A developmental switch in the signaling cascades for LTP induction

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 · 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

The molecular basis of CaMKII function in synaptic and behavioural memory

Lisman, J., Schulman, H., & Cline, H. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn753 · Cited by 1,860 · see citing works

Autophosphorylation at Thr ²⁸⁶ of the α Calcium-Calmodulin Kinase II in LTP and Learning

Giese, K. P., Fedorov, N. B., Filipkowski, R. K., & Silva, A. J. (1998) · Science · doi:10.1126/science.279.5352.870 · Cited by 1,055 · see citing works

Dendritic spines: cellular specializations imparting both stability and flexibility to synaptic function.

Harris, K., & Kater, S. (1994) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.17.030194.002013 · Cited by 1,032 · see citing works

Synaptogenesis Via Dendritic Filopodia in Developing Hippocampal Area CA1

Fiala, J. C., Feinberg, M., Popov, V., & Harris, K. M. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-21-08900.1998 · Cited by 758 · see citing works

Molecular Psychology: Roles for the ERK MAP Kinase Cascade in Memory

Adams, J. P., & Sweatt, J. D. (2002) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.42.082701.145401 · Cited by 588 · see citing works

Postsynaptic CAMP pathway gates early LTP in hippocampal CA1 region

Blitzer, R. D., Wong, T., Nouranifar, R., Iyengar, R., & Landau, E. M. (1995) · Neuron · doi:10.1016/0896-6273(95)90018-7 · Cited by 325 · see citing works

Increased transmitter release at excitatory synapses produced by direct activation of adenylate cyclase in rat hippocampal slices

Chavez-Noriega, L., & Stevens, C. F. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-01-00310.1994 · Cited by 300 · see citing works

Characterization of a calmodulin kinase II inhibitor protein in brain

Chang, B. H., Mukherji, S., & Soderling, T. R. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.18.10890 · Cited by 227 · see citing works

LTP and activity-dependent synaptogenesis: the more alike they are, the more different they become

Constantine‐Paton, M., & Cline, H. T. (1998) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(98)80017-2 · Cited by 225 · see citing works

NMDA Receptor Activation Increases Cyclic AMP in Area CA1 of the Hippocampus via Calcium/Calmodulin Stimulation of Adenylyl Cyclase

Chetkovich, D. M., & Sweatt, J. D. (1993) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1993.tb09836.x · Cited by 212 · see citing works

Changes in the subcellular distribution of calmodulin-kinase II during brain development

Kelly, P. T., & Vernon, P. J. (1985) · Developmental Brain Research · doi:10.1016/0165-3806(85)90265-2 · Cited by 95 · see citing works

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 · see citing works

[57] Reconstitution of calmodulin-sensitive adenylate cyclase from bovine brain with phospholipids, calmodulin, and β-adrenergic receptors

Rosenberg, G. B., Minocherhomjee, A.-E.-V. M., & Storm, D. R. (1987) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(87)39126-8 · Cited by 46 · 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

AMPA receptor trafficking at excitatory synapses

Bredt, D. S., & Nicoll, R. A. (2003) · Neuron · doi:10.1016/s0896-6273(03)00640-8 · Cited by 1,150 · 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

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

The AMPA Receptor Code of Synaptic Plasticity

Diering, G. H., & Huganir, R. L. (2018) · Neuron · doi:10.1016/j.neuron.2018.10.018 · Cited by 844 · 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

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

Seminars in Cell & Developmental Biology

Lee, H., & Kirkwood, A. (2011) · Cited by 692 · see citing works

Regulation of NMDA receptor subunit expression and its implications for LTD, LTP, and metaplasticity

Yashiro, K., & Philpot, B. D. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.07.046 · Cited by 649 · see citing works

Effects of secreted oligomers of amyloid β‐protein on hippocampal synaptic plasticity: a potent role for trimers

Townsend, M., Shankar, G. M., Mehta, T., Walsh, D. M., & Selkoe, D. J. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2005.103754 · Cited by 619 · see citing works

Calmodulin-kinases: modulators of neuronal development and plasticity.

Wayman, G. A., Lee, Y.-S., Tokumitsu, H., Silva, A., & Soderling, T. R. (2008) · Neuron · doi:10.1016/j.neuron.2008.08.021 · Cited by 567 · see citing works

PSD-95 is required for activity-driven synapse stabilization.

