Potentiated Transmission and Prevention of Further LTP by Increased CaMKII activity in Postsynaptic Hippocampal Slice Neurons

Selective impairment of learning and blockade of long-term potentiation by an N-methyl-D-aspartate receptor antagonist, AP5

Morris, R. G. M., Anderson, E., Lynch, G. S., & Baudry, M. (1986) · Nature · doi:10.1038/319774a0 · Cited by 3,640

Excitatory amino acids in synaptic transmission in the Schaffer collateral-commissural pathway of the rat hippocampus

Collingridge, G. L., Kehl, S. J., & McLennan, H. (1983) · The Journal of Physiology · doi:10.1113/jphysiol.1983.sp014478 · Cited by 2,413

NMDA-receptor activation increases cytoplasmic calcium concentration in cultured spinal cord neurones

MacDermott, A. B., Mayer, M. L., Westbrook, G. L., Smith, S. J., & Barker, J. L. (1986) · Nature · doi:10.1038/321519a0 · Cited by 1,835

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

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

An essential role for postsynaptic calmodulin and protein kinase activity in long-term potentiation

Malenka, R. C., Kauer, J. A., Perkel, D. J., Mauk, M. D., Kelly, P. T., Nicoll, R. A., & Waxham, M. N. (1989) · Nature · doi:10.1038/340554a0 · Cited by 1,025

Long-term potentiation in the hippocampus involves activation of N-methyl-D-aspartate receptors

Harris, E. W., Ganong, A. H., & Cotman, C. W. (1984) · Brain Research · doi:10.1016/0006-8993(84)90275-0 · Cited by 905

Regulation of brain Type II Ca2+/calmodulin-dependent protein kinase by autophosphorylation: A Ca2+-triggered molecular switch

Miller, S. (1986) · Cell · doi:10.1016/0092-8674(86)90008-5 · Cited by 864

Presynaptic enhancement shown by whole-cell recordings of long-term potentiation in hippocampal slices

Malinow, R., & Tsien, R. W. (1990) · Nature · doi:10.1038/346177a0 · Cited by 797

NEURONAL Ca2+/CALMODULIN-DEPENDENT PROTEIN KINASES

Hanson, P. I., & Schulman, H. (1992) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.61.070192.003015 · Cited by 728

Alphaviral gene transfer in neurobiology

Ehrengruber, M. U. (2002) · Brain Research Bulletin · doi:10.1016/s0361-9230(02)00858-4 · Cited by 24

Lobe Specific Ca2+-Calmodulin Nano-Domain in Neuronal Spines: A Single Molecule Level Analysis

Kubota, Y., & Waxham, M. (2010) · PLoS Comput. Biol. · doi:10.1371/journal.pcbi.1000987 · Cited by 24

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 24

Restoration of decaying long-term potentiation in the hippocampal formation by stimulation of neuromodulatory nuclei in freely moving rats

Ézrokhi, V. L., Zosimovskiĭ, V. A., Korshunov, V. A., & Markevich, V. A. (1999) · Neuroscience · doi:10.1016/s0306-4522(98)00232-2 · Cited by 23

Ubiquitous Molecular Substrates for Associative Learning and Activity-Dependent Neuronal Facilitation

Matzel, L. D., Talk, A. C., Muzzio, I. A., & Rogers, R. F. (1998) · Reviews in the Neurosciences · doi:10.1515/revneuro.1998.9.3.129 · Cited by 23

Site-Selective Autophosphorylation of Ca2+/Calmodulin-Dependent Protein Kinase II as a Synaptic Encoding Mechanism

Coomber, C. J. (1998) · Neural Computation · doi:10.1162/089976698300017070 · Cited by 22

Learning-induced Glutamate Receptor Phosphorylation Resembles That Induced by Long Term Potentiation

Shukla, K. P., Kim, J., Blundell, J. J., & Powell, C. M. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m702906200 · Cited by 22

