Inhibitory Autophosphorylation of CaMKII Controls PSD Association, Plasticity, and Learning

Derivation of completely cell culture-derived mice from early-passage embryonic stem cells.

Nagy, A., Rossant, J., Nagy, R., Abramow-Newerly, W., & Roder, J. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.18.8424 · Cited by 2,328

Genetic enhancement of learning and memory in mice

Tang, Y., Shimizu, E., Dubé, G., Rampon, C., Kerchner, G. A., Zhuo, M., Liu, G., & Tsien, J. Z. (1999) · Nature · doi:10.1038/43432 · Cited by 1,878

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

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

Control of memory formation through regulated expression of a CaMKII transgene

Mayford, M., Bach, M. E., Huang, Y.-Y., Wang, L., Hawkins, R. D., & Kandel, E. R. (1996) · Science · doi:10.1126/science.274.5293.1678 · Cited by 1,550

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

Impaired Spatial Learning in α-Calcium-Calmodulin Kinase II Mutant Mice

Silva, A. J., Paylor, R. E., Wehner, J. M., & Tonegawa, S. (1992) · Science · doi:10.1126/science.1321493 · Cited by 1,366

A mechanism for the Hebb and the anti-Hebb processes underlying learning and memory.

Lisman, J. (1989) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.86.23.9574 · Cited by 1,127

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

Synaptic Plasticity: The Subcellular Location of CaMKII Controls Plasticity

Fox, K. D. (2003) · Current Biology · doi:10.1016/s0960-9822(03)00077-0 · Cited by 15

Signal transduction mechanisms in memory disorders

Shalin, S. C., Egli, R. E., Birnbaum, S. G., Roth, T. L., Levenson, J. M., & Sweatt, J. D. (2006) · Progress in brain research · doi:10.1016/s0079-6123(06)57003-7 · Cited by 14

The CaMKIIα hub ligand Ph-HTBA promotes neuroprotection after focal ischemic stroke by a distinct molecular interaction

Griem‐Krey, N., Gauger, S. J., Gowing, E. K., Thiesen, L., Frølund, B., Clarkson, A. N., & Wellendorph, P. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.113895 · Cited by 14

Developmental changes of CaMKII localization, activity and function during postembryonic CNS remodelling in Manduca sexta

Burkert, P., & Duch, C. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04562.x · Cited by 15

Differential Involvement of Kinase Activity of Ca2+/Calmodulin-Dependent Protein Kinase IIα in Hippocampus- and Amygdala-Dependent Memory Revealed by Kinase-Dead Knock-In Mouse

Yamagata, Y., Yanagawa, Y., & Imoto, K. (2018) · eNeuro · doi:10.1523/eneuro.0133-18.2018 · Cited by 12

Regulation of Multifunctional Calcium/Calmodulin Stimulated Protein Kinases by Molecular Targeting

Skelding, K. A., & Rostas, J. A. P. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-12457-1_26 · 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

CaMKIIα as a Promising Drug Target for Ischemic Grey Matter

Griem‐Krey, N., Clarkson, A. N., & Wellendorph, P. (2022) · Brain Sciences · doi:10.3390/brainsci12121639 · Cited by 11

In vivo evaluation of cellular activity in αCaMKII heterozygous knockout mice using manganese-enhanced magnetic resonance imaging (MEMRI)

Hattori, S., Hagihara, H., Ohira, K., Aoki, I., Saga, T., Suhara, T., Higuchi, M., & Miyakawa, T. (2013) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2013.00076 · Cited by 11

Special Considerations When Using Mice for In Vivo Electrophysiology and Long-Term Studies of Hippocampal Synaptic Plasticity During Behavior

Manahan‐Vaughan, D. (2018) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-812028-6.00003-3 · Cited by 11

Analysis of organelles within the nervous system: impact on brain and organelle functions

Tribl, F., Meyer, H. E., & Marcus, K. (2008) · Expert Review of Proteomics · doi:10.1586/14789450.5.2.333 · Cited by 11

The Cognitive Enhancer SGS742 Does not Involve Major Known Signaling Cascades in OF1 Mice

Sunyer, B., Shim, K., Höger, H., & Lubec, G. (2008) · Neurochemical Research · doi:10.1007/s11064-008-9596-x · Cited by 7

CaMKII Requirement for in Vivo Insular Cortex LTP Maintenance and CTA Memory Persistence

Juárez-Muñoz, Y., Ramos-Languren, L. E., & Escobar, M. L. (2017) · Frontiers in Pharmacology · doi:10.3389/fphar.2017.00822 · Cited by 9

