Molecular Mechanisms of Early and Late LTP

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 · see citing works

Glutamate neurotoxicity and diseases of the nervous system

Choi, D. W. (1988) · Neuron · doi:10.1016/0896-6273(88)90162-6 · Cited by 8,152 · see citing works

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 7,460 · see citing works

The Organization of Behavior; A Neuropsychological Theory.

Attneave, F., B., M., & Hebb, D. O. (1950) · The American Journal of Psychology · doi:10.2307/1418888 · Cited by 5,146 · see citing works

The Organization of Behavior: A Neuropsychological Theory

(1950) · JAMA · doi:10.1001/jama.1950.02910470083028 · Cited by 4,271 · see citing works

LTP and LTD

Malenka, R. C., & Bear, M. F. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.012 · Cited by 3,968 · see citing works

The molecular biology of memory storage: a dialogue between genes and synapses

Kandel, E. R. (2001) · Science · doi:10.1126/science.1067020 · Cited by 3,917 · see citing works

Glutamate Receptor Ion Channels: Structure, Regulation, and Function

Traynelis, S. F., Wollmuth, L. P., McBain, C. J., Menniti, F. S., Vance, K. M., Ogden, K. K., Hansen, K. B., Yuan, H., Myers, S. J., & Dingledine, R. (2010) · Pharmacological Reviews · doi:10.1124/pr.109.002451 · Cited by 3,568 · see citing works

Long-Term Potentiation--A Decade of Progress?

Malenka, R. C., & Nicoll, A. R. A. (1999) · Science · doi:10.1126/science.285.5435.1870 · Cited by 2,729 · see citing works

Neurotrophin regulation of neural circuit development and function

Park, H., & Poo, M.-M. (2013) · Nature Reviews Neuroscience · doi:10.1038/nrn3379 · Cited by 2,060 · see citing works

Neurotrophin signal transduction in the nervous system

Kaplan, D. R., & Miller, F. D. (2000) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(00)00092-1 · Cited by 1,944 · see citing works

Deficient long-term memory in mice with a targeted mutation of the cAMP-responsive element-binding protein

Bourtchuladze, R., Frenguelli, B., Blendy, J., Cioffi, D., Schutz, G., & Silva, A. J. (1994) · Cell · doi:10.1016/0092-8674(94)90400-6 · Cited by 1,800 · see citing works

Synaptic tagging and long-term potentiation

Frey, U., & Morris, R. G. M. (1997) · Nature · doi:10.1038/385533a0 · Cited by 1,736 · see citing works

Driving AMPA receptors into synapses by LTP and CaMKII: requirement for GluR1 and PDZ domain interaction

Hayashi, Y., Shi, S.-H., Esteban, J. A., Piccini, A., Poncer, J.-C., & Malinow, R. (2000) · Science · doi:10.1126/science.287.5461.2262 · Cited by 1,524 · see citing works

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 · see citing works

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 · see citing works

Sensitivity of CaM Kinase II to the Frequency of Ca ²⁺ Oscillations

De Koninck, P., & Schulman, H. (1998) · Science · doi:10.1126/science.279.5348.227 · Cited by 1,269 · see citing works

Evidence for silent synapses: Implications for the expression of LTP

Isaac, J. T. R., Nicoll, R. A., & Malenka, R. C. (1995) · Neuron · doi:10.1016/0896-6273(95)90046-2 · Cited by 1,233 · see citing works

Effects of cAMP simulate a late stage of LTP in hippocampal CA1 neurons

Frey, U., Huang, Y.-Y., & Kandel, E. R. (1993) · Science · doi:10.1126/science.8389057 · Cited by 1,218 · see citing works

Genetic Demonstration of a Role for PKA in the Late Phase of LTP and in Hippocampus-Based Long-Term Memory

Abel, T., Nguyen, P. V., Barad, M., Deuel, T. A. S., Kandel, E. R., & Bourtchouladze, R. (1997) · Cell · doi:10.1016/s0092-8674(00)81904-2 · Cited by 1,217 · see citing works

Cleavage of proBDNF by tPA/Plasmin Is Essential for Long-Term Hippocampal Plasticity

Pang, P. T., Teng, H. K., Zaitsev, E., Woo, N. T., Sakata, K., Zhen, S., Teng, K. K., Yung, W.-H., Hempstead, B. L., & Lu, B. (2004) · Science · doi:10.1126/science.1100135 · Cited by 1,136 · see citing works

Mechanisms of CaMKII action in long-term potentiation

Lisman, J., Yasuda, R., & Raghavachari, S. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3192 · Cited by 1,134 · see citing works

Regulation of distinct AMPA receptor phosphorylation sites during bidirectional synaptic plasticity

Lee, H.-K., Barbarosie, M., Kameyama, K., Bear, M. F., & Huganir, R. L. (2000) · Nature · doi:10.1038/35016089 · Cited by 1,116 · see citing works

Subunit-Specific Rules Governing AMPA Receptor Trafficking to Synapses in Hippocampal Pyramidal Neurons

Shi, S.-H., Hayashi, Y., Esteban, J. A., & Malinow, R. (2001) · Cell · doi:10.1016/s0092-8674(01)00321-x · Cited by 1,094 · see citing works

Type-Specific Regulation of Adenylyl Cyclase by G Protein βγ Subunits

Tang, W.-J., & Gilman, A. G. (1991) · Science · doi:10.1126/science.1962211 · Cited by 1,091 · see citing works

cAMP Activates MAP Kinase and Elk-1 through a B-Raf- and Rap1-Dependent Pathway

Vossler, M. R., Yao, H. W., York, R. D., Pan, M., Rim, C. S., & Stork, P. A. (1997) · Cell · doi:10.1016/s0092-8674(00)80184-1 · Cited by 1,044 · see citing works

Rapid increase of an immediate early gene messenger RNA in hippocampal neurons by synaptic NMDA receptor activation

Cole, A. J., Saffen, D. W., Baraban, J. M., & Worley, P. F. (1989) · Nature · doi:10.1038/340474a0 · Cited by 1,010 · see citing works

Mitogen-activated protein kinases in synaptic plasticity and memory

Sweatt, J. D. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.04.001 · Cited by 990 · see citing works

A requirement for the immediate early gene Zif268 in the expression of late LTP and long-term memories

Jones, M. W., Errington, M. L., French, P. J., Fine, A., Bliss, T., Garel, S., Charnay, P., Bozon, B., Laroche, S., & Davis, S. (2001) · Nature Neuroscience · doi:10.1038/85138 · Cited by 899 · see citing works

PKA phosphorylation of AMPA receptor subunits controls synaptic trafficking underlying plasticity

Esteban, J. A., Shi, S.-H., Wilson, C., Nuriya, M., Huganir, R. L., & Malinow, R. (2003) · Nature Neuroscience · doi:10.1038/nn997 · Cited by 894 · see citing works

Requirement of a Critical Period of Transcription for Induction of a Late Phase of LTP

Nguyen, P. V., Abel, T., & Kandel, E. R. (1994) · Science · doi:10.1126/science.8066450 · Cited by 888 · see citing works

GRIP: a synaptic PDZ domain-containing protein that interacts with AMPA receptors

Dong, H., O’Brien, R., Fung, E. T., Lanahan, A. A., Worley, P. F., & Huganir, R. L. (1997) · Nature · doi:10.1038/386279a0 · Cited by 871 · see citing works

