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Rhes Deletion Is Neuroprotective in the 3-Nitropropionic Acid Model of Huntington's Disease

Although the mutated protein causing Huntington's disease (HD) is expressed throughout the body, the major pathology of HD is localized to the striatum of the brain. We previously reported that the striatal-enriched protein Rhes binds the mutated huntingtin protein and enhances its cytotoxicity...

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Detalhes bibliográficos
Main Authors: Mealer, Robert G., Subramaniam, Srinivasa, Snyder, Solomon H.
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3667505/
https://ncbi.nlm.nih.gov/pubmed/23447628
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.3730-12.2013
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