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Mitochondrial Dysfunction in Huntington’s Disease; Interplay Between HSF1, p53 and PGC-1α Transcription Factors

Huntington’s disease (HD) is a neurodegenerative disease caused by an expanded CAG repeat in the huntingtin (HTT) gene, causing the protein to misfold and aggregate. HD progression is characterized by motor impairment and cognitive decline associated with the preferential loss of striatal medium spi...

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Bibliografski detalji
Izdano u:Front Cell Neurosci
Glavni autori: Intihar, Taylor A., Martinez, Elisa A., Gomez-Pastor, Rocio
Format: Artigo
Jezik:Inglês
Izdano: Frontiers Media S.A. 2019
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6433789/
https://ncbi.nlm.nih.gov/pubmed/30941017
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2019.00103
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