These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
23. Microsatellite instability and expression of MLH1 and MSH2 in normal and malignant endometrial and ovarian epithelium in hereditary nonpolyposis colorectal cancer family members. Ichikawa Y; Lemon SJ; Wang S; Franklin B; Watson P; Knezetic JA; Bewtra C; Lynch HT Cancer Genet Cytogenet; 1999 Jul; 112(1):2-8. PubMed ID: 10432927 [TBL] [Abstract][Full Text] [Related]
24. Evaluation of microsatellite instability and immunohistochemistry for the prediction of germ-line MSH2 and MLH1 mutations in hereditary nonpolyposis colon cancer families. Wahlberg SS; Schmeits J; Thomas G; Loda M; Garber J; Syngal S; Kolodner RD; Fox E Cancer Res; 2002 Jun; 62(12):3485-92. PubMed ID: 12067992 [TBL] [Abstract][Full Text] [Related]
25. Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer. Viel A; Genuardi M; Capozzi E; Leonardi F; Bellacosa A; Paravatou-Petsotas M; Pomponi MG; Fornasarig M; Percesepe A; Roncucci L; Tamassia MG; Benatti P; Ponz de Leon M; Valenti A; Covino M; Anti M; Foletto M; Boiocchi M; Neri G Genes Chromosomes Cancer; 1997 Jan; 18(1):8-18. PubMed ID: 8993976 [TBL] [Abstract][Full Text] [Related]
26. Tumor buds show reduced expression of laminin-5 gamma 2 chain in DNA mismatch repair deficient colorectal cancer. Shinto E; Baker K; Tsuda H; Mochizuki H; Ueno H; Matsubara O; Foulkes WD; Jass JR Dis Colon Rectum; 2006 Aug; 49(8):1193-202. PubMed ID: 16773493 [TBL] [Abstract][Full Text] [Related]
27. 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]
28. Mutation analysis of the MLH1, MSH2 and MSH6 genes in patients with double primary cancers of the colorectum and the endometrium: a population-based study in northern Sweden. Cederquist K; Emanuelsson M; Göransson I; Holinski-Feder E; Müller-Koch Y; Golovleva I; Grönberg H Int J Cancer; 2004 Apr; 109(3):370-6. PubMed ID: 14961575 [TBL] [Abstract][Full Text] [Related]
29. Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. Aaltonen LA; Salovaara R; Kristo P; Canzian F; Hemminki A; Peltomäki P; Chadwick RB; Kääriäinen H; Eskelinen M; Järvinen H; Mecklin JP; de la Chapelle A N Engl J Med; 1998 May; 338(21):1481-7. PubMed ID: 9593786 [TBL] [Abstract][Full Text] [Related]
30. A polymorphism in the ATM gene modulates the penetrance of hereditary non-polyposis colorectal cancer. Maillet P; Chappuis PO; Vaudan G; Dobbie Z; Müller H; Hutter P; Sappino AP Int J Cancer; 2000 Dec; 88(6):928-31. PubMed ID: 11093816 [TBL] [Abstract][Full Text] [Related]
31. Mean age of tumor onset in hereditary nonpolyposis colorectal cancer (HNPCC) families correlates with the presence of mutations in DNA mismatch repair genes. Pensotti V; Radice P; Presciuttini S; Calistri D; Gazzoli I; Grimalt Perez A; Mondini P; Buonsanti G; Sala P; Rossetti C; Ranzani GN; Bertario L; Pierotti MA Genes Chromosomes Cancer; 1997 Jul; 19(3):135-42. PubMed ID: 9218993 [TBL] [Abstract][Full Text] [Related]