Ehrlich, I., Klein, M., Rumpel, S., & Malinow, R. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0609307104 · Cited by 470 · 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

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

Glutamate induces de novo growth of functional spines in developing cortex

Kwon, H.-B., & Sabatini, B. L. (2011) · Nature · doi:10.1038/nature09986 · Cited by 368 · see citing works

Protein kinase A regulates calcium permeability of NMDA receptors

Skeberdis, V. A., Chevaleyre, V., Lau, C. G., Goldberg, J. H., Pettit, D. L., Suadicani, S. O., Lin, Y., Bennett, M. V. L., Yuste, R., Castillo, P. E., et al. (2006) · Nature Neuroscience · doi:10.1038/nn1664 · Cited by 332 · 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

Ube3a is required for experience-dependent maturation of the neocortex

Yashiro, K., Riday, T. T., Condon, K. H., Roberts, A. C., Bernardo, D. R., Prakash, R., Weinberg, R. J., Ehlers, M. D., & Philpot, B. D. (2009) · Nature Neuroscience · doi:10.1038/nn.2327 · Cited by 328 · see citing works

Synaptic Plasticity and AMPA Receptor Trafficking

Malenka, R. C. (2003) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1300.001 · Cited by 324 · see citing works

Lack of NMDA Receptor Subtype Selectivity for Hippocampal Long-Term Potentiation

Berberich, S., Punnakkal, P., Jensen, V., Pawlak, V., Seeburg, P. H., Hvalby, Ø., & Köhr, G. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.1905-05.2005 · Cited by 304 · see citing works

Calcium/calmodulin-dependent protein kinase II and synaptic plasticity

Colbran, R. J., & Brown, A. M. (2004) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2004.05.008 · Cited by 307 · see citing works

Distinct Modes of AMPA Receptor Suppression at Developing Synapses by GluN2A and GluN2B: Single-Cell NMDA Receptor Subunit Deletion In Vivo

Gray, J. A., Shi, Y. S., Usui, H., During, M. J., Sakimura, K., & Nicoll, R. A. (2011) · Neuron · doi:10.1016/j.neuron.2011.08.007 · Cited by 303 · see citing works

Age matters

McCutcheon, J. E., & Marinelli, M. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.06648.x · Cited by 279 · see citing works

Selective control of inhibitory synapse development by Slitrk3-PTPδ trans-synaptic interaction

Takahashi, H., Katayama, K.-I., Sohya, K., Miyamoto, H., Prasad, T., Matsumoto, Y., Ota, M., Yasuda, H., Tsumoto, T., Aruga, J., et al. (2012) · Nature Neuroscience · doi:10.1038/nn.3040 · Cited by 250 · see citing works

LTP forms 1, 2 and 3: different mechanisms for the ‘long’ in long-term potentiation

Raymond, C. R. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.01.007 · Cited by 237 · see citing works

Plasticity of Inhibition

Kullmann, D. M., Moreau, A. W., Bakiri, Y., & Nicholson, E. (2012) · Neuron · doi:10.1016/j.neuron.2012.07.030 · Cited by 234 · see citing works

Synaptic plasticity and phosphorylation

Lee, H. (2006) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2006.06.003 · Cited by 215 · see citing works

Coactivation of Pre- and Postsynaptic Signaling Mechanisms Determines Cell-Specific Spike-Timing-Dependent Plasticity

Tzounopoulos, T., Rubio, M. E., Keen, J. E., & Trussell, L. O. (2007) · Neuron · doi:10.1016/j.neuron.2007.03.026 · Cited by 213 · see citing works

Autonomous CaMKII Mediates Both LTP and LTD Using a Mechanism for Differential Substrate Site Selection

Coultrap, S. J., Freund, R. K., O’Leary, H., Sanderson, J. L., Roche, K. W., Dell’Acqua, M. L., & Bayer, K. U. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.01.005 · Cited by 207 · see citing works

Calcium/calmodulin-dependent kinase II and Alzheimer’s disease

Ghosh, A., & Giese, K. P. (2015) · Molecular Brain · doi:10.1186/s13041-015-0166-2 · Cited by 205 · see citing works

Circuit and Plasticity Defects in the Developing Somatosensory Cortex of<i>Fmr1</i>Knock-Out Mice

