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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: The Federation of American Societies for Experimental Biology 2010
Assuntos:
Research Communications
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados