Matches in DBpedia 2016-04 for { ?s ?p "Tau tubulin kinase 2 is a protein in humans that is encoded by the TTBK2 gene.This gene encodes a serine-threonine kinase that putatively phosphorylates tau and tubulin proteins. Mutations in this gene cause spinocerebellar ataxia type 11 (SCA11); a neurodegenerative disease characterized by progressive ataxia and atrophy of the cerebellum and brainstem."@en }
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- TTBK2 abstract "Tau tubulin kinase 2 is a protein in humans that is encoded by the TTBK2 gene.This gene encodes a serine-threonine kinase that putatively phosphorylates tau and tubulin proteins. Mutations in this gene cause spinocerebellar ataxia type 11 (SCA11); a neurodegenerative disease characterized by progressive ataxia and atrophy of the cerebellum and brainstem.".
- Q18051430 abstract "Tau tubulin kinase 2 is a protein in humans that is encoded by the TTBK2 gene.This gene encodes a serine-threonine kinase that putatively phosphorylates tau and tubulin proteins. Mutations in this gene cause spinocerebellar ataxia type 11 (SCA11); a neurodegenerative disease characterized by progressive ataxia and atrophy of the cerebellum and brainstem.".
- TTBK2 comment "Tau tubulin kinase 2 is a protein in humans that is encoded by the TTBK2 gene.This gene encodes a serine-threonine kinase that putatively phosphorylates tau and tubulin proteins. Mutations in this gene cause spinocerebellar ataxia type 11 (SCA11); a neurodegenerative disease characterized by progressive ataxia and atrophy of the cerebellum and brainstem.".
- Q18051430 comment "Tau tubulin kinase 2 is a protein in humans that is encoded by the TTBK2 gene.This gene encodes a serine-threonine kinase that putatively phosphorylates tau and tubulin proteins. Mutations in this gene cause spinocerebellar ataxia type 11 (SCA11); a neurodegenerative disease characterized by progressive ataxia and atrophy of the cerebellum and brainstem.".