DNA Repair and Ultraviolet Mutagenesis in Cells From a New Patient With Xeroderma Pigmentosum Group G and Cockayne Syndrome Resemble Xeroderma Pigmentosum Cells
- 1 October 1996
- journal article
- case report
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 107 (4) , 647-653
- https://doi.org/10.1111/1523-1747.ep12584287
Abstract
No abstract availableKeywords
This publication has 37 references indexed in Scilit:
- The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIHCell, 1995
- Mammalian DNA nucleotide excision repair reconstituted with purified protein componentsCell, 1995
- Nucleotide excision repair syndromes: molecular basis and clinical symptomsPhilosophical Transactions Of The Royal Society B-Biological Sciences, 1995
- Correction of xeroderma pigmentosum complementation group D mutant cell phenotypes by chromosome and gene transfer: involvement of the human ERCC2 DNA repair gene.Proceedings of the National Academy of Sciences, 1992
- 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
- Clinical and biochemical studies in three patients with severe early infantile Cockayne syndromeHuman Genetics, 1989
- A Mild Form of Xeroderma Pigmentosum Assigned to Complementation Group G and Its Repair HeterogeneityJournal of Investigative Dermatology, 1985
- A seventh complementation group in excision-deficient xeroderma pigmentosumMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1979
- (30) Xeroderma pigmentosum—a unique variant with neurological involvementBritish Journal of Dermatology, 1978
- Cockayne's Syndrome Fibroblasts Have Increased Sensitivity to Ultraviolet Light But Normal Rates of Unscheduled DNA SynthesisJournal of Investigative Dermatology, 1978