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The British Journal of Dermatology|July 30, 2013
Patients with xeroderma pigmentosum complementation groups C, E and V do not have abnormal sunburn reactionsM Sethi, A R Lehmann, H Fawcett, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 24, 1997
Photocarcinogenesis and inhibition of intercellular adhesion molecule 1 expression in cells of DNA-repair-defective individualsC Ahrens, M Grewe, M Berneburg, et al.
The Journal of Investigative Dermatology|January 1, 1990
Immune function, mutant frequency, and cancer risk in the DNA repair defective genodermatoses xeroderma pigmentosum, Cockayne's syndrome, and trichothiodystrophyP G Norris, G A Limb, A S Hamblin, et al.
Clinical Dysmorphology|January 1, 1994
Syndromes associated with trichothiodystrophyJ L Tolmie, D de Berker, R Dawber, et al.
Carcinogenesis|August 1, 1994
Correction by the ERCC2 gene of UV sensitivity and repair deficiency phenotype in a subset of trichothiodystrophy cellsM Mezzina, E Eveno, O Chevallier-Lagente, et al.
Journal of Cell Science. Supplement|January 1, 1987
A gamma-ray-resistant derivative of an ataxia telangiectasia cell line obtained following DNA-mediated gene transferM H Green, J E Lowe, C F Arlett, et al.
Cancer Research|February 10, 2000
The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defectM Berneburg, P H Clingen, S A Harcourt, et al.
Cancer Research|November 1, 1988
Trichothiodystrophy, a human DNA repair disorder with heterogeneity in the cellular response to ultraviolet lightA R Lehmann, C F Arlett, B C Broughton, et al.
The EMBO Journal|March 4, 2000
UV damage causes uncontrolled DNA breakage in cells from patients with combined features of XP-D and Cockayne syndromeM Berneburg, J E Lowe, T Nardo, et al.
The British Journal of Dermatology|June 24, 2006
A novel mutation in the XPA gene associated with unusually mild clinical features in a patient who developed a spindle cell melanomaR U Sidwell, A Sandison, J Wing, et al.
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