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PUBMED FOR HANDHELDS

Journal Abstract Search


320 related items for PubMed ID: 21063410

  • 21. First evidence for digenic inheritance in hereditary colorectal cancer by mutations in the base excision repair genes.
    Morak M, Massdorf T, Sykora H, Kerscher M, Holinski-Feder E.
    Eur J Cancer; 2011 May; 47(7):1046-55. PubMed ID: 21195604
    [Abstract] [Full Text] [Related]

  • 22. Risk of colorectal cancer for carriers of mutations in MUTYH, with and without a family history of cancer.
    Win AK, Dowty JG, Cleary SP, Kim H, Buchanan DD, Young JP, Clendenning M, Rosty C, MacInnis RJ, Giles GG, Boussioutas A, Macrae FA, Parry S, Goldblatt J, Baron JA, Burnett T, Le Marchand L, Newcomb PA, Haile RW, Hopper JL, Cotterchio M, Gallinger S, Lindor NM, Tucker KM, Winship IM, Jenkins MA.
    Gastroenterology; 2014 May; 146(5):1208-11.e1-5. PubMed ID: 24444654
    [Abstract] [Full Text] [Related]

  • 23. Increased colorectal cancer incidence in obligate carriers of heterozygous mutations in MUTYH.
    Jones N, Vogt S, Nielsen M, Christian D, Wark PA, Eccles D, Edwards E, Evans DG, Maher ER, Vasen HF, Hes FJ, Aretz S, Sampson JR.
    Gastroenterology; 2009 Aug; 137(2):489-94, 494.e1; quiz 725-6. PubMed ID: 19394335
    [Abstract] [Full Text] [Related]

  • 24. Characteristics of MUTYH variants in Japanese colorectal polyposis patients.
    Takao M, Yamaguchi T, Eguchi H, Tada Y, Kohda M, Koizumi K, Horiguchi SI, Okazaki Y, Ishida H.
    Int J Clin Oncol; 2018 Jun; 23(3):497-503. PubMed ID: 29330641
    [Abstract] [Full Text] [Related]

  • 25. High prevalence of the c.1227_1228dup (p.Glu410GlyfsX43) mutation in Tunisian families affected with MUTYH-associated-polyposis.
    Abdelmaksoud-Dammak R, Miladi-Abdennadher I, Amouri A, Tahri N, Ayadi L, Khabir A, Frikha F, Gargouri A, Mokdad-Gargouri R.
    Fam Cancer; 2012 Sep; 11(3):503-8. PubMed ID: 22744763
    [Abstract] [Full Text] [Related]

  • 26. MUTYH-associated polyposis (MAP).
    Nielsen M, Morreau H, Vasen HF, Hes FJ.
    Crit Rev Oncol Hematol; 2011 Jul; 79(1):1-16. PubMed ID: 20663686
    [Abstract] [Full Text] [Related]

  • 27.
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  • 28. Risk of colorectal cancer for people with a mutation in both a MUTYH and a DNA mismatch repair gene.
    Win AK, Reece JC, Buchanan DD, Clendenning M, Young JP, Cleary SP, Kim H, Cotterchio M, Dowty JG, MacInnis RJ, Tucker KM, Winship IM, Macrae FA, Burnett T, Le Marchand L, Casey G, Haile RW, Newcomb PA, Thibodeau SN, Lindor NM, Hopper JL, Gallinger S, Jenkins MA.
    Fam Cancer; 2015 Dec; 14(4):575-83. PubMed ID: 26202870
    [Abstract] [Full Text] [Related]

  • 29. The thorough screening of the MUTYH gene in a large French cohort of sporadic colorectal cancers.
    Küry S, Buecher B, Robiou-du-Pont S, Scoul C, Colman H, Lelièvre B, Olschwang S, Le Houérou C, Le Neel T, Faroux R, Ollivry J, Lafraise B, Chupin LD, Bézieau S.
    Genet Test; 2007 Dec; 11(4):373-9. PubMed ID: 17931073
    [Abstract] [Full Text] [Related]

  • 30. Increased frequency of disease-causing MYH mutations in colon cancer families.
    Peterlongo P, Mitra N, Sanchez de Abajo A, de la Hoya M, Bassi C, Bertario L, Radice P, Glogowski E, Nafa K, Caldes T, Offit K, Ellis NA.
    Carcinogenesis; 2006 Nov; 27(11):2243-9. PubMed ID: 16774938
    [Abstract] [Full Text] [Related]

