Frataxin activates mitochondrial energy conversion and oxidative phosphorylation

Friedreich's ataxia (FA) is an autosomal recessive disease caused by decreased expression of the mitochondrial protein frataxin. The biological function of frataxin is unclear. The homologue of frataxin in yeast, YFH1, is required for cellular respiration and was suggested to regulate mitochond...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Ristow, Michael, Pfister, Markus F., Yee, Andrew J., Schubert, Markus, Michael, Laura, Zhang, Chen-Yu, Ueki, Kojhiro, Michael, M. Dodson, Lowell, Bradford B., Kahn, C. Ronald
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: The National Academy of Sciences 2000
Pynciau:
Biological Sciences
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC17325/
https://ncbi.nlm.nih.gov/pubmed/11035806
Tagiau: Ychwanegu Tag
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