Effects of XPD Mutations on Ultraviolet-Induced Apoptosis in Relation to Skin Cancer-Proneness in Repair-Deficient Syndromes
- 1 November 2001
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 117 (5) , 1162-1170
- https://doi.org/10.1046/j.0022-202x.2001.01533.x
Abstract
No abstract availableKeywords
This publication has 50 references indexed in Scilit:
- Proneness to UV-induced apoptosis in human fibroblasts defective in transcription coupled repair is associated with the lack of Mdm2 transactivationOncogene, 2000
- Genomic heterogeneity of nucleotide excision repairGene, 2000
- Nucleotide excision repair and human syndromesCarcinogenesis: Integrative Cancer Research, 2000
- Damage recognition in nucleotide excision repair of DNAGene, 1999
- Protein complexes in nucleotide excision repairMutation Research/DNA Repair, 1999
- Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIHNature Genetics, 1998
- Analysis of Mutations in the XPD Gene in Italian Patients with Trichothiodystrophy: Site of Mutation Correlates with Repair Deficiency, but Gene Dosage Appears to Determine Clinical SeverityAmerican Journal of Human Genetics, 1998
- Defective Global Genome Repair in XPC Mice Is Associated with Skin Cancer Susceptibility But Not with Sensitivity to UVB Induced Erythema and EdemaJournal of Investigative Dermatology, 1998
- Characterization of defective nucleotide excision repair in XPC mutant miceMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1997
- Evidence for detective repair of cyclobutane pyrimidine dimers with normal repair of other DNA photoproducts in a transcriptionally active gene transfected into Cockayne syndrome cellsMutation Research/DNA Repair, 1991