Controlled and localized genetic manipulation in the brain

Aronoff, R., & Petersen, C. C. H. (2006) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2006.tb00403.x · Cited by 22

MODULATION OF GLUTAMATE RECEPTORS BY CALCIUM/CALMODULIN-DEPENDENT PROTEIN KINASE II

Soderling, T. R. (1996) · Neurochemistry International · doi:10.1016/0197-0186(95)00098-4 · Cited by 22

Current Studies on a Working Model of CaM Kinase II in Hippocampal Long-Term Potentiation and Memory

Fukunaga, K., & Eishichi, M. (1999) · The Japanese Journal of Pharmacology · doi:10.1254/jjp.79.7 · Cited by 21

Postsynaptic kinase signaling underlies inhibitory synaptic plasticity in the lateral superior olive

Kotak, V. C., & Sanes, D. H. (2002) · Journal of Neurobiology · doi:10.1002/neu.10107 · Cited by 21

Interplay between hippocampal TACR3 and systemic testosterone in regulating anxiety-associated synaptic plasticity

Wojtas, M. N., Diaz-González, M., Stavtseva, N. S., Shoam, Y., Verma, P., Buberman, A., Izhak, I., Geva, A., Basch, R., Ouro, A., et al. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02361-z · Cited by 20

Involvement of protein kinases in the upregulation of acetylcholine release at endplates of alpha‐bungarotoxin‐treated rats.

Plomp, J. J., & Molenaar, P. C. (1996) · The Journal of Physiology · doi:10.1113/jphysiol.1996.sp021373 · Cited by 20

Stabilization of Dendritic mRNAs by Nitric Oxide Allows Localized, Activity‐dependent Enhancement of Hippocampal Protein Synthesis

MORRIS, B. J. (1997) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1997.tb01650.x · Cited by 20

AcuteIn VivoGenetic Rescue Demonstrates That Phosphorylation of RIM1α Serine 413 Is Not Required for Mossy Fiber Long-Term Potentiation

Yang, Y., & Calakos, N. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.4285-09.2010 · Cited by 19

Distinct expressions for synaptic potentiation induced by calcium through voltage-gated calcium and N-methyl-d-aspartate receptor channels in the hippocampal CA1 region

Chen, H.-X., Hanse, E., Pananceau, M., & Gustafsson, B. (1998) · Neuroscience · doi:10.1016/s0306-4522(98)00042-6 · Cited by 19

Boosting Psychotherapy With Noninvasive Brain Stimulation: The Whys and Wherefores of Modulating Neural Plasticity to Promote Therapeutic Change

Saccenti, D., Lauro, L. J. R., Crespi, S. A., Moro, A. S., Vergallito, A., Grgič, R. G., Pretti, N., Lamanna, J., & Ferro, M. (2024) · Neural Plasticity · doi:10.1155/np/7853199 · Cited by 16

Propagation of CaMKII translocation waves in heterogeneous spiny dendrites

Bressloff, P. C. (2012) · Journal of Mathematical Biology · doi:10.1007/s00285-012-0542-9 · Cited by 17

Enriching the environment of αCaMKIIT286A mutant mice reveals that LTD occurs in memory processing but must be subsequently reversed by LTPPreprint

Parsley, S. L., Pilgram, S. M., Soto, F., Giese, K.-P., & Edwards, F. A. (2007) · Learning & Memory · doi:10.1101/lm.356607 · Cited by 18

Recruitment of the SNX17-Retriever recycling pathway regulates synaptic function and plasticity

Rivero-Ríos, P., Tsukahara, T., Uygun, T., Chen, A., Chavis, G. D., Giridharan, S. S. P., Iwase, S., Sutton, M. A., & Weisman, L. S. (2023) · Journal of Cell Biology · doi:10.1083/jcb.202207025 · Cited by 17

Levothyroxin replacement therapy restores hypothyroidism induced impairment of L-LTP induction: critical role of CREB.