A Requirement for the Mitogen-activated Protein Kinase Cascade in Hippocampal Long Term Potentiation

English, J. D., & Sweatt, J. D. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.31.19103 · Cited by 860 · see citing works

A Brief History of Long-Term Potentiation

Nicoll, R. A. (2017) · Neuron · doi:10.1016/j.neuron.2016.12.015 · Cited by 841 · see citing works

Synaptic Activation Causes the mRNA for the IEG Arc to Localize Selectively near Activated Postsynaptic Sites on Dendrites

Steward, O., Wallace, C. S., Lyford, G. L., & Worley, P. F. (1998) · Neuron · doi:10.1016/s0896-6273(00)80591-7 · Cited by 811 · see citing works

Phosphorylation of the AMPA Receptor GluR1 Subunit Is Required for Synaptic Plasticity and Retention of Spatial Memory

Lee, H.-K., Takamiya, K., Han, J.-S., Man, H., Kim, C.-H., Rumbaugh, G., Yu, S., Ding, L., He, C., Petralia, R. S., et al. (2003) · Cell · doi:10.1016/s0092-8674(03)00122-3 · Cited by 802 · see citing works

Arc/Arg3.1 interacts with the endocytic machinery to regulate AMPA receptor trafficking

Chowdhury, S., Shepherd, J. D., Okuno, H., Lyford, G., Petralia, R. S., Plath, N., Kuhl, D., Huganir, R. L., & Worley, P. F. (2006) · Neuron · doi:10.1016/j.neuron.2006.08.033 · Cited by 792 · see citing works

Importance of AMPA Receptors for Hippocampal Synaptic Plasticity But Not for Spatial Learning

Zamanillo, D., Sprengel, R., Hvalby, Ø., Jensen, V., Burnashev, N., Rozov, A., Kaiser, K. M. M., Köster, H. J., Borchardt, T., Worley, P., et al. (1999) · Science · doi:10.1126/science.284.5421.1805 · Cited by 791 · see citing works

Ras and Rap control AMPA receptor trafficking during synaptic plasticity

Zhu, J. J., Qin, Y., Zhao, M., Van Aelst, L., & Malinow, R. (2002) · Cell · doi:10.1016/s0092-8674(02)00897-8 · Cited by 769 · see citing works

Synapse-Specific, Long-Term Facilitation of Aplysia Sensory to Motor Synapses: A Function for Local Protein Synthesis in Memory Storage

Martin, K. C., Casadio, A., Zhu, H., Yaping, E., Rose, J. C., Chen, M., Bailey, C. H., & Kandel, E. R. (1997) · Cell · doi:10.1016/s0092-8674(00)80484-5 · Cited by 743 · see citing works

Interaction with the NMDA receptor locks CaMKII in an active conformation

Bayer, K.-U., De Koninck, P., Leonard, A. S., Hell, J. W., & Schulman, H. (2001) · Nature · doi:10.1038/35081080 · Cited by 732 · see citing works

NMDA Receptor Subunit Composition Controls Synaptic Plasticity by Regulating Binding to CaMKII

Barria, A., & Malinow, R. (2005) · Neuron · doi:10.1016/j.neuron.2005.08.034 · Cited by 709 · see citing works

Two components of long-term potentiation induced by different patterns of afferent activation

Grover, L. M., & Teyler, T. J. (1990) · Nature · doi:10.1038/347477a0 · Cited by 708 · see citing works

Role of AMPA Receptor Cycling in Synaptic Transmission and Plasticity

Lüscher, C., Xia, H., Beattie, E. C., Carroll, R. C., von Zastrow, M., Malenka, R. C., & Nicoll, R. A. (1999) · Neuron · doi:10.1016/s0896-6273(00)81119-8 · Cited by 692 · see citing works

LTP Inhibits LTD in the Hippocampus via Regulation of GSK3β

Peineau, S., Taghibiglou, C., Bradley, C. A., Wong, T. P., Liu, L., Lu, J., Lo, E., Wu, D., Saule, E., Bouschet, T., et al. (2007) · Neuron · doi:10.1016/j.neuron.2007.01.029 · Cited by 690 · see citing works

Preferential localization of polyribosomes under the base of dendritic spines in granule cells of the dentate gyrus

Steward, O., & Levy, W. (1982) · The Journal of Neuroscience · doi:10.1523/jneurosci.02-03-00284.1982 · Cited by 676 · see citing works

Synaptic plasticity at hippocampal mossy fibre synapses

Nicoll, R. A., & Schmitz, D. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1786 · Cited by 653 · see citing works

Synaptic enhancement in fascia dentata: Cooperativity among coactive afferents

McNaughton, B. L., Douglas, R. M., & Goddard, G. V. (1978) · Brain Research · doi:10.1016/0006-8993(78)90030-6 · Cited by 647 · see citing works

Structural and Molecular Remodeling of Dendritic Spine Substructures during Long-Term Potentiation

Bosch, M., Castro, J., Saneyoshi, T., Matsuno, H., Sur, M., & Hayashi, Y. (2014) · Neuron · doi:10.1016/j.neuron.2014.03.021 · Cited by 637 · see citing works

Protein synthesis and neurotrophin-dependent structural plasticity of single dendritic spines

Tanaka, J.-I., Horiike, Y., Matsuzaki, M., Miyazaki, T., Ellis-Davies, G. C. R., & Kasai, H. (2008) · Science · doi:10.1126/science.1152864 · Cited by 615 · see citing works

Silent synapses and the emergence of a postsynaptic mechanism for LTP

Kerchner, G. A., & Nicoll, R. A. (2008) · Nature reviews. Neuroscience · doi:10.1038/nrn2501 · Cited by 602 · see citing works

Regulation of AMPA receptor trafficking and synaptic plasticity

Anggono, V., & Huganir, R. L. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.12.006 · Cited by 588 · see citing works

DNA binding site of the growth factor-inducible protein Zif268.

Christy, B. A., & Nathans, D. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.22.8737 · Cited by 572 · see citing works

A Neuronal Isoform of the Aplysia CPEB Has Prion-Like Properties

Si, K., Lindquist, S. L., & Kandel, E. R. (2003) · Cell · doi:10.1016/s0092-8674(03)01020-1 · Cited by 565 · see citing works

Local, persistent activation of Rho GTPases during plasticity of single dendritic spines

Murakoshi, H., Wang, H., & Yasuda, R. (2011) · Nature · doi:10.1038/nature09823 · Cited by 564 · see citing works

Phosphorylation of the AMPA receptor subunit GluR2 differentially regulates its interaction with PDZ domain-containing proteins

Chung, H. J., Xia, J., Scannevin, R. H., Zhang, X., & Huganir, R. L. (2000) · The Journal of Neuroscience · doi:10.1523/jneurosci.20-19-07258.2000 · Cited by 558 · see citing works

Synapses as associative memory elements in the hippocampal formation

Levy, W. B., & Steward, O. (1979) · Brain Research · doi:10.1016/0006-8993(79)91003-5 · Cited by 557 · see citing works

Synaptic secretion of BDNF after high‐frequency stimulation of glutamatergic synapses

Hartmann, M., Heumann, R., & Leßmann, V. (2001) · The EMBO Journal · doi:10.1093/emboj/20.21.5887 · Cited by 513 · see citing works