Bureau, I., Shepherd, G. M. G., & Svoboda, K. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.1076-08.2008 · Cited by 201 · see citing works

Chapter 6 Regulation of hippocampus-dependent memory by cyclic AMP-dependent protein kinase

Abel, T., & Nguyen, P. V. (2008) · Progress in Brain Research · doi:10.1016/s0079-6123(07)00006-4 · Cited by 198 · see citing works

LRRK2 regulates synaptogenesis and dopamine receptor activation through modulation of PKA activity

Parisiadou, L., Yu, J. H., Sgobio, C., Xie, C., Liu, G., Sun, L., Gu, X., Lin, X. Z., Crowley, N. A., Lovinger, D. M., et al. (2014) · Nature Neuroscience · doi:10.1038/nn.3636 · Cited by 201 · 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

Presynaptic NMDA Receptors: Newly Appreciated Roles in Cortical Synaptic Function and Plasticity

Corlew, R., Brasier, D. J., Feldman, D. E., & Philpot, B. D. (2008) · The Neuroscientist · doi:10.1177/1073858408322675 · Cited by 185 · see citing works

Developmental Switch in the Contribution of Presynaptic and Postsynaptic NMDA Receptors to Long-Term Depression

Corlew, R., Wang, Y., Ghermazien, H., Erişir, A., & Philpot, B. D. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.5494-06.2007 · Cited by 184 · see citing works

Modulation of neurotransmitter release by the second messenger-activated protein kinases: Implications for presynaptic plasticity

Leenders, A. G. M., & SHENG, Z. (2004) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2004.10.012 · Cited by 182 · see citing works

Developmental Switch in Synaptic Mechanisms of Hippocampal Metabotropic Glutamate Receptor-Dependent Long-Term Depression

Nosyreva, E. D., & Huber, K. M. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3652-04.2005 · Cited by 182 · see citing works

The developmental stages of synaptic plasticity

Löhmann, C., & Kessels, H. W. H. G. (2013) · The Journal of Physiology · doi:10.1113/jphysiol.2012.235119 · Cited by 176 · see citing works

Intracellular Domains of NMDA Receptor Subtypes Are Determinants for Long-Term Potentiation Induction

Köhr, G., Jensen, V., Koester, H. J., Mihaljević, A. L., Utvik, J. K., Kvello, A., Ottersen, O. P., Seeburg, P. H., Sprengel, R., & Hvalby, Ø. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-34-10791.2003 · Cited by 181 · see citing works

A Critical Role for GluN2B-Containing NMDA Receptors in Cortical Development and Function

Wang, C.-C., Held, R. G., Chang, S.-C., Yang, L., Delpire, E., Ghosh, A., & Hall, B. J. (2011) · Neuron · doi:10.1016/j.neuron.2011.09.023 · Cited by 180 · see citing works

AMPA-silent synapses in brain development and pathology

Hanse, E., Seth, H., & Riebe, I. (2013) · Nature reviews. Neuroscience · doi:10.1038/nrn3642 · Cited by 175 · see citing works

An Autism-Linked Mutation Disables Phosphorylation Control of UBE3A

Yi, J. J., Berrios, J., Newbern, J. M., Snider, W. D., Philpot, B. D., Hahn, K. M., & Zylka, M. J. (2015) · Cell · doi:10.1016/j.cell.2015.06.045 · Cited by 177 · see citing works

Developmental regulation of cognitive abilities: Modified composition of a molecular switch turns on associative learning

Dumas, T. C. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2005.08.002 · Cited by 169 · see citing works

Age‐dependent requirement of AKAP150‐anchored PKA and GluR2‐lacking AMPA receptors in LTP

Lü, Y., Allen, M., Halt, A. R., Weisenhaus, M., Dallapiazza, R. F., Hall, D. D., Usachev, Y. M., McKnight, G. S., & Hell, J. W. (2007) · The EMBO Journal · doi:10.1038/sj.emboj.7601884 · Cited by 166 · see citing works

The neural rejuvenation hypothesis of cocaine addiction

Dong, Y., & Nestler, E. J. (2014) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2014.05.005 · Cited by 163 · see citing works

Epilepsy and autism spectrum disorders: are there common developmental mechanisms?

