The DOI matches its Crossref record; 43 of the 43 references it cites were found in a registry or an index.
Inhibitory Autophosphorylation of CaMKII Controls PSD Association, Plasticity, and Learning
Open accessAbstract
To investigate the function of the alpha calcium-calmodulin-dependent kinase II (alphaCaMKII) inhibitory autophosphorylation at threonines 305 and/or 306, we generated knockin mice that express alphaCaMKII that cannot undergo inhibitory phosphorylation. In addition, we generated mice that express the inhibited form of alphaCaMKII, which resembles the persistently phosphorylated kinase at these sites. Our data demonstrate that blocking inhibitory phosphorylation increases CaMKII in the postsynaptic density (PSD), lowers the threshold for hippocampal long-term potentiation (LTP), and results in hippocampal-dependent learning that seems more rigid and less fine-tuned. Mimicking inhibitory phosphorylation dramatically decreased the association of CaMKII with the PSD and blocked both LTP and learning. These data demonstrate that inhibitory phosphorylation has a critical role in plasticity and learning.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“However, T305A/T306A mutations increase CaMKII levels in PSDs and lower the threshold for LTP (87).”
From Synaptic memory and CaMKII (2023) · cites this paper as [87]
In the citing paper
“the results with the genetic deletion of CaMKIIα are more variable, some showing roughly a 50% block (87, 204–206) but some showing a complete block (121, 207, 208).”
From Synaptic memory and CaMKII (2023) · cites this paper as [87]
Citations
Cites
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
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
Self-citationControl 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
Self-citationImpaired 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
Self-citationA 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
Self-citationRegulatory 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
Cited by
Sorted by citations
Long-Term Potentiation and Memory
Lynch, M. A. (2004) · Physiological Reviews · doi:10.1152/physrev.00014.2003 · Cited by 2,074
Mechanisms of CaMKII action in long-term potentiation
Lisman, J., Yasuda, R., & Raghavachari, S. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3192 · Cited by 1,134
Calmodulin-kinases: modulators of neuronal development and plasticity.
Wayman, G. A., Lee, Y.-S., Tokumitsu, H., Silva, A., & Soderling, T. R. (2008) · Neuron · doi:10.1016/j.neuron.2008.08.021 · Cited by 567
Self-citationMolecular mechanisms underlying emotional learning and memory in the lateral amygdala
Rodrigues, S. M., Schafe, G. E., & LeDoux, J. E. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.014 · Cited by 491
Neurofibromin Regulation of ERK Signaling Modulates GABA Release and Learning
Cui, Y., Costa, R. M., Murphy, G. G., Elgersma, Y., Zhu, Y., Gutmann, D. H., Parada, L. F., Módy, I., & Silva, A. J. (2008) · Cell · doi:10.1016/j.cell.2008.09.060 · Cited by 445
Self-citationTrinidad, J. C., Barkan, D. T., Gulledge, B. F., Thalhammer, A., Šali, A., Schoepfer, R., & Burlingame, A. L. (2012) · Molecular & Cellular Proteomics · doi:10.1074/mcp.o112.018366 · Cited by 437
Ca2+/Calmodulin-dependent Protein Kinases
Swulius, M. T., & Waxham, M. N. (2008) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-008-8086-2 · Cited by 411
CaM Kinase: Still Inspiring at 40
Bayer, K. U., & Schulman, H. (2019) · Neuron · doi:10.1016/j.neuron.2019.05.033 · Cited by 314
Wiltgen, B. J., Brown, R. A. M., Talton, L. E., & Silva, A. J. (2004) · Neuron · doi:10.1016/j.neuron.2004.09.015 · Cited by 324
