Is Persistent Activity of Calcium/Calmodulin-Dependent Kinase Required for the Maintenance of 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

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

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

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

Involvement of a calcineurin/ inhibitor-1 phosphatase cascade in hippocampal long-term depression

Mulkey, R. M., Endo, S., Shenolikar, S., & Malenka, R. C. (1994) · Nature · doi:10.1038/369486a0 · Cited by 1,083

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

Regulatory phosphorylation of AMPA-type glutamate receptors by CaM-KII during long-term potentiation

Barria, A., Muller, D., Derkach, V., Griffith, L. C., & Soderling, T. R. (1997) · Science · doi:10.1126/science.276.5321.2042 · Cited by 1,049

LTP promotes formation of multiple spine synapses between a single axon terminal and a dendrite

Toni, N., Buchs, P.-A., Nikonenko, I., Bron, C. R., & Muller, D. (1999) · Nature · doi:10.1038/46574 · Cited by 949

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

Ca 2+ /calmodulin-kinase II enhances channel conductance of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionate type glutamate receptors

Derkach, V., Barria, A., & Soderling, T. R. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.6.3269 · Cited by 842

Regulatory mechanisms of AMPA receptors in synaptic plasticity

Derkach, V. A., Oh, M. C., Guire, E. S., & Soderling, T. R. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2055 · Cited by 708

Activation of CaMKII in single dendritic spines during long-term potentiation

Lee, S.-J. R., Escobedo-Lozoya, Y., Szatmari, E. M., & Yasuda, R. (2009) · Nature · doi:10.1038/nature07842 · Cited by 685

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 520

Untitled work

Lisman (2001) · doi:10.1016/s0896-6273(01)00364-6 · Cited by 480

CaMKII: a central molecular organizer of synaptic plasticity, learning and memory

Yasuda, R., Hayashi, Y., & Hell, J. W. (2022) · Nature Reviews Neuroscience · doi:10.1038/s41583-022-00624-2 · Cited by 431

Neural plasticity and behavior – sixty years of conceptual advances

Sweatt, J. D. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13580 · Cited by 362

CaMKII regulation in information processing and storage

Coultrap, S. J., & Bayer, K. U. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.05.003 · Cited by 323

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 311

Transition from Reversible to Persistent Binding of CaMKII to Postsynaptic Sites and NR2B

Bayer, K. U., LeBel, É., McDonald, G. L., O’Leary, H., Schulman, H., & Koninck, P. D. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3116-05.2006 · Cited by 259

Phosphatidylinositol 3-Kinase Is Required for the Expression But Not for the Induction or the Maintenance of Long-Term Potentiation in the Hippocampal CA1 Region

Sanna, P. P., Cammalleri, M., Berton, F., Simpson, C., Lütjens, R., Bloom, F. E., & Francesconi, W. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-09-03359.2002 · Cited by 254

Role of the CaMKII/NMDA Receptor Complex in the Maintenance of Synaptic Strength

Sanhueza, M., Fernandez-Villalobos, G., Stein, I. S., Kasumova, G., Zhang, P., Bayer, K. U., Otmakhov, N., Hell, J. W., & Lisman, J. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.1250-11.2011 · Cited by 248

Molecular bases of long-term memories: a question of persistence

Dudai, Y. (2002) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(02)00305-7 · Cited by 233

Persistent Phosphorylation by Protein Kinase Mζ Maintains Late-Phase Long-Term Potentiation

Serrano, P. A., Yao, Y., & Sacktor, T. C. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.5132-04.2005 · Cited by 226

Computational principles of memory

Chaudhuri, R., & Fiete, I. (2016) · Nature Neuroscience · doi:10.1038/nn.4237 · Cited by 213

The Roles of CaMKII and F-Actin in the Structural Plasticity of Dendritic Spines: A Potential Molecular Identity of a Synaptic Tag?

