Long-term complementation of DNA repair deficient human primary fibroblasts by retroviral transduction of the XPD gene

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

Jaap Venema, L.H.F. Mullenders, A.T. Natarajan et al. · Proceedings of the National Academy of Sciences · 1990 · 556 citations

Life Sciences, Genetics, Molecular Genetics +16

Preferential DNA repair of an active gene in human cells.

Isabel Mellon, Vilhelm A. Bohr, Charles A. Smith et al. · Proceedings of the National Academy of Sciences · 1986 · 450 citations

Life Sciences, Genetics, Molecular Biology +13

A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndrome

Geert Weeda, Reinier C.A. van Ham, Wim Vermeulen et al. · Cell · 1990 · 438 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domain

Kiyoji Tanaka, Naoyuki Miura, Ichiro Satokata et al. · Nature · 1990 · 393 citations

Life Sciences, Genetics, Molecular Genetics +13

Genetic Heterogeneity of Xeroderma Pigmentosum demonstrated by Somatic Cell Hybridization

E.A. de Weerd-Kastelein, W. Keijzer, D. Bootsma · Nature New Biology · 1972 · 320 citations

Life Sciences, Genetics, Molecular Genetics +16