Cockayne syndrome group B protein promotes mitochondrial DNA stability by supporting the DNA repair association with the mitochondrial membrane

Cockayne syndrome (CS) is a human premature aging disorder associated with severe developmental deficiencies and neurodegeneration, and phenotypically it resembles some mitochondrial DNA (mtDNA) diseases. Most patients belong to complementation group B, and the CS group B (CSB) protein plays a role...

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Bibliografiska uppgifter
Huvudupphovsmän: Aamann, Maria D., Sorensen, Martin M., Hvitby, Christina, Berquist, Brian R., Muftuoglu, Meltem, Tian, Jingyan, de Souza-Pinto, Nadja C., Scheibye-Knudsen, Morten, Wilson, David M., Stevnsner, Tinna, Bohr, Vilhelm A.
Materialtyp: Artigo
Språk:Inglês
Publicerad: The Federation of American Societies for Experimental Biology 2010
Ämnen:
Research Communications
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC2887265/
https://ncbi.nlm.nih.gov/pubmed/20181933
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1096/fj.09-147991
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