Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy: do the genes explain the diseases?
Open Access
- 31 May 1996
- journal article
- review article
- Published by Elsevier BV in Trends in Genetics
- Vol. 12 (5), 187-192
- https://doi.org/10.1016/0168-9525(96)10021-4
Abstract
No abstract availableKeywords
This publication has 30 references indexed in Scilit:
- Isolation of a cDNA encoding a UV-damaged DNA binding factor defective in xeroderma pigmentosum group E cellsMutation Research/DNA Repair, 1996
- Transcription-Coupled Repair and Human DiseaseScience, 1994
- Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophyNature Genetics, 1994
- Dual role of TFIIH in DNA excision repair and in transcription by RNA polymerase IINature, 1994
- Nucleotide excision repair II: from yeast to mammalsTrends in Genetics, 1993
- A Drosophila model for xeroderma pigmentosum and Cockayne's syndrome: haywire encodes the fly homolog of ERCC3, a human excision repair geneCell, 1992
- The XPD complementation group: Insights into xeroderma pigmentosum, Cockayne's syndrome and trichothiodystrophyMutation Research/DNA Repair, 1992
- Trichothiodystrophy: Review of sulfur-deficient brittle hair syndromes and association with the ectodermal dysplasiasJournal of the American Academy of Dermatology, 1990
- Relationship between pyrimidine dimers, 6-4 photoproducts, repair synthesis and cell survival: Studies using cells from patients with trichothiodystrophyMutation Research/DNA Repair, 1990
- The Cockayne syndrome—An inherited multisystem disorder with cutaneous photosensitivity and defective repair of DNA Comparison with xeroderma pigmentosumThe American Journal of Dermatopathology, 1985