CaMKIIβ Functions As an F-Actin Targeting Module that Localizes CaMKIIα/β Heterooligomers to Dendritic Spines

Control of memory formation through regulated expression of a CaMKII transgene

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Deficient Hippocampal Long-Term Potentiation in α-Calcium-Calmodulin Kinase II Mutant Mice

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

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

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

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Rapid Actin-Based Plasticity in Dendritic Spines

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Evidence for a Role of Dendritic Filopodia in Synaptogenesis and Spine Formation

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

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Contrasting properties of two forms of long-term potentiation in the hippocampus

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The Multifunctional Calcium/Calmodulin-Dependent Protein Kinase: From Form to Function

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Calcium/Calmodulin-Dependent Protein Kinase II Mediates Hippocampal Glutamatergic Plasticity During Benzodiazepine Withdrawal

Shen, G., Sickle, B. J. V., & Tietz, E. I. (2010) · Neuropsychopharmacology · doi:10.1038/npp.2010.61 · Cited by 26

Differential roles for CaM kinases in mediating excitation–morphogenesis coupling during formation and maturation of neuronal circuits

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The Long 3′UTR mRNA ofCaMKIIIs Essential for Translation-Dependent Plasticity of Spontaneous Release inDrosophila melanogaster

Kuklin, E. A., Alkins, S., Bakthavachalu, B., Genco, M. C., Sudhakaran, I. P., Raghavan, K. V., Ramaswami, M., & Griffith, L. C. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.1313-17.2017 · Cited by 24

Photoreceptor regulated expression of Ca2+/Calmodulin-dependent protein kinase II in the mouse retina

Liu, O. L., Li, G., McCall, M. A., & Cooper, N. G. F. (2000) · Molecular Brain Research · doi:10.1016/s0169-328x(00)00203-5 · Cited by 23

Studying the Protein Organization of the Postsynaptic Density by a Novel Solid Phase- and Chemical Cross-linking-based Technology

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"MEMORY BYTES" — MOLECULAR MATCH FOR CaMKII PHOSPHORYLATION ENCODING OF MICROTUBULE LATTICES

Hameroff, S. R., Craddock, T. J. A., & Tuszyński, J. A. (2010) · Journal of Integrative Neuroscience · doi:10.1142/s0219635210002482 · Cited by 23

Spatiotemporal maps of CaMKII in dendritic spines

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δ Ca2+/Calmodulin‐Dependent Protein Kinase IIIsozyme‐Specific Induction of Neurite Outgrowth in P19 Embryonal Carcinoma Cells

Johnson, L. D., Willoughby, C. A., Burke, S. H., Paik, D. S., Jenkins, K. J., & Tombes, R. M. (2000) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2000.0752380.x · Cited by 21

The multi-PDZ domain protein MUPP1 is a cytoplasmic ligand for the membrane-spanning proteoglycan NG2

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Proteomics on the role of muscone in the “consciousness-restoring resuscitation” effect of musk on ischemic stroke

Han, B., Zhao, Y., Yao, J., Li, N., Fang, T., Wang, Y., Meng, Z., & Liu, W. (2022) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2022.115475 · Cited by 20

Ganglioside/protein kinase signals triggering cytoskeletal actin reorganization

Higashi, H., & Chen, N. H. (2003) · Glycoconjugate Journal · doi:10.1023/b:glyc.0000016742.88750.1a · Cited by 20

The identification of a second actin-binding region in spinophilin/neurabin II

Barnes, A. P., Smith, F. D., VanDongen, H. M. A., VanDongen, A. M. J., & Milgram, S. L. (2004) · Molecular Brain Research · doi:10.1016/j.molbrainres.2003.12.020 · Cited by 20

Analysis of Protein Complex Hierarchy in Living Cells

Piljić, A., & Schultz, C. (2008) · ACS Chemical Biology · doi:10.1021/cb8002539 · Cited by 19

Immunohistochemical study of Ca2+/calmodulin-dependent protein kinase II in the Drosophila brain using a specific monoclonal antibody

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Identification of the isoforms of Ca2+/calmodulin‐dependent protein kinase II and expression of brain‐derived neurotrophic factor mRNAs in the substantia nigra