Brooks-Kayal, A. (2010) · Brain and Development · doi:10.1016/j.braindev.2010.04.010 · Cited by 162 · see citing works

AMPA and NMDA glutamate receptor trafficking: multiple roads for reaching and leaving the synapse

Groc, L., & Choquet, D. (2006) · Cell and Tissue Research · doi:10.1007/s00441-006-0254-9 · Cited by 158 · see citing works

Ras and Rap Signaling in Synaptic Plasticity and Mental Disorders

Stornetta, R. L., & Zhu, J. (2010) · The Neuroscientist · doi:10.1177/1073858410365562 · Cited by 159 · see citing works

Brain‐derived neurotrophic factor stimulates the neural differentiation of human umbilical cord blood‐derived mesenchymal stem cells and survival of differentiated cells through MAPK/ERK and PI3K/Akt‐dependent signaling pathways

Lim, J. Y., Park, S., Oh, J. H., Kim, S. M., Jeong, C. H., Jun, J. A., Lee, K., Oh, W., Lee, J., & Jeun, S. (2008) · Journal of Neuroscience Research · doi:10.1002/jnr.21669 · Cited by 158 · see citing works

Maturation of Long-Term Potentiation Induction Rules in Rodent Hippocampus: Role of GABAergic Inhibition

Meredith, R. M., Floyer-Lea, A., & Paulsen, O. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-35-11142.2003 · Cited by 158 · see citing works

Cocaine-induced potentiation of synaptic strength in dopamine neurons: Behavioral correlates in GluRA(–/–) mice

Dong, Y., Saal, D., Thomas, M., Faust, R., Bonci, A., Robinson, T., & Malenka, R. C. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401553101 · Cited by 158 · see citing works

Recruitment of Calcium-Permeable AMPA Receptors during Synaptic Potentiation Is Regulated by CaM-Kinase I

Guire, E. S., Oh, M. C., Soderling, T. R., & Derkach, V. A. (2008) · Journal of Neuroscience · doi:10.1523/jneurosci.0384-08.2008 · Cited by 151 · see citing works

Presynaptic Spike Timing-Dependent Long-Term Depression in the Mouse Hippocampus

Andrade‐Talavera, Y., Duque‐Feria, P., Paulsen, O., & Moreno, A. R. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhw172 · Cited by 147 · see citing works

Mouse Genetic Approaches to Investigating Calcium/Calmodulin-Dependent Protein Kinase II Function in Plasticity and Cognition: Table 1.

Elgersma, Y., Sweatt, J. D., & Giese, K.-P. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3622-04.2004 · Cited by 150 · see citing works

A Juvenile form of Postsynaptic Hippocampal Long‐Term Potentiation in Mice Deficient for the AMPA Receptor Subunit GluR‐A

Jensen, V., Kaiser, K. M. M., Borchardt, T., Adelmann, G., Rozov, A. V., Burnashev, N., Brix, C., Frotscher, M., Andersen, P. N., Hvalby, Ø., et al. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.053637 · Cited by 139 · see citing works

Regulation of NMDA receptor Ca2+ signalling and synaptic plasticity

Lau, C. G., Takeuchi, K., Rodenas-Ruano, A., Takayasu, Y., Murphy, J., Bennett, M. V. L., & Zukin, R. S. (2009) · Biochemical Society Transactions · doi:10.1042/bst0371369 · Cited by 138 · see citing works

Correlated Synaptic Inputs Drive Dendritic Calcium Amplification and Cooperative Plasticity during Clustered Synapse Development

Lee, K. F. H., Soares, C., Thivierge, J., & Béïque, J.-C. (2016) · Neuron · doi:10.1016/j.neuron.2016.01.012 · Cited by 131 · see citing works

Surface dynamics of GluN2B‐NMDA receptors controls plasticity of maturing glutamate synapses

Dupuis, J. P., Ladépêche, L., Seth, H., Bard, L., Varela, J. A., Mikasová, L., Bouchet, D., Rogemond, V., Honnorat, J., Hanse, E., et al. (2014) · The EMBO Journal · doi:10.1002/embj.201386356 · Cited by 132 · see citing works

Temporally distinct demands for classic cadherins in synapse formation and maturation

Bozdagi, O., Valcin, M., Poskanzer, K. E., Tanaka, H., & Benson, D. L. (2004) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2004.08.008 · Cited by 131 · see citing works

