ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genes
- 11 December 1992
- journal article
- research article
- Published by Elsevier
- Vol. 71 (6) , 939-953
- https://doi.org/10.1016/0092-8674(92)90390-x
Abstract
No abstract availableKeywords
This publication has 70 references indexed in Scilit:
- SSL2, a suppressor of a stem-loop mutation in the HIS4 leader encodes the yeast homolog of human ERCC-3Cell, 1992
- Localization of the nucleotide excision repair gene ERCC6 to human chromosome 10q11–q21Genomics, 1992
- Basic local alignment search toolJournal of Molecular Biology, 1990
- Site-specific DNA repair at the nucleosome level in a yeast minichromosomeCell, 1990
- Summary of complementation groups of UV-sensitive CHO cell mutants isolated by large-scale screeningMutagenesis, 1989
- Transformation of DNA repair-deficient human diploid fibroblasts with a simian virus 40 plasmidExperimental Cell Research, 1987
- Sensitive determination of pyrimidine dimers in DNA of UV-irradiated mammalian cells Introduction of T4 endonuclease V into frozen and thawed cellsMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1981
- Genetic control of diploid recovery after γ-irradiation in the yeast Saccharomyces cerevisiaeMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1980
- The influence of the wavelength of ultraviolet radiation on survival, mutation induction and DNA repair in irradiated chinese hamster cellsMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1980
- A seventh complementation group in excision-deficient xeroderma pigmentosumMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1979