Self-citationCalcium/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
van Woerden, G. M., Harris, K. D., Hojjati, M. R., Gustin, R. M., Qiu, S., de Avila Freire, R., Jiang, Y.-H., Elgersma, Y., & Weeber, E. J. (2007) · Nature Neuroscience · doi:10.1038/nn1845 · Cited by 281
Self-citationRellos, P., Pike, A. C. W., Niesen, F. H., Salah, E., Lee, W. H., von Delft, F., & Knapp, S. (2010) · PLoS Biology · doi:10.1371/journal.pbio.1000426 · Cited by 279
Autophosphorylated CaMKIIα Acts as a Scaffold to Recruit Proteasomes to Dendritic Spines
Bingol, B., Wang, C.-F., Arnott, D., Cheng, D., Peng, J., & Sheng, M. (2010) · Cell · doi:10.1016/j.cell.2010.01.024 · Cited by 268
Weeber, E. J., Jiang, Y., Elgersma, Y., Varga, A. W., Carrasquillo, Y., Brown, S. E., Christian, J. M., Mirnikjoo, B., Silva, A. J., Beaudet, A. L., et al. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-07-02634.2003 · Cited by 262
Self-citationOtmakhov, N., Tao-Cheng, J.-H., Carpenter, S., Asrican, B., Dosemeci, A., Reese, T. S., & Lisman, J. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.2350-04.2004 · Cited by 258
Chao, L. H., Stratton, M. M., Lee, I., Rosenberg, O. S., Levitz, J., Mandell, D. J., Kortemme, T., Groves, J. T., Schulman, H., & Kuriyan, J. (2011) · Cell · doi:10.1016/j.cell.2011.07.038 · Cited by 258
Targeting of calcium/calmodulin-dependent protein kinase II
Colbran, R. J. (2004) · Biochemical Journal · doi:10.1042/bj20031547 · Cited by 241
The roles of protein kinases in learning and memoryPreprint
Giese, K.-P., & Mizuno, K. (2013) · Learning & Memory · doi:10.1101/lm.028449.112 · Cited by 238
Self-citationTime and tide in cerebellar memory formation
Zeeuw, C. I. D., & Yeo, C. H. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.10.008 · Cited by 232
αCaMKII Is Essential for Cerebellar LTD and Motor Learning
Hansel, C., de Jeu, M. T. G., Belmeguenaï, A., Houtman, S. H., Buitendijk, G. H. S., Andreev, D., Zeeuw, C. I. D., & Elgersma, Y. (2006) · Neuron · doi:10.1016/j.neuron.2006.08.013 · Cited by 225
Self-citationSynaptic plasticity and phosphorylation
Lee, H. (2006) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2006.06.003 · Cited by 222
Coultrap, S. J., Freund, R. K., O’Leary, H., Sanderson, J. L., Roche, K. W., Dell’Acqua, M. L., & Bayer, K. U. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.01.005 · Cited by 207
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
Kushner, S. A., Elgersma, Y., Murphy, G. G., Jaarsma, D., van Woerden, G. M., Hojjati, M. R., Cui, Y., LeBoutillier, J. C., Marrone, D. F., Choi, E. S., et al. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2836-05.2005 · Cited by 193
Self-citationCaMKII Isoforms in Learning and Memory: Localization and Function
Zalcman, G., Federman, N., & Romano, A. G. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00445 · Cited by 185
De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability
Küry, S., van Woerden, G. M., Besnard, T., Proietti Onori, M., Latypova, X., Towne, M. C., Cho, M. T., Prescott, T. E., Ploeg, M. A., Sanders, S., et al. (2017) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2017.10.003 · Cited by 185
Incontro, S., Díaz-Alonso, J., Iafrati, J., Vieira, M., Asensio, C. S., Sohal, V. S., Roche, K. W., Bender, K. J., & Nicoll, R. A. (2018) · Nature Communications · doi:10.1038/s41467-018-04439-7 · Cited by 171
Calmodulin kinases: essential regulators in health and disease
Takemoto‐Kimura, S., Suzuki, K., Horigane, S., Kamijo, S., Inoue, M., Sakamoto, M., Fujii, H., & Bito, H. (2017) · Journal of Neurochemistry · doi:10.1111/jnc.14020 · Cited by 175
Hudmon, A., LeBel, E., Roy, H., Sik, A., Schulman, H., Waxham, M. N., & De Koninck, P. (2005) · The Journal of Neuroscience · doi:10.1523/jneurosci.4698-04.2005 · Cited by 159
