Showing results (581-590 of 663) with videos related to
Sort By:
Pageof 67
Nucleic Acids Research|September 22, 2017
Phosphorylation regulates human polη stability and damage bypass throughout the cell cycleFederica Bertoletti, Valentina Cea, Chih-Chao Liang, 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.Nucleic Acids Research|October 9, 2015
Chromatin association of the SMC5/6 complex is dependent on binding of its NSE3 subunit to DNAKaterina Zabrady, Marek Adamus, Lucie Vondrova, et al.Veterinary Immunology and Immunopathology|December 1, 1992
Immunization-induced decrease of the CD4+:CD8+ ratio in cats experimentally infected with feline immunodeficiency virusR Lehmann, B von Beust, E Niederer, et al.Molecular Biology of the Cell|April 28, 2006
Postreplication repair and PCNA modification in Schizosaccharomyces pombeJonathan Frampton, Anja Irmisch, Catherine M Green, 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.Molecular Cell|February 18, 2010
Regulation of translesion synthesis DNA polymerase eta by monoubiquitinationMarzena Bienko, Catherine M Green, Simone Sabbioneda, et al.The British Journal of Dermatology|September 1, 1991
Long-term survival and preservation of natural killer cell activity in a xeroderma pigmentosum patient with spontaneous regression and multiple deposits of malignant melanomaA V Anstey, C F Arlett, J Cole, 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.Pageof 67