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

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

A Review of Aspects of Synaptic Plasticity in Hippocampus via mT Extremely Low‐Frequency Magnetic Fields

Dong, L., Xia, P., Tian, L., Tian, C.-X., Zhao, W., Zhao, L., Duan, J., Zhao, Y., & Zheng, Y. (2023) · Bioelectromagnetics · doi:10.1002/bem.22437 · Cited by 9

α-Calcium Calmodulin Kinase II Modulates the Temporal Structure of Hippocampal Bursting Patterns

Cho, J., Bhatt, R., Elgersma, Y., & Silva, A. J. (2012) · PLoS ONE · doi:10.1371/journal.pone.0031649 · Cited by 10

Long-Term Potentiation and Memory

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

Förster resonance energy transfer-based kinase mutation phenotyping reveals an aberrant facilitation of Ca2+/calmodulin-dependent CaMKIIα activity in de novo mutations related to intellectual disability

Fujii, H., Kidokoro, H., Kondo, Y., Kawaguchi, M., Horigane, S., Natsume, J., Takemoto‐Kimura, S., & Bito, H. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.970031 · Cited by 8

Adult Camk2a Gene Reinstatement Restores the Learning and Plasticity Deficits of Camk2a Knockout Mice

Rigter, P. M. F., Wallaard, I., Jolfaei, M. A., Kingma, J., Post, L. C., Elgersma, M., Elgersma, Y., & van Woerden, G. M. (2022) · iScience · doi:10.1016/j.isci.2022.105303 · Cited by 10

Pharmacological Enhancement of Adult Hippocampal Neurogenesis Improves Behavioral Pattern Separation in Young and Aged Male Mice

Chang, W.-L., Tegang, K., Samuels, B. A., Saxe, M., Wichmann, J., David, D. J. P., Mendez‐David, I., Augustin, A., Fischer, H., Golling, S., et al. (2024) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2024.100419 · Cited by 10

Genes Responsible for H2S Production and Metabolism Are Involved in Learning and Memory in Drosophila melanogaster

Zatsepina, O. G., Chuvakova, L. N., Nikitina, E. A., Rezvykh, A. P., Zakluta, A. S., Sarantseva, S. V., Surina, N. V., Ksenofontov, A. L., Baratova, L. A., Shilova, V. Y., et al. (2022) · Biomolecules · doi:10.3390/biom12060751 · Cited by 8

Mechanisms of Activation and Subunit Release in Ca2+/Calmodulin-Dependent Protein Kinase II

Pullara, F., Asciutto, E. K., & General, I. J. (2017) · The Journal of Physical Chemistry B · doi:10.1021/acs.jpcb.7b09214 · Cited by 8

A familial case of CAMK2B mutation with variable expressivity

Heiman, P., Drewes, S., & Ghaloul‐Gonzalez, L. (2021) · SAGE Open Medical Case Reports · doi:10.1177/2050313x21990982 · 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

Phosphorylation at Ser26 in the ATP-binding site of Ca2+/calmodulin-dependent kinase II as a mechanism for switching off the kinase activity

Yilmaz, M., Gangopadhyay, S. S., Leavis, P. C., Grabarek, Z., & Morgan, K. G. (2013) · Bioscience Reports · doi:10.1042/bsr20120116 · Cited by 7

Molecular Mechanism of Learning and Memory Based on the Research for Ca2+/Calmodulin-dependent Protein Kinase II

Yamauchi, T. (2007) · YAKUGAKU ZASSHI · doi:10.1248/yakushi.127.1173 · Cited by 7

Ca2+/calmodulin‐dependent protein kinase II is reversibly autophosphorylated, inactivated and made sedimentable by acute neuronal excitation in rats in vivo

Yamagata, Y., & Obata, K. (2004) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2004.02753.x · Cited by 7

Genetic Engineering Cures Mice of Neurological Deficits: Prospects for Treating Angelman Syndrome

Elgersma, Y. (2007) · Pharmacogenomics · doi:10.2217/14622416.8.6.539 · Cited by 7

A hyper-activatable CAMK2A variant associated with intellectual disability causes exaggerated long-term potentiation and learning impairments

Pan, M., Liu, P.-W., Ozawa, Y., Arima‐Yoshida, F., Dong, G., Sawahata, M., Mori, D., Nagase, M., Fujii, H., Ueda, S., et al. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03316-4 · Cited by 5

Aberrant extracellular dopamine clearance in the prefrontal cortex exhibits ADHD ‐like behavior in NCX 3 heterozygous mice

