Disruption of mouse ERCC1 results in a novel repair syndrome with growth failure, nuclear abnormalities and senescence
Open Access
- 1 June 1997
- journal article
- research article
- Published by Elsevier in Current Biology
- Vol. 7 (6) , 427-439
- https://doi.org/10.1016/s0960-9822(06)00190-4
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Synergistic interactions between XPC and p53 mutations in double-mutant mice: neural tube abnormalities and accelerated UV radiation-induced skin cancerCurrent Biology, 1996
- High incidence of ultraviolet-B-or chemical-carcinogen-induced skin tumours in mice lacking the xeroderma pigmentosum group A geneNature, 1995
- Increased susceptibility to ultraviolet-B and carcinogens of mice lacking the DNA excision repair gene XPANature, 1995
- Human nucleotide excision repair syndromes: Molecular clues to unexpected intricaciesEuropean Journal Of Cancer, 1994
- Detection of Endogenous Malondialdehyde-Deoxyguanosine Adducts in Human LiverScience, 1994
- A case of xeroderma pigmentosum complementation group F with neurological abnormalitiesBritish Journal of Dermatology, 1993
- Removal of Nonhomologous DNA Ends in Double-Strand Break Recombination: the Role of the Yeast Ultraviolet Repair Gene RAD1Science, 1992
- The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through IMutation Research/DNA Repair, 1989
- Molecular characterization of the human excision repair gene : cDNA cloning and amino acid homology with the yeast DNA repair geneCell, 1986
- Repair of ultraviolet radiation damage in xeroderma pigmentosum cells belonging to complementation group FMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1981