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6. Clinical features and mismatch repair gene mutation screening in Chinese patients with hereditary nonpolyposis colorectal carcinoma. Liu SR; Zhao B; Wang ZJ; Wan YL; Huang YT World J Gastroenterol; 2004 Sep; 10(18):2647-51. PubMed ID: 15309712 [TBL] [Abstract][Full Text] [Related]
7. Hypermethylation of the hMLH1 promoter in colon cancer with microsatellite instability. Cunningham JM; Christensen ER; Tester DJ; Kim CY; Roche PC; Burgart LJ; Thibodeau SN Cancer Res; 1998 Aug; 58(15):3455-60. PubMed ID: 9699680 [TBL] [Abstract][Full Text] [Related]
8. Mutations of hMLH1 and hMSH2 in patients with suspected hereditary nonpolyposis colorectal cancer: correlation with microsatellite instability and abnormalities of mismatch repair protein expression. Scartozzi M; Bianchi F; Rosati S; Galizia E; Antolini A; Loretelli C; Piga A; Bearzi I; Cellerino R; Porfiri E J Clin Oncol; 2002 Mar; 20(5):1203-8. PubMed ID: 11870161 [TBL] [Abstract][Full Text] [Related]
9. hMLH1 and hMSH2 expression in human hepatocellular carcinoma. Wang L; Bani-Hani A; Montoya DP; Roche PC; Thibodeau SN; Burgart LJ; Roberts LR Int J Oncol; 2001 Sep; 19(3):567-70. PubMed ID: 11494037 [TBL] [Abstract][Full Text] [Related]
10. Germline, somatic and epigenetic events underlying mismatch repair deficiency in colorectal and HNPCC-related cancers. Yuen ST; Chan TL; Ho JW; Chan AS; Chung LP; Lam PW; Tse CW; Wyllie AH; Leung SY Oncogene; 2002 Oct; 21(49):7585-92. PubMed ID: 12386821 [TBL] [Abstract][Full Text] [Related]
11. Mutational analysis of promoters of mismatch repair genes hMSH2 and hMLH1 in hereditary nonpolyposis colorectal cancer and early onset colorectal cancer patients: identification of three novel germ-line mutations in promoter of the hMSH2 gene. Shin KH; Shin JH; Kim JH; Park JG Cancer Res; 2002 Jan; 62(1):38-42. PubMed ID: 11782355 [TBL] [Abstract][Full Text] [Related]
12. Causes of microsatellite instability in colorectal tumors: implications for hereditary non-polyposis colorectal cancer screening. Potocnik U; Glavac D; Golouh R; Ravnik-Glavac M Cancer Genet Cytogenet; 2001 Apr; 126(2):85-96. PubMed ID: 11376800 [TBL] [Abstract][Full Text] [Related]
13. Association between family history and mismatch repair in colorectal cancer. Coggins RP; Cawkwell L; Bell SM; Crockford GP; Quirke P; Finan PJ; Bishop DT Gut; 2005 May; 54(5):636-42. PubMed ID: 15831908 [TBL] [Abstract][Full Text] [Related]
14. Prevalence of germline mutations of hMLH1, hMSH2, hPMS1, hPMS2, and hMSH6 genes in 75 French kindreds with nonpolyposis colorectal cancer. Wang Q; Lasset C; Desseigne F; Saurin JC; Maugard C; Navarro C; Ruano E; Descos L; Trillet-Lenoir V; Bosset JF; Puisieux A Hum Genet; 1999; 105(1-2):79-85. PubMed ID: 10480359 [TBL] [Abstract][Full Text] [Related]
15. Loss of hMSH2 and hMSH6 expression is frequent in sporadic endometrial carcinomas with microsatellite instability: a population-based study. Stefansson I; Akslen LA; MacDonald N; Ryan A; Das S; Jacobs IJ; Salvesen HB Clin Cancer Res; 2002 Jan; 8(1):138-43. PubMed ID: 11801550 [TBL] [Abstract][Full Text] [Related]
16. Screening for defective DNA mismatch repair in stage II and III colorectal cancer patients. Chai SM; Zeps N; Shearwood AM; Grieu F; Charles A; Harvey J; Goldblatt J; Joseph D; Iacopetta B Clin Gastroenterol Hepatol; 2004 Nov; 2(11):1017-25. PubMed ID: 15551255 [TBL] [Abstract][Full Text] [Related]
17. hMLH1, hMSH2 and hMSH6 mutations in hereditary non-polyposis colorectal cancer families from southern Sweden. Planck M; Koul A; Fernebro E; Borg A; Kristoffersson U; Olsson H; Wenngren E; Mangell P; Nilbert M Int J Cancer; 1999 Oct; 83(2):197-202. PubMed ID: 10471527 [TBL] [Abstract][Full Text] [Related]
18. Novel hMLH1 and hMSH2 germline mutations in African Americans with colorectal cancer. Weber TK; Chin HM; Rodriguez-Bigas M; Keitz B; Gilligan R; O'Malley L; Urf E; Diba N; Pazik J; Petrelli NJ JAMA; 1999 Jun 23-30; 281(24):2316-20. PubMed ID: 10386556 [TBL] [Abstract][Full Text] [Related]
19. Immunohistochemistry for hMLH1 and hMSH2: a practical test for DNA mismatch repair-deficient tumors. Marcus VA; Madlensky L; Gryfe R; Kim H; So K; Millar A; Temple LK; Hsieh E; Hiruki T; Narod S; Bapat BV; Gallinger S; Redston M Am J Surg Pathol; 1999 Oct; 23(10):1248-55. PubMed ID: 10524526 [TBL] [Abstract][Full Text] [Related]
20. Microsatellite mutations of transforming growth factor-beta receptor type II and caspase-5 occur in human precursor T-cell lymphoblastic lymphomas/leukemias in vivo but are not associated with hMSH2 or hMLH1 promoter methylation. Scott S; Kimura T; Ichinohasama R; Bergen S; Magliocco A; Reimer C; Kerviche A; Sheridan D; DeCoteau JF Leuk Res; 2003 Jan; 27(1):23-34. PubMed ID: 12479849 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]