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Mutation Research|March 1, 1991
UV mutation spectra in cell lines from patients with Cockayne's syndrome and ataxia telangiectasia, using the shuttle vector pZ189W J Muriel, J R Lamb, A R LehmannMutagenesis|November 1, 1990
Possible methodologies for the detection and study of DNA sequence changes following mutagen exposure: magnetic enrichment in mutant DNAB A Bridges, A M Carr, A R LehmannMutation Research|July 1, 1988
Inactivation by nitrogen mustard of plasmids introduced into normal and Fanconi's anaemia cellsS W Dean, H R Sykes, A R LehmannTrends in Genetics : TIG|September 2, 1998
Splitting the ATM: distinct repair and checkpoint defects in ataxia-telangiectasiaP A Jeggo, A M Carr, A R LehmannJournal of Molecular Biology|January 20, 1991
Molecular analysis of ultraviolet-induced mutations in a xeroderma pigmentosum cell lineG Dorado, H Steingrimsdottir, C F Arlett, et al.Nucleic Acids Research|March 25, 1992
Mutations which alter splicing in the human hypoxanthine-guanine phosphoribosyltransferase geneH Steingrimsdottir, G Rowley, G Dorado, et al.Nature Genetics|June 1, 1994
Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophyB C Broughton, H Steingrimsdottir, C A Weber, et al.Human Molecular Genetics|April 18, 2000
Identical mutations in the CSB gene associated with either Cockayne syndrome or the DeSanctis-cacchione variant of xeroderma pigmentosumS Colella, T Nardo, E Botta, et al.Human Genetics|April 1, 1996
Genetic analysis of twenty-two patients with Cockayne syndromeM Stefanini, H Fawcett, E Botta, et al.Carcinogenesis|August 1, 1983
Similar rate of O6-ethylguanine elimination from DNA in normal human fibroblast and xeroderma pigmentosum cell strains not transformed by SV40I A Teo, A R Lehmann, R Müller, et al.Pageof 13