Disruption of Dendritic Translation of CaMKIIα Impairs Stabilization of Synaptic Plasticity and Memory Consolidation

Miller, S., Yasuda, M., Coats, J., Jones, Y., Martone, M. E., & Mayford, M. R. (2002) · Neuron · doi:10.1016/s0896-6273(02)00978-9 · Cited by 507 · see citing works

AMPA Receptor Incorporation into Synapses during LTP: The Role of Lateral Movement and Exocytosis

Makino, H., & Malinow, R. (2009) · Neuron · doi:10.1016/j.neuron.2009.08.035 · Cited by 501 · see citing works

Enhancement of the Glutamate Response by cAMP-Dependent Protein Kinase in Hippocampal Neurons

Greengard, P., Jen, J. C., Nairn, A. C., & Stevens, C. F. (1991) · Science · doi:10.1126/science.1716001 · Cited by 498 · see citing works

Neurotrophins and Time: Different Roles for TrkB Signaling in Hippocampal Long-Term Potentiation

Kang, H., Welcher, A. A., Shelton, D., & Schuman, E. M. (1997) · Neuron · doi:10.1016/s0896-6273(00)80378-5 · Cited by 481 · see citing works

Recruitment of long-lasting and protein kinase A-dependent long-term potentiation in the CA1 region of hippocampus requires repeated tetanization.Preprint

Huang, Y.-Y., & Kandel, E. R. (1994) · Learning & Memory · doi:10.1101/lm.1.1.74 · Cited by 476 · see citing works

Myosin Vb mobilizes recycling endosomes and AMPA receptors for postsynaptic plasticity

Wang, Z., Edwards, J. G., Riley, N., Provance, D. W., Karcher, R., Li, X.-D., Davison, I. G., Ikebe, M., Mercer, J. A., Kauer, J. A., et al. (2008) · Cell · doi:10.1016/j.cell.2008.09.057 · Cited by 470 · see citing works

Spine Ca²⁺Signaling in Spike-Timing-Dependent Plasticity

Nevian, T., & Sakmann, B. (2006) · The Journal of Neuroscience · doi:10.1523/jneurosci.1749-06.2006 · Cited by 458 · see citing works

Calcium/calmodulin-dependent kinase II and long-term potentiation enhance synaptic transmission by the same mechanism

Lledo, P. M., Hjelmstad, G. O., Mukherji, S., Soderling, T. R., Malenka, R. C., & Nicoll, R. A. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.24.11175 · Cited by 456 · see citing works

Sustained Arc/Arg3.1 Synthesis Controls Long-Term Potentiation Consolidation through Regulation of Local Actin Polymerization in the Dentate GyrusIn Vivo

Messaoudi, E., Kanhema, T., Soule, J. D., Tiron, A., Dagytė, G., da Silva, B., & Bramham, C. R. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2883-07.2007 · Cited by 452 · see citing works

The Arc of synaptic memory

Bramham, C. R., Alme, M. N., Bittins, M., Kuipers, S. D., Nair, R. R., Pai, B., Panja, D., Schubert, M., Soule, J., Tiron, A., et al. (2010) · Experimental Brain Research · doi:10.1007/s00221-009-1959-2 · Cited by 452 · see citing works

Phosphorylation of the α-Amino-3-hydroxy-5-methylisoxazole4-propionic Acid Receptor GluR1 Subunit by Calcium/ Calmodulin-dependent Kinase II

Mammen, A. L., Kameyama, K., Roche, K. W., & Huganir, R. L. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.51.32528 · Cited by 441 · see citing works

A Neuronal Isoform of CPEB Regulates Local Protein Synthesis and Stabilizes Synapse-Specific Long-Term Facilitation in Aplysia

Si, K., Giustetto, M., Etkin, A., Hsu, R., Janisiewicz, A. M., Miniaci, M. C., Kim, J., Zhu, H., & Kandel, E. R. (2003) · Cell · doi:10.1016/s0092-8674(03)01021-3 · Cited by 432 · see citing works

How does PKMζ maintain long-term memory?

Sacktor, T. C. (2011) · Nature Reviews Neuroscience · doi:10.1038/nrn2949 · Cited by 431 · see citing works

Long-Term Potentiation: From CaMKII to AMPA Receptor Trafficking

Herring, B. E., & Nicoll, R. A. (2016) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021014-071753 · Cited by 425 · see citing works

Structural plasticity of dendritic spines

Bosch, M., & Hayashi, Y. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.09.002 · Cited by 415 · see citing works

Postsynaptic Membrane Fusion and Long-Term Potentiation

Lledo, P.-M., Zhang, X., Südhof, T. C., Malenka, R. C., & Nicoll, R. A. (1998) · Science · doi:10.1126/science.279.5349.399 · Cited by 413 · see citing works

The Expanding Social Network of Ionotropic Glutamate Receptors: TARPs and Other Transmembrane Auxiliary Subunits

Jackson, A. C., & Nicoll, R. A. (2011) · Neuron · doi:10.1016/j.neuron.2011.04.007 · Cited by 410 · see citing works

CaMKII Triggers the Diffusional Trapping of Surface AMPARs through Phosphorylation of Stargazin

Opazo, P., Labrecque, S., Tigaret, C. M., Frouin, A., Wiseman, P. W., Koninck, P. D., & Choquet, D. (2010) · Neuron · doi:10.1016/j.neuron.2010.06.007 · Cited by 403 · see citing works

Structural Components of Synaptic Plasticity and Memory ConsolidationPreprint

Bailey, C. H., Kandel, E. R., & Harris, K. M. (2015) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a021758 · Cited by 393 · see citing works

Identification of the Ca2+/Calmodulin-dependent Protein Kinase II Regulatory Phosphorylation Site in the α-Amino-3-hydroxyl-5-methyl4-isoxazole-propionate-type Glutamate Receptor

Barría, A., Derkach, V. A., & Soderling, T. R. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.52.32727 · Cited by 392 · see citing works

Calcium/calmodulin-dependent protein kinase II is associated with the <i>N</i> -methyl- <scp>d</scp> -aspartate receptor

Leonard, A. S., Lim, I. A., Hemsworth, D. E., Horne, M. C., & Hell, J. W. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.6.3239 · Cited by 385 · see citing works

Synaptic incorporation of AMPA receptors during LTP is controlled by a PKC phosphorylation site on GluR1

Boehm, J., Kang, M.-G., Johnson, R. C., Esteban, J., Huganir, R. L., & Malinow, R. (2006) · Neuron · doi:10.1016/j.neuron.2006.06.013 · Cited by 382 · see citing works

Aplysia CPEB can form prion-like multimers in sensory neurons that contribute to long-term facilitation.

