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Mutation Research|February 15, 1996
Rodent complementation group 8 (ERCC8) corresponds to Cockayne syndrome complementation group AT Itoh, T Shiomi, N Shiomi, et al.
Nucleic Acids Research|May 9, 2001
Cloning the human and mouse MMS19 genes and functional complementation of a yeast mms19 deletion mutantL Queimado, M Rao, R A Schultz, et al.
Molecular and Cellular Biology|June 1, 1994
Yeast nucleotide excision repair proteins Rad2 and Rad4 interact with RNA polymerase II basal transcription factor b (TFIIH)A J Bardwell, L Bardwell, N Iyer, et al.
The Journal of Biological Chemistry|September 28, 2000
Fidelity and processivity of DNA synthesis by DNA polymerase kappa, the product of the human DINB1 geneE Ohashi, K Bebenek, T Matsuda, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1991
Functional complementation of ataxia-telangiectasia group D (AT-D) cells by microcell-mediated chromosome transfer and mapping of the AT-D locus to the region 11q22-23C Lambert, R A Schultz, M Smith, et al.
Molecular and Cellular Biology|October 12, 2000
Proapoptotic p53-interacting protein 53BP2 is induced by UV irradiation but suppressed by p53C D Lopez, Y Ao, L H Rohde, et al.
Antimicrobial Agents and Chemotherapy|September 1, 1992
Outbreak of ceftazidime resistance due to a novel extended-spectrum beta-lactamase in isolates from cancer patientsL Naumovski, J P Quinn, D Miyashiro, et al.
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