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Abnormal mitochondrial dynamics, mitochondrial loss and mutant huntingtin oligomers in Huntington's disease: implications for selective neuronal damage

The purpose of our study was to determine the relationship between mutant huntingtin (Htt) and mitochondrial dynamics in the progression of Huntington's disease (HD). We measured the mRNA levels of electron transport chain genes, and mitochondrial structural genes, Drp1 (dynamin-related protein...

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Detalhes bibliográficos
Main Authors: Shirendeb, Ulziibat, Reddy, Arubala P., Manczak, Maria, Calkins, Marcus J., Mao, Peizhong, Tagle, Danilo A., Hemachandra Reddy, P.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3049363/
https://ncbi.nlm.nih.gov/pubmed/21257639
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddr024
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