Molecular characterization of an acidic region deletion mutant of Cockayne syndrome group B protein

Cockayne syndrome (CS) is a human genetic disorder characterized by post-natal growth failure, neurological abnormalities and premature aging. CS cells exhibit high sensitivity to UV light, delayed RNA synthesis recovery after UV irradiation and defective transcription-coupled repair (TCR). Two gene...

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Veröffentlicht in:	Nucleic Acids Res
Hauptverfasser:	Sunesen, Morten, Selzer, Rebecca R., Brosh, Robert M., Balajee, Adayabalam S., Stevnsner, Tinna, Bohr, Vilhelm A.
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	Oxford University Press 2000
Schlagworte:	Article
Online-Zugang:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC108419/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10931931/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/28.16.3151
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