A striatal-enriched intronic GPCR modulates huntingtin levels and toxicity

Huntington's disease (HD) represents an important model for neurodegenerative disorders and proteinopathies. It is mainly caused by cytotoxicity of the mutant huntingtin protein (Htt) with an expanded polyQ stretch. While Htt is ubiquitously expressed, HD is characterized by selective neurodege...

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Detalles Bibliográficos
Autores principales: Yao, Yuwei, Cui, Xiaotian, Al-Ramahi, Ismael, Sun, Xiaoli, Li, Bo, Hou, Jiapeng, Difiglia, Marian, Palacino, James, Wu, Zhi-Ying, Ma, Lixiang, Botas, Juan, Lu, Boxun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
Materias:
Human Biology and Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4372774/
https://www.ncbi.nlm.nih.gov/pubmed/25738228
http://dx.doi.org/10.7554/eLife.05449

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4372774/
https://www.ncbi.nlm.nih.gov/pubmed/25738228
http://dx.doi.org/10.7554/eLife.05449

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