Evidence for Proteasome Involvement in Polyglutamine Disease: Localization to Nuclear Inclusions in SCA3/MJD and Suppression of Polyglutamine Aggregation in vitro-Reference-Cited by-同舟云学术

Evidence for Proteasome Involvement in Polyglutamine Disease: Localization to Nuclear Inclusions in SCA3/MJD and Suppression of Polyglutamine Aggregation in vitro

Published:1999-04-01 Issue:4 Volume:8 Page:673-682
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Chai Y.,Koppenhafer S. L.,Shoesmith S. J.,Perez M. K.,Paulson H. L.

Publisher

Oxford University Press (OUP)

Subject

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

Reference52 articles.

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4. Glutamine repeats as polar zippers: their possible role in inherited neurodegenerative diseases.

5. Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

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