QR-Code

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...

Ausführliche Beschreibung

Gespeichert in:
Veröffentlicht in:Nucleic Acids Res
Hauptverfasser: Selzer, Rebecca R., Nyaga, Simon, Tuo, Jingsheng, May, Alfred, Muftuoglu, Meltem, Christiansen, Mette, Citterio, Elisabetta, Brosh, Robert M., Bohr, Vilhelm A.
Format: Artigo
Sprache:Inglês
Veröffentlicht: Oxford University Press 2002
Schlagworte:
Article
Online-Zugang: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
Tags: Tag hinzufügen
Keine Tags, Fügen Sie das erste Tag hinzu!

Ähnliche Einträge