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390 related items for PubMed ID: 8137274
1. Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients. Aaltonen LA, Peltomäki P, Mecklin JP, Järvinen H, Jass JR, Green JS, Lynch HT, Watson P, Tallqvist G, Juhola M. Cancer Res; 1994 Apr 01; 54(7):1645-8. PubMed ID: 8137274 [Abstract] [Full Text] [Related]
2. Multiple epithelial and nonepithelial tumors in hereditary nonpolyposis colorectal cancer: characterization of germline and somatic mutations of the MSH2 gene and heterogeneity of replication error phenotypes. Huang RL, Chao CF, Ding DC, Yu CP, Chang CC, Lai HC, Yu MH, Liu HS, Chu TY. Cancer Genet Cytogenet; 2004 Sep 01; 153(2):108-14. PubMed ID: 15350299 [Abstract] [Full Text] [Related]
3. Exon 3 beta-catenin mutations are specifically associated with colorectal carcinomas in hereditary non-polyposis colorectal cancer syndrome. Johnson V, Volikos E, Halford SE, Eftekhar Sadat ET, Popat S, Talbot I, Truninger K, Martin J, Jass J, Houlston R, Atkin W, Tomlinson IP, Silver AR. Gut; 2005 Feb 01; 54(2):264-7. PubMed ID: 15647192 [Abstract] [Full Text] [Related]
4. Genomic DNA-based hMSH2 and hMLH1 mutation screening in 32 Eastern United States hereditary nonpolyposis colorectal cancer pedigrees. Weber TK, Conlon W, Petrelli NJ, Rodriguez-Bigas M, Keitz B, Pazik J, Farrell C, O'Malley L, Oshalim M, Abdo M, Anderson G, Stoler D, Yandell D. Cancer Res; 1997 Sep 01; 57(17):3798-803. PubMed ID: 9288790 [Abstract] [Full Text] [Related]
5. Analysis of somatic molecular changes, clinicopathological features, family history, and germline mutations in colorectal cancer families: evidence for efficient diagnosis of HNPCC and for the existence of distinct groups of non-HNPCC families. Johnson V, Lipton LR, Cummings C, Eftekhar Sadat AT, Izatt L, Hodgson SV, Talbot IC, Thomas HJ, Silver AJ, Tomlinson IP. J Med Genet; 2005 Oct 01; 42(10):756-62. PubMed ID: 15788729 [Abstract] [Full Text] [Related]
6. A search for germline APC mutations in early onset colorectal cancer or familial colorectal cancer with normal DNA mismatch repair. Boardman LA, Schmidt S, Lindor NM, Burgart LJ, Cunningham JM, Price-Troska T, Snow K, Ahlquist DA, Thibodeau SN. Genes Chromosomes Cancer; 2001 Feb 01; 30(2):181-6. PubMed ID: 11135435 [Abstract] [Full Text] [Related]
7. Molecular analysis of colorectal cancer tumors from patients with mismatch repair proficient hereditary nonpolyposis colorectal cancer suggests novel carcinogenic pathways. Sánchez-de-Abajo A, de la Hoya M, van Puijenbroek M, Tosar A, López-Asenjo JA, Díaz-Rubio E, Morreau H, Caldes T. Clin Cancer Res; 2007 Oct 01; 13(19):5729-35. PubMed ID: 17908962 [Abstract] [Full Text] [Related]
8. Comprehensive characterization of HNPCC-related colorectal cancers reveals striking molecular features in families with no germline mismatch repair gene mutations. Abdel-Rahman WM, Ollikainen M, Kariola R, Järvinen HJ, Mecklin JP, Nyström-Lahti M, Knuutila S, Peltomäki P. Oncogene; 2005 Feb 24; 24(9):1542-51. PubMed ID: 15674332 [Abstract] [Full Text] [Related]
9. A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancer. Froggatt NJ, Green J, Brassett C, Evans DG, Bishop DT, Kolodner R, Maher ER. J Med Genet; 1999 Feb 24; 36(2):97-102. PubMed ID: 10051005 [Abstract] [Full Text] [Related]