Belmeguenaï, A., Hosy, E., Bengtsson, F., Pedroarena, C. M., Piochon, C., Teuling, E., He, Q., Ohtsuki, G., de Jeu, M. T. G., Elgersma, Y., et al. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.3226-10.2010 · Cited by 158
Self-citationChocyk, A., Bobula, B., Dudys, D., Przyborowska, A., Majcher-Maślanka, I., Hess, G., & Wędzony, K. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12208 · Cited by 153
Visualization of Synaptic Ca2+/Calmodulin-Dependent Protein Kinase II Activity in Living Neurons
Takao, K., Okamoto, K., Nakagawa, T., Neve, R. L., Nagai, T., Miyawaki, A., Hashikawa, T., Kobayashi, S., & Hayashi, Y. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.0085-05.2005 · Cited by 146
Elgersma, Y., Sweatt, J. D., & Giese, K.-P. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3622-04.2004 · Cited by 150
Self-citationYamagata, Y., Kobayashi, S., Umeda, T., Inoue, A., Sakagami, H., Fukaya, M., Watanabe, M., Hatanaka, N., Totsuka, M., Yagi, T., et al. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.0707-09.2009 · Cited by 146
Optical induction of plasticity at single synapses reveals input-specific accumulation of αCaMKII
Zhang, Y.-P., Holbro, N., & Oertner, T. G. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0802940105 · Cited by 140
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
Rodrigues, S. M., Farb, C. R., Bauer, E. P., LeDoux, J. E., & Schafe, G. E. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.5303-03.2004 · Cited by 134
Griffith, L. C. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3604-04.2004 · Cited by 132
βCaMKII controls the direction of plasticity at parallel fiber–Purkinje cell synapses
van Woerden, G. M., Hoebeek, F. E., Gao, Z., Nagaraja, R. Y., Hoogenraad, C. C., Kushner, S. A., Hansel, C., Zeeuw, C. I. D., & Elgersma, Y. (2009) · Nature Neuroscience · doi:10.1038/nn.2329 · Cited by 132
Self-citationMolecular Switches at the Synapse Emerge from Receptor and Kinase Traffic
Hayer, A., & Bhalla, U. S. (2005) · PLoS Computational Biology · doi:10.1371/journal.pcbi.0010020 · Cited by 127
Stephenson, J. R., Wang, X., Perfitt, T. L., Parrish, W. P., Shonesy, B. C., Marks, C. R., Mortlock, D. P., Nakagawa, T., Sutcliffe, J. S., & Colbran, R. J. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.2068-16.2017 · Cited by 127
Nicoll, R. A., & Schulman, H. (2023) · Physiological Reviews · doi:10.1152/physrev.00034.2022 · Cited by 126
“Interestingly, the results with the genetic deletion of CaMKII a are more variable, some showing roughly a 50% block (87, 204 – 206) but some showing a complete block (121, 207, 208).”
BackgroundPi, H. J., Otmakhov, N., Lemelin, D., De Koninck, P., & Lisman, J. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0133-10.2010 · Cited by 125
Jiang, X., Lautermilch, N., Watari, H., Westenbroek, R., Scheuer, T., & Catterall, W. (2008) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.0710213105 · Cited by 106
Borgesius, N. Z., van Woerden, G. M., Buitendijk, G. H. S., Keijzer, N., Jaarsma, D., Hoogenraad, C. C., & Elgersma, Y. (2011) · Journal of Neuroscience · doi:10.1523/jneurosci.5105-10.2011 · Cited by 124
Self-citationStratton, M., Lee, I.-H., Bhattacharyya, M., Christensen, S. M., Chao, L. H., Schulman, H., Groves, J. T., & Kuriyan, J. (2014) · eLife · doi:10.7554/elife.01610 · Cited by 114
Fields, R. D., Lee, P. R., & Cohen, J. E. (2005) · Cell Calcium · doi:10.1016/j.ceca.2005.01.011 · Cited by 113
Bhattacharyya, M., Stratton, M. M., Going, C. C., McSpadden, E. D., Huang, Y., Susa, A. C., Elleman, A., Cao, Y. M., Pappireddi, N., Burkhardt, P., et al. (2016) · eLife · doi:10.7554/elife.13405 · Cited by 112
