203 related articles for article (PubMed ID: 12072462)
21. Sequence analysis of the mismatch repair gene hMSH6 in the germline of patients with familial and sporadic colorectal cancer.
Plaschke J; Kruppa C; Tischler R; Bocker T; Pistorius S; Dralle H; Rüschoff J; Saeger HD; Fishel R; Schackert HK
Int J Cancer; 2000 Mar; 85(5):606-13. PubMed ID: 10699937
[TBL] [Abstract][Full Text] [Related]
22. Loss of DNA mismatch repair proteins in skin tumors from patients with Muir-Torre syndrome and MSH2 or MLH1 germline mutations: establishment of immunohistochemical analysis as a screening test.
Mathiak M; Rütten A; Mangold E; Fischer HP; Ruzicka T; Friedl W; Propping P; Kruse R
Am J Surg Pathol; 2002 Mar; 26(3):338-43. PubMed ID: 11859205
[TBL] [Abstract][Full Text] [Related]
23. Two mismatch repair gene mutations found in a colon cancer patient--which one is pathogenic?
Kariola R; Otway R; Lönnqvist KE; Raevaara TE; Macrae F; Vos YJ; Kohonen-Corish M; Hofstra RM; Nyström-Lahti M
Hum Genet; 2003 Feb; 112(2):105-9. PubMed ID: 12522549
[TBL] [Abstract][Full Text] [Related]
24. Hereditary and somatic DNA mismatch repair gene mutations in sporadic endometrial carcinoma.
Chadwick RB; Pyatt RE; Niemann TH; Richards SK; Johnson CK; Stevens MW; Meek JE; Hampel H; Prior TW; de la Chapelle A
J Med Genet; 2001 Jul; 38(7):461-6. PubMed ID: 11474654
[No Abstract] [Full Text] [Related]
25. Oncogenic pathway of sporadic colorectal cancer with novel germline missense mutations in the hMSH2 gene.
Yamada K; Zhong X; Kanazawa S; Koike J; Tsujita K; Hemmi H
Oncol Rep; 2003; 10(4):859-66. PubMed ID: 12792735
[TBL] [Abstract][Full Text] [Related]
26. [HNPCC syndrome, microsatellite instability and NF1 gene alteration].
Puisieux A
Bull Cancer; 1999 Oct; 86(10):812-4. PubMed ID: 10572231
[TBL] [Abstract][Full Text] [Related]
27. DNA mismatch repair and the significance of a sebaceous skin tumor for visceral cancer prevention.
Kruse R; Ruzicka T
Trends Mol Med; 2004 Mar; 10(3):136-41. PubMed ID: 15102357
[TBL] [Abstract][Full Text] [Related]
28. Bethesda guidelines: relation to microsatellite instability and MLH1 promoter methylation in patients with colorectal cancer.
Raedle J; Trojan J; Brieger A; Weber N; Schäfer D; Plotz G; Staib-Sebler E; Kriener S; Lorenz M; Zeuzem S
Ann Intern Med; 2001 Oct; 135(8 Pt 1):566-76. PubMed ID: 11601928
[TBL] [Abstract][Full Text] [Related]
29. Impact of microsatellite testing and mismatch repair protein expression on the clinical interpretation of genetic testing in hereditary non-polyposis colorectal cancer.
Ward R; Meldrum C; Williams R; Mokany E; Scott R; Turner J; Hawkins N; Burgess B; Groombridge C; Spigelman A
J Cancer Res Clin Oncol; 2002 Aug; 128(8):403-11. PubMed ID: 12200596
[TBL] [Abstract][Full Text] [Related]
30. Allelic imbalance at the DNA mismatch repair loci, hMSH2, hMLH1, hPMS1, hPMS2 and hMSH3, in squamous cell carcinoma of the head and neck.
