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182 related items for PubMed ID: 25590978

  • 1. Racial variation in frequency and phenotypes of APC and MUTYH mutations in 6,169 individuals undergoing genetic testing.
    Inra JA, Steyerberg EW, Grover S, McFarland A, Syngal S, Kastrinos F.
    Genet Med; 2015 Oct; 17(10):815-21. PubMed ID: 25590978
    [Abstract] [Full Text] [Related]

  • 2. Prevalence and phenotypes of APC and MUTYH mutations in patients with multiple colorectal adenomas.
    Grover S, Kastrinos F, Steyerberg EW, Cook EF, Dewanwala A, Burbidge LA, Wenstrup RJ, Syngal S.
    JAMA; 2012 Aug 01; 308(5):485-492. PubMed ID: 22851115
    [Abstract] [Full Text] [Related]

  • 3. MUTYH hotspot mutations in unselected colonoscopy patients.
    Casper M, Plotz G, Juengling B, Zeuzem S, Lammert F, Raedle J.
    Colorectal Dis; 2012 May 01; 14(5):e238-44. PubMed ID: 22469480
    [Abstract] [Full Text] [Related]

  • 4. Clinical characterization and mutation spectrum in patients with familial adenomatous polyposis in China.
    Li N, Kang Q, Yang L, Zhao XJ, Xue LJ, Wang X, Li AQ, Li CG, Sheng JQ.
    J Gastroenterol Hepatol; 2019 Sep 01; 34(9):1497-1503. PubMed ID: 31062380
    [Abstract] [Full Text] [Related]

  • 5. Clinical characterization and mutation spectrum in Hispanic families with adenomatous polyposis syndromes.
    Cruz-Correa M, Diaz-Algorri Y, Mendez V, Vazquez PJ, Lozada ME, Freyre K, Lathroum L, Gonzalez-Pons M, Hernandez-Marrero J, Giardiello F, Rodriguez-Quilichini S.
    Fam Cancer; 2013 Sep 01; 12(3):555-62. PubMed ID: 23460355
    [Abstract] [Full Text] [Related]

  • 6. Contribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in Hungary.
    Papp J, Kovacs ME, Matrai Z, Orosz E, Kásler M, Børresen-Dale AL, Olah E.
    Fam Cancer; 2016 Jan 01; 15(1):85-97. PubMed ID: 26446593
    [Abstract] [Full Text] [Related]

  • 7. Multi-gene panel testing confirms phenotypic variability in MUTYH-Associated Polyposis.
    Sutcliffe EG, Bartenbaker Thompson A, Stettner AR, Marshall ML, Roberts ME, Susswein LR, Wang Y, Klein RT, Hruska KS, Solomon BD.
    Fam Cancer; 2019 Apr 01; 18(2):203-209. PubMed ID: 30604180
    [Abstract] [Full Text] [Related]

  • 8. Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposis.
    Nielsen M, Hes FJ, Nagengast FM, Weiss MM, Mathus-Vliegen EM, Morreau H, Breuning MH, Wijnen JT, Tops CM, Vasen HF.
    Clin Genet; 2007 May 01; 71(5):427-33. PubMed ID: 17489848
    [Abstract] [Full Text] [Related]

  • 9. Presentation and Follow-up of Familial Adenomatous Polyposis: Differences Between APC and MUTYH Mutations.
    Bademci R, Bollo J, Ramón Y Cajal T, Martínez MC, Hernández MP, Targarona EM.
    Cir Esp (Engl Ed); 2020 Oct 01; 98(8):465-471. PubMed ID: 32505560
    [Abstract] [Full Text] [Related]

  • 10. Increased risk for colorectal adenomas and cancer in mono-allelic MUTYH mutation carriers: results from a cohort of North-African Jews.
    Rosner G, Bercovich D, Daniel YE, Strul H, Fliss-Isakov N, Ben-Yehoiada M, Santo E, Halpern Z, Kariv R.
    Fam Cancer; 2015 Sep 01; 14(3):427-36. PubMed ID: 25822476
    [Abstract] [Full Text] [Related]