Si, K., Choi, Y.-B., White-Grindley, E., Majumdar, A., & Kandel, E. (2010) · Cell · doi:10.1016/j.cell.2010.01.008 · Cited by 380 · see citing works

Mechanism and Regulation of Calcium/Calmodulin-dependent Protein Kinase II Targeting to the NR2B Subunit of the N-Methyl-d-aspartate Receptor

Strack, S., McNeill, R. B., & Colbran, R. J. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m001471200 · Cited by 356 · see citing works

BDNF and its pro-peptide are stored in presynaptic dense core vesicles in brain neurons

Dieni, S., Matsumoto, T., Dekkers, M. P. J., Rauskolb, S., Ionescu, M. S., Deogracias, R., Gundelfinger, E. D., Kojima, M., Nestel, S., Frotscher, M., et al. (2012) · The Journal of Cell Biology · doi:10.1083/jcb.201201038 · Cited by 346 · see citing works

Mechanisms, locations, and kinetics of synaptic BDNF secretion: An update

Leßmann, V., & Brigadski, T. (2009) · Neuroscience Research · doi:10.1016/j.neures.2009.06.004 · Cited by 340 · see citing works

Complexin Controls the Force Transfer from SNARE Complexes to Membranes in Fusion

Maximov, A., Tang, J., Yang, X., Pang, Z. P., & Südhof, T. C. (2009) · Science · doi:10.1126/science.1166505 · Cited by 339 · see citing works

BDNF mechanisms in late LTP formation: A synthesis and breakdown

Panja, D., & Bramham, C. R. (2014) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.06.024 · Cited by 336 · see citing works

Some Forms of cAMP-Mediated Long-Lasting Potentiation Are Associated with Release of BDNF and Nuclear Translocation of Phospho-MAP Kinase

Patterson, S. L., Pittenger, C., Morozov, A., Martin, K. C., Scanlin, H., Drake, C., & Kandel, E. R. (2001) · Neuron · doi:10.1016/s0896-6273(01)00443-3 · Cited by 334 · see citing works

Gene Expression Profiling of Facilitated L-LTP in VP16-CREB Mice Reveals that BDNF Is Critical for the Maintenance of LTP and Its Synaptic Capture

Barco, Á., Patterson, S., Alarcón, J. M., Gromova, P., Mata, M., Morozov, A., & Kandel, E. R. (2005) · Neuron · doi:10.1016/j.neuron.2005.09.005 · Cited by 332 · see citing works

MAPK, CREB and zif268 are all required for the consolidation of recognition memory

Bozon, B., Kelly, A. M., Josselyn, S. A., Silva, A. J., Davis, S., & Laroche, S. (2003) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2002.1224 · Cited by 327 · see citing works

Autocrine BDNF-TrkB signalling within a single dendritic spine

Harward, S. C., Hedrick, N. G., Hall, C. E., Parra-Bueno, P., Milner, T. A., Pan, E., Laviv, T., Hempstead, B. L., Yasuda, R., & McNamara, J. O. (2016) · Nature · doi:10.1038/nature19766 · Cited by 325 · see citing works

Regulation of hippocampal synaptic plasticity by cyclic AMP-dependent protein kinases

Nguyen, P., & Woo, N. H. (2003) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2003.12.003 · Cited by 324 · see citing works

Hippocampal LTP and contextual learning require surface diffusion of AMPA receptors

Penn, A. C., Zhang, C. L., Georges, F., Royer, L., Breillat, C., Hosy, E., Petersen, J. D., Humeau, Y., & Choquet, D. (2017) · Nature · doi:10.1038/nature23658 · Cited by 324 · see citing works

LTP requires a reserve pool of glutamate receptors independent of subunit type

Granger, A. J., Shi, Y., Lu, W., Cerpas, M., & Nicoll, R. A. (2013) · Nature · doi:10.1038/nature11775 · Cited by 313 · see citing works

PKM-ζ is not required for hippocampal synaptic plasticity, learning and memory

Volk, L. J., Bachman, J. L., Johnson, R., Yu, Y., & Huganir, R. L. (2013) · Nature · doi:10.1038/nature11802 · Cited by 310 · see citing works

Inverse synaptic tagging of inactive synapses via dynamic interaction of Arc/Arg3.1 with CaMKIIβ

Okuno, H., Akashi, K., Ishii, Y., Yagishita-Kyo, N., Suzuki, K., Nonaka, M., Kawashima, T., Fujii, H., Takemoto-Kimura, S., Abe, M., et al. (2012) · Cell · doi:10.1016/j.cell.2012.02.062 · Cited by 310 · see citing works

PSD-95 family MAGUKs are essential for anchoring AMPA and NMDA receptor complexes at the postsynaptic density

Chen, X., Levy, J. M., Hou, A., Winters, C., Azzam, R., Sousa, A. A., Leapman, R. D., Nicoll, R. A., & Reese, T. S. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1517045112 · Cited by 310 · see citing works

Visualization of changes in presynaptic function during long-term synaptic plasticity

Zakharenko, S. S., Zablow, L., & Siegelbaum, S. A. (2001) · Nature Neuroscience · doi:10.1038/89498 · Cited by 305 · see citing works

Correlations between immediate early gene induction and the persistence of long-term potentiation

Abraham, W. C., Mason, S. E., Demmer, J., Williams, J. M., Richardson, C. L., Tate, W. P., Lawlor, P. A., & Dragunow, M. (1993) · Neuroscience · doi:10.1016/0306-4522(93)90369-q · Cited by 303 · see citing works

Endocytic Trafficking and Recycling Maintain a Pool of Mobile Surface AMPA Receptors Required for Synaptic Potentiation

Petrini, E. M., Lü, J., Cognet, L., Lounis, B., Ehlers, M., & Choquet, D. (2009) · Neuron · doi:10.1016/j.neuron.2009.05.025 · Cited by 301 · see citing works

Constitutive expression of zif268 in neocortex is regulated by synaptic activity.

Worley, P. F., Christy, B. A., Nakabeppu, Y., Bhat, R. V., Cole, A. J., & Baraban, J. M. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.12.5106 · Cited by 298 · see citing works

Multiple forms of LTP in hippocampal CA3 neurons use a common postsynaptic mechanism

Yeckel, M. F., Kapur, A., & Johnston, D. (1999) · Nature Neuroscience · doi:10.1038/10180 · Cited by 295 · see citing works

Mechanism of Ca2+/calmodulin-dependent kinase II regulation of AMPA receptor gating

Kristensen, A. S., Jenkins, M. A., Banke, T. G., Schousboe, A., Makino, Y., Johnson, R. C., Huganir, R., & Traynelis, S. F. (2011) · Nature Neuroscience · doi:10.1038/nn.2804 · Cited by 286 · see citing works

Critical Role of Amyloid-like Oligomers of Drosophila Orb2 in the Persistence of Memory

Majumdar, A., Cesario, W. C., White‐Grindley, E., Jiang, H., Ren, F., Khan, M. R., Li, L., Choi, E. M.-L., Kannan, K. S., Guo, F., et al. (2012) · Cell · doi:10.1016/j.cell.2012.01.004 · Cited by 281 · see citing works

Rapid dispersion of SynGAP from synaptic spines triggers AMPA receptor insertion and spine enlargement during LTP

Araki, Y., Zeng, M., Zhang, M., & Huganir, R. L. (2015) · Neuron · doi:10.1016/j.neuron.2014.12.023 · Cited by 271 · see citing works

Spike-Time-Dependent Plasticity and Heterosynaptic Competition Organize Networks to Produce Long Scale-Free Sequences of Neural Activity

Fiete, I., Senn, W., Wang, C. Z.-H., & Hahnloser, R. H. R. (2010) · Neuron · doi:10.1016/j.neuron.2010.02.003 · Cited by 269 · see citing works

PKMζ Maintains Late Long-Term Potentiation by N -Ethylmaleimide-Sensitive Factor/GluR2-Dependent Trafficking of Postsynaptic AMPA Receptors

