- TTBK2 kinase substrate specificity and the impact of spinocerebellar-ataxia-causing mutations on expression, activity, localization and development
[作者:Bouskila, M; Esoof, N; Gay, L; Fang, EH; Deak, M; Begley, MJ; Cantley, LC; Prescott, A; Storey, KG; Alessi, DR,期刊:Biochemical Journal, 页码:157-167 , 文章类型: Article,,卷期:2011年437-Part 1]
- Mutations that truncate the C-terminal non-catalytic moiety of TTBK2 (tau tubulin kinase 2) cause the inherited, autosomal dominant, SCA11 (spinocerebellar ataxia type 11) movement disorder. In the present study we first...
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