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Ubiquilin-1 overexpression increases the lifespan and delays accumulation of Huntingtin aggregates in the R6/2 mouse model of Huntington's disease.

Huntington's Disease (HD) is a neurodegenerative disorder that is caused by abnormal expansion of a polyglutamine tract in huntingtin (htt) protein. The expansion leads to increased htt aggregation and toxicity. Factors that aid in the clearance of mutant huntingtin proteins should relieve the toxic...

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Autores principales: Nathaniel Safren, Amina El Ayadi, Lydia Chang, Chantelle E Terrillion, Todd D Gould, Darren F Boehning, Mervyn J Monteiro
Formato: Artigo
Lenguaje:Inglês
Publicado: Public Library of Science (PLoS) 2014-01-01
Colección:PLoS ONE
Acceso en línea:http://europepmc.org/articles/PMC3903676?pdf=render
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