  • 31. MUTYH gene variants and breast cancer in a Dutch case–control study.
    Out AA, Wasielewski M, Huijts PE, van Minderhout IJ, Houwing-Duistermaat JJ, Tops CM, Nielsen M, Seynaeve C, Wijnen JT, Breuning MH, van Asperen CJ, Schutte M, Hes FJ, Devilee P.
    Breast Cancer Res Treat; 2012 Jul; 134(1):219-27. PubMed ID: 22297469
    [Abstract] [Full Text] [Related]

  • 32. Low frequency of AXIN2 mutations and high frequency of MUTYH mutations in patients with multiple polyposis.
    Lejeune S, Guillemot F, Triboulet JP, Cattan S, Mouton C, PAFNORD Group, Porchet N, Manouvrier S, Buisine MP.
    Hum Mutat; 2006 Oct; 27(10):1064. PubMed ID: 16941501
    [Abstract] [Full Text] [Related]

  • 33. Association between monoallelic MUTYH mutation and colorectal cancer risk: a meta-regression analysis.
    Win AK, Hopper JL, Jenkins MA.
    Fam Cancer; 2011 Mar; 10(1):1-9. PubMed ID: 21061173
    [Abstract] [Full Text] [Related]

  • 34. Contribution of common monoallelic MUTYH gene variants in German patients with familial colorectal cancer.
    Grünhage F, Jungck M, Lamberti C, Schulte-Witte H, Plassmann D, Becker U, Rahner N, Aretz S, Friedrichs N, Buettner R, Sauerbruch T, Lammert F.
    Cancer Biomark; 2008 Mar; 4(2):55-61. PubMed ID: 18503156
    [Abstract] [Full Text] [Related]

  • 35. Frequent mutation in North African patients with MUTYH-associated polyposis.
    Lefevre JH, Colas C, Coulet F, Baert-Desurmont S, Mongin C, Tiret E, Frebourg T, Soubrier F, Parc Y.
    Clin Genet; 2011 Oct; 80(4):389-93. PubMed ID: 21443744
    [Abstract] [Full Text] [Related]

  • 36. Association of MUTYH Gln324His and APEX1 Asp148Glu with colorectal cancer and smoking in a Japanese population.
    Kasahara M, Osawa K, Yoshida K, Miyaishi A, Osawa Y, Inoue N, Tsutou A, Tabuchi Y, Tanaka K, Yamamoto M, Shimada E, Takahashi J.
    J Exp Clin Cancer Res; 2008 Sep 30; 27(1):49. PubMed ID: 18823566
    [Abstract] [Full Text] [Related]

  • 37. Cost-utility analysis of genetic screening in families of patients with germline MUTYH mutations.
    Nielsen M, Hes FJ, Vasen HF, van den Hout WB.
    BMC Med Genet; 2007 Jul 02; 8():42. PubMed ID: 17605803
    [Abstract] [Full Text] [Related]

  • 38. Efficacy of immune checkpoint blockade in MUTYH-associated hereditary colorectal cancer.
    Volkov NM, Yanus GA, Ivantsov AO, Moiseenko FV, Matorina OG, Bizin IV, Moiseyenko VM, Imyanitov EN.
    Invest New Drugs; 2020 Jun 02; 38(3):894-898. PubMed ID: 31377904
    [Abstract] [Full Text] [Related]

  • 39. An in-frame exon-skipping MUTYH mutation is associated with early-onset colorectal cancer.
    Fostira F, Papademitriou C, Efremidis A, Yannoukakos D.
    Dis Colon Rectum; 2010 Aug 02; 53(8):1197-201. PubMed ID: 20628285
    [Abstract] [Full Text] [Related]

  • 40. The value of MUTYH testing in patients with early onset microsatellite stable colorectal cancer referred for hereditary nonpolyposis colon cancer syndrome testing.
    Riegert-Johnson DL, Johnson RA, Rabe KG, Wang L, Thomas B, Baudhuin LM, Thibodeau SN, Boardman LA.
    Genet Test; 2007 Aug 02; 11(4):361-5. PubMed ID: 18294051
    [Abstract] [Full Text] [Related]


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