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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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Bibliografische gegevens
Hoofdauteurs: Shirendeb, Ulziibat, Reddy, Arubala P., Manczak, Maria, Calkins, Marcus J., Mao, Peizhong, Tagle, Danilo A., Hemachandra Reddy, P.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Oxford University Press 2011
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Online toegang: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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