Inagaki, R., Kita, S., Niwa, N., Fukunaga, K., Iwamoto, T., & Moriguchi, S. (2024) · FEBS Journal · doi:10.1111/febs.17339 · Cited by 6

Deletion of CaMKIIα disrupts glucose metabolism, glutamate uptake, and synaptic energetics in the cerebral cortex

Andersen, J. V., Westi, E. W., Griem‐Krey, N., Skotte, N. H., Schousboe, A., Aldana, B. I., & Wellendorph, P. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.15814 · Cited by 6

Translational Control Mechanisms in Synaptic Plasticity and Memory ☆

Costa‐Mattioli, M., & Klann, E. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21110-3 · Cited by 6

Physical interactions driving the activation/inhibition of calcium/calmodulin dependent protein kinase II

Asciutto, E. K., Pantano, S., & General, I. J. (2021) · Journal of Molecular Graphics and Modelling · doi:10.1016/j.jmgm.2021.107875 · 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

Large‐scale study of phosphoproteins involved in long‐term potentiation in the rat dentate gyrus in vivo

Chardonnet, S., Maréchal, P. L., Cheval, H., Caër, J. L., Decottignies, P., Laprévôte, O., Laroche, S., & Davis, S. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06280.x · Cited by 5

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

Interaction Between Cav2.1α1 and CaMKII in Cav2.1α1 Mutant Mice, Rolling Nagoya

Takahashi, E., Niimi, K., & Itakura, C. (2009) · Journal of Molecular Neuroscience · doi:10.1007/s12031-009-9216-5 · 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

Arc ubiquitination regulates endoplasmic reticulum-mediated Ca2+ release and CaMKII signaling

Ghane, M. A., Wei, W., Yakout, D. W., Allen, Z. D., Miller, C. L., Dong, B., Yang, J. J., Fang, N., & Mabb, A. M. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1091324 · Cited by 4

Loss of CAMK2G affects intrinsic and motor behavior but has minimal impact on cognitive behavior

Rigter, P. M. F., de Konink, C., & van Woerden, G. M. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.1086994 · Cited by 4

Spatiomolecular mapping reveals anatomical organization of heterogeneous cell types in the human nucleus accumbens

Ravichandran, P., Bach, S. V., Phillips, R. A., Valentine, M. R., Eagles, N. J., Du, Y., Rosario, I. D., AlGrain, H. A., Maguire, S. E., Miller, R. A., et al. (2026) · Neuron · doi:10.1016/j.neuron.2026.06.002 · Cited by 5

Role of densin‐180 in mouse ventral hippocampal neurons in 24‐hr retention of contextual fear conditioning

Kim, C., Kim, S., Kim, S., Roh, J., Jin, H., & Song, B. (2020) · Brain and Behavior · doi:10.1002/brb3.1891 · Cited by 3

Postsynaptic Targeting of Protein Kinases and Phosphatases

Strack, S., & Hell, J. W. (2008) · Springer eBooks · doi:10.1007/978-0-387-77232-5_16 · Cited by 3

Ca2+/Calmodulin-Dependent Protein Kinase II Signaling in Vascular Smooth Muscle

House, S. J., Zachar, M. M., Ginnan, R. G., Riper, D. A. V., & Singer, H. A. (2008) · Springer eBooks · doi:10.1007/978-0-387-09552-3_18 · Cited by 3

The Role of the Postsynaptic Density and the Spine Cytoskeleton in Synaptic Plasticity

Marcora, E. M., Carlisle, H. J., & Kennedy, M. B. (2008) · Elsevier eBooks · doi:10.1016/b978-012370509-9.00036-x · Cited by 4

Effects of citicoline administration on synaptic proteins in rapid eye movement sleep-deprived rats.

Çakır, A., Öcalan, B., Koç, C., Süyen, G. G., Cansev, M., & Kahveci, N. (2022) · PubMed Central · doi:10.22038/ijbms.2022.60756 · Cited by 2

Oxidation of CaMKIIα cysteines inhibits autonomous activation induced by phosphorylation

Rocco-Machado, N., Deng, M., He, Y., & Levine, R. L. (2024) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2024.110268 · Cited by 2

Esketamine-mediated alleviation of electroconvulsive shock-induced memory impairment is associated with the regulation of mGluR5 in depressive-like rats

Shen, Y., Wei, R., Liu, D., Lv, F., Ren, L., & Min, S. (2025) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2025.173955 · Cited by 3

Two selected models of missense mutations in mice for the study of learning behaviour

Mohajeri, M. H., & Giese, K.-P. (2011) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2011.12.003 · 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

Genetic Mechanisms of Memory Disorders (Excluding Alzheimer's Disease)