Kamata, A., Takeuchi, Y., & Fukunaga, K. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03531.x · Cited by 19

Studies of signal transduction events using chimeras to green fluorescent protein

Meyer, T., & Oancea, E. (2000) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(00)27298-4 · Cited by 19

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

GABAA Receptor Subunit Transcriptional Regulation, Expression Organization, and Mediated Calmodulin Signaling in Prefrontal Cortex of Rats Showing Testosterone-Mediated Impulsive Behavior

Agrawal, J., & Dwivedi, Y. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.600099 · Cited by 18

Synaptic activity and F-actin coordinately regulate CaMKIIα localization to dendritic postsynaptic sites in developing hippocampal slices

Ahmed, R., Zha, X., Green, S. H., & Dailey, M. E. (2005) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2005.08.020 · Cited by 18

N-methyl-d-aspartate receptor dependent transcriptional regulation of two calcium/calmodulin-dependent protein kinase type II isoforms in rodent cerebral cortex

Murray, K. D., Isackson, P. J., & Jones, E. G. (2003) · Neuroscience · doi:10.1016/j.neuroscience.2003.07.015 · Cited by 18

Interleukin-10 prevents the hypoxia-induced decreases in expressions of AMPA receptor subunit GluA1 and alpha subunit of Ca2+/calmodulin-dependent protein kinase II in hippocampal neurons

Savina, T. A., Shchipakina, T., Levin, S. G., & Godukhin, O. V. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2012.11.023 · Cited by 17

Non-canonical heterogeneous cellular distribution and co-localization of CaMKIIα and CaMKIIβ in the spinal superficial dorsal horn

Larsson, M. (2017) · Brain Structure and Function · doi:10.1007/s00429-017-1566-0 · Cited by 17

Sustained CaMKII Delta Gene Expression Is Specifically Required for Long-Lasting Memories in Mice

Zalcman, G., Federman, N., Fiszbein, A., de la Fuente, V., Ameneiro, L., Schor, I. E., & Romano, A. G. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1144-3 · Cited by 18

Opposite regulation of inhibitory synaptic plasticity by α and β subunits of Ca2+/calmodulin‐dependent protein kinase II

Nagasaki, N., Hirano, T., & Kawaguchi, S. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2014.280230 · Cited by 16

Neuronal CaMKII acts as a structural kinase

Lin, Y., & Redmond, L. (2009) · Communicative & Integrative Biology · doi:10.4161/cib.2.1.7426 · Cited by 16

Distinct roles of α- and βCaMKII in controlling long-term potentiation of GABAA-receptor mediated transmission in murine Purkinje cells

Gao, Z., van Woerden, G. M., Elgersma, Y., Zeeuw, C. I. D., & Hoebeek, F. E. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00016 · Cited by 16

A Model of NMDA Receptor Control of F-actin Treadmilling in Synaptic Spines and Their Growth

Bennett, M. R., Farnell, L., & Gibson, W. G. (2010) · Bulletin of Mathematical Biology · doi:10.1007/s11538-010-9614-4 · Cited by 17

Molecular basis of interactions between CaMKII and α-actinin-2 that underlie dendritic spine enlargement

Curtis, A. J., Zhu, J., Penny, C. J., & Gold, M. G. (2023) · eLife · doi:10.7554/elife.85008 · Cited by 15

Modelling the dynamics of CaMKII–NMDAR complex related to memory formation in synapses: The possible roles of threonine 286 autophosphorylation of CaMKII in long term potentiation

He, Y., Kulasiri, D., & Samarasinghe, S. (2014) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2014.11.001 · Cited by 14

Systems biology of synaptic plasticity: A review on N-methyl-d-aspartate receptor mediated biochemical pathways and related mathematical models

He, Y., Kulasiri, D., & Samarasinghe, S. (2014) · Biosystems · doi:10.1016/j.biosystems.2014.06.005 · Cited by 15

Spine Remodeling and Synaptic Modification

Wang, X., & Zhou, Q. (2010) · Molecular Neurobiology · doi:10.1007/s12035-009-8093-9 · Cited by 18

Dendritic spine morphology and dynamics in health and disease

Webb, D. J., Lee, S. N., & Zhang, H. (2015) · Cell Health and Cytoskeleton · doi:10.2147/chc.s82214 · Cited by 17

