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Reversal of a full-length mutant huntingtin neuronal cell phenotype by chemical inhibitors of polyglutamine-mediated aggregation

BACKGROUND: Huntington's disease (HD) is an inherited neurodegenerative disorder triggered by an expanded polyglutamine tract in huntingtin that is thought to confer a new conformational property on this large protein. The propensity of small amino-terminal fragments with mutant, but not wild-t...

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Detalhes bibliográficos
Main Authors: Wang, Jin, Gines, Silvia, MacDonald, Marcy E, Gusella, James F
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2005
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC548150/
https://ncbi.nlm.nih.gov/pubmed/15649316
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2202-6-1
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