  • 11. Somatic c.34G>T KRAS mutation: a new prescreening test for MUTYH-associated polyposis?
    Aimé A, Coulet F, Lefevre JH, Colas C, Cervera P, Flejou JF, Lascols O, Soubrier F, Parc Y.
    Cancer Genet; 2015 Sep 01; 208(7-8):390-5. PubMed ID: 26056087
    [Abstract] [Full Text] [Related]

  • 12. MUTYH-associated polyposis - variability of the clinical phenotype in patients with biallelic and monoallelic MUTYH mutations and report on novel mutations.
    Morak M, Laner A, Bacher U, Keiling C, Holinski-Feder E.
    Clin Genet; 2010 Oct 01; 78(4):353-63. PubMed ID: 20618354
    [Abstract] [Full Text] [Related]

  • 13. Declining detection rates for APC and biallelic MUTYH variants in polyposis patients, implications for DNA testing policy.
    Terlouw D, Suerink M, Singh SS, Gille HJJP, Hes FJ, Langers AMJ, Morreau H, Vasen HFA, Vos YJ, van Wezel T, Tops CM, Ten Broeke SW, Nielsen M.
    Eur J Hum Genet; 2020 Feb 01; 28(2):222-230. PubMed ID: 31527860
    [Abstract] [Full Text] [Related]

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  • 15. 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 01; 27(10):1064. PubMed ID: 16941501
    [Abstract] [Full Text] [Related]

  • 16. Novel mutations and phenotypic associations identified through APC, MUTYH, NTHL1, POLD1, POLE gene analysis in Indian Familial Adenomatous Polyposis cohort.
    Khan N, Lipsa A, Arunachal G, Ramadwar M, Sarin R.
    Sci Rep; 2017 May 22; 7(1):2214. PubMed ID: 28533537
    [Abstract] [Full Text] [Related]

  • 17. Heterogeneous molecular mechanisms underlie attenuated familial adenomatous polyposis.
    Cattaneo F, Molatore S, Mihalatos M, Apessos A, Venesio T, Bione S, Grignani P, Nasioulas G, Ranzani GN.
    Genet Med; 2007 Dec 22; 9(12):836-41. PubMed ID: 18091433
    [Abstract] [Full Text] [Related]

  • 18. Correlation between mutations and mRNA expression of APC and MUTYH genes: new insight into hereditary colorectal polyposis predisposition.
    Aceto GM, Fantini F, De Iure S, Di Nicola M, Palka G, Valanzano R, Di Gregorio P, Stigliano V, Genuardi M, Battista P, Cama A, Curia MC.
    J Exp Clin Cancer Res; 2015 Oct 28; 34():131. PubMed ID: 26511139
    [Abstract] [Full Text] [Related]

  • 19. APC or MUTYH mutations account for the majority of clinically well-characterized families with FAP and AFAP phenotype and patients with more than 30 adenomas.
    Filipe B, Baltazar C, Albuquerque C, Fragoso S, Lage P, Vitoriano I, Mão de Ferro S, Claro I, Rodrigues P, Fidalgo P, Chaves P, Cravo M, Nobre Leitão C.
    Clin Genet; 2009 Sep 28; 76(3):242-55. PubMed ID: 19793053
    [Abstract] [Full Text] [Related]

  • 20. Characterizing germline APC and MUTYH variants in Ashkenazi Jews compared to other individuals.
    Ukaegbu C, Levi Z, Fehlmann TD, Uno H, Chittenden A, Inra JA, Grover S, Kastrinos F, Syngal S, Yurgelun MB.
    Fam Cancer; 2021 Apr 28; 20(2):111-116. PubMed ID: 32743790
    [Abstract] [Full Text] [Related]

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