Okamoto, K., Bosch, M., & Hayashi, Y. (2009) · Physiology · doi:10.1152/physiol.00029.2009 · Cited by 213

Identification of Compartment- and Process-Specific Molecules Required for “Synaptic Tagging” during Long-Term Potentiation and Long-Term Depression in Hippocampal CA1

Sajikumar, S., Navakkode, S., & Frey, J. U. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4940-06.2007 · Cited by 194

Dual Mechanism of a Natural CaMKII Inhibitor

Vest, R. S., Davies, K. D., O’Leary, H., Port, J. D., & Bayer, K. U. (2007) · Molecular Biology of the Cell · doi:10.1091/mbc.e07-02-0185 · Cited by 188

Properties and Mechanisms of LTP Maintenance

Abraham, W. C., & Williams, J. M. (2003) · The Neuroscientist · doi:10.1177/1073858403259119 · Cited by 189

The CaMKII/NMDAR complex as a molecular memory

Sanhueza, M., & Lisman, J. (2013) · Molecular Brain · doi:10.1186/1756-6606-6-10 · Cited by 166

CaMKII Autophosphorylation Is Necessary for Optimal Integration of Ca 2+ Signals during LTP Induction, but Not Maintenance

Chang, J.-Y., Parra-Bueno, P., Laviv, T., Szatmari, E. M., Lee, S.-J. R., & Yasuda, R. (2017) · Neuron · doi:10.1016/j.neuron.2017.04.041 · Cited by 161

CaMKII "Autonomy" Is Required for Initiating But Not for Maintaining Neuronal Long-Term Information Storage

Buard, I., Coultrap, S. J., Freund, R. K., Lee, Y.-S., Dell'Acqua, M. L., Silva, A. J., & Bayer, K. U. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.1469-10.2010 · Cited by 160

Activity-driven postsynaptic translocation of CaMKII

Merrill, M. A., Chen, Y., Strack, S., & Hell, J. W. (2005) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2005.10.003 · Cited by 155

CaMKII in cerebral ischemia

Coultrap, S. J., Vest, R. S., Ashpole, N. M., Hudmon, A., & Bayer, K. U. (2011) · Acta Pharmacologica Sinica · doi:10.1038/aps.2011.68 · Cited by 148

A Temporary Gating of Actin Remodeling during Synaptic Plasticity Consists of the Interplay between the Kinase and Structural Functions of CaMKII

Kim, K., Lakhanpal, G., Lu, H. E., Khan, M., Suzuki, A., Kato Hayashi, M., Narayanan, R., Luyben, T. T., Matsuda, T., Nagai, T., et al. (2015) · Neuron · doi:10.1016/j.neuron.2015.07.023 · Cited by 145

STDP in a Bistable Synapse Model Based on CaMKII and Associated Signaling Pathways

Graupner, M., & Brunel, N. (2005) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0030221 · Cited by 147

Kinetics of Endogenous CaMKII Required for Synaptic Plasticity Revealed by Optogenetic Kinase Inhibitor

Murakoshi, H., Shin, M. E., Parra-Bueno, P., Szatmari, E. M., Shibata, A. C. E., & Yasuda, R. (2017) · Neuron · doi:10.1016/j.neuron.2017.02.036 · Cited by 140

CaMKII

Shonesy, B. C., Jalan‐Sakrikar, N., Cavener, V. S., & Colbran, R. J. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-420170-5.00003-9 · Cited by 140

Cognitive neuroepigenetics: A role for epigenetic mechanisms in learning and memory

Day, J. J., & Sweatt, J. D. (2010) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2010.12.008 · Cited by 137

Synaptic memory and CaMKII

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

Effective Post-insult Neuroprotection by a Novel Ca2+/ Calmodulin-dependent Protein Kinase II (CaMKII) Inhibitor

Vest, R. S., O’Leary, H., Coultrap, S. J., Kindy, M. S., & Bayer, K. U. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.088617 · Cited by 120

Roles of CaMKII, PKA, and PKC in the Induction and Maintenance of LTP of C-Fiber-Evoked Field Potentials in Rat Spinal Dorsal Horn

Yang, H.-W., Hu, X.-D., Zhang, H., Xin, W., Li, M.-T., Zhang, T., Zhou, L., & Liu, X. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00735.2003 · Cited by 116

The NMDA receptor complex: a multifunctional machine at the glutamatergic synapse

Fan, X., Jin, W. Y., & Wang, Y. T. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00160 · Cited by 124

Postsynaptic signaling networks: Cellular cogwheels underlying long-term plasticity

Blitzer, R. D., Iyengar, R., & Landau, E. M. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.02.031 · Cited by 117

Autonomous activity of CaMKII is only transiently increased following the induction of long‐term potentiation in the rat hippocampus

Lengyel, I., Voss, K., Cammarota, M., Bradshaw, K., Brent, V., Murphy, K., Giese, K., Rostas, J. A., & Bliss, T. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03748.x · Cited by 112

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 101

Neuromodulators and Long-Term Synaptic Plasticity in Learning and Memory: A Steered-Glutamatergic Perspective