The proteomes of neurotransmitter receptor complexes form modular networks with distributed functionality underlying plasticity and behaviour

Pocklington, A. J., Cumiskey, M. A., Armstrong, J. D., & Grant, S. G. N. (2006) · Molecular Systems Biology · doi:10.1038/msb4100041 · Cited by 130 · see citing works

Activity regulates cell death within cortical interneurons through a Calcineurin-dependent mechanism

Priya, R., Paredes, M. F., Karayannis, T., Yusuf, N., Liu, X., Jaglin, X., Graef, I., Alvarez-Buylla, A., & Fishell, G. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.01.007 · Cited by 127 · see citing works

Subcellular Dynamics of Type II PKA in Neurons

Zhong, H., Sia, G.-M., Sato, T., Gray, N. W., Mao, T., Khuchua, Z. A., Huganir, R. L., & Svoboda, K. (2009) · Neuron · doi:10.1016/j.neuron.2009.03.013 · Cited by 125 · see citing works

Synaptic memory and CaMKII

Nicoll, R. A., & Schulman, H. (2023) · Physiological Reviews · doi:10.1152/physrev.00034.2022 · Cited by 126 · see citing works

Genotype–phenotype relationship in three cases with overlapping 19p13.12 microdeletions

Bonaglia, M. C., Marelli, S., Novara, F., Commodaro, S., Borgatti, R., Minardo, G., Memo, L., Mangold, E., Beri, S., Zucca, C., et al. (2010) · European Journal of Human Genetics · doi:10.1038/ejhg.2010.115 · Cited by 125 · see citing works

A Local Reduction in Cortical GABAergic Synapses after a Loss of Endogenous Brain-Derived Neurotrophic Factor, as Revealed by Single-Cell Gene Knock-Out Method

Kohara, K., Yasuda, H., Huang, Y. Y., Adachi, N., Sohya, K., & Tsumoto, T. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1943-07.2007 · Cited by 124 · see citing works

Basic roles of key molecules connected with NMDAR signaling pathway on regulating learning and memory and synaptic plasticity

Wang, H., & Peng, R. (2016) · Military Medical Research · doi:10.1186/s40779-016-0095-0 · Cited by 121 · see citing works

Neurosteroid-Induced Plasticity of Immature Synapses via Retrograde Modulation of Presynaptic NMDA Receptors

Mameli, M., Carta, M., Partridge, L. D., & Valenzuela, C. F. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3877-04.2005 · Cited by 124 · see citing works

The Role of Nitric Oxide and GluR1 in Presynaptic and Postsynaptic Components of Neocortical Potentiation

Hardingham, N. R., & Fox, K. D. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0652-06.2006 · Cited by 123 · see citing works

Effect of varied gestational stress on acquisition of spatial memory, hippocampal LTP and synaptic proteins in juvenile male rats

Yaka, R., Salomon, S., Matzner, H., & Weinstock, M. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.01.018 · Cited by 120 · see citing works

Dominant role of the GluR2 subunit in regulation of AMPA receptors by CaMKII

Oh, M. C., & Derkach, V. A. (2005) · Nature Neuroscience · doi:10.1038/nn1476 · Cited by 118 · see citing works

Orexins/hypocretins cause sharp wave- and θ-related synaptic plasticity in the hippocampus via glutamatergic, gabaergic, noradrenergic, and cholinergic signaling

Selbach, O., Doreulee, N., Bohla, C., Eriksson, K. S., Sergeeva, O. A., Poelchen, W., Brown, R. E., & Haas, H. L. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.05.012 · Cited by 112 · see citing works

A mechanism underlying AMPA receptor trafficking during cerebellar long-term potentiation

Kakegawa, W., & Yuzaki, M. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0508910102 · Cited by 109 · see citing works

Adenylyl cyclase I regulates AMPA receptor trafficking during mouse cortical 'barrel' map development

Lu, H., She, W.-C., Plas, D. T., Neumann, P. E., Janz, R., & Crair, M. C. (2003) · Nature Neuroscience · doi:10.1038/nn1106 · Cited by 108 · see citing works

Slow Presynaptic and Fast Postsynaptic Components of Compound Long-Term Potentiation

