The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA.

Cells from patients with Cockayne syndrome (CS) are hypersensitive to UV-irradiation but have an apparently normal ability to remove pyrimidine dimers from the genome overall. We have measured the repair of pyrimidine dimers in defined DNA sequences in three normal and two CS cell strains. When comp...

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Detalles Bibliográficos

Publicado en:	Proc Natl Acad Sci U S A
Autores principales:	Venema, J, Mullenders, L H, Natarajan, A T, van Zeeland, A A, Mayne, L V
Formato:	Artigo
Lenguaje:	Inglês
Publicado:	National Academy of Sciences 1990
Materias:	Research Article
Acceso en línea:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC54186/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2352945/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.87.12.4707
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