Huang, S., Treviño, M., He, K., Ardiles, Á. O., Pasquale, R. D., Guo, Y., Palacios, A. G., Huganir, R. L., & Kirkwood, A. (2012) · Neuron · doi:10.1016/j.neuron.2011.11.023 · Cited by 112
Azriel-Tamir, H., Sharir, H., Schwartz, B., & Hershfinkel, M. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m406581200 · Cited by 111
Nelson, A., Gittis, A. H., & du Lac, S. (2005) · Neuron · doi:10.1016/j.neuron.2005.04.009 · Cited by 108
Complexin II is essential for normal neurological function in mice
Glynn, D. (2003) · Human Molecular Genetics · doi:10.1093/hmg/ddg249 · Cited by 108
Mouse models of genetic effects on cognition: Relevance to schizophrenia
Papaleo, F., Lipska, B. K., & Weinberger, D. R. (2011) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.04.025 · Cited by 107
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
Self-citationRegulation of the Ca2+/CaM-Responsive Pool of CaMKII by Scaffold-Dependent Autophosphorylation
Lu, C. S., Hodge, J. J. L., Mehren, J. E., Sun, X. X., & Griffith, L. C. (2003) · Neuron · doi:10.1016/s0896-6273(03)00786-4 · Cited by 100
Centonze, D., Usiello, A., Costa, C., Picconi, B., Erbs, E., Bernardi, G., Borrelli, E., & Calabresi, P. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1274-04.2004 · Cited by 96
Novel insights into CaMKII function and regulation during memory formation
Lucchesi, W., Mizuno, K., & Giese, K.-P. (2010) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2010.10.009 · Cited by 106
Self-citationCerebellar and extracerebellar involvement in mouse eyeblink conditioning: the ACDC model
Boele, H. (2009) · Frontiers in Cellular Neuroscience · doi:10.3389/neuro.03.019.2009 · Cited by 94
Structural Insights into the Regulation of Ca2+/Calmodulin-Dependent Protein Kinase II (CaMKII)
Bhattacharyya, M., Karandur, D., & Kuriyan, J. (2020) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a035147 · Cited by 95
Yiu, A. P., Rashid, A. J., & Josselyn, S. A. (2011) · Neuropsychopharmacology · doi:10.1038/npp.2011.107 · Cited by 99
Dopamine depletion alters phosphorylation of striatal proteins in a model of Parkinsonism
Brown, A. M., Deutch, A. Y., & Colbran, R. J. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04190.x · Cited by 96
Lü, W., Isozaki, K., Roche, K. W., & Nicoll, R. A. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1016289107 · Cited by 97
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
Self-citationEmotional tagging—A simple hypothesis in a complex reality
Bergado, J. A., Lucas, M., & Richter‐Levin, G. (2011) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2011.03.004 · Cited by 98
Hansen, N., & Manahan‐Vaughan, D. (2014) · Cerebral Cortex · doi:10.1093/cercor/bht429 · Cited by 96
Translocation of CaM kinase II to synaptic sites in vivo
Gleason, M. R., Higashijima, S., Dallman, J. E., Liu, K., Mandel, G., & Fetcho, J. R. (2003) · Nature Neuroscience · doi:10.1038/nn1011 · Cited by 90
Rostas, J. A. P., & Skelding, K. A. (2023) · Cells · doi:10.3390/cells12030401 · Cited by 85
Robison, A. J., Bartlett, R. K., Bass, M. A., & Colbran, R. J. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m508189200 · Cited by 84
CAMK2-Dependent Signaling in Neurons Is Essential for Survival
Kool, M. J., Onori, M. P., Borgesius, N. Z., van de Bree, J. E., Elgersma, M., Nio, E., Bezstarosti, K., Buitendijk, G. H. S., Jolfaei, M. A., Demmers, J., et al. (2019) · Journal of Neuroscience · doi:10.1523/jneurosci.1341-18.2019 · Cited by 79
Self-citationO’Leary, H., Liu, W. H., Rorabaugh, J. M., Coultrap, S. J., & Bayer, K. U. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.233668 · Cited by 77