Yao, Y., Kelly, M. T., Sajikumar, S., Serrano, P. A., Tian, D., Bergold, P. J., Frey, J. U., & Sacktor, T. C. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0223-08.2008 · Cited by 268 · see citing works

Function of the Drosophila CPEB protein Orb2 in long-term courtship memory

Keleman, K., Krüttner, S., Alenius, M., & Dickson, B. J. (2007) · Nature Neuroscience · doi:10.1038/nn1996 · Cited by 266 · see citing works

Specific Roles of AMPA Receptor Subunit GluR1 (GluA1) Phosphorylation Sites in Regulating Synaptic Plasticity in the CA1 Region of Hippocampus

Lee, H.-K., Takamiya, K., He, K., Song, L., & Huganir, R. L. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00835.2009 · Cited by 261 · see citing works

Motor protein–dependent transport of AMPA receptors into spines during long-term potentiation

Correia, S. S., Bassani, S., Brown, T. C., Lisé, M.-F., Backos, D. S., El-Husseini, A., Passafaro, M., & Esteban, J. A. (2008) · Nature Neuroscience · doi:10.1038/nn2063 · Cited by 260 · see citing works

Prkcz null mice show normal learning and memory

Lee, A. M., Kanter, B. R., Wang, D., Lim, J. P., Zou, M. E., Qiu, C., McMahon, T., Dadgar, J., Fischbach-Weiss, S., & Messing, R. O. (2013) · Nature · doi:10.1038/nature11803 · Cited by 259 · see citing works

Arg3.1/Arc mRNA Induction by Ca2+and cAMP Requires Protein Kinase A and Mitogen-Activated Protein Kinase/Extracellular Regulated Kinase Activation

Waltereit, R., Dammermann, B., Wulff, P., Scafidi, J., Staubli, U. V., Kauselmann, G., Bundman, M. C., & Kuhl, D. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-15-05484.2001 · Cited by 259 · see citing works

How long will long-term potentiation last?

Abraham, W. C. (2003) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2002.1222 · Cited by 258 · see citing works

The role of immediate early genes in the stabilization of long-term potentiation

Abraham, W. C., Dragunow, M., & Tate, W. P. (1991) · Molecular Neurobiology · doi:10.1007/bf02935553 · Cited by 254 · see citing works

Synaptic transmission and plasticity in the absence of AMPA glutamate receptor GluR2 and GluR3

Meng, Y., Zhang, Y., & Jia, Z. (2003) · Neuron · doi:10.1016/s0896-6273(03)00368-4 · Cited by 251 · see citing works

Rap1 Couples cAMP Signaling to a Distinct Pool of p42/44MAPK Regulating Excitability, Synaptic Plasticity, Learning, and Memory

Morozov, A., Muzzio, I. A., Bourtchouladze, R., Van-Strien, N., Lapidus, K. A. B., Yin, D., Winder, D. G., Adams, J. P., Sweatt, J. D., & Kandel, E. R. (2003) · Neuron · doi:10.1016/s0896-6273(03)00404-5 · Cited by 237 · see citing works

LTP Requires a Unique Postsynaptic SNARE Fusion Machinery

Jurado, S., Goswami, D., Zhang, Y., Molina, A. J. M., Südhof, T. C., & Malenka, R. C. (2013) · Neuron · doi:10.1016/j.neuron.2012.11.029 · Cited by 232 · see citing works

CPEB3 and CPEB4 in neurons: analysis of RNA‐binding specificity and translational control of AMPA receptor GluR2 mRNA

Huang, Y., Kan, M.-C., Lin, C., & Richter, J. D. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601322 · Cited by 229 · see citing works

MAP kinase-mediated signalling to nucleosomes and immediate-early gene induction

Thomson, S., Mahadevan, L. C., & Clayton, A. L. (1999) · Seminars in Cell and Developmental Biology · doi:10.1006/scdb.1999.0302 · Cited by 228 · see citing works

The Persistence of Hippocampal-Based Memory Requires Protein Synthesis Mediated by the Prion-like Protein CPEB3

Fioriti, L., Myers, C., Huang, Y.-Y., Li, X., Stephan, J. S., Trifilieff, P., Colnaghi, L., Kosmidis, S., Drisaldi, B., Pavlopoulos, E., et al. (2015) · Neuron · doi:10.1016/j.neuron.2015.05.021 · Cited by 221 · see citing works

Synaptic tagging — who's it?

Martin, K. C., & Kosik, K. S. (2002) · Nature reviews. Neuroscience · doi:10.1038/nrn942 · Cited by 219 · see citing works

Chapter 2 PKMζ, LTP maintenance, and the dynamic molecular biology of memory storage

Sacktor, T. C. (2008) · Progress in Brain Research · doi:10.1016/s0079-6123(07)00002-7 · Cited by 208 · see citing works

Association of the Kinesin Motor KIF1A with the Multimodular Protein Liprin-α

Shin, H., Wyszynski, M. W., Huh, K. H., Valtschanoff, J. G., Lee, J.-R., Ko, J., Streuli, M., Weinberg, R. J., Sheng, M., & Kim, E. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m211874200 · Cited by 207 · see citing works

NSF ATPase and α-/β-SNAPs Disassemble the AMPA Receptor-PICK1 Complex

Hanley, J. G., Khatri, L., Hanson, P. I., & Ziff, E. B. (2002) · Neuron · doi:10.1016/s0896-6273(02)00638-4 · Cited by 197 · see citing works

Postsynaptic synaptotagmins mediate AMPA receptor exocytosis during LTP

Wu, D., Bacaj, T., Morishita, W., Goswami, D., Arendt, K. L., Xu, W., Chen, L., Malenka, R. C., & Südhof, T. C. (2017) · Nature · doi:10.1038/nature21720 · Cited by 195 · see citing works

Two previously undescribed members of the mouse CPEB family of genes and their inducible expression in the principal cell layers of the hippocampus

Theis, M., Si, K., & Kandel, E. R. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1133424100 · Cited by 194 · see citing works

A three-step model for the synaptic recruitment of AMPA receptors

Opazo, P., & Choquet, D. (2011) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2010.08.014 · Cited by 190 · see citing works

Neuralized1 Activates CPEB3: A Function for Nonproteolytic Ubiquitin in Synaptic Plasticity and Memory Storage

Pavlopoulos, E., Trifilieff, P., Chevaleyre, V., Fioriti, L., Zairis, S., Pagano, A., Malleret, G., & Kandel, E. R. (2011) · Cell · doi:10.1016/j.cell.2011.09.056 · Cited by 189 · see citing works

The Transcription Factor Zif268/Egr1, Brain Plasticity, and Memory

Veyrac, A., Besnard, A., Caboche, J., Davis, S., & Laroche, S. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-420170-5.00004-0 · Cited by 184 · see citing works

Arc protein: a flexible hub for synaptic plasticity and cognition

Nikolaienko, O., Patil, S. S., Eriksen, M. S., & Bramham, C. R. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.09.006 · Cited by 183 · see citing works

Tyrosine phosphorylation and regulation of the AMPA receptor by SRC family tyrosine kinases

Hayashi, T., & Huganir, R. L. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.0799-04.2004 · Cited by 177 · see citing works

Correlation between the induction of an immediate early gene,zif/268, and long-term potentiation in the dentate gyrus