Nunn J; Nagini S; Risk JM; Prime W; Maloney P; Liloglou T; Jones AS; Rogers SR; Gosney JR; Woolgar J; Field JK
Oral Oncol; 2003 Feb; 39(2):115-29. PubMed ID: 12509964
[TBL] [Abstract][Full Text] [Related]
31. The colon cancer burden of genetically defined hereditary nonpolyposis colon cancer.
Samowitz WS; Curtin K; Lin HH; Robertson MA; Schaffer D; Nichols M; Gruenthal K; Leppert MF; Slattery ML
Gastroenterology; 2001 Oct; 121(4):830-8. PubMed ID: 11606497
[TBL] [Abstract][Full Text] [Related]
32. Family history characteristics, tumor microsatellite instability and germline MSH2 and MLH1 mutations in hereditary colorectal cancer.
Bapat BV; Madlensky L; Temple LK; Hiruki T; Redston M; Baron DL; Xia L; Marcus VA; Soravia C; Mitri A; Shen W; Gryfe R; Berk T; Chodirker BN; Cohen Z; Gallinger S
Hum Genet; 1999 Feb; 104(2):167-76. PubMed ID: 10190329
[TBL] [Abstract][Full Text] [Related]
33. Spectrum of germ-line MLH1 and MSH2 mutations in Austrian patients with hereditary nonpolyposis colorectal cancer.
Wolf B; Henglmueller S; Janschek E; Ilencikova D; Ludwig-Papst C; Bergmann M; Mannhalter C; Wrba F; Karner-Hanusch J
Wien Klin Wochenschr; 2005 Apr; 117(7-8):269-77. PubMed ID: 15926618
[TBL] [Abstract][Full Text] [Related]
34. Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis.
de Leon MP; Pedroni M; Benatti P; Percesepe A; Di Gregorio C; Foroni M; Rossi G; Genuardi M; Neri G; Leonardi F; Viel A; Capozzi E; Boiocchi M; Roncucci L
Gut; 1999 Jul; 45(1):32-8. PubMed ID: 10369701
[TBL] [Abstract][Full Text] [Related]
35. The relative roles of three DNA repair pathways in preventing Caenorhabditis elegans mutation accumulation.
Denver DR; Feinberg S; Steding C; Durbin MD; Lynch M
Genetics; 2006 Sep; 174(1):57-65. PubMed ID: 16783005
[TBL] [Abstract][Full Text] [Related]
36. Microsatellite instability in gynecological sarcomas and in hMSH2 mutant uterine sarcoma cell lines defective in mismatch repair activity.
Risinger JI; Umar A; Boyer JC; Evans AC; Berchuck A; Kunkel TA; Barrett JC
Cancer Res; 1995 Dec; 55(23):5664-9. PubMed ID: 7585651
[TBL] [Abstract][Full Text] [Related]
37. Novel germline mutation (300-305delAGTTGA) in the human MSH2 gene in hereditary non-polyposis colorectal cancer (HNPCC).
Glasl S; Papatheodorou L; Baretton G; Jung C; Gross M
Hum Mutat; 2000 Jul; 16(1):91-2. PubMed ID: 10874318
[TBL] [Abstract][Full Text] [Related]
38. Mutation rate and spectrum in obligately outcrossing Caenorhabditis elegans mutation accumulation lines subjected to RNAi-induced knockdown of the mismatch repair gene msh-2.
Katju V; Konrad A; Deiss TC; Bergthorsson U
G3 (Bethesda); 2022 Jan; 12(1):. PubMed ID: 34849777
[TBL] [Abstract][Full Text] [Related]
39. Mutator phenotype in Msh2-deficient murine embryonic fibroblasts.
Reitmair AH; Risley R; Bristow RG; Wilson T; Ganesh A; Jang A; Peacock J; Benchimol S; Hill RP; Mak TW; Fishel R; Meuth M
Cancer Res; 1997 Sep; 57(17):3765-71. PubMed ID: 9288785
[TBL] [Abstract][Full Text] [Related]
40. Mismatch repair and microsatellite instability in esophageal cancer cells.
Uchida N; Kumimoto H; Nishizawa K; Tokumasu S; Harada H; Shimada Y; Ishizaki K
Int J Cancer; 2001 Mar; 91(5):687-91. PubMed ID: 11267981
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