Bazzari, A. H., & Parri, H. R. (2019) · Brain Sciences · doi:10.3390/brainsci9110300 · Cited by 107

Memory Erasure Experiments Indicate a Critical Role of CaMKII in Memory Storage

Rossetti, T., Banerjee, S., Kim, C., Leubner, M., Lamar, C., Gupta, P., Lee, B., Neve, R., & Lisman, J. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.010 · Cited by 94

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 95

Ca2+ and synaptic plasticity

Cavazzini, M., Bliss, T., & Emptage, N. J. (2005) · Cell Calcium · doi:10.1016/j.ceca.2005.06.013 · Cited by 93

LTP and adaptation to inactivity: Overlapping mechanisms and implications for metaplasticity

Thiagarajan, T. C., Lindskog, M., Malgaroli, A., & Tsien, R. W. (2007) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.07.030 · Cited by 99

Signalling pathways underlying structural plasticity of dendritic spines

Patterson, M., & Yasuda, R. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01328.x · Cited by 76

PKG and PKA Signaling in LTP at GABAergic Synapses

Nugent, F. S., Niehaus, J. L., & Kauer, J. A. (2009) · Neuropsychopharmacology · doi:10.1038/npp.2009.5 · Cited by 73

Environmental noise degrades hippocampus-related learning and memory

Zhang, Y., Zhu, M., Sun, Y., Tang, B., Zhang, G., An, P., Cheng, Y., Shan, Y., Merzenich, M. M., & Zhou, X. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2017841117 · Cited by 69

Synaptic memory requires CaMKII

Tao, W., Lee, J., Chen, X., Díaz-Alonso, J., Zhou, J., Pleasure, S., & Nicoll, R. A. (2021) · eLife · doi:10.7554/elife.60360 · Cited by 72

A Model of the Roles of Essential Kinases in the Induction and Expression of Late Long-Term Potentiation

Smolen, P., Baxter, D. A., & Byrne, J. H. (2006) · Biophysical Journal · doi:10.1529/biophysj.105.072470 · Cited by 61

The molecular memory code and synaptic plasticity: A synthesis

Gershman, S. J. (2023) · Biosystems · doi:10.1016/j.biosystems.2022.104825 · Cited by 62

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

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

Effects of olanzapine on brain-derived neurotrophic factor gene promoter activity in SH-SY5Y neuroblastoma cells

Lee, J. G., Cho, H. Y., Park, S. W., Seo, M. K., & Kim, Y. H. (2010) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2010.05.013 · Cited by 56

Regulation of synaptic plasticity in memory and memory decline with aging

Foster, T. C. (2002) · Progress in brain research · doi:10.1016/s0079-6123(02)38083-x · Cited by 51

Genetic inhibition of CaMKII in dorsal striatal medium spiny neurons reduces functional excitatory synapses and enhances intrinsic excitability

Klug, J. R., Mathur, B. N., Kash, T. L., Wang, H.-D., Matthews, R. T., Robison, A. J., Anderson, M. E., Deutch, A. Y., Lovinger, D. M., Colbran, R. J., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0045323 · Cited by 49

Translational switch for long‐term maintenance of synaptic plasticity

Aslam, N., Kubota, Y., Wells, D. G., & Shouval, H. Z. (2009) · Molecular Systems Biology · doi:10.1038/msb.2009.38 · Cited by 46

CaMKII is differentially localized in synaptic regions of kenyon cells within the mushroom bodies of the honeybee brain

Pasch, E., Muenz, T. S., & Rößler, W. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22683 · Cited by 45

Neurobiological and Pharmacological Validity of Curcumin in Ameliorating Memory Performance of Senescence-Accelerated Mice

Sun, C. Y., Qi, S. S., Zhou, P., Cui, H. R., Chen, S. X., Dai, K. Y., & Tang, M. L. (2013) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2013.02.002 · Cited by 44

A revised view of the role of CaMKII in learning and memory

Bayer, K. U., & Giese, K.-P. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01809-x · Cited by 51

Endothelial CaMKII as a regulator of eNOS activity and NO-mediated vasoreactivity

Murthy, S., Koval, O. M., Diaz, J. M. R., Kumar, S., Nuno, D. W., Scott, J. A., Allamargot, C., Zhu, L. J., Broadhurst, K., Santhana, V., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0186311 · Cited by 43