Alzoubi, K., & Alkadhi, K. (2014) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2013.10.011 · Cited by 21

AMPA Receptors: potential implications in development and disease

Franciosi, S. (2001) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000911 · Cited by 16

Chronic psychosocial stress exposes Alzheimer s disease phenotype in a novel at-risk model

Karim, A. A. (2011) · Frontiers in Bioscience-Elite · doi:10.2741/371 · Cited by 18

Posttranslational Regulation of Ionotropic Glutamate Receptors and Synaptic Plasticity

Bi, X., Standley, S., & Baudry, M. (1998) · International review of neurobiology · doi:10.1016/s0074-7742(08)60612-1 · Cited by 16

A role for calcium/calmodulin-dependent protein kinase II in cardiac disease and arrhythmia.

Hund, T., & Rudy, Y. (2006) · Handbook of Experimental Pharmacology · doi:10.1007/3-540-29715-4_7 · Cited by 20

Long-term potentiation can be induced in the CA1 region of hippocampus in the absence of αCaMKII T286-autophosphorylation

Villers, A., Giese, K. P., & Ris, L. (2014) · Learning & Memory · doi:10.1101/lm.035972.114 · Cited by 16

Rapid gene transfer into cultured hippocampal neurons and acute hippocampal slices using adenoviral vectors

Griesbeck, O., Körte, M., Gravel, C., Bonhoeffer, T., & Thoenen, H. (1997) · Molecular Brain Research · doi:10.1016/s0169-328x(96)00246-x · Cited by 16

Visualizing synapse formation and remodeling: recent advances in real-time imaging of CNS synapses

Umeda, T., & Okabe, S. (2001) · Neuroscience Research · doi:10.1016/s0168-0102(01)00243-7 · Cited by 15

Basic mechanisms of plasticity and learning

Mancini, A., de Iure, A., & Picconi, B. (2022) · Handbook of clinical neurology · doi:10.1016/b978-0-12-819410-2.00002-3 · Cited by 16

Neural population dynamics of computing with synaptic modulations

Aitken, K., & Mihalaş, Ş. (2023) · eLife · doi:10.7554/elife.83035 · Cited by 17

In vivo expression of ganglionic long-term potentiation in superior cervical ganglia from hypertensive aged rats.

Alzoubi, K., Aleisa, A., & Alkadhi, K. (2010) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2008.06.007 · Cited by 15

Long-term potentiation induction—a synaptic catch mechanism released by extracellular phosphorylation

Fujii, S., Kuroda, Y., Ito, K., & Kato, H. (2000) · Neuroscience · doi:10.1016/s0306-4522(99)00559-x · Cited by 13

The Activation of Calcium/Calmodulin-Dependent Protein Kinase II After Glutamate or Potassium Stimulation in Hippocampal Slices

Tan, S.-E., & Chen, S. S. (1997) · Brain Research Bulletin · doi:10.1016/s0361-9230(97)00004-x · Cited by 13

The Function of CaM Kinase II in Synaptic Plasticity and Spine Formation

Fukunaga, K., Shioda, N., & Miyamoto, E. (2009) · Springer eBooks · doi:10.1007/978-0-387-30370-3_9 · Cited by 12

Chronic psychosocial stress impairs early LTP but not late LTP in the dentate gyrus of at-risk rat model of Alzheimer׳s disease

Alkadhi, K. A., & Tran, T. T. (2014) · Brain Research · doi:10.1016/j.brainres.2014.09.014 · Cited by 12

N-terminal myristoylation alters the calcium binding pathways in neuronal calcium sensor-1

Chandra, K., Ramakrishnan, V., Sharma, Y., & Chary, K. (2010) · JBIC Journal of Biological Inorganic Chemistry · doi:10.1007/s00775-010-0705-3 · Cited by 8

CaMKII mediates stimulus specificity in early odor preference learning in rats.

