【摘 要】
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Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant neurologic disorder caused by ATTCT expansion in the ATXN10 gene.Previously we have presented da
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Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant neurologic disorder caused by ATTCT expansion in the ATXN10 gene.Previously we have presented data that Ataxin-10, the gene product of ATXN10, is phosphorylated by Plk1 at S77 and T82, and participates in cytokinesis.Herein we further identify that Aurora B coimmunoprecipates with and phosphorylates Ataxin-10 at S12.
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