Inactivation of Pif1 helicase causes a mitochondrial myopathy in mice

Mutations in genes coding for mitochondrial helicases such as TWINKLE and DNA2 are involved in mitochondrial myopathies with mtDNA instability in both human and mouse. We show that inactivation of Pif1, a third member of the mitochondrial helicase family, causes a similar phenotype in mouse. pif1−/−...

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發表在:Mitochondrion
Main Authors: Bannwarth, Sylvie, Berg-Alonso, Laetitia, Augé, Gaëlle, Fragaki, Konstantina, Kolesar, Jill E., Lespinasse, Françoise, Lacas-Gervais, Sandra, Burel-Vandenbos, Fanny, Villa, Elodie, Belmonte, Frances, Michiels, Jean-François, Ricci, Jean-Ehrland, Gherardi, Romain, Harrington, Lea, Kaufman, Brett A., Paquis-Flucklinger, Véronique
格式: Artigo
語言:Inglês
出版: 2016
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Article
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC5454384/
https://ncbi.nlm.nih.gov/pubmed/26923168
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mito.2016.02.005
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