Modarresi, S., Mukherjee, B., McLean, J., Harley, C., & Yuan, Q. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00176.2016 · Cited by 11

Two independent forms of activity-dependent potentiation regulate electrical transmission at mixed synapses on the Mauthner cell

Cachope, R., & Pereda, A. E. (2012) · Brain Research · doi:10.1016/j.brainres.2012.05.059 · Cited by 11

Brain Plasticity and the Neural Cell Adhesion Molecule (NCAM)

Rønn, L. C. B., Pedersen, N. M., Jahnsen, H., Berezin, V., & Bock, E. (1997) · Advances in experimental medicine and biology · doi:10.1007/978-1-4757-9551-6_22 · Cited by 11

Chapter 21 Control of retinotectal axon arbor growth by postsynaptic CaMKII

Zou, D., & Cline, H. T. (1996) · Progress in brain research · doi:10.1016/s0079-6123(08)62548-0 · Cited by 11

Proteins Involved in the Trafficking and Functional Synaptic Expression of AMPA and KA Receptors

Rue, S. A. D. L., & Henley, J. M. (2002) · The Scientific World JOURNAL · doi:10.1100/tsw.2002.97 · Cited by 10

Chronic neuronal excitation leads to dual metaplasticity in the signaling for structural long-term potentiation

Ueda, H. H., Nagasawa, Y., Sato, A., Onda, M., & Murakoshi, H. (2022) · Cell Reports · doi:10.1016/j.celrep.2021.110153 · Cited by 11

Autophosphorylation of F-actin binding domain of CaMKIIβ is required for fear learning

Kim, K., Suzuki, A., Kojima, H., Kawamura, M., Miya, K., Abe, M., Yamada, I., Furuse, T., Wakana, S., Sakimura, K., et al. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.12.003 · Cited by 11

Long-Term Potentiation and Memory

(2012) · Springer eBooks · doi:10.1007/springerreference_169302 · Cited by 10

Learning Invariance from Natural Images Inspired by Observations in the Primary Visual Cortex

Teichmann, M., Wiltschut, J., & Hamker, F. H. (2012) · Neural Computation · doi:10.1162/neco_a_00268 · Cited by 10

Modulation of dendritic spines by protein phosphatase-1

Platholi, J., & Hemmings, H. C. (2020) · Advances in pharmacology · doi:10.1016/bs.apha.2020.10.001 · Cited by 8

The role of hippocampal CaMKII in resilience to trauma-related psychopathology

Hazra, S., Hazra, J. D., Bar-On, R. A., Duan, Y., Edut, S., Cao, X., & Richter‐Levin, G. (2022) · Neurobiology of Stress · doi:10.1016/j.ynstr.2022.100506 · Cited by 9

Interactions between αCaMKII and calmodulin in living cells: conformational changes arising from CaM -dependent and -independent relationships

Kato, K.-I., Iwamoto, T., & Kida, S. (2013) · Molecular Brain · doi:10.1186/1756-6606-6-37 · Cited by 8

A Novel CaMKII Inhibitory Peptide Blocks Relapse to Morphine Seeking by Influencing Synaptic Plasticity in the Nucleus Accumbens Shell

Liu, Z., Zhang, J., Miao, L., Kong, Q., Liu, X., & Yu, L. (2022) · Brain Sciences · doi:10.3390/brainsci12080985 · Cited by 8

Caffeine improved spatial learning and memory deficit in sleep deprived female rat

Esmaeilpour, K., Sheibani, V., & Saadati, H. (2015) · Cited by 8

Carbonyl compounds cross-link cellular proteins and activate protein-tyrosine kinase p60c-Src

Akhand, A. A., Kato, M., Suzuki, H., Liu, W., Du, J., Hamaguchi, M., Miyata, T., Kurokawa, K., & Nakashima, I. (1999) · Journal of Cellular Biochemistry · doi:10.1002/(sici)1097-4644(19990101)72:1 · Cited by 63

Neural Analysis of Learning in Simple Systems

Krasne, F. (2002) · Wiley eBooks · doi:10.1002/0471214426.pas0304 · Cited by 8

Cellular mechanisms of visual cortical plasticity: a game of cat and mouse.Preprint

