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Biochemical Society Transactions|July 27, 2005
Functional consequences of DNA mismatch repair missense mutations in murine models and their impact on cancer predispositionS J Scherer, E Avdievich, W EdelmannProceedings of the National Academy of Sciences of the United States of America|December 15, 1992
Organization of the human skeletal myosin heavy chain gene clusterS J Yoon, S H Seiler, R Kucherlapati, et al.Genomics|December 1, 1996
Physical mapping of the human neurotensin gene (NTS) between markers D12S1444 and D12S81 on chromosome 12q21I Marondel, B Renault, J Lieman, et al.Nucleic Acids Research|September 25, 1995
Unequal homologous recombination of human DNA on a yeast artificial chromosomeC Campbell, I Marondel, K Montgomery, et al.Nature Genetics|December 30, 1999
Cardiac defects and renal failure in mice with targeted mutations in Pkd2G Wu, G S Markowitz, L Li, et al.Genomics|November 1, 1995
Localization of the human achaete-scute homolog gene (ASCL1) distal to phenylalanine hydroxylase (PAH) and proximal to tumor rejection antigen (TRA1) on chromosome 12q22-q23B Renault, J Lieman, D Ward, et al.Cell|June 16, 1989
A recombination hotspot in the LTR of a mouse retrotransposon identified in an in vitro systemW Edelmann, B Kröger, M Goller, et al.Proceedings of the National Academy of Sciences of the United States of America|July 1, 1980
Genetic analysis of epidermal growth factor action: assignment of human epidermal growth factor receptor gene to chromosome 7R L Davies, V A Grosse, R Kucherlapati, et al.Genetics|October 1, 1985
Homologous recombination between autonomously replicating plasmids in mammalian cellsD Ayares, J Spencer, F Schwartz, et al.The Journal of Experimental Medicine|February 9, 2000
Somatic hypermutation in MutS homologue (MSH)3-, MSH6-, and MSH3/MSH6-deficient mice reveals a role for the MSH2-MSH6 heterodimer in modulating the base substitution patternM Wiesendanger, B Kneitz, W Edelmann, et al.Pageof 15