Inherited defects in DNA repair and susceptibility to DNA-damaging agents
- 31 December 1992
- journal article
- review article
- Published by Elsevier in Toxicology Letters
- Vol. 64-65, 141-148
- https://doi.org/10.1016/0378-4274(92)90183-k
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Identification of splicing mutations of the last nucleotides of exons, a nonsense mutation, and a missense mutation of the XPAC gene as causes of group A xeroderma pigmentosumMutation Research/DNA Repair, 1992
- Three nonsense mutations responsible for group A xeroderma pigmentosumMutation Research/DNA Repair, 1992
- Gene specific DNA repairCarcinogenesis: Integrative Cancer Research, 1991
- Analysis of a human DNA excision repair gene involved in group A xeroderma pigmentosum and containing a zinc-finger domainNature, 1990
- A presumed DNA helicase encoded by ERCC-3 is involved in the human repair disorders xeroderma pigmentosum and Cockayne's syndromeCell, 1990
- Molecular cloning and biological characterization of the human excision repair gene ERCC-3.Molecular and Cellular Biology, 1990
- The residual repair capacity of xeroderma pigmentosum complementation group C fibroblasts is highly specific for transcriptionally active DNANucleic Acids Research, 1990
- Nucleotide excision repair in Escherichia coli.Microbiological Reviews, 1990
- Xeroderma pigmentosum. Cutaneous, ocular, and neurologic abnormalities in 830 published casesArchives of Dermatology, 1987
- Defective Repair Replication of DNA in Xeroderma PigmentosumNature, 1968