Protein kinase Cγ, a protein causative for dominant ataxia, negatively regulates nuclear import of recessive-ataxia-related aprataxin-Reference-Cited by-同舟云学术

Protein kinase Cγ, a protein causative for dominant ataxia, negatively regulates nuclear import of recessive-ataxia-related aprataxin

Published:2009-06-26 Issue:19 Volume:18 Page:3533-3543
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Asai Hirohide,Hirano Makito,Shimada Keiji,Kiriyama Takao,Furiya Yoshiko,Ikeda Masanori,Iwamoto Takaaki,Mori Toshio,Nishinaka Kazuto,Konishi Noboru,Udaka Fukashi,Ueno Satoshi

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/18/19/3533/17246939/ddp298.pdf

Reference28 articles.

1. Impaired motor coordination correlates with persistent multiple climbing fiber innervation in PKC gamma mutant mice;Chen;Cell,1995

2. Mutant protein kinase Cgamma found in spinocerebellar ataxia type 14 is susceptible to aggregation and causes cell death;Seki;J. Biol. Chem.,2005

3. The clinical and genetic spectrum of spinocerebellar ataxia 14;Chen;Neurology,2005

4. Activation of mutant protein kinase Cgamma leads to aberrant sequestration and impairment of its cellular function;Doran;Biochem. Biophys. Res. Commun.,2008

5. Protein kinase C gamma mutations in spinocerebellar ataxia 14 increase kinase activity and alter membrane targeting;Verbeek;Brain,2005

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