An ERCC5 gene with homology to yeast RAD2 is involved in group G xeroderma pigmentosum
- 1 March 1994
- journal article
- Published by Elsevier in Mutation Research/DNA Repair
- Vol. 314 (2), 167-175
- https://doi.org/10.1016/0921-8777(94)90080-9
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Education, Culture, Sports, Science and Technology
- Japan Science and Technology Agency
This publication has 21 references indexed in Scilit:
- Identical defects in DNA repair in xeroderma pigmentosum group G and rodent ERCC group 5Nature, 1993
- Complementation of the DNA repair defect in xeroderma pigmentosum group G cells by a human cDNA related to yeast RAD2Nature, 1993
- ERCC6, a member of a subfamily of putative helicases, is involved in Cockayne's syndrome and preferential repair of active genesCell, 1992
- Precise Localization of the Excision Repair Gene, ERCC5, to Human Chromosome 13q32.3-q33.1 by Direct R-Banding Fluorescencein situHybridizationJapanese Journal of Cancer Research, 1992
- 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
- The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through IMutation Research/DNA Repair, 1989
- Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA PolymeraseScience, 1988
- [12] Unidirectional digestion with exonuclease III in DNA sequence analysisMethods in Enzymology, 1987
- Isolation of biologically active ribonucleic acid from sources enriched in ribonucleaseBiochemistry, 1979