Gordon, J. A. (1997) · Learning & Memory · doi:10.1101/lm.4.3.245 · Cited by 8

Rapid sequential clustering of NMDARs, CaMKII, and AMPARs upon activation of NMDARs at developing synapses

Chen, Y., Liu, S., Jacobi, A. A., Jeng, G., Ulrich, J. D., Stein, I. S., Patriarchi, T., & Hell, J. W. (2024) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2024.1291262 · Cited by 9

Expression of gLTP in Sympathetic Ganglia from Stress-hypertensive Rats: Molecular Evidence

Alzoubi, K. H., Aleisa, A. M., & Alkadhi, K. A. (2008) · Journal of Molecular Neuroscience · doi:10.1007/s12031-008-9054-x · Cited by 7

Chronic Nicotine Treatment Reverses Hypothyroidism-Induced Impairment of L-LTP Induction Phase: Critical Role of CREB

Alzoubi, K., & Alkadhi, K. (2013) · Molecular Neurobiology · doi:10.1007/s12035-013-8594-4 · Cited by 7

Expression of gLTP in Sympathetic Ganglia of Obese Zucker Rats In Vivo: Molecular Evidence

Alzoubi, K., Aleisa, A., & Alkadhi, K. (2008) · Journal of Molecular Neuroscience · doi:10.1007/s12031-008-9110-6 · Cited by 7

Transduction of hippocampal CA1 by adenovirus in vivo

Kammesheidt, A., Ito, K., Katō, K., Villarreal, L. P., & Sumikawa, K. (1996) · Brain Research · doi:10.1016/0006-8993(96)00715-9 · Cited by 7

Temporal-Specific Sex and Injury-Dependent Changes on Neurogranin-Associated Synaptic Signaling After Controlled Cortical Impact in Rats

Svirsky, S. E., Henchir, J. J., Li, Y., Carlson, S. W., & Dixon, C. E. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04043-5 · Cited by 7

Maternal gastrointestinal nematode infection alters hippocampal neuroimmunity, promotes synaptic plasticity, and improves resistance to direct infection in offspring

Noel, S. C., Madranges, J. F., Gothié, J. M., Ewald, J., Milnerwood, A. J., Kennedy, T. E., & Scott, M. E. (2024) · Scientific Reports · doi:10.1038/s41598-024-60865-2 · Cited by 7

Synaptic Plasticity and Cognitive Ability in Experimental Adult-Onset Hypothyroidism

Alkadhi, K. A. (2024) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.123.001887 · Cited by 6

Ionotropic Glutamate Receptors in Synaptic Plasticity

Pelkey, K. A., & McBain, C. J. (2008) · Humana Press eBooks · doi:10.1007/978-1-59745-055-3_5 · Cited by 5

CaMKII autophosphorylation but not downstream kinase activity is required for synaptic memoryPreprint

Chen, X., Cai, Q., Zhou, J., Pleasure, S. J., Schulman, H., Zhang, M., & Nicoll, R. A. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.25.554912 · Cited by 7

Thyroidectomy and PTU-Induced Hypothyroidism: Effect of L-Thyroxine on Suppression of Spatial and Non-Spatial Memory Related Signaling Molecules

Alzoubi, K. H., & Alkadhi, K. A. (2022) · Current Molecular Pharmacology · doi:10.2174/1874467215666220920122039 · Cited by 5

LTD – Synaptic Depression and Memory Storage

Hansel, C., & Bear, M. F. (2008) · Elsevier eBooks · doi:10.1016/b978-012370509-9.00017-6 · Cited by 6

Sleep, Synaptic Plasticity, and Memory

Golbert, D. C. F., Souza, A. C., Filho, D. A., & Ribeiro, S. T. G. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21118-8 · Cited by 5

Deciphering Ca2+-controlled biochemical computation governing neural circuit dynamics via multiplex imaging

