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Journal Abstract Search

1480 related items for PubMed ID: 16116158

  • 1. Use of molecular tumor characteristics to prioritize mismatch repair gene testing in early-onset colorectal cancer.
    Southey MC, Jenkins MA, Mead L, Whitty J, Trivett M, Tesoriero AA, Smith LD, Jennings K, Grubb G, Royce SG, Walsh MD, Barker MA, Young JP, Jass JR, St John DJ, Macrae FA, Giles GG, Hopper JL.
    J Clin Oncol; 2005 Sep 20; 23(27):6524-32. PubMed ID: 16116158
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  • 7. 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 Sep 20; 105(1-2):79-85. PubMed ID: 10480359
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  • 8. Microsatellite instability and novel mismatch repair gene mutations in northern Chinese population with hereditary non-polyposis colorectal cancer.
    Sheng JQ, Chan TL, Chan YW, Huang JS, Chen JG, Zhang MZ, Guo XL, Mu H, Chan AS, Li SR, Yuen ST, Leung SY.
    Chin J Dig Dis; 2006 Sep 20; 7(4):197-205. PubMed ID: 17054581
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  • 10. 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 01; 21(23):4364-70. PubMed ID: 14645426
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  • 13. Evaluating the performance of clinical criteria for predicting mismatch repair gene mutations in Lynch syndrome: a comprehensive analysis of 3,671 families.
    Steinke V, Holzapfel S, Loeffler M, Holinski-Feder E, Morak M, Schackert HK, Görgens H, Pox C, Royer-Pokora B, von Knebel-Doeberitz M, Büttner R, Propping P, Engel C, German HNPCC Consortium.
    Int J Cancer; 2014 Jul 01; 135(1):69-77. PubMed ID: 24493211
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  • 14. Characterization of mutator phenotype in familial colorectal cancer patients not fulfilling amsterdam criteria.
    Kim JC, Lee KH, Ka IH, Koo KH, Roh SA, Kim HC, Yu CS, Kim TW, Chang HM, Gong GY, Kim JS.
    Clin Cancer Res; 2004 Sep 15; 10(18 Pt 1):6159-68. PubMed ID: 15448003
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  • 16. 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 01; 20(5):1203-8. PubMed ID: 11870161
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  • 17. Feasibility of screening for Lynch syndrome among patients with colorectal cancer.
    Hampel H, Frankel WL, Martin E, Arnold M, Khanduja K, Kuebler P, Clendenning M, Sotamaa K, Prior T, Westman JA, Panescu J, Fix D, Lockman J, LaJeunesse J, Comeras I, de la Chapelle A.
    J Clin Oncol; 2008 Dec 10; 26(35):5783-8. PubMed ID: 18809606
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  • 18. The contribution of the hereditary nonpolyposis colorectal cancer syndrome to the development of ovarian cancer.
    Malander S, Rambech E, Kristoffersson U, Halvarsson B, Ridderheim M, Borg A, Nilbert M.
    Gynecol Oncol; 2006 May 10; 101(2):238-43. PubMed ID: 16360201
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  • 19. Microsatellite instability testing in colorectal carcinoma: choice of markers affects sensitivity of detection of mismatch repair-deficient tumors.
    Hatch SB, Lightfoot HM, Garwacki CP, Moore DT, Calvo BF, Woosley JT, Sciarrotta J, Funkhouser WK, Farber RA.
    Clin Cancer Res; 2005 Mar 15; 11(6):2180-7. PubMed ID: 15788665
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  • 20. Microsatellite instability analysis and/or immunostaining for the diagnosis of hereditary nonpolyposis colorectal cancer?
    Halvarsson B, Lindblom A, Rambech E, Lagerstedt K, Nilbert M.
    Virchows Arch; 2004 Feb 15; 444(2):135-41. PubMed ID: 14652751
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