Abstract
Background: Tau is hyperphosphorylated in the tauopathies. Targeting Tau kinases CDK5 and GSK3β represents a potential therapeutic approach. Results: Inhibitors of Tau kinases are neuroprotective, decrease PHF-1 immunoreactivity, and induce recovery of memory by fear conditioning. Conclusion: Diaminothiazoles as CDK5 and GSK3β inhibitors improve the tauopathy in mouse models. Significance: Dual kinase inhibition can be critical for efficacy when treating tauopathies. © 2013 by The American Society for Biochemistry and Molecular Biology, Inc.
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CITATION STYLE
Zhang, X., Hernandez, I., Rei, D., Mair, W., K. Laha, J., Cornwell, M. E., … Kosik, K. S. (2013). Diaminothiazoles modify tau phosphorylation and improve the tauopathy in mouse models. Journal of Biological Chemistry, 288(30), 22042–22056. https://doi.org/10.1074/jbc.M112.436402
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