Tsui, J., Inagaki, M., & Schulman, H. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m407653200 · Cited by 78
Cooke, S. F., Wu, J., Plattner, F., Errington, M., Rowan, M., Peters, M., Hirano, A., Bradshaw, K. D., Anwyl, R., Bliss, T. V. P., et al. (2006) · The Journal of Physiology · doi:10.1113/jphysiol.2006.111559 · Cited by 77
Self-citationMechanisms of Ca2+/calmodulin-dependent kinase II activation in single dendritic spines
Chang, J.-Y., Nakahata, Y., Hayano, Y., & Yasuda, R. (2019) · Nature Communications · doi:10.1038/s41467-019-10694-z · Cited by 77
Christian, D., Alexander, N. J., Diaz, M. R., Robinson, S. L., & McCool, B. A. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2012.02.017 · Cited by 76
CaMKII holoenzyme mechanisms that govern the LTP versus LTD decision
Cook, S. G., Buonarati, O. R., Coultrap, S. J., & Bayer, K. U. (2021) · Science Advances · doi:10.1126/sciadv.abe2300 · Cited by 74
Calcium/Calmodulin-Dependent Protein Kinase II: An Unforgettable Kinase
Griffith, L. C. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.2888-04.2004 · Cited by 77
Baucum, A. J., Shonesy, B. C., Rose, K. L., & Colbran, R. J. (2015) · ACS Chemical Neuroscience · doi:10.1021/cn500337u · Cited by 72
Schulman, H. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.3606-04.2004 · Cited by 71
Lee, I., Eriksson, P., Fredriksson, A., Buratovic, S., & Viberg, H. (2015) · Toxicology · doi:10.1016/j.tox.2015.06.010 · Cited by 75
CaMKII, an Enzyme on the Move: Regulation of Temporospatial Localization
Griffith, L. C. (2003) · Molecular Interventions · doi:10.1124/mi.3.7.386 · Cited by 68
Inducible and Selective Erasure of Memories in the Mouse Brain via Chemical-Genetic Manipulation
Cao, X., Wang, H., Mei, B., An, S., Yin, L., Wang, L. P., & Tsien, J. Z. (2008) · Neuron · doi:10.1016/j.neuron.2008.08.027 · Cited by 69
Hasegawa, S., Furuichi, T., Yoshida, T., Endoh, K., Kato, K., Sado, M., Maeda, R., Kitamoto, A., Miyao, T., Suzuki, R., et al. (2009) · Molecular Brain · doi:10.1186/1756-6606-2-6 · Cited by 67
CASK and CaMKII function in the mushroom body α′/β′ neurons during Drosophila memory formation
Malik, B. R., Gillespie, J. M., & Hodge, J. J. L. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00052 · Cited by 66
Sałaciak, K., Koszałka, A., Żmudzka, E., & Pytka, K. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094307 · Cited by 67
Zhang, L., Kirschstein, T., Sommersberg, B., Merkens, M., Manahan‐Vaughan, D., Elgersma, Y., & Beck, H. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2086-05.2005 · Cited by 63
Self-citationMatsuo, N. (2009) · Frontiers in Behavioral Neuroscience · doi:10.3389/neuro.08.020.2009 · Cited by 62
The Synaptic Proteome during Development and Plasticity of the Mouse Visual Cortex
Dahlhaus, M., Li, K. W., van der Schors, R. C., Saiepour, M. H., van Nierop, P., Heimel, J. A., Hermans, J. M., Loos, M., Smit, A. B., & Levelt, C. N. (2011) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m110.005413 · Cited by 60
CaMKIIβ in Neuronal Development and Plasticity: An Emerging Candidate in Brain Diseases
Nicole, O., & Pacary, E. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21197272 · Cited by 65
Woolfrey, K. M., O’Leary, H., Goodell, D. J., Robertson, H. R., Horne, E. A., Coultrap, S. J., Dell’Acqua, M. L., & Bayer, K. U. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.m117.813808 · Cited by 56
Flexible linkers in CaMKII control the balance between activating and inhibitory autophosphorylation
Bhattacharyya, M., Lee, Y. K., Muratcioglu, S., Qiu, B., Nyayapati, P., Schulman, H., Groves, J. T., & Kuriyan, J. (2020) · eLife · doi:10.7554/elife.53670 · Cited by 58