Sensitizing exposure to amphetamine increases AMPA receptor phosphorylation without increasing cell surface expression in the rat nucleus accumbens

Wang, Q., Li, D., Bubula, N., Campioni, M. R., McGehee, D. S., & Vezina, P. (2017) · Neuropharmacology · doi:10.1016/j.neuropharm.2017.02.018 · Cited by 16

The role of calcium and CaMKII in sleep

Wang, Y., Minami, Y., Ode, K. L., & Ueda, H. R. (2022) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2022.1059421 · Cited by 16

Binding of Filamentous Actin to CaMKII as Potential Regulation Mechanism of Bidirectional Synaptic Plasticity by β CaMKII in Cerebellar Purkinje Cells

Pinto, T. M., Schilstra, M. J., Roque, A. C., & Steuber, V. (2020) · Scientific Reports · doi:10.1038/s41598-020-65870-9 · Cited by 14

Electron tomographic structure and protein composition of isolated rat cerebellar, hippocampal and cortical postsynaptic densities

Farley, M. M., Swulius, M. T., & Waxham, M. N. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.07.062 · Cited by 14

Chronic membrane depolarization-induced morphological alteration of developing neurons

Sohya, K., Kitamura, A., & Akaneya, Y. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2006.11.045 · Cited by 15

CaMKIIβ is localized in dendritic spines as both drebrin‐dependent and drebrin‐independent pools

Yamazaki, H., Sasagawa, Y., Yamamoto, H., Bito, H., & Shirao, T. (2018) · Journal of Neurochemistry · doi:10.1111/jnc.14449 · Cited by 14

SK Channel Modulates Synaptic Plasticity by Tuning CaMKIIα/β Dynamics

Shrestha, A., Sultana, R., Lee, C. C., & Ogundele, O. M. (2019) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2019.00018 · Cited by 13

Protein phosphatases regulate the growth of developing neurites

Monroe, J. D., & Heathcote, R. D. (2013) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2013.01.005 · Cited by 15

Network, Cellular, and Molecular Mechanisms Underlying Long-Term Memory Formation

Carasatorre, M., & Ramı́rez-Amaya, V. (2012) · Current topics in behavioral neurosciences · doi:10.1007/7854_2012_229 · Cited by 14

Transient viral‐mediated overexpression of α‐calcium/calmodulin‐dependent protein kinase II in the nucleus accumbens shell leads to long‐lasting functional upregulation of α‐amino‐3‐hydroxyl‐5‐methyl‐4‐isoxazole‐propionate receptors: dopamine type‐1 receptor and protein kinase A dependence

Singer, B. F., Loweth, J. A., Neve, R. L., & Vezina, P. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07155.x · Cited by 13

Understanding the pathogenetic mechanisms underlying altered neuronal function associated with CAMK2B mutations

Borghi, R., Trivisano, M., Specchio, N., Tartaglia, M., & Compagnucci, C. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105299 · Cited by 13

Visual-mediated regulation of retinal CaMKII and its GluR1 substrate is age-dependent

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Developmentally regulated expression of CaMKII and iGluRs in the rat retina

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

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CaMKIIβ knockdown decreases store-operated calcium entry in hippocampal dendritic spines

Zernov, N., Борисович, Б. И., & Александровна, П. Е. (2022) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2022.01.001 · Cited by 12

Developmental restoration of LTP deficits in heterozygous CaMKIIα KO mice

Goodell, D. J., Benke, T. A., & Bayer, K. U. (2016) · Journal of Neurophysiology · doi:10.1152/jn.00518.2016 · Cited by 12

Local and Relayed Effects of Deep Brain Stimulation of the Pedunculopontine Nucleus

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Role of β isoform‐specific insertions of Ca2+/calmodulin‐dependent protein kinase II

Urushihara, M., & Yamauchi, T. (2001) · European Journal of Biochemistry · doi:10.1046/j.1432-1327.2001.02410.x · Cited by 12

Gene expression profile of Dclk1+ cells in intestinal tumors

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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

Two splice variants of CaMKII-anchoring protein are present in the sarcoplasmic reticulum of rabbit fast-twitch muscle

