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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...

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書誌詳細
主要な著者: 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
フォーマット: Artigo
言語:Inglês
出版事項: The National Academy of Sciences 2000
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC17325/
https://ncbi.nlm.nih.gov/pubmed/11035806
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