Long-Term Potentiation Is Mediated by Multiple Kinase Cascades Involving CaMKII or Either PKA or p42/44 MAPK in the Adult Rat Dentate Gyrus In Vitro

Wu, J., Rowan, M. J., & Anwyl, R. (2006) · Journal of Neurophysiology · doi:10.1152/jn.01235.2005 · Cited by 44

Ionotropic Glutamate Receptors in Spinal Nociceptive Processing

Larsson, M. (2009) · Molecular Neurobiology · doi:10.1007/s12035-009-8086-8 · Cited by 45

Regulation of CaMKII In vivo: The Importance of Targeting and the Intracellular Microenvironment

Skelding, K. A., & Rostas, J. A. P. (2009) · Neurochemical Research · doi:10.1007/s11064-009-9985-9 · Cited by 37

CaMKII Activation State Underlies Synaptic Labile Phase of LTP and Short-Term Memory Formation

Wang, H., Feng, R., Wang, L. P., Li, F. R., Cao, X., & Tsien, J. Z. (2008) · Current Biology · doi:10.1016/j.cub.2008.08.064 · Cited by 35

CaMKII autophosphorylation is the only enzymatic event required for synaptic memory

Chen, X., Cai, Q., Zhou, J., Pleasure, S. J., Schulman, H., Zhang, M., & Nicoll, R. A. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2402783121 · Cited by 41

Protein kinase signaling in synaptic plasticity and memory.

Mayford, M. (2007) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2007.05.001 · Cited by 38

A Significant but Rather Mild Contribution of T286 Autophosphorylation to Ca2+/CaM-Stimulated CaMKII Activity

Coultrap, S. J., Barcomb, K., & Bayer, K. U. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037176 · Cited by 33

Studying Signal Transduction in Single Dendritic SpinesPreprint

Yasuda, R. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005611 · Cited by 33

Changes of learning, memory and levels of CaMKII, CaM mRNA, CREB mRNA in the hippocampus of chronic multiple-stressed rats

Sun, C., Qi, S., Lou, X., Sun, S., Wang, X., Dai, K.-Y., Hu, S., & Liu, N.-B. (2006) · Chinese Medical Journal · doi:10.1097/00029330-200601020-00008 · Cited by 31

Neuroprotective Effect of Dichloromethane Extraction From Piper nigrum L. and Piper longum L. on Permanent Focal Cerebral Ischemia Injury in Rats

Hua, S., Wang, B., Chen, R., Zhang, Y., Zhang, Y., Li, T., Dong, L., & Fu, X. (2018) · Journal of Stroke and Cerebrovascular Diseases · doi:10.1016/j.jstrokecerebrovasdis.2018.11.018 · Cited by 31

Pain and learning in a spinal system: Contradictory outcomes from common origins

Baumbauer, K. M., Young, E. E., & Joynes, R. L. (2009) · Brain Research Reviews · doi:10.1016/j.brainresrev.2009.05.004 · Cited by 28

Effects of high-speed railway noise on the synaptic ultrastructure and phosphorylated-CaMKII expression in the central nervous system of SD rats

Di, G., & Zheng, Y. (2012) · Environmental Toxicology and Pharmacology · doi:10.1016/j.etap.2012.11.012 · Cited by 28

Arsenic downregulates gene expression at the postsynaptic density in mouse cerebellum, including genes responsible for long-term potentiation and depression

Zhang, C., Li, S., Sun, Y., Dong, W., Piao, F., Piao, Y., liu, S., Guan, H., & Yu, S.-B. (2014) · Toxicology Letters · doi:10.1016/j.toxlet.2014.05.007 · Cited by 28

A Model of Late Long-Term Potentiation Simulates Aspects of Memory Maintenance

Smolen, P. D. (2007) · PLoS ONE · doi:10.1371/journal.pone.0000445 · Cited by 27

Long-Term Potentiation of Excitatory Synapses on Neocortical Somatostatin-Expressing Interneurons

Chen, H.-X., Jiang, M., Akakın, D., & Roper, S. N. (2009) · Journal of Neurophysiology · doi:10.1152/jn.00641.2009 · Cited by 28

The Delicate Bistability of CaMKII

Michalski, P. J. (2013) · Biophysical Journal · doi:10.1016/j.bpj.2013.06.038 · Cited by 24

Modulation of CaM Kinase II Activity Is Coincident with Induction of Status Epilepticus in the Rat Pilocarpine Model