Damiani, E., Sacchetto, R., Salviati, L., & Margreth, A. (2003) · Biochemical and Biophysical Research Communications · doi:10.1016/s0006-291x(03)00110-4 · Cited by 11

Overexpression of βCaMKII impairs behavioral flexibility and NMDAR-dependent long-term depression in the dentate gyrus

Yin, P., Xu, H., Wang, Q., Wang, J., Yin, L., Xu, M., Xie, Z., Liu, W., & Cao, X. (2016) · Neuropharmacology · doi:10.1016/j.neuropharm.2016.12.013 · Cited by 10

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

Characterization of mouse neuronal Ca2+/calmodulin kinase II inhibitor α

Saha, S., Datta, K., & Rangarajan, P. N. (2007) · Brain Research · doi:10.1016/j.brainres.2007.02.018 · Cited by 10

Binding of CaMKII to the giant muscle protein projectin: stimulation of CaMKII activity by projectin

Fährmann, M., Erfmann, M., & Beinbrech, G. (2002) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/s0304-4165(01)00251-3 · Cited by 10

Traveling Waves in One-Dimensional Excitable Media

Bressloff, P. C. (2013) · Lecture notes on mathematical modelling in the life sciences · doi:10.1007/978-1-4614-8866-8_2 · Cited by 8

Effects of Camk2b Overexpression and Underexpression on the Proteome of Rat Hippocampal Neurons

Yang, C., Zhang, M., Li, S., Yi, F., Huang, H., Xie, H., Liu, H., Huang, R., & Zhou, J. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.08.019 · Cited by 9

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

Structural and functional characterization of the IgSF21-neurexin2α complex and its related signaling pathways in the regulation of inhibitory synapse organization

Chofflet, N., Naito, Y., Pastore, A. J., Padmanabhan, N., Nguyen, P. T., Poitras, C., Feller, B., Yi, N., Prooijen, J. V., Khaled, H., et al. (2024) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2024.1371145 · Cited by 9

Proteomic measures of gamma oscillations

Byrum, S. D., Washam, C. L., Tackett, A. J., García‐Rill, E., Bisagno, V., & Urbano, F. J. (2019) · Heliyon · doi:10.1016/j.heliyon.2019.e02265 · Cited by 8

Is MYND Domain-Mediated Assembly of SMYD3 Complexes Involved in Calcium Dependent Signaling?

Zhang, Y., Li, C., & Yang, Z. (2019) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2019.00121 · Cited by 8

Predicting protein–protein interactions in the post synaptic density

Bar-Shira, O., & Chechik, G. (2013) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2013.04.004 · Cited by 7

Conformational coupling by trans-phosphorylation in calcium calmodulin dependent kinase II

Pandini, A., Schulman, H., & Khan, S. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006796 · Cited by 7

Proteomic Analysis of Dendritic Filopodia-Rich Fraction Isolated by Telencephalin and Vitronectin Interaction

Furutani, Y., & Yoshihara, Y. (2018) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2018.00027 · Cited by 7

ERK1/2-Dependent Phosphorylation of GABAB1(S867/T872), Controlled by CaMKIIβ, Is Required for GABAB Receptor Degradation under Physiological and Pathological Conditions

Bhat, M. A., Grampp, T., & Benke, D. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241713436 · Cited by 7

Channel-interacting PDZ protein, ‘CIPP’, interacts with proteins involved in cytoskeletal dynamics

Alpi, E., Landi, E., Barilari, M., Serresi, M., Salvadori, P. A., Bachi, A., & Dente, L. (2009) · Biochemical Journal · doi:10.1042/bj20081387 · Cited by 7

Studying the protein–protein interactions in the postsynaptic density by means of immunoabsorption and chemical crosslinking

Chang, C., Peng, S., Cheng, W., Liu, S., Cheng, H., Huang, S., & Chang, Y. (2007) · PROTEOMICS - CLINICAL APPLICATIONS · doi:10.1002/prca.200700327 · Cited by 7

Stimulation-induced changes in diffusion and structure of calmodulin and calmodulin-dependent protein kinase II proteins in neurons

Heidarinejad, M., Nakamura, H., & Inoue, T. (2018) · Neuroscience Research · doi:10.1016/j.neures.2018.01.003 · Cited by 7

