HACE1 is essential for astrocyte mitochondrial function and influences Huntington disease phenotypes in vivo
Author:
Affiliation:
1. Department of Medical Genetics, Centre for Molecular Medicine and Therapeutics (CMMT), CFRI, University of British Columbia, Vancouver, BC V5Z 4H4, Canada
Funder
Canadian Institutes of Health Research
CIHR
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/27/2/239/24325598/ddx394.pdf
Reference73 articles.
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2. Antioxidants in Huntington’s disease;Johri;Biochim. Biophys. Acta,2012
3. Mechanisms of synaptic dysfunction and excitotoxicity in Huntington’s disease;Sepers;Drug Discov. Today,2014
4. Elevated NADPH oxidase activity contributes to oxidative stress and cell death in Huntington’s disease;Valencia;Hum. Mol. Genet,2013
5. Huntington’s disease;Zuccato;Handb. Exp. Pharmacol,2014
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