Singleton, M. W., Holbert, W. H., Lee, A. T., Bracey, J. M., & Churn, S. B. (2005) · Epilepsia · doi:10.1111/j.1528-1167.2005.19205.x · Cited by 26

Chapter 1 Molecular memory traces

Sossin, W. S. (2008) · Progress in brain research · doi:10.1016/s0079-6123(07)00001-5 · Cited by 26

Impaired spatial learning related with decreased expression of calcium/calmodulin-dependent protein kinase IIα and cAMP-response element binding protein in the pentylenetetrazol-kindled rats

Wang, P., Wang, W., Sun-Zhang, Wang, H.-X., Yan-Lou, & Yue-hui, F. (2008) · Brain Research · doi:10.1016/j.brainres.2008.07.103 · Cited by 25

Ca2+/Calmodulin-Dependent Protein Kinase II (CaMKII)

Coultrap, S. J., & Bayer, K. U. (2012) · Neuromethods · doi:10.1007/978-1-61779-824-5_4 · Cited by 22

Postsynaptic Application of a cAMP Analogue Reverses Long-Term Potentiation in Hippocampal CA1 Pyramidal Neurons

Otmakhov, N., & Lisman, J. E. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.87.6.3018 · Cited by 22

Enzymatic Activity of CaMKII Is Not Required for Its Interaction with the Glutamate Receptor Subunit GluN2B

Barcomb, K., Coultrap, S. J., & Bayer, K. U. (2013) · Molecular Pharmacology · doi:10.1124/mol.113.089045 · Cited by 22

Propofol and Ketamine-induced Anesthetic Depth-dependent Decrease of CaMKII Phosphorylation Levels in Rat Hippocampus and Cortex

Cui, X., Li, J., Li, T., Ji, F., Bu, X., Zhang, N., & Zhang, B. (2009) · Journal of Neurosurgical Anesthesiology · doi:10.1097/ana.0b013e31819ac2c0 · Cited by 21

LTP expression mediated by autonomous activity of GluN2B-bound CaMKII

Rumian, N. L., Barker, C. M., Larsen, M. E., Tullis, J. E., Freund, R. K., Taslimi, A., Coultrap, S. J., Tucker, C. L., Dell’Acqua, M. L., & Bayer, K. U. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114866 · Cited by 20

Rostral Ganglia Are Required for Induction But Not Expression of Crayfish Escape Reflex Habituation: Role of Higher Centers in Reprogramming Low-Level Circuits

Shirinyan, D., Teshiba, T. M., Taylor, K., O’Neill, P.-K., Lee, S. C., & Krasne, F. B. (2005) · Journal of Neurophysiology · doi:10.1152/jn.00914.2005 · Cited by 20

Differential involvement of Ca2+/calmodulin‐dependent protein kinases and mitogen‐activated protein kinases in the dopamine D1/D5 receptor‐mediated potentiation in hippocampal CA1 pyramidal neurons

Shetty, M., & Sajikumar, S. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2016.07.020 · Cited by 16

Spatiotemporal Regulation of Signaling In and Out of Dendritic Spines: CaMKII and Ras

Lee, S.-J. R., & Yasuda, R. (2009) · The Open Neuroscience Journal · doi:10.2174/1874082000903020117 · Cited by 21

A New Principle for Information Storage in an Enzymatic Pathway Model

Delord, B., Berry, H., Guigon, E., & Genet, S. (2005) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0030124 · Cited by 21

Lateralized hippocampal effects of vasoactive intestinal peptide on learning and memory in rats in a model of depression

Velikova, M., Belcheva, S. P., Belcheva, I., Negrev, N., & Tashev, R. E. (2011) · Psychopharmacology · doi:10.1007/s00213-011-2600-1 · Cited by 18

Dysfunction of Ca2+/CaM kinase IIα cascades in the amygdala in post-traumatic stress disorder

Shi (2009) · International Journal of Molecular Medicine · doi:10.3892/ijmm_00000294 · Cited by 17

Long-Term Potentiation: Mechanisms of Induction and Maintenance

Blitzer, R. D. (2005) · Science s STKE · doi:10.1126/stke.3092005tr26 · Cited by 19

Simulations suggest pharmacological methods for rescuing long-term potentiation

Smolen, P., Baxter, D. A., & Byrne, J. H. (2014) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2014.07.006 · Cited by 13

Axonal localization of delta Ca2+/calmodulin‐dependent protein kinase II in developing P19 neurons

