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Molecular Carcinogenesis|August 4, 1998
p53 mutations in cutaneous lesions induced in the hairless mouse by a solar ultraviolet light simulatorS Queille, S Seite, S Tison, et al.Journal of Virology|January 9, 1999
Amplification of the inflammatory cellular redox state by human immunodeficiency virus type 1-immunosuppressive tat and gp160 proteinsA Lachgar, N Sojic, S Arbault, et al.Oncogene|May 13, 2008
Overexpression of matrix metalloproteinase 1 in dermal fibroblasts from DNA repair-deficient/cancer-prone xeroderma pigmentosum group C patientsM Fréchet, E Warrick, C Vioux, et al.Cell|April 29, 2000
Transcription-coupled repair of 8-oxoguanine: requirement for XPG, TFIIH, and CSB and implications for Cockayne syndromeF Le Page, E E Kwoh, A Avrutskaya, et al.Journal of Molecular Biology|October 20, 1992
Mutagenicity of a unique apurinic/apyrimidinic site in mammalian cellsA Gentil, J B Cabral-Neto, R Mariage-Samson, et al.Carcinogenesis|August 30, 2000
Molecular cloning and characterization of the human KIN17 cDNA encoding a component of the UVC response that is conserved among metazoansP Kannouche, P Mauffrey, G Pinon-Lataillade, et al.Oncogene|March 27, 2007
Frequent alteration of DNA damage signalling and repair pathways in human colorectal cancers with microsatellite instabilityC Miquel, S Jacob, S Grandjouan, et al.Journal of the National Cancer Institute|November 18, 2000
Association between INK4a-ARF and p53 mutations in skin carcinomas of xeroderma pigmentosum patientsN Soufir, L Daya-Grosjean, de La Salmonière P, et al.Human Molecular Genetics|May 20, 1999
The relative expression of mutated XPB genes results in xeroderma pigmentosum/Cockayne's syndrome or trichothiodystrophy cellular phenotypesL Riou, L Zeng, O Chevallier-Lagente, et al.American Journal of Human Genetics|February 1, 1996
Defects in the DNA repair and transcription gene ERCC2(XPD) in trichothiodystrophyK Takayama, E P Salazar, B C Broughton, et al.Pageof 21