Kaas, G. A., Hawkins, K. E., & Sweatt, J. D. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21125-5 · Cited by 3

Translational Control Mechanisms in Synaptic Plasticity and Memory

Costa‐Mattioli, M., Sonenberg, N., & Klann, E. (2008) · Elsevier eBooks · doi:10.1016/b978-012370509-9.00037-1 · Cited by 2

Calcium-Calmodulin Kinase II (CaMKII) in Learning and Memory

Waxham, M. N. (2009) · Elsevier eBooks · doi:10.1016/b978-008045046-9.00818-4 · Cited by 2

Bidirectional changes in excitability upon loss of both CAMK2A and CAMK2BPreprint

Kool, M. J., Bodde, H. E., Elgersma, Y., & van Woerden, G. M. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.06.07.494679 · Cited by 2

Molecular control of temporal integration matches decision-making to motivational statePreprint

Gautham, A. K., Miner, L. E., Franco, M. N., Thornquist, S. C., & Crickmore, M. A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.03.01.582988 · Cited by 2

A Modeling and Analysis Study Reveals That CaMKII in Synaptic Plasticity Is a Dominant Affecter in CaM Systems in a T286 Phosphorylation-Dependent Manner

Stevens-Bullmore, H., Kulasiri, D., & Samarasinghe, S. (2022) · Molecules · doi:10.3390/molecules27185974 · Cited by 2

CaMKIIα hub ligands are unable to reverse known phenotypes in Angelman syndrome mice

Gauger, S. J., Lie, M. E. K., Wallaard, I., Tian, Y., Marek, A., Frølund, B., van Woerden, G. M., Elgersma, Y., Kornum, B. R., & Wellendorph, P. (2024) · Basic & Clinical Pharmacology & Toxicology · doi:10.1111/bcpt.14112 · Cited by 1

Phosphoproteomic Analysis of Cortical Tissue from Mice Lacking Both CaMKIIα and CaMKIIβ Identifies Novel In Vivo Substrates

Rigter, P. M. F., Bezstarosti, K., Koc, O. C., Perfitt, T. L., Demmers, J., Colbran, R. J., Stratton, M. M., Elgersma, Y., & van Woerden, G. M. (2026) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.5c00779 · Cited by 1

Prescient Synapses: Gating Future Neuronal Consciousness Through Synaptic Tagging and Metaplasticity

Connor, S. A., & Nguyen, P. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1761-7_11 · Cited by 1

[Signal transduction, pillar of the neurobiological integration of memory. An alternative view to the cholinergic hypothesis].

Mansilla‐Olivares, A. (2005) · PubMed · Cited by 1

Transcriptome profiling reveals major structural genes, transcription factors and biosynthetic pathways in refractory epilepsy in tropical region of China

Ben, X., Zhang, P., Li, C., Zou, Q., Cai, Y., Wang, S., Li, C., Feng, R., & Li, Q. (2025) · BMC Neurology · doi:10.1186/s12883-025-04216-2 · Cited by 1

Ca-CaM Protein Kinase 2

Kennedy, M., & Knuesel, I. (2008) · xPharm: The Comprehensive Pharmacology Reference · doi:10.1016/b978-008055232-3.60533-1 · Cited by 1

Upregulation of CaMKIIβ and Nogo-C mRNA in schizophrenia and the prevalence of CAA insert in the 3'UTR of the Nogo gene.

Novak, G. (2008) · TSpace (University of Toronto) · Cited by 1

Intrinsic and synaptic determinants of receptive field plasticity in Purkinje cells of the mouse cerebellumPreprint

Lin, T., Busch, S. E., & Hansel, C. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.07.19.549760 · Cited by 1

Pharmacological Enhancement of Adult Hippocampal Neurogenesis Improves Behavioral Pattern Separation in Young and Aged MicePreprint

Chang, W.-L., Tegang, K., Samuels, B. A., Saxe, M., Wichmann, J., David, D. J. P., Mendez‐David, I., Augustin, A., Fischer, H., Golling, S., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.02.01.578406 · Cited by 1

The role of CaMKII in cerebellar learning

Andreev, D. (2006)

Optical analysis of synaptic plasticity in rat hippocampus

Zhang, Y. (2008) · edoc (University of Basel) · doi:10.5451/unibas-004414662

When more is not more

Wells, W. A. (2002) · The Journal of Cell Biology · doi:10.1083/jcb1595rr1

Plasticity in eye movement control

Luo, C. (2005) · EUR Research Repository (Erasmus University Rotterdam)

