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Potential Transfer of Polyglutamine and CAG-Repeat RNA in Extracellular Vesicles in Huntington’s Disease: Background and Evaluation in Cell Culture

In Huntington’s disease (HD) the imperfect expanded CAG repeat in the first exon of the HTT gene leads to the generation of a polyglutamine (polyQ) protein, which has some neuronal toxicity, potentially mollified by formation of aggregates. Accumulated research, reviewed here, implicates both the po...

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Publicado en:Cell Mol Neurobiol
Autores principales: Zhang, Xuan, Abels, Erik R., Redzic, Jasmina S., Margulis, Julia, Finkbeiner, Steve, Breakefield, Xandra O.
Formato: Artigo
Lenguaje:Inglês
Publicado: 2016
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC5844350/
https://ncbi.nlm.nih.gov/pubmed/26951563
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10571-016-0350-7
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