32. Molecular characterization of the spectrum of genomic deletions in the mismatch repair genes MSH2, MLH1, MSH6, and PMS2 responsible for hereditary nonpolyposis colorectal cancer (HNPCC). van der Klift H; Wijnen J; Wagner A; Verkuilen P; Tops C; Otway R; Kohonen-Corish M; Vasen H; Oliani C; Barana D; Moller P; Delozier-Blanchet C; Hutter P; Foulkes W; Lynch H; Burn J; Möslein G; Fodde R Genes Chromosomes Cancer; 2005 Oct; 44(2):123-38. PubMed ID: 15942939 [TBL] [Abstract][Full Text] [Related]
33. Hereditary nonpolyposis colorectal cancer in young colorectal cancer patients: high-risk clinic versus population-based registry. Terdiman JP; Levin TR; Allen BA; Gum JR; Fishbach A; Conrad PG; Miller GA; Weinberg V; Bachman R; Bergoffen J; Stembridge A; Toribara NW; Sleisenger MH; Kim YS Gastroenterology; 2002 Apr; 122(4):940-7. PubMed ID: 11910346 [TBL] [Abstract][Full Text] [Related]
34. Novel MLH1 and MSH2 germline mutations in the first HNPCC families identified in Slovakia. Bartosova Z; Fridrichova I; Bujalkova M; Wolf B; Ilencikova D; Krizan P; Hlavcak P; Palaj J; Lukac L; Lukacova M; Böör A; Haider R; Jiricny J; Nyström-Lahti M; Marra G Hum Mutat; 2003 Apr; 21(4):449. PubMed ID: 12655568 [TBL] [Abstract][Full Text] [Related]
35. Genetic testing for hereditary nonpolyposis colorectal cancer. Hoedema R; Monroe T; Bos C; Palmer S; Kim D; Marvin M; Luchtefeld M Am Surg; 2003 May; 69(5):387-91; discussion 391-2. PubMed ID: 12769209 [TBL] [Abstract][Full Text] [Related]
36. Immunohistochemistry and microsatellite instability testing for selecting MLH1, MSH2 and MSH6 mutation carriers in hereditary non-polyposis colorectal cancer. Caldés T; Godino J; Sanchez A; Corbacho C; De la Hoya M; Lopez Asenjo J; Saez C; Sanz J; Benito M; Ramon Y Cajal S; Diaz-Rubio E Oncol Rep; 2004 Sep; 12(3):621-9. PubMed ID: 15289847 [TBL] [Abstract][Full Text] [Related]
37. Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer. Mangold E; Pagenstecher C; Friedl W; Mathiak M; Buettner R; Engel C; Loeffler M; Holinski-Feder E; Müller-Koch Y; Keller G; Schackert HK; Krüger S; Goecke T; Moeslein G; Kloor M; Gebert J; Kunstmann E; Schulmann K; Rüschoff J; Propping P Int J Cancer; 2005 Sep; 116(5):692-702. PubMed ID: 15849733 [TBL] [Abstract][Full Text] [Related]
38. Mutations in MLH1 are more frequent than in MSH2 in sporadic colorectal cancers with microsatellite instability. Herfarth KK; Kodner IJ; Whelan AJ; Ivanovich JL; Bracamontes JR; Wells SA; Goodfellow PJ Genes Chromosomes Cancer; 1997 Jan; 18(1):42-9. PubMed ID: 8993979 [TBL] [Abstract][Full Text] [Related]
39. Hereditary nonpolyposis colorectal cancer: frequent occurrence of large genomic deletions in MSH2 and MLH1 genes. Wang Y; Friedl W; Lamberti C; Jungck M; Mathiak M; Pagenstecher C; Propping P; Mangold E Int J Cancer; 2003 Feb; 103(5):636-41. PubMed ID: 12494471 [TBL] [Abstract][Full Text] [Related]
40. [Clinical features and hMSH2/hMLH1 germline mutation screening of Chinese hereditary nonpolyposis colorectal cancer patients]. Liu SR; Wang ZJ; Zhao B; Wan YL; Huang YT Zhonghua Yi Xue Za Zhi; 2004 May; 84(9):714-7. PubMed ID: 15200905 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]