Fujii, H., & Bito, H. (2022) · Neuroscience Research · doi:10.1016/j.neures.2022.04.004 · Cited by 6

Phosphorylation of Glutamate Receptors

Lee, H., & Huganir, R. L. (1999) · Handbook of experimental pharmacology · doi:10.1007/978-3-662-08022-1_2 · Cited by 5

Model Systems for Assessing Cognitive Function: Implications for HIV-1 Infection and Drugs of Abuse

Zink, W. E., Boyle, J., Persidsky, Y., Xiong, H., & Gendelman, H. E. (2006) · Kluwer Academic Publishers eBooks · doi:10.1007/0-306-47611-8_2 · Cited by 5

Conditional Transgenesis and Recombination to Study the Molecular Mechanisms of Brain Plasticity and Memory

Baumgärtel, K., Fernández, C., Johansson, T., & Mansuy, I. M. (2007) · Springer eBooks · doi:10.1007/978-3-540-35109-2_13 · Cited by 5

Differential regulation of MAP2 and αCamKII expression in hippocampal neurones by forskolin and calcium ionophore treatment

Alier, K. A., & MORRIS, B. J. (2004) · Molecular Brain Research · doi:10.1016/j.molbrainres.2003.11.018 · Cited by 4

Calcium Regulation of Cytosolic Enzymes

Schulman, H. (1998) · Springer eBooks · doi:10.1007/978-1-4899-1901-4_3 · Cited by 4

Potentiation of phosphoinositide-derived signals during LTP in intact rat brain

Kusuki, T., Imahori, Y., Fujii, R., Inokuchi, K., Kimura, M., & Ueda, S. (1998) · Neuroreport · doi:10.1097/00001756-199806220-00032 · Cited by 4

KN‐62: A Specific Ca2+/calmodulin‐dependent Protein Kinase Inhibitor as a Putative Function‐searching Probe for Intracellular Signal Transduction

Hidaka, H., & Okazaki, K. (1996) · Cardiovascular Drug Reviews · doi:10.1111/j.1527-3466.1996.tb00315.x · Cited by 4

CaMKII Kinase Activity, Targeting and Control of Cellular Functions: Effect of Single and Double Phosphorylation of CaMKIIα

Majeed, A., Pearsall, E., Carpenter, H., Brzozowski, J. S., Dickson, P. W., Rostas, J. A. P., & Skelding, K. A. (2014) · NOVA (University of Newcastle Australia) · Cited by 5

Brain Disrupting Actions of Prenatal Diethylstilbestrol Exposure in Mice - Behavioral, Neurochemical and Electrophysiological Studies

Takahama, K., Kaitsuka, T., Shirasaki, T., & Soeda, F. (2003) · Eisei kagaku · doi:10.1248/jhs.49.423 · Cited by 3

Learning Mutants

Matzel, L. D. (2002) · doi:10.1002/0471214426.pas0305 · Cited by 3

LOV2-based photoactivatable CaMKII and its application to single synapses: Local Optogenetics

Nagasawa, Y., Ueda, H. H., Kawabata, H., & Murakoshi, H. (2023) · Biophysics and Physicobiology · doi:10.2142/biophysico.bppb-v20.0027 · Cited by 2

Synaptic Triad in the Neostriatum

Klug, J. R., Deutch, A. Y., Colbran, R. J., & Winder, D. J. (2011) · Frontiers in neuroscience · doi:10.1201/b11284-5 · Cited by 2

CaMKII: A Master Functional and Structural Molecule in Synaptic Plasticity and Memory

Sanhueza, M., & Fernandez, G. (2015) · Springer eBooks · doi:10.1007/978-3-319-24364-1_3 · Cited by 2

Dynamism of Postsynaptic Proteins as the Mechanism of Synaptic Plasticity

Futai, K., & Hayashi, Y. (2003) · Springer eBooks · doi:10.1007/978-1-4615-0039-1_3 · Cited by 2