Bayazitov, I. T., Richardson, R. J., Fricke, R. G., & Zakharenko, S. S. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.3077-07.2007 · Cited by 102 · see citing works

Latent sex differences in molecular signaling that underlies excitatory synaptic potentiation in the hippocampus

Jain, A., Huang, G. Z., & Woolley, C. S. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.1897-18.2018 · Cited by 103 · see citing works

Reversal of Synaptic Memory by Ca2+/Calmodulin-Dependent Protein Kinase II Inhibitor

Sanhueza, M., McIntyre, C., & Lisman, J. E. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.5049-06.2007 · Cited by 100 · 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

Role of the Neurogranin Concentrated in Spines in the Induction of Long-Term Potentiation

Zhabotinsky, A. M., Camp, R. N., Epstein, I. R., & Lisman, J. E. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.0729-06.2006 · Cited by 95 · see citing works

Mechanism for long-term memory formation when synaptic strengthening is impaired

Radwanska, K., Medvedev, N. I., Pereira, G. S., Engmann, O., Thiede, N., Moraes, M. F. D., Villers, A., Irvine, E. E., Maunganidze, N. S., Pyza, E. M., et al. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1109680108 · Cited by 97 · see citing works

Long-Term Potentiation in the Hippocampal CA1 Region Does Not Require Insertion and Activation of GluR2-Lacking AMPA Receptors

Gray, E. E., Fink, A. E., Sariñana, J., Vissel, B., & O’Dell, T. J. (2007) · Journal of Neurophysiology · doi:10.1152/jn.00473.2007 · Cited by 94 · see citing works

Late postnatal maturation of excitatory synaptic transmission permits adult‐like expression of hippocampal‐dependent behaviors

Dumas, T. C. (2005) · Hippocampus · doi:10.1002/hipo.20077 · Cited by 94 · see citing works

Differential regulation of local mRNA dynamics and translation following long-term potentiation and depression

Donlin-Asp, P., Polisseni, C., Klimek, R., Heckel, A., & Schuman, E. M. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2017578118 · Cited by 92 · see citing works

αCaMKII autophosphorylation: a fast track to memory

Irvine, E. E., von Hertzen, L. S. J., Plattner, F., & Giese, K.-P. (2006) · Trends in Neurosciences · doi:10.1016/j.tins.2006.06.009 · Cited by 92 · see citing works

Prostaglandin E2-Induced Masculinization of Brain and Behavior Requires Protein Kinase A, AMPA/Kainate, and Metabotropic Glutamate Receptor Signaling

Wright, C. L., & McCarthy, M. M. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.3603-09.2009 · Cited by 90 · see citing works

Regulation of AMPA receptor recruitment at developing synapses

Hall, B. J., & Ghosh, A. (2008) · Trends in Neurosciences · doi:10.1016/j.tins.2007.11.010 · Cited by 91 · see citing works

A Highly Sensitive A-Kinase Activity Reporter for Imaging Neuromodulatory Events in Awake Mice

Ma, L., Jongbloets, B. C., Xiong, W.-H., Melander, J. B., Qin, M., Lameyer, T. J., Harrison, M. F., Zemelman, B. V., Mao, T., & Zhong, H. (2018) · Neuron · doi:10.1016/j.neuron.2018.07.020 · Cited by 88 · see citing works

Orexins/hypocretins control bistability of hippocampal long‐term synaptic plasticity through co‐activation of multiple kinases

Selbach, O., Bohla, C., Barbara, A. B., Doreulee, N., Eriksson, K. S., Sergeeva, O. A., & Haas, H. L. (2009) · Acta Physiologica · doi:10.1111/j.1748-1716.2009.02021.x · Cited by 87 · see citing works

Seizures and Antiepileptic Drugs: Does Exposure Alter Normal Brain Development?

