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Huntingtin Expression Stimulates Endosomal–Lysosomal Activity, Endosome Tubulation, and Autophagy

An expansion of polyglutamines in the N terminus of huntingtin causes Huntington's disease (HD) and results in the accrual of mutant protein in the nucleus and cytoplasm of affected neurons. How mutant huntingtin causes neurons to die is unclear, but some recent observations suggest that an aut...

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Détails bibliographiques
Publié dans:J Neurosci
Auteurs principaux: Kegel, Kimberly B., Kim, Manho, Sapp, Ellen, McIntyre, Charmian, Castaño, José G., Aronin, Neil, DiFiglia, Marian
Format: Artigo
Langue:Inglês
Publié: Society for Neuroscience 2000
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Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6772788/
https://ncbi.nlm.nih.gov/pubmed/11007884
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.20-19-07268.2000
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