Richardson, C. L., Tate, W. P., Mason, S. E., Lawlor, P. A., Dragunow, M., & Abraham, W. C. (1992) · Brain Research · doi:10.1016/0006-8993(92)90938-6 · Cited by 171 · see citing works

The CaMKII/NMDA receptor complex controls hippocampal synaptic transmission by kinase-dependent and independent mechanisms

Incontro, S., Díaz-Alonso, J., Iafrati, J., Vieira, M., Asensio, C. S., Sohal, V. S., Roche, K. W., Bender, K. J., & Nicoll, R. A. (2018) · Nature Communications · doi:10.1038/s41467-018-04439-7 · Cited by 171 · see citing works

TARP Phosphorylation Regulates Synaptic AMPA Receptors through Lipid Bilayers

Sumioka, A., Yan, D., & Tomita, S. (2010) · Neuron · doi:10.1016/j.neuron.2010.04.035 · Cited by 167 · see citing works

Compensation for PKMζ in long-term potentiation and spatial long-term memory in mutant mice

Tsokas, P., Hsieh, C., Yao, Y., Lesburguères, E., Wallace, E. J. C., Tcherepanov, A., Jothianandan, D., Hartley, B. R., Pan, L., Rivard, B., et al. (2016) · eLife · doi:10.7554/elife.14846 · Cited by 166 · see citing works

GRASP-1

Ye, B., Liao, D., Zhang, X., Zhang, P., Dong, H., & Huganir, R. L. (2000) · Neuron · doi:10.1016/s0896-6273(00)81198-8 · Cited by 155 · see citing works

Arc in the nucleus regulates PML-dependent GluA1 transcription and homeostatic plasticity

Korb, E., Wilkinson, C. L., Delgado, R. N., Lovero, K. L., & Finkbeiner, S. M. (2013) · Nature Neuroscience · doi:10.1038/nn.3429 · Cited by 145 · see citing works

Regulation of Protein Kinase Mζ Synthesis by Multiple Kinases in Long-Term Potentiation

Kelly, M., Crary, J. F., & Sacktor, T. C. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.5612-06.2007 · Cited by 144 · see citing works

Glutamate Release Monitored with Astrocyte Transporter Currents during LTP

Diamond, J. S., Bergles, D. E., & Jahr, C. E. (1998) · Neuron · doi:10.1016/s0896-6273(00)80551-6 · Cited by 143 · see citing works

Long-Term Potentiation: Evidence Against an Increase in Transmitter Release Probability in the CA1 Region of the Hippocampus

Manabe, T., & Nicoll, R. A. (1994) · Science · doi:10.1126/science.7916483 · Cited by 140 · see citing works

Translational Control in the Brain in Health and Disease

Sossin, W. S., & Costa-Mattioli, M. (2019) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a032912 · Cited by 138 · see citing works

Long-lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path

Bliss, T. V. P., & Lømo, T. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010273 · Cited by 135 · see citing works

Activity-regulated cytoskeletal-associated protein is localized to recently activated excitatory synapses

Moga, D. E., Calhoun, M. E., Chowdhury, A., Worley, P., Morrison, J. H., & Shapiro, M. L. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.02.004 · Cited by 134 · see citing works

Postsynaptic Complexin Controls AMPA Receptor Exocytosis during LTP

Ahmad, M., Polepalli, J. S., Goswami, D., Yang, X., Kaeser-Woo, Y. J., Südhof, T. C., & Malenka, R. C. (2012) · Neuron · doi:10.1016/j.neuron.2011.11.020 · Cited by 133 · see citing works

TrkB as a Potential Synaptic and Behavioral Tag

Lü, Y., Ji, Y., Ganesan, S., Schloesser, R. J., Martinowich, K., Sun, M., Mei, F., Chao, M. V., & Lu, B. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.2707-11.2011 · Cited by 130 · see citing works

Autonomous CaMKII can promote either long-term potentiation or long-term depression, depending on the state of T305/T306 phosphorylation

Pi, H. J., Otmakhov, N., Lemelin, D., De Koninck, P., & Lisman, J. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0133-10.2010 · Cited by 125 · see citing works

Monitoring Glutamate Release during LTP with Glial Transporter Currents

Lüscher, C., Malenka, R. C., & Nicoll, R. A. (1998) · Neuron · doi:10.1016/s0896-6273(00)80552-8 · Cited by 123 · see citing works

Dual Regulation of miRNA Biogenesis Generates Target Specificity in Neurotrophin-Induced Protein Synthesis

Huang, Y. A., Ruiz, C. R., Eyler, E. C. H., Lin, K., & Meffert, M. K. (2012) · Cell · doi:10.1016/j.cell.2012.01.036 · Cited by 122 · see citing works

Positioning of AMPA Receptor-Containing Endosomes Regulates Synapse Architecture

da Silva, M. E., Adrian, M., Schätzle, P., Lipka, J., Watanabe, T., Cho, S., Futai, K., Wierenga, C. J., Kapitein, L. C., & Hoogenraad, C. C. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.09.062 · Cited by 122 · see citing works

CaMKII Phosphorylation of TARPγ-8 Is a Mediator of LTP and Learning and Memory

Park, J., Chávez, A. E., Mineur, Y. S., Morimoto-Tomita, M., Lutzu, S., Kim, K. S., Picciotto, M. R., Castillo, P. E., & Tomita, S. (2016) · Neuron · doi:10.1016/j.neuron.2016.09.002 · Cited by 121 · see citing works

SUMOylation Is an Inhibitory Constraint that Regulates the Prion-like Aggregation and Activity of CPEB3

Drisaldi, B., Colnaghi, L., Fioriti, L., Rao, N., Myers, C., Snyder, A. M., Metzger, D. J., Tarasoff, J., Konstantinov, E., Fraser, P. E., et al. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.04.061 · Cited by 120 · see citing works

Intersubunit capture of regulatory segments is a component of cooperative CaMKII activation

Chao, L. H., Pellicena, P., Deindl, S., Barclay, L. A., Schulman, H., & Kuriyan, J. (2010) · Nature Structural &amp; Molecular Biology · doi:10.1038/nsmb.1751 · Cited by 119 · see citing works

Convergent CaMK and RacGEF signals control dendritic structure and function

Penzes, P., Cahill, M. E., Jones, K. A., & Srivastava, D. P. (2008) · Trends in Cell Biology · doi:10.1016/j.tcb.2008.07.002 · Cited by 118 · see citing works

Loss of Cdc42 leads to defects in synaptic plasticity and remote memory recall

Kim, I. H., Wang, H., Soderling, S. H., & Yasuda, R. (2014) · eLife · doi:10.7554/elife.02839 · Cited by 116 · see citing works

Mouse cytoplasmic polyadenylylation element binding protein: An evolutionarily conserved protein that interacts with the cytoplasmic polyadenylylation elements of c- mos mRNA

Gebauer, F., & Richter, J. D. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.25.14602 · Cited by 115 · see citing works

Novel Translational Control in Arc-dependent Long Term Potentiation Consolidation in Vivo

Panja, D., Dagytė, G., Bidinosti, M., Wibrand, K., Kristiansen, Å.-M., Sonenberg, N., & Bramham, C. R. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.056077 · Cited by 113 · see citing works

Long‐term potentiation in the rat dentate gyrus is associated with enhanced Arc/Arg3.1 protein expression in spines, dendrites and glia

