The ATPase Domain but Not the Acidic Region of Cockayne Syndrome Group B Gene Product Is Essential for DNA Repair

Cockayne syndrome (CS) is a human genetic disorder characterized by UV sensitivity, developmental abnormalities, and premature aging. Two of the genes involved, CSA and CSB, are required for transcription-coupled repair (TCR), a subpathway of nucleotide excision repair that removes certain lesions r...

Täydet tiedot

Bibliografiset tiedot

Julkaisussa:	Mol Biol Cell
Päätekijät:	Brosh, Robert M., Balajee, Adayabalam S., Selzer, Rebecca R., Sunesen, Morten, De Santis, Luca Proietti, Bohr, Vilhelm A.
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	American Society for Cell Biology 1999
Aiheet:	Article
Linkit:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC25641/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10564257/ https://ncbi.nlm.nih.govhttps://doi.org/10.1091/mbc.10.11.3583
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