Aus der Klinik und Poliklinik für Psychiatrie und Psychotherapie der Ludwig-Maximilians-Universität München

Möller, H. (2004)

Angelman syndrome (AS) is a severe neurological disorder that is associated with prominent movement and balance impairments that are widely considered to be due to defects of cerebellar origin. Here, using the cerebellar-specific vestibulo- ocular reflex (VOR) paradigm, we determined that cerebellar function is only mildly impaired in the Ube3a

Bruinsma, C. F., Schonewille, M., Gao, Z., Judson, M. C., Philpot, B. D., Hoebeek, F. E., van Woerden, G. M., Zeeuw, C. I. D., & Elgersma, Y. (2015)

Role of CaMKII and the GluN2B subunit of the NMDAR in dorsal striatal glutamatergic synaptic transmission, MSN morphology and striatal-based behaviors

Klug, J. R. (2012)

Roles of CaMKII in Learning and Memory ☆

Stephenson, J. R., & Colbran, R. J. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809324-5.21106-1

Interaction of the neuronal gap junction protein Connexin 36 with alpha Calcium/Calmodulin-dependent protein Kinase II

Akintürk, S. S. (2012) · Dokumentenrepositorium der RUB (Ruhr University Bochum)

The role of Ca2+/calmodulin-dependent kinase II in normal and abnormal early postnatal development

Gustin, R. M. (2010)

Investigation of CaMKII activation: a model of self-regulation

Hoffman, L. (2011)

Characterizing the TrkB Receptor as a Therapeutic Target for Treating Angelman Syndrome

Lau, K. A. (2020) · doi:10.26300/7gnr-qj74

Essential regulatory functions of CaMKII T286 phosphorylation in LTP and two distinct forms of LTDPreprint

Cook, S. G., Rumian, N. L., & Bayer, K. U. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.01.03.474759

The Cerebellum

Meyer, M. A. (2016) · Springer eBooks · doi:10.1007/978-3-319-39581-4_11

Calcium | Calcium/Calmodulin-Dependent Protein Kinase II

Hudmon, A., & Schulman, H. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-819460-7.00099-2

Adult Camk2a Gene Reinstatement Restores the Learning and Plasticity Deficits of Camk2a Knockout MicePreprint

Rigter, P. M. F., Wallaard, I., Jolfaei, M. A., Kingma, J., Post, L. C., Elgersma, M., Elgersma, Y., & van Woerden, G. M. (2022) · SSRN Electronic Journal · doi:10.2139/ssrn.4143785

Synaptic Tagging and Metaplasticity as Mediators of Neuronal Consciousness

Maity, S., & Connor, S. A. (2024) · Springer eBooks · doi:10.1007/978-3-031-54864-2_11

Simultaneous loss of CAMK2A and CAMK2B reveals endogenous in vivo substratesPreprint

Rigter, P. M. F., Bezstarosti, K., Koc, O. C., Perfitt, T. L., Demmers, J., Colbran, R. J., Stratton, M. M., Elgersma, Y., & van Woerden, G. M. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.11.17.624016

CaMKII mechanisms in plasticity, learning and memory: Approaches and concepts

Bayer, K. U., Brown, C. N., & Giese, K.-P. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15754-7.00057-2

Calcium/calmodulin-dependent protein kinase II in Schistosoma: Relation to praziquantel action and resistance

Abou-El-Naga, I. F. (2025) · Molecular and Biochemical Parasitology · doi:10.1016/j.molbiopara.2025.111686

Angelman Syndrome

Banko, J. L., & Weeber, E. J. (2008) · Elsevier eBooks · doi:10.1016/b978-012370509-9.00027-9

Conséquences d’une perturbation de l’expérience sensorimotrice sur la plasticité synaptique du cortex cérébral : implication de deux modifications post-traductionnelles, la phosphorylation et la O-GlcNAcylation

Fourneau, J. (2018) · theses.fr (ABES) · doi:10.70675/6324f6b7z65d0z4f8aza022zfaaa24669376

Protein Kinases and Synaptogenesis

Meier, J. C. (2006) · Springer eBooks · doi:10.1007/978-0-387-32562-0_22

Genetic Manipulation of Learning and Memory

Dunning, J. (2006) · Elsevier eBooks · doi:10.1016/b978-012397632-1/50014-9

Role of inhibitory autophosphorylation of calcium/calmodulin-dependent kinase II (αCAMKII) in persistent (>24h) hippocampal LTP and in LTD facilitated by novel object-place learning and recognition in mice

Goh, J. J., & Manahan‐Vaughan, D. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.01.022 · Cited by 20

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

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