Protein Phosphatase 2B Dual Function Facilitates Synaptic Integrity and Motor Learning

Lin, Z., Wu, B., Paul, M. W., Li, K. W., Yao, Y., Smal, I., Onori, M. P., Hasanbegović, H., Bezstarosti, K., Demmers, J., et al. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.1741-20.2021 · Cited by 6

Calcium/Calmodulin-Dependent Protein Kinase II

Kennedy, M. B. (2010) · Elsevier eBooks · doi:10.1016/b978-0-12-374145-5.00075-9 · Cited by 6

Calcium/calmodulin‐dependent protein kinase IIβ isoform is expressed in motor neurons during axon outgrowth and is part of slow axonal transport

Lund, L. M., & McQuarrie, I. G. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10162 · Cited by 6

Super-resolution imaging reveals the relationship between CaMKIIβ and drebrin within dendritic spines.

Yamazaki, H., Koganezawa, N., Yokoo, H., Sekino, Y., & Shirao, T. (2023) · Neurosciences research · doi:10.1016/j.neures.2023.08.002 · Cited by 5

Initiation and Regulation of CNS Autoimmunity: Balancing Immune Surveillance and Inflammation in the CNS

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Cyclin Y, a novel actin-binding protein, regulates spine plasticity through the cofilin-actin pathway

Hwang, H., Hur, Y.-N., Sohn, H., Seo, J., Hong, J., Cho, E., Choi, Y., Lee, S., Song, S., Lee, A.-R., et al. (2020) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2020.101915 · Cited by 5

Hub stability in the calcium calmodulin-dependent protein kinase II

Chien, C.-T. H., Puhl, H. L., Vogel, S. S., Molloy, J. E., Chiu, W., & Khan, S. (2024) · Communications Biology · doi:10.1038/s42003-024-06423-y · Cited by 5

Differential subcellular distribution of Ca2+/calmodulin‐dependent protein kinase II isoforms in the striatum and NG108‐15 cells

Takeuchi, Y., Nomura, K., & Fukunaga, K. (2004) · Journal of Neuroscience Research · doi:10.1002/jnr.20010 · Cited by 5

Aversive Olfactory Conditioning

Parma, V., Wilson, D. A., & Lundström, J. N. (2017) · Springer eBooks · doi:10.1007/978-3-319-26932-0_41 · Cited by 5

Alternative splicing in the variable domain of CaMKIIβ affects the level of F-actin association in developing neurons.

Zheng, J., Redmond, L., Xu, C., Kuang, J., & Liao, W. (2014) · PubMed Central · Cited by 4

Alpha calcium/calmodulin dependent protein kinase II in learning-dependent plasticity of mouse somatosensory cortex.

Skibinska-Kijek, A., Radwańska, A., & Kossut, M. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2007.11.012 · Cited by 6

Bioinformatic search for Ca2+- and calmodulin-dependent protein kinases potentially associated with the regulation of plant cytoskeleton

Novozhylov, D. O., Karpov, P. A., & Blume, Y. B. (2017) · Cytology and Genetics · doi:10.3103/s0095452717040053 · Cited by 4

Global sensitivity analysis of a model related to memory formation in synapses: Model reduction based on epistemic parameter uncertainties and related issues

Kulasiri, D., Liang, J., He, Y., & Samarasinghe, S. (2017) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2017.02.003 · Cited by 3

Multi-physics modeling and finite-element formulation of neuronal dendrite growth with electrical polarization

Wang, S., Wang, X., & Holland, M. A. (2023) · Brain Multiphysics · doi:10.1016/j.brain.2023.100071 · Cited by 3

Waves in Excitable Neural Fields

Bressloff, P. C. (2013) · Lecture notes on mathematical modelling in the life sciences · doi:10.1007/978-1-4614-8866-8_7 · 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

Neural Field Model of Binocular Rivalry Waves

Bressloff, P. C. (2013) · Lecture notes on mathematical modelling in the life sciences · doi:10.1007/978-1-4614-8866-8_8 · 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

CaMKII: Mechanisms of a Prototypical Memory Model

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The Synaptic Protein Network Associated with Ionotropic Glutamate Receptors

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