Marsh, E. D., Brooks‐Kayal, A. R., & Porter, B. E. (2006) · Epilepsia · doi:10.1111/j.1528-1167.2006.00894.x · Cited by 86 · see citing works

Nobiletin, a citrus flavonoid with neurotrophic action, augments protein kinase A-mediated phosphorylation of the AMPA receptor subunit, GluR1, and the postsynaptic receptor response to glutamate in murine hippocampus

Matsuzaki, K., Miyazaki, K.-I., Sakai, S., Yawo, H., Nakata, N., Moriguchi, S., Fukunaga, K., Yokosuka, A., Sashida, Y., Mimaki, Y., et al. (2007) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2007.09.028 · Cited by 86 · see citing works

Developmental regulation of protein interacting with C kinase 1 (PICK1) function in hippocampal synaptic plasticity and learning

Volk, L., Kim, C.-H., Takamiya, K., Yu, Y., & Huganir, R. L. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1016103107 · Cited by 85 · see citing works

Dendritic spine geometry and spine apparatus organization govern the spatiotemporal dynamics of calcium

Bell, M. K., Bartol, T., B, T. J. S. A., & Rangamani, P. (2019) · The Journal of General Physiology · doi:10.1085/jgp.201812261 · Cited by 80 · see citing works

SynGAP Regulates Protein Synthesis and Homeostatic Synaptic Plasticity in Developing Cortical Networks

Wang, C.-C., Held, R. G., & Hall, B. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0083941 · Cited by 84 · see citing works

CAMK2-Dependent Signaling in Neurons Is Essential for Survival

Kool, M. J., Onori, M. P., Borgesius, N. Z., van de Bree, J. E., Elgersma, M., Nio, E., Bezstarosti, K., Buitendijk, G. H. S., Jolfaei, M. A., Demmers, J., et al. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1341-18.2019 · Cited by 77 · see citing works

At Immature Mossy-Fiber–CA3 Synapses, Correlated Presynaptic and Postsynaptic Activity Persistently Enhances GABA Release and Network Excitability via BDNF and cAMP-Dependent PKA

Sivakumaran, S., Mohajerani, M. H., & Cherubini, E. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.5019-08.2009 · Cited by 84 · see citing works

AMPAR trafficking in synapse maturation and plasticity

Bassani, S., Folci, A., Zapata, J., & Passafaro, M. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1309-1 · Cited by 81 · see citing works

Activity-Dependent Netrin-1 Secretion Drives Synaptic Insertion of GluA1-Containing AMPA Receptors in the Hippocampus

Glasgow, S. D., Labrecque, S., Beamish, I. V., Aufmkolk, S., Gibon, J., Han, D. C., Harris, S. N., Dufresne, P., Wiseman, P. W., McKinney, R. A., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.09.028 · Cited by 80 · see citing works

Multiple, Developmentally Regulated Expression Mechanisms of Long-Term Potentiation at CA1 Synapses

Palmer, M. J., Isaac, J. T. R., & Collingridge, G. L. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.0170-04.2004 · Cited by 78 · see citing works

Molecular mechanisms of cognitive and behavioral comorbidities of epilepsy in children

Brooks‐Kayal, A. R. (2011) · Epilepsia · doi:10.1111/j.1528-1167.2010.02906.x · Cited by 79 · see citing works

AMPA receptor regulation during synaptic plasticity in hippocampus and neocortex

Lee, H., & Kirkwood, A. (2011) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2011.06.007 · Cited by 769 · see citing works

The development of long-term potentiation in hippocampus and neocortex

Teyler, T. J., Perkins, A. T., & Harris, K. M. (1989) · Neuropsychologia · doi:10.1016/0028-3932(89)90088-2 · Cited by 52 · see citing works

Neonatal isolation accelerates the developmental switch in the signalling cascades for long‐term potentiation induction

Huang, C., Chou, P., Yang, C., & Hsu, K. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.098160 · Cited by 23 · see citing works

Developmental regulation of the late phase of long-term potentiation (L-LTP) and metaplasticity in hippocampal area CA1 of the rat

Cao, G., & Harris, K. M. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00780.2011 · Cited by 47 · see citing works

An in vivo study of the ontogeny of long-term potentiation (LTP) in the CA1 region and in the dentate gyrus of the rat hippocampal formation

Bekenstein, J. W., & Lothman, E. W. (1991) · Developmental Brain Research · doi:10.1016/0165-3806(91)90084-v · Cited by 82 · see citing works

Stereotypical changes in the pattern and duration of long-term potentiation expressed at postnatal days 11 and 15 in the rat hippocampus.

Jackson, P., Suppes, T., & Harris, K. (1993) · Journal of Neurophysiology · doi:10.1152/jn.1993.70.4.1412 · Cited by 46 · see citing works