Rodent complementation group 8 (ERCC8) corresponds to Cockayne syndrome complementation group A
- 15 February 1996
- journal article
- Published by Elsevier in Mutation Research/DNA Repair
- Vol. 362 (2) , 167-174
- https://doi.org/10.1016/0921-8777(95)00046-1
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- A new UV-sensitive syndrome not belonging to any complementation groups of xeroderma pigmentosum or Cockayne syndrome: siblings showing biochemical characteristics of Cockayne syndrome without typical clinical manifestationsPublished by Elsevier ,2002
- An ERCC5 gene with homology to yeast RAD2 is involved in group G xeroderma pigmentosumMutation Research/DNA Repair, 1994
- Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5Nature, 1993
- Establishment of a monoclonal antibody recognizing cyclobutane-type thymine dimers in DNA: a comparative study with 64M-1 antibody specific for (6-4) photoproductsMutation Research/DNA Repair, 1991
- Isolation of the functional human excision repair gene ERCC5 by intercosmid recombinationGenomics, 1990
- A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndromeCell, 1990
- Stable replication of plasmids derived from Epstein–Barr virus in various mammalian cellsNature, 1985
- Molecular cloning of a human DNA repair geneNature, 1984
- Three complementation groups in Cockayne syndromeMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1982
- Induction of Directional Chromosome Elimination in Somatic Cell HybridsNature, 1971