Protein Fate in Neurodegenerative Proteinopathies: Polyglutamine Diseases Join the (Mis)Fold-Reference-Cited by-同舟云学术

Protein Fate in Neurodegenerative Proteinopathies: Polyglutamine Diseases Join the (Mis)Fold

Published:1999-02 Issue:2 Volume:64 Page:339-345
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Paulson Henry L.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference37 articles.

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4. Truncated N-terminal fragments of huntingtin with expanded glutamine repeats form nuclear and cytoplasmic aggregates in cell culture;Cooper;Hum Mol Genet,1998

5. Chaperone suppression of ataxin-1 aggregation and altered subcellular proteosome localization imply protein misfolding in SCA1;Cummings;Nat Genet,1998

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