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Journal of Medical Genetics|July 17, 2008
Cerebro-oculo-facio-skeletal syndrome: three additional cases with CSB mutations, new diagnostic criteria and an approach to investigationV Laugel, C Dalloz, E S Tobias, et al.Carcinogenesis|May 1, 1995
Development of a new easy complementation assay for DNA repair deficient human syndromes using cloned repair genesM Carreau, E Eveno, X Quilliet, 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.American Journal of Human Genetics|October 1, 1993
A new nucleotide-excision-repair gene associated with the disorder trichothiodystrophyM Stefanini, W Vermeulen, G Weeda, et al.Molecular Carcinogenesis|April 2, 2004
INK4a-ARF mutations in skin carcinomas from UV irradiated hairless miceN Soufir, S Queille, K Mollier, et al.Journal of Controlled Release : Official Journal of the Controlled Release Society|August 10, 2010
Transmembrane diffusion of gemcitabine by a nanoparticulate squalenoyl prodrug: an original drug delivery pathwayL Bildstein, C Dubernet, V Marsaud, et al.Mutation Research|January 1, 1990
Relationship between pyrimidine dimers, 6-4 photoproducts, repair synthesis and cell survival: studies using cells from patients with trichothiodystrophyB C Broughton, A R Lehmann, S A Harcourt, et al.Journal of Hepatology|December 2, 1998
Induction of apoptosis in rat hepatocarcinoma cells by expression of IGF-I antisense c-DNAS Ellouk-Achard, S Djenabi, G A De Oliveira, et al.Proceedings of the National Academy of Sciences of the United States of America|August 5, 1997
Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription geneE M Taylor, B C Broughton, E Botta, et al.The British Journal of Dermatology|August 23, 2008
Xeroderma pigmentosum group C in a French Caucasian patient with multiple melanoma and unusual long-term survivalS Jacobelli, N Soufir, J J Lacapere, et al.Pageof 21