wang, X., Cheng, H., & Bi, G. (2017) · Nature Communications · doi:10.1038/s41467-017-00043-3 · Cited by 73

Possible role of intramembrane receptor-receptor interactions in memory and learning via formation of long-lived heteromeric complexes: focus on motor learning in the basal ganglia

Agnati, L. F., Franzén, O. G., Ferré, S., Leo, G., Franco, R., & Fuxé, K. (2003) · Journal of neural transmission. Supplementum · doi:10.1007/978-3-7091-0643-3_1 · Cited by 72

Isoform‐specific distribution of the plasma membrane Ca2+ ATPase in the rat brain

Burette, A., Rockwood, J. M., Strehler, E. E., & Weinberg, R. J. (2003) · The Journal of Comparative Neurology · doi:10.1002/cne.10933 · Cited by 72

Building new motor responses: eyelid conditioning revisited

Delgado-Garcia, J. M., & Gruart, A. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.05.003 · Cited by 72

NT-3 Evokes an LTP-Like Facilitation of AMPA/Kainate Receptor–Mediated Synaptic Transmission in the Neonatal Rat Spinal Cord

Arvanov, V. L., Seebach, B. S., & Mendell, L. M. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.84.2.752 · Cited by 73

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

The Effects of NR2 Subunit-Dependent NMDA Receptor Kinetics on Synaptic Transmission and CaMKII Activation

Santucci, D. M., & Raghavachari, S. (2008) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000208 · Cited by 73

Emergence of Input Specificity of LTP during Development of Retinotectal Connections In Vivo

Tao, H. W., Zhang, L. I., Engert, F., & Poo, M.-M. (2001) · Neuron · doi:10.1016/s0896-6273(01)00393-2 · Cited by 71

Freud-1/Aki1, a Novel PDK1-Interacting Protein, Functions as a Scaffold To Activate the PDK1/Akt Pathway in Epidermal Growth Factor Signaling

Nakamura, A., Naito, M., Tsuruo, T., & Fujita, N. (2008) · Molecular and Cellular Biology · doi:10.1128/mcb.00114-08 · Cited by 71

Low-frequency stimulation induces a new form of LTP, metabotropic glutamate (mGlu5) receptor- and PKA-dependent, in the CA1 area of the rat hippocampus

Lanté, F., Ferreira, M. D. J., Guiramand, J., Récasens, M., & Vignes, M. (2005) · Hippocampus · doi:10.1002/hipo.20146 · Cited by 77

Behavioral and genetic evidence for a novel animal model of Attention-Deficit/Hyperactivity Disorder Predominantly Inattentive Subtype

Sagvolden, T., DasBanerjee, T., Zhang‐James, Y., Middleton, F. A., & Faraone, S. V. (2008) · Behavioral and Brain Functions · doi:10.1186/1744-9081-4-56 · Cited by 72

The Jewels of Our Genome: The Search for the Genomic Changes Underlying the Evolutionarily Unique Capacities of the Human Brain

Sikela, J. M. (2006) · PLoS Genetics · doi:10.1371/journal.pgen.0020080 · Cited by 72

Acupuncture Attenuated Vascular Dementia–Induced Hippocampal Long-Term Potentiation Impairments via Activation of D1/D5 Receptors

Yang, Y., Li, H., Yang, J., Wang, X., Shi, G., Yan, C.-Q., Ma, S., Zhu, W. X., Li, Q., Li, T.-R., et al. (2017) · Stroke · doi:10.1161/strokeaha.116.014696 · Cited by 71

Actin-Dependent Activation of Presynaptic Silent Synapses Contributes to Long-Term Synaptic Plasticity in Developing Hippocampal Neurons

Yao, J., Qi, J., & Chen, G. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1183-06.2006 · Cited by 71

Developmental synaptic plasticity at the thalamocortical input to barrel cortex: Mechanisms and roles

Daw, M. I., Scott, H. L., & Isaac, J. T. R. (2007) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2007.01.001 · Cited by 70

From sensorimotor learning to memory cells in prefrontal and temporal association cortex: A neurocomputational study of disembodiment

Friedemann Pulvermüller, A., & Garagnani, M. (2014) · Cortex · doi:10.1016/j.cortex.2014.02.015 · Cited by 74

Phase Change Random Access Memory for Neuro‐Inspired Computing

Wang, Q., Niu, G., Ren, W., Wang, R., Chen, X.-G., Li, X., Ye, Z., Xie, Y., Song, S., & Song, Z. (2021) · Advanced Electronic Materials · doi:10.1002/aelm.202001241 · Cited by 71

Dopamine D4-receptor modulation of cortical neuronal network activity and emotional processing: Implications for neuropsychiatric disorders

Lauzon, N. M., & Laviolette, S. R. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.11.037 · Cited by 72

Ca2+ and mitochondria as substrates for deficits in synaptic plasticity in normal brain ageing

Toescu, E. C., & Verkhratsky, A. (2004) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2004.tb00273.x · Cited by 70

Distinct roles of astroglia and neurons in synaptic plasticity and memory

Liu, J., Zhang, M., Wang, Q., Wu, D., Jie, W., Hu, N.-Y., Lan, J.-Z., Zeng, K., Li, S.-J., Li, X., et al. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01332-6 · Cited by 70

Synaptic Depression Mediates Bistability in Neuronal Networks with Recurrent Inhibitory Connectivity

