Differential requirement for the ATPase domain of the Cockayne syndrome group B gene in the processing of UV-induced DNA damage and 8-oxoguanine lesions in human cells

Cockayne syndrome (CS) is a rare inherited human genetic disorder characterized by UV sensitivity, developmental abnormalities and premature aging. The cellular and molecular phenotypes of CS include increased sensitivity to oxidative and UV-induced DNA lesions. The CSB protein is thought to play a...

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Detalhes bibliográficos

Publicado no:	Nucleic Acids Res
Principais autores:	Selzer, Rebecca R., Nyaga, Simon, Tuo, Jingsheng, May, Alfred, Muftuoglu, Meltem, Christiansen, Mette, Citterio, Elisabetta, Brosh, Robert M., Bohr, Vilhelm A.
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Oxford University Press 2002
Assuntos:	Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC100288/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11809892/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/30.3.782
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