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.
222 related articles for article (PubMed ID: 14749686)
1. Immunoassay for wild-type protein in lymphocytes predicts germline mutations in patients at risk for hereditary colorectal cancer. Fields JZ; Gao Z; Gao Z; Lewis M; Maimonis P; Harvey J; Lynch HT; Boman BM J Lab Clin Med; 2004 Jan; 143(1):59-66. PubMed ID: 14749686 [TBL] [Abstract][Full Text] [Related]
2. The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas. Cunningham JM; Kim CY; Christensen ER; Tester DJ; Parc Y; Burgart LJ; Halling KC; McDonnell SK; Schaid DJ; Walsh Vockley C; Kubly V; Nelson H; Michels VV; Thibodeau SN Am J Hum Genet; 2001 Oct; 69(4):780-90. PubMed ID: 11524701 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Clinical findings with implications for genetic testing in families with clustering of colorectal cancer. Wijnen JT; Vasen HF; Khan PM; Zwinderman AH; van der Klift H; Mulder A; Tops C; Møller P; Fodde R N Engl J Med; 1998 Aug; 339(8):511-8. PubMed ID: 9709044 [TBL] [Abstract][Full Text] [Related]
6. [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]
7. Association of colonic and endometrial carcinomas in Portuguese families with hereditary nonpolyposis colorectal carcinoma significantly increases the probability of detecting a pathogenic mutation in mismatch repair genes, primarily the MSH2 gene. Lage PA; Albuquerque C; Sousa RG; Cravo ML; Salazar M; Francisco I; Maia L; Claro I; Suspiro A; Rodrigues P; Raposo H; Fidalgo PA; Nobre-Leitão C Cancer; 2004 Jul; 101(1):172-7. PubMed ID: 15222003 [TBL] [Abstract][Full Text] [Related]
8. Germline mutations of hMLH1 and hMSH2 genes in patients with suspected hereditary nonpolyposis colorectal cancer and sporadic early-onset colorectal cancer. Yuan Y; Han HJ; Zheng S; Park JG Dis Colon Rectum; 1998 Apr; 41(4):434-40. PubMed ID: 9559627 [TBL] [Abstract][Full Text] [Related]
9. Detection of DNA mismatch repair proteins in fresh human blood lymphocytes--towards a novel method for hereditary non-polyposis colorectal cancer (Lynch syndrome) screening. Hassen S; Boman BM; Ali N; Parker M; Somerman C; Ali-Khan Catts ZJ; Ali AA; Fields JZ J Exp Clin Cancer Res; 2011 Oct; 30(1):100. PubMed ID: 22017758 [TBL] [Abstract][Full Text] [Related]
10. Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium. Plaschke J; Engel C; Krüger S; Holinski-Feder E; Pagenstecher C; Mangold E; Moeslein G; Schulmann K; Gebert J; von Knebel Doeberitz M; Rüschoff J; Loeffler M; Schackert HK J Clin Oncol; 2004 Nov; 22(22):4486-94. PubMed ID: 15483016 [TBL] [Abstract][Full Text] [Related]
11. Accuracy of revised Bethesda guidelines, microsatellite instability, and immunohistochemistry for the identification of patients with hereditary nonpolyposis colorectal cancer. Piñol V; Castells A; Andreu M; Castellví-Bel S; Alenda C; Llor X; Xicola RM; Rodríguez-Moranta F; Payá A; Jover R; Bessa X; JAMA; 2005 Apr; 293(16):1986-94. PubMed ID: 15855432 [TBL] [Abstract][Full Text] [Related]
12. [The first molecular analysis of a Hungarian HNPCC family: a novel MSH2 germline mutation]. Czakó L; Tiszlavicz L; Takács R; Baradnay G; Lonovics J; Cserni G; Závodná K; Bartosova Z Orv Hetil; 2005 May; 146(20):1009-16. PubMed ID: 15945244 [TBL] [Abstract][Full Text] [Related]
13. MLH1 and MSH2 protein immunohistochemistry is useful for detection of hereditary non-polyposis colorectal cancer in young patients. Paraf F; Gilquin M; Longy M; Gilbert B; Gorry P; Petit B; Labrousse F Histopathology; 2001 Sep; 39(3):250-8. PubMed ID: 11532035 [TBL] [Abstract][Full Text] [Related]
14. Germline hMSH2 and hMLH1 gene mutations in incomplete HNPCC families. Wang Q; Desseigne F; Lasset C; Saurin JC; Navarro C; Yagci T; Keser I; Bagci H; Luleci G; Gelen T; Chayvialle JA; Puisieux A; Ozturk M Int J Cancer; 1997 Dec; 73(6):831-6. PubMed ID: 9399661 [TBL] [Abstract][Full Text] [Related]
15. Clinical and molecular characteristics of hereditary non-polyposis colorectal cancer families in Southeast Asia. Lee SC; Guo JY; Lim R; Soo R; Koay E; Salto-Tellez M; Leong A; Goh BC Clin Genet; 2005 Aug; 68(2):137-45. PubMed ID: 15996210 [TBL] [Abstract][Full Text] [Related]
16. MLH1 and MSH2 constitutional mutations in colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancer. Genuardi M; Anti M; Capozzi E; Leonardi F; Fornasarig M; Novella E; Bellacosa A; Valenti A; Gasbarrini GB; Roncucci L; Benatti P; Percesepe A; Ponz de Leòn M; Coco C; de Paoli A; Valentini M; Boiocchi M; Neri G; Viel A Int J Cancer; 1998 Mar; 75(6):835-9. PubMed ID: 9506527 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Prediction of the outcome of genetic testing in HNPCC kindreds using the revised Amsterdam criteria and immunohistochemistry. Stormorken AT; Müller W; Lemkemeyer B; Apold J; Wijnen JT; Fodde R; Möslein G; Møller P Fam Cancer; 2001; 1(3-4):169-73. PubMed ID: 14574174 [TBL] [Abstract][Full Text] [Related]
19. Molecular screening for hereditary nonpolyposis colorectal cancer: a prospective, population-based study. Percesepe A; Borghi F; Menigatti M; Losi L; Foroni M; Di Gregorio C; Rossi G; Pedroni M; Sala E; Vaccina F; Roncucci L; Benatti P; Viel A; Genuardi M; Marra G; Kristo P; Peltomäki P; Ponz de Leon M J Clin Oncol; 2001 Oct; 19(19):3944-50. PubMed ID: 11579115 [TBL] [Abstract][Full Text] [Related]
20. Toward new strategies to select young endometrial cancer patients for mismatch repair gene mutation analysis. Berends MJ; Wu Y; Sijmons RH; van der Sluis T; Ek WB; Ligtenberg MJ; Arts NJ; ten Hoor KA; Kleibeuker JH; de Vries EG; Mourits MJ; Hollema H; Buys CH; Hofstra RM; van der Zee AG J Clin Oncol; 2003 Dec; 21(23):4364-70. PubMed ID: 14645426 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]