Long-term complementation of DNA repair deficient human primary fibroblasts by retroviral transduction of the XPD gene
- 1 December 1996
- journal article
- Published by Elsevier in Mutation Research/DNA Repair
- Vol. 364 (3), 161-169
- https://doi.org/10.1016/s0921-8777(96)00024-9
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Stable SV40-transformation and characterisation of some DNA repair properties of fibroblasts from a trichothiodystrophy patientBiochimie, 1995
- Nucleotide excision repair syndromes: molecular basis and clinical symptomsPhilosophical Transactions Of The Royal Society B-Biological Sciences, 1995
- Correction by the ERCC2 gene of UV sensitivity and repair deficiency phenotype in a subset of trichothiodystrophy cellsCarcinogenesis: Integrative Cancer Research, 1994
- Complementation of the DNA repair defect in xeroderma pigmentosum group G cells by a human cDNA related to yeast RAD2Nature, 1993
- Genes controlling nucleotide excision repair in eukaryotic cellsBioEssays, 1993
- Expression cloning of a human DNA repair gene involved in xeroderma pigmentosum group CNature, 1992
- 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
- Trichothiodystrophy: Review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasiasJournal of the American Academy of Dermatology, 1990
- An immortalized xeroderma pigmentosum, group C, cell line which replicates SV40 shuttle vectorsMutation Research/DNA Repair Reports, 1987