Biochemical Mechanisms for Short-Term Information Storage at the Cellular Level

Sweatt, J. D. (2003) · Elsevier eBooks · doi:10.1016/b978-012678957-7/50009-8 · Cited by 2

Ca2+-Independent Autophosphorylation of Postsynaptic Density-Associated Ca2+/Calmodulin-Dependent Protein Kinase

Dosemeci, A., & Choi, C. (1997) · Neurochemical Research · doi:10.1023/a:1027373404145 · Cited by 1

Homeostasis of dendritic spines in hippocampal CA1 cells

Mestrallet, C. A. (2011) · UCL Discovery (University College London) · Cited by 2

AMPA receptors in synaptic plasticity and learning and memory

Kim, K., & Park, M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15754-7.00056-0 · Cited by 1

PI(3)P coordinates SNX17- and SNX27-dependent protein recycling for long-term synaptic plasticity

Rivero-Ríos, P., Uygun, T., Chavis, G. D., Lee, H., Duan, B., Sutton, M. A., & Weisman, L. S. (2025) · Journal of Cell Biology · doi:10.1083/jcb.202411198 · Cited by 1

CaMKII monomers are sufficient for GluN2B binding, co-condensation, and synaptic potentiation

Brown, C. N., Barker, C. M., Miller, C. N., Chao, F.-Y., Aoto, J. N., Coultrap, S. J., & Bayer, K. U. (2026) · Molecular Cell · doi:10.1016/j.molcel.2026.08.029 · Cited by 2

Phosphorylation of Non-NMDA Glutamate Receptor Ion Channels

Soderling, T. R. (1997) · Humana Press eBooks · doi:10.1007/978-1-4612-3962-8_5 · Cited by 1

The role of CaMKII in cerebellar learning

Andreev, D. (2006)

In vivo visualization of CaMKII activity in ocular dominance plasticity

Kwok, S. M. (2009) · DSpace@MIT (Massachusetts Institute of Technology)

Identification of novel target genes for the plasticity-related transcription factor Zif268

McDade, D. M. (2007) · Enlighten: Theses (The University of Glasgow)

Brain circuit dynamics related to extremes in trait anxiety in mice

Avrabos, C. (2012) · Elektronische Hochschulschriften der LMU München (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.14994

Extracellular Signal-Regulated Kinase as an Integrative Synapse-to-Nucleus Signal

Zhai, S. (2013) · DukeSpace (Duke University)

Developmentally Regulated Induction and Expression Mechanisms of Long-Term Potentiation at Hippocampal CA3 CA1 Synapses

Luchkina, N. V. (2015) · Työväentutkimus Vuosikirja

Neuronal adaptations in rat hippocampal CA1 neurons during withdrawal from prolonged flurazepam exposure : glutamatergic system remodeling.

Song, J. H. (2007) · OhioLink ETD Center (Ohio Library and Information Network)

Glutamate Receptors in the Medial Temporal Lobe Following Bilateral Vestibular Deafferentation

Wilson, G. (2011) · Otago University Research Archive (University of Otago)

Establishment and validation of hippocampal LTP for characterization of memory enhancing drugs as potential treatment of Alzheimers disease

Würzburg, J.-M.-U. (2011)

Ca²⁺/calmodulin dependent protein kinase II subcellular re-distribution and activation of protein phosphatase after a brief pentylenetertrazol seizure : potential role in kindling.

Dong, Y. (2003) · OhioLink ETD Center (Ohio Library and Information Network)

VitroMAPK in the Adult Rat Dentate Gyrus In Kinase Cascades Involving CaMKII or Either PKA Long-Term Potentiation Is Mediated by Multiple

Rowan, M. J., Anwyl, R., Morishita, W., Malenka, R. C., Pu, Z., Krugers, H. J., Joëls, M., Obrietan, K. H., Karelina, K., Hansen, K. F., et al. (2015)

Synapse- and cell-specific plasticity in the mature hippocampus

Queenan, B. N. (2014) · DigitalGeorgetown (Georgetown University Library)

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