Tian, Y., Yabuki, Y., Moriguchi, S., Fukunaga, K., Mao, P., Hong, L., Lu, Y., Wang, R., Ahmed, M. M., Liao, M., et al. (2013) · Journal of Pineal Research · doi:10.1111/jpi.12081 · Cited by 56
Ishida, A., Shigeri, Y., Taniguchi, T., & Kameshita, I. (2003) · Pharmacology and Therapeutics · doi:10.1016/j.pharmthera.2003.09.003 · Cited by 52
Steinkellner, T., Yang, J., Montgomery, T., Chen, W., Winkler, M.-T., Sučić, S., Lübec, G., Freissmuth, M., Elgersma, Y., Sitte, H. H., et al. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.367219 · Cited by 56
Self-citationOhmae, S., Takemoto‐Kimura, S., Okamura, M., Adachi-Morishima, A., Nonaka, M., Fuse, T., Kida, S., Tanji, M., Furuyashiki, T., Arakawa, Y., et al. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m513212200 · Cited by 55
Interplay of enzymatic and structural functions of Ca MKII in long‐term potentiation
Kim, K., Saneyoshi, T., Hosokawa, T., Okamoto, K., & Hayashi, Y. (2016) · Journal of Neurochemistry · doi:10.1111/jnc.13672 · Cited by 53
In Vivo Amphetamine Action is Contingent on αCaMKII
Steinkellner, T., Mus, L., Eisenrauch, B., Constantinescu, A., Leo, D., Konrad, L. K., Rickhag, M., Sørensen, G., Efimova, E. V., Kong, E., et al. (2014) · Neuropsychopharmacology · doi:10.1038/npp.2014.124 · Cited by 53
Dateki, M., Horii, T., Kasuya, Y., Mochizuki, R., Nagao, Y., Ishida, J., Sugiyama, F., Tanimoto, K., Yagami, K., Imai, H., et al. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m414033200 · Cited by 53
CASK regulates CaMKII autophosphorylation in neuronal growth, calcium signaling, and learning
Gillespie, J. M., & Hodge, J. J. L. (2013) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2013.00027 · Cited by 53
Autonomous CaMKII requires further stimulation by Ca 2+ /calmodulin for enhancing synaptic strength
Barcomb, K., Buard, I., Coultrap, S. J., Kulbe, J. R., O'Leary, H., Benke, T. A., & Bayer, K. U. (2014) · The FASEB Journal · doi:10.1096/fj.14-250407 · Cited by 52
Mohanan, A. G., Gunasekaran, S., Jacob, R. S., & Omkumar, R. V. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.855752 · Cited by 55
Metadata
- Authors
- Elgersma, Y., Fedorov, N. B., Ikonen, S., Choi, E. S., Elgersma, M., Carvalho, O. M., Giese, K. P., & Silva, A. J.
- Affiliations
- University of California, Los Angeles (US)
- Corresponding author
- Silva, Alcino J
- Venue
- Neuron
- Publisher
- Elsevier BV
- Published
- 2002-10
- Volume
- 36
- Issue
- 3
- Pages
- 493-505
- ISSN
- 0896-6273 (ISSN-L)
- OpenAlex
- W2035831063
- Cited by
- 290
- References
- 43
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 17 · 2023: 11 · 2022: 14 · 2021: 9 · 2020: 10 · 2019: 7 · 2018: 11 · 2017: 15 · 2016: 8 · 2015: 8 · 2014: 18 · 2013: 12 · 2012: 18
- FWCI
- 5.11
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Neuron (publishedVersion)
- PubMed (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Research Portal (King's College London) (submittedVersion)
- Funders
- National Institute on Aging (AG 13622)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Keywords
- CaMKII, postsynaptic density, long-term potentiation, hippocampal plasticity, hippocampus-dependent learning, knock-in mice, synaptic plasticity
- MeSH terms
- Animals, Electric Stimulation, Female, Hippocampus, Learning, Male, Membrane Potentials, Mice, Transgenic, Synaptic Transmission, Organ Culture Techniques, Phosphorylation, Synaptic Membranes, Gene Expression Regulation, Enzymologic, Presynaptic Terminals, Long-Term Potentiation, Calcium-Calmodulin-Dependent Protein Kinases, Excitatory Amino Acid Antagonists, Maze Learning, Long-Term Synaptic Depression, Mice, Calcium-Calmodulin-Dependent Protein Kinase Type 2
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review