Rodríguez, J. J., Davies, H. A., Silva, A. T., De Souza, I. E. J., Peddie, C. J., Colyer, F. M., Lancashire, C. L., Fine, A., Errington, M. L., Bliss, T. V. P., et al. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04068.x · Cited by 113 · see citing works

Genetic Dissection of Presynaptic and Postsynaptic BDNF-TrkB Signaling in Synaptic Efficacy of CA3-CA1 Synapses

Lin, P.-Y., Kavalali, E. T., & Monteggia, L. M. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.07.020 · Cited by 112 · see citing works

Neuron Specific Rab4 Effector GRASP-1 Coordinates Membrane Specialization and Maturation of Recycling Endosomes

Hoogenraad, C. C., Popa, I., Futai, K., Martínez-Sanchez, E., Wulf, P. S., van Vlijmen, T., Dortland, B. R., Oorschot, V. M. J., Govers, R., Monti, M., et al. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000283 · Cited by 108 · see citing works

PKCλ is critical in AMPA receptor phosphorylation and synaptic incorporation during LTP

Ren, S., Yan, J., Zhang, X., Bu, Y.-F., Pan, W.-W., Yao, W., Tian, T., & Lü, W. (2013) · The EMBO Journal · doi:10.1038/emboj.2013.60 · Cited by 107 · see citing works

The Role of Functional Prion-Like Proteins in the Persistence of MemoryPreprint

Si, K., & Kandel, E. R. (2016) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a021774 · Cited by 107 · see citing works

Dendritic Transport and Localization of Protein Kinase Mζ mRNA

Muslimov, I. A., Nimmrich, V., Hernandez, A. I., Tcherepanov, A., Sacktor, T. C., & Tiedge, H. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m409240200 · Cited by 106 · see citing works

Drosophila CPEB Orb2A Mediates Memory Independent of Its RNA-Binding Domain

Krüttner, S., Stepien, B. K., Noordermeer, J. N., Mommaas, M., Mechtler, K., Dickson, B. J., & Keleman, K. (2012) · Neuron · doi:10.1016/j.neuron.2012.08.028 · Cited by 103 · see citing works

Lengthening of the Stargazin Cytoplasmic Tail Increases Synaptic Transmission by Promoting Interaction to Deeper Domains of PSD-95

Hafner, A.-S., Penn, A. C., Grillo-Bosch, D., Retailleau, N., Poujol, C., Philippat, A., Coussen, F., Sainlos, M., Opazo, P., & Choquet, D. (2015) · Neuron · doi:10.1016/j.neuron.2015.03.013 · Cited by 101 · see citing works

Multiple cellular cascades participate in long-term potentiation and in hippocampus-dependent learning

Baudry, M., Zhu, G., Liu, Y., Wang, Y., Briz, V., & Bi, X. (2014) · Brain Research · doi:10.1016/j.brainres.2014.11.033 · Cited by 100 · see citing works

Kalirin and Trio proteins serve critical roles in excitatory synaptic transmission and LTP

Herring, B. E., & Nicoll, R. A. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1600179113 · Cited by 98 · see citing works

CaMKII control of spine size and synaptic strength: Role of phosphorylation states and nonenzymatic action

Pi, H. J., Otmakhov, N., Gaamouch, F. E., Lemelin, D., Koninck, P. D., & Lisman, J. E. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1009268107 · Cited by 94 · see citing works

Plasma membrane insertion of the AMPA receptor GluA2 subunit is regulated by NSF binding and Q/R editing of the ion pore

Araki, Y., Lin, D.-T., & Huganir, R. L. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1006584107 · Cited by 92 · see citing works

Calpain-2-Mediated PTEN Degradation Contributes to BDNF-Induced Stimulation of Dendritic Protein Synthesis

Briz, V., Hsu, Y., Li, Y., Lee, E., Bi, X., & Baudry, M. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4907-12.2013 · Cited by 85 · see citing works

Pin1 and PKMζ Sequentially Control Dendritic Protein Synthesis

Westmark, P. R., Westmark, C. J., Wang, S., Levenson, J. M., O’Riordan, K. J., Bürger, C., & Malter, J. S. (2010) · Science Signaling · doi:10.1126/scisignal.2000451 · Cited by 84 · see citing works

Synaptic Orb2A Bridges Memory Acquisition and Late Memory Consolidation in Drosophila

Krüttner, S., Traunmüller, L., Dag, U., Jandrasits, K., Stepien, B. K., Iyer, N., Fradkin, L. G., Noordermeer, J. N., Mensh, B. D., & Keleman, K. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.05.037 · Cited by 83 · see citing works

A molecular brake controls the magnitude of long-term potentiation

Wang, Y., Zhu, G., Briz, V., Hsu, Y., Bi, X., & Baudry, M. (2014) · Nature Communications · doi:10.1038/ncomms4051 · Cited by 82 · see citing works

An Increase in Basal BDNF Provokes Hyperactivation of the Akt-Mammalian Target of Rapamycin Pathway and Deregulation of Local Dendritic Translation in a Mouse Model of Down's Syndrome

Troca-Marín, J. A., Alves-Sampaio, A., & Montesinos, M. L. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.0011-11.2011 · Cited by 79 · see citing works

Activity-Regulated Cytoskeleton-Associated Protein Controls AMPAR Endocytosis through a Direct Interaction with Clathrin-Adaptor Protein 2

daSilva, L. L. P., Wall, M. J., de Almeida, L. P., Wauters, S. C., Januário, Y. C., Müller, J., & Corrêa, S. A. L. (2016) · eNeuro · doi:10.1523/eneuro.0144-15.2016 · Cited by 79 · see citing works

Genomic profiling of the neuronal target genes of the plasticity‐related transcription factor – Zif268

Allan, B., James, A. B., AnnMarie, A., Conway, Brian, J., & Morris (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03400.x · Cited by 78 · see citing works

Metabotropic Glutamate Receptors Induce a Form of LTP Controlled by Translation and Arc Signaling in the Hippocampus

Wang, H., Ardiles, Á. O., Yang, S., Tran, T., Posada‐Duque, R., Valdivia, G., Baek, M., Chuang, Y.-A., Palacios, A. G., Gallagher, M., et al. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0878-15.2016 · Cited by 76 · see citing works

A model for regulation by SynGAP-α1 of binding of synaptic proteins to PDZ-domain 'Slots' in the postsynaptic density

Walkup, W. G., Mastro, T. L., Schenker, L. T., Vielmetter, J., Hu, R., Iancu, A., Reghunathan, M., Bannon, B. D., & Kennedy, M. B. (2016) · eLife · doi:10.7554/elife.16813 · Cited by 76 · see citing works

Drosophila Orb2 targets genes involved in neuronal growth, synapse formation, and protein turnover

Mastushita-Sakai, T., White‐Grindley, E., Samuelson, J., Seidel, C. W., & Si, K. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1004433107 · Cited by 72 · see citing works

MicroRNA-22 Gates Long-Term Heterosynaptic Plasticity in Aplysia through Presynaptic Regulation of CPEB and Downstream Targets

Fiumara, F., Rajasethupathy, P., Antonov, I., Kosmidis, S., Sossin, W. S., & Kandel, E. R. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.05.034 · Cited by 71 · see citing works

PICK1 regulates AMPA receptor endocytosis via direct interactions with AP2 α-appendage and dynamin