Faison, M. O., Perozzi, E. F., Caran, N., Stewart, J. K., & Tombes, R. M. (2002) · International Journal of Developmental Neuroscience · doi:10.1016/s0736-5748(02)00107-7 · Cited by 14

Phosphorylation of Ca2+/calmodulin-dependent protein kinase type ii and the α-amino-3-hydroxy-5-methyl-4-isoxazole propionate (ampa) receptor in response to a threonine-devoid diet

Sharp, J. W., Ross, C. M., Koehnle, T. J., & Gietzen, D. W. (2004) · Neuroscience · doi:10.1016/j.neuroscience.2004.03.066 · Cited by 14

Overexpression cdc42 attenuates isoflurane-induced neurotoxicity in developmental brain of rats

Fang, X., Li, S., Han, Q., Zhao, Y., Gao, J., Yan, J., & Luo, A. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.06.108 · Cited by 13

Co-localization of phosphorylated extracellular signal-regulated protein kinases 1/2 (ERK1/2) and phosphorylated eukaryotic initiation factor 2α (eIF2α) in response to a threonine-devoid diet

Sharp, J. W., Ross‐Inta, C., Hao, S., Rudell, J. B., & Gietzen, D. W. (2005) · The Journal of Comparative Neurology · doi:10.1002/cne.20817 · Cited by 13

Ocular dominance plasticity is stably maintained in the absence of α calcium calmodulin kinase II (αCaMKII) autophosphorylation

Taha, S. A., & Stryker, M. P. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0508185102 · Cited by 12

Reciprocal activation within a kinase effector complex: A mechanism for the persistence of molecular memory

Saneyoshi, T. (2021) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2021.01.018 · Cited by 9

Mathematical Modeling and Analysis of Intracellular Signaling Pathways

Smolen, P. D., Baxter, D. A., & Byrne, J. H. (2004) · Elsevier eBooks · doi:10.1016/b978-012148660-0/50015-9 · Cited by 10

STDP in a bistable synapse model based on CaMKII and associated signaling pathways

Graupner, M., & Brunel, N. (2005) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0030221.eor · Cited by 10

Administration of a Ca2+/calmodulin-dependent protein kinase II (CaMKII) inhibitor prevents the learning deficit observed in spinal rats after noncontingent shock administration.

Baumbauer, K. M., Young, E. E., Hoy, K. C., Abood, A., & Joynes, R. L. (2007) · Behavioral Neuroscience · doi:10.1037/0735-7044.121.3.570 · Cited by 10

Experimental study of effect of corticosterone on primary cultured hippocampal neurons and their Ca2+/CaMK II expression

Sun, C., Liu, N.-B., Li, H.-L., Zhang, M.-H., Liu, S.-C., Liu, X.-Q., Li, X.-H., & Hong, X.-P. (2008) · Journal of Huazhong University of Science and Technology. Medical Sciences · doi:10.1007/bf02911349 · Cited by 8

Translational switch for long term maintenance of synaptic plasticity

Aslam, N., Kubota, Y., & Shouval, H. Z. (2008) · BMC Neuroscience · doi:10.1186/1471-2202-9-s1-p102 · Cited by 9

Hippocampal levels of ChAT, PKA, phospho-PKA and phospho-CaMKIIα but not CaMKIIα positively correlate with spatial learning skills in rats

Gökçek-Saraç, Ç., Adalı, O., & Jakubowska-Doğru, E. (2013) · Neuroscience Letters · doi:10.1016/j.neulet.2013.04.046 · Cited by 8

Neural Analysis of Learning in Simple Systems

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

Autophosphorylation versus dephosphorylation of Ca 2+ /calmodulin-dependent protein kinase II: switching characteristics and implication for the induction of LTP

Okamoto, H., & Ichikawa, K. (1997)

Autophosphorylation Versus Dephosphorylation of Ca2+/Calmodulin-Dependent Protein Kinase II

Okamoto, H., & Ichikawa, K. (1997) · Springer eBooks · doi:10.1007/978-1-4757-9800-5_5

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

Chapter 5 The involvement of PKC and multifunctional CaM kinase II of the postsynaptic neuron in induction and maintenance of long-term potentiation

Feng, T. P. (1995) · Progress in Brain Research · doi:10.1016/s0079-6123(08)63283-5 · Cited by 31

Potentiated transmission and prevention of further LTP by increased CaMKII activity in postsynaptic hippocampal slice neurons

Pettit, D. L., Perlman, S., & Malinow, R. (1994) · Science · doi:10.1126/science.7997883 · Cited by 329