Manor, Y., & Farzan Nadim, A. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-23-09460.2001 · Cited by 69

Long term recordings with microelectrode arrays: Studies of transcription-dependent neuronal plasticity and axonal regeneration

Hofmann, F., & Bading, H. (2006) · Journal of Physiology-Paris · doi:10.1016/j.jphysparis.2005.12.005 · Cited by 69

Bi-directional modulation of AMPA receptor unitary conductance by synaptic activity

Lüthi, A., Wikström, M. A., Palmer, M. J., Matthews, P., Benke, T. A., Isaac, J. T. R., & Collingridge, G. L. (2004) · BMC Neuroscience · doi:10.1186/1471-2202-5-44 · Cited by 71

Postsynaptic Application of a Peptide Inhibitor of cAMP-Dependent Protein Kinase Blocks Expression of Long-Lasting Synaptic Potentiation in Hippocampal Neurons

Duffy, S. N., & Nguyen, P. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-04-01142.2003 · Cited by 69

Strongly Improved Stability and Faster Convergence of Temporal Sequence Learning by Using Input Correlations Only

Porr, B., & Wörgötter, F. (2006) · Neural Computation · doi:10.1162/neco.2006.18.6.1380 · Cited by 68

Dissection of bidirectional synaptic plasticity into saturable unidirectional processes.

O'Connor, D. H., Wittenberg, G. M., & Wang, S. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00047.2005 · Cited by 82

A-kinase anchoring proteins and neuronal signaling mechanismsPreprint

Carnegie, G. K., & Scott, J. D. (2003) · Genes & Development · doi:10.1101/gad.1095803 · Cited by 72

AMPA receptor trafficking and synaptic plasticity: major unanswered questions.

Sheng, M., & Hyoung Lee, S. (2003) · Neuroscience Research · doi:10.1016/s0168-0102(03)00040-3 · Cited by 71

Shank3-Rich2 Interaction Regulates AMPA Receptor Recycling and Synaptic Long-Term Potentiation

Raynaud, F., Janossy, A., Dahl, J., Bertaso, F., Perroy, J., Varrault, A., Vidal, M., Worley, P. F., Boeckers, T. M., Bockaert, J., et al. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2725-12.2013 · Cited by 71

Localization and signaling of the receptor protein tyrosine kinase Tyro3 in cortical and hippocampal neurons

Prieto, A. L., O’Dell, S., Varnum, B. C., & Lai, C. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2007.09.047 · Cited by 71

ZD7288 inhibits postsynaptic glutamate receptor‐mediated responses at hippocampal perforant path–granule cell synapses

Chen, C. (2004) · European Journal of Neuroscience · doi:10.1111/j.0953-816x.2003.03174.x · Cited by 68

Postsynaptic conversion of silent synapses during LTP affects synaptic gain and transmission dynamics

Poncer, J. C., & Malinow, R. (2001) · Nature Neuroscience · doi:10.1038/nn719 · Cited by 68

The Cadherin Family of Cell Adhesion Molecules: Multiple Roles in Synaptic Plasticity

Huntley, G. W., Gil, O. D., & Bozdagi, O. (2002) · The Neuroscientist · doi:10.1177/1073858402008003008 · Cited by 69

Ischemia induces short‐ and long‐term remodeling of synaptic activity in the hippocampus

Crépel, V., Epsztein, J., & Ben‐Ari, Y. (2003) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2003.tb00242.x · Cited by 67

Developmental nicotine exposure induced alterations in behavior and glutamate receptor function in hippocampus

Parameshwaran, K., Buabeid, M. A., Karuppagounder, S. S., Uthayathas, S., Thiruchelvam, K., Shonesy, B. C., Dityatev, A. E., Escobar, M. E., Dhanasekaran, M., & Suppiramaniam, V. D. (2011) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-011-0805-4 · Cited by 68

Extinguishing trace fear engages the retrosplenial cortex rather than the amygdala

Kwapis, J. L., Jarome, T. J., Lee, J. L. C., Gilmartin, M. R., & Helmstetter, F. J. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.09.007 · Cited by 66

Inducible and Selective Erasure of Memories in the Mouse Brain via Chemical-Genetic Manipulation

Cao, X., Wang, H., Mei, B., An, S., Yin, L., Wang, L. P., & Tsien, J. Z. (2008) · Neuron · doi:10.1016/j.neuron.2008.08.027 · Cited by 69

Transgenic up-regulation of alpha-CaMKII in forebrain leads to increased anxiety-like behaviors and aggression

Hasegawa, S., Furuichi, T., Yoshida, T., Endoh, K., Kato, K., Sado, M., Maeda, R., Kitamoto, A., Miyao, T., Suzuki, R., et al. (2009) · Molecular Brain · doi:10.1186/1756-6606-2-6 · Cited by 67

The roles of STP and LTP in synaptic encoding

Volianskis, A., Collingridge, G. L., & Jensen, M. S. (2013) · PeerJ · doi:10.7717/peerj.3 · Cited by 66

Low-Frequency Repetitive Transcranial Magnetic Stimulation Ameliorates Cognitive Function and Synaptic Plasticity in APP23/PS45 Mouse Model of Alzheimer’s Disease

Huang, Z., Tan, T., Du, Y., Chen, L., Fu, M., Yu, Y., Zhang, L., Song, W., & Dong, Z. (2017) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2017.00292 · Cited by 67

Presenilin Attenuates Receptor-Mediated Signaling and Synaptic Function

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