Showing results (1-10 of 20) with videos related to
Sort By:
Pageof 2
Current Opinion in Genetics & Development|April 8, 2000
Mismatch repair defects in cancerJ Jiricny, M Nyström-LahtiThe Journal of Biological Chemistry|November 5, 1999
Identification of hMutLbeta, a heterodimer of hMLH1 and hPMS1M Räschle, G Marra, M Nyström-Lahti, et al.International Journal of Cancer|December 20, 1995
Life-time risk of different cancers in hereditary non-polyposis colorectal cancer (HNPCC) syndromeM Aarnio, J P Mecklin, L A Aaltonen, et al.British Journal of Cancer|September 9, 2004
MSH6 missense mutations are often associated with no or low cancer susceptibilityR Kariola, H Hampel, W L Frankel, et al.Genes, Chromosomes & Cancer|October 27, 1999
Missense and nonsense mutations in codon 659 of MLH1 cause aberrant splicing of messenger RNA in HNPCC kindredsM Nyström-Lahti, M Holmberg, P Fidalgo, et al.Nature|October 24, 1985
Pseudoautosomal DNA sequences in the pairing region of the human sex chromosomesM C Simmler, F Rouyer, G Vergnaud, et al.Nature Genetics|December 1, 1994
Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancerA Hemminki, P Peltomäki, J P Mecklin, et al.Human Mutation|April 13, 1999
Mutation sharing, predominant involvement of the MLH1 gene and description of four novel mutations in hereditary nonpolyposis colorectal cancer. Mutations in brief no. 144. OnlineM Holmberg, P Kristo, R B Chadwicks, et al.Proceedings of the National Academy of Sciences of the United States of America|October 27, 1999
Epigenetic phenotypes distinguish microsatellite-stable and -unstable colorectal cancersS A Kuismanen, M T Holmberg, R Salovaara, et al.Proceedings of the National Academy of Sciences of the United States of America|June 21, 2001
Tolerance of human MSH2+/- lymphoblastoid cells to the methylating agent temozolomideG Marra, S D'Atri, C Corti, et al.Pageof 2