Fiuza, M., Rostosky, C. M., Parkinson, G. T., Bygrave, A. M., Halemani, N., Baptista, M., Milosevic, I., & Hanley, J. G. (2017) · Journal of Cell Biology · doi:10.1083/jcb.201701034 · Cited by 71 · see citing works

PDZ binding of TARPγ-8 controls synaptic transmission but not synaptic plasticity

Sumioka, A., Brown, T. E., Kato, A. S., Bredt, D. S., Kauer, J. A., & Tomita, S. (2011) · Nature Neuroscience · doi:10.1038/nn.2952 · Cited by 68 · see citing works

Dynamic Arc SUMOylation and Selective Interaction with F-Actin-Binding Protein Drebrin A in LTP Consolidation In Vivo

Nair, R. R., Patil, S. S., Tiron, A., Kanhema, T., Panja, D., Schiro, L., Parobczak, K., Wilczynski, G. M., & Bramham, C. R. (2017) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2017.00008 · Cited by 68 · see citing works

GRASP1 Regulates Synaptic Plasticity and Learning through Endosomal Recycling of AMPA Receptors

Chiu, S.-L., Diering, G. H., Ye, B., Takamiya, K., Chen, C.-M., Jiang, Y., Niranjan, T., Schwartz, C. E., Wang, T., & Huganir, R. L. (2017) · Neuron · doi:10.1016/j.neuron.2017.02.031 · Cited by 66 · see citing works

Ca2+/calmodulin sensitivity may be common to all forms of neural adenylate cyclase.

Eliot, L., Dudai, Y., Kandel, E. R., & Abrams, T. W. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.23.9564 · Cited by 65 · see citing works

LTP requires postsynaptic PDZ-domain interactions with glutamate receptor/auxiliary protein complexes

Sheng, N., Bemben, M. A., Díaz-Alonso, J., Tao, W., Shi, Y. S., & Nicoll, R. A. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1800719115 · Cited by 65 · see citing works

Postsynaptic localization and regulation of AMPA receptors and Cav1.2 by β2 adrenergic receptor/PKA and Ca2+/CaMKII signaling

Patriarchi, T., Buonarati, O. R., & Hell, J. W. (2018) · The EMBO Journal · doi:10.15252/embj.201899771 · Cited by 65 · see citing works

Persistent increased PKMζ in long-term and remote spatial memory

Hsieh, C., Tsokas, P., Serrano, P. A., Hernandez, A. I., Tian, D., Cottrell, J. E., Shouval, H. Z., Fenton, A. A., & Sacktor, T. C. (2016) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.07.008 · Cited by 61 · see citing works

Distinct Roles of PKCι/λ and PKMζ in the Initiation and Maintenance of Hippocampal Long-Term Potentiation and Memory

Wang, S., Sheng, T., Ren, S., Tian, T., & Lü, W. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.07.030 · Cited by 52 · see citing works

CPEB2 Activates GRASP1 mRNA Translation and Promotes AMPA Receptor Surface Expression, Long-Term Potentiation, and Memory

Lu, W.-H., Yeh, N.-H., & Huang, Y. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.10.073 · Cited by 49 · see citing works

Nuclear Arc Interacts with the Histone Acetyltransferase Tip60 to Modify H4K12 Acetylation

Wee, C. L., Teo, S., Oey, N. E., Wright, G. D., VanDongen, H. M. A., & VanDongen, A. M. J. (2014) · eNeuro · doi:10.1523/eneuro.0019-14.2014 · Cited by 46 · see citing works

Regulation of spine structural plasticity by Arc/Arg3.1

Newpher, T. M., Harris, S. C., Pringle, J., Hamilton, C., & Soderling, S. H. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.09.022 · Cited by 44 · see citing works

Inverse synaptic tagging: An inactive synapse-specific mechanism to capture activity-induced Arc/arg3.1 and to locally regulate spatial distribution of synaptic weights

Okuno, H., Minatohara, K., & Bito, H. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.09.025 · Cited by 43 · see citing works

Recent Findings on AMPA Receptor Recycling

Moretto, E., & Passafaro, M. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00286 · Cited by 38 · see citing works

Stimulus-evoked ERK-dependent phosphorylation of activity-regulated cytoskeleton-associated protein (Arc) regulates its neuronal subcellular localization

Nikolaienko, O., Eriksen, M. S., Patil, S. S., Bito, H., & Bramham, C. R. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.07.026 · Cited by 37 · see citing works

A Rapid Induction Mechanism for Lin28a in Trophic Responses

Amen, A. M., Ruiz, C. R., Shi, J., Subramanian, M. P., Pham, D. L., & Meffert, M. K. (2017) · Molecular Cell · doi:10.1016/j.molcel.2016.12.025 · Cited by 33 · see citing works

Intact Ras function is required for sustained activation and nuclear translocation of extracellular signal-regulated kinases in nerve growth factor-stimulated PC12 cells

Boglári, G., Erhardt, P., Cooper, G. M., et al. (1998) · European Journal of Cell Biology · doi:10.1016/s0171-9335(98)80046-0 · Cited by 26 · see citing works

GRIP1 Binds to ApoER2 and EphrinB2 to Induce Activity-Dependent AMPA Receptor Insertion at the Synapse

Pfennig, S., Foss, F., Bissen, D., Harde, E., Treeck, J. C., Segarra, M., & Acker‐Palmer, A. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.09.019 · Cited by 24 · see citing works

Phosphorylation of synaptic GTPase-activating protein (synGAP) by polo-like kinase (Plk2) alters the ratio of its GAP activity toward HRas, Rap1 and Rap2 GTPases

Walkup, W. G., Sweredoski, M. J., Graham, R. L., Hess, S. Y., & Kennedy, M. B. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.07.087 · Cited by 22 · see citing works

Increased PKMζ activity impedes lateral movement of GluA2-containing AMPA receptors

Yu, N., Uhm, H., Shim, J.-H., Choi, J., Bae, S., Sacktor, T. C., Hohng, S., & Kaang, B. (2017) · Molecular Brain · doi:10.1186/s13041-017-0334-7 · Cited by 18 · see citing works

PKCλ: a new player in LTP coming to the rescue of PKCζ's faltering role in LTP?

Matt, L., & Hell, J. W. (2013) · The EMBO Journal · doi:10.1038/emboj.2013.81 · Cited by 7 · see citing works

Neurochemistry of Childhood Anxiety Disorders

Havel, L. K., Mehta, P., Gautam, A., Danielyan, E., & Saxena, K. (2022) · Springer eBooks · doi:10.1007/978-3-031-14080-8_5 · Cited by 1 · see citing works

The History of Neurochemistry as Revealed by the Journal of Neurochemistry

Curzon, G. (1993) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1993.tb02189.x · Cited by 9 · see citing works

[Present-day marginal problems of neurochemistry. 3d International Congress of Neurochemistry].

(1973) · PubMed

A History of the Origin and Development of Japanese Society for Neurochemistry: International Cooperation to Overcome Dementia and Mental Illness

Mikoshiba, K. (2022) · Neurochemical Research · doi:10.1007/s11064-022-03705-x

The origins and early history of neurochemistry and its societies

Boullerne, A. I., Foley, P., Turner, A. J., et al. (2019) · Journal of Neurochemistry · doi:10.1111/jnc.14839 · Cited by 4 · see citing works