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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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Main Authors: Shirendeb, Ulziibat, Reddy, Arubala P., Manczak, Maria, Calkins, Marcus J., Mao, Peizhong, Tagle, Danilo A., Hemachandra Reddy, P.
Formáid: Artigo
Teanga:Inglês
Foilsithe: Oxford University Press 2011
Ábhair:
Rochtain Ar Líne: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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