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Journal Abstract Search

397 related items for PubMed ID: 26056087

  • 1. 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; 208(7-8):390-5. PubMed ID: 26056087
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  • 2. Identification of patients with (atypical) MUTYH-associated polyposis by KRAS2 c.34G > T prescreening followed by MUTYH hotspot analysis in formalin-fixed paraffin-embedded tissue.
    van Puijenbroek M, Nielsen M, Tops CM, Halfwerk H, Vasen HF, Weiss MM, van Wezel T, Hes FJ, Morreau H.
    Clin Cancer Res; 2008 Jan 01; 14(1):139-42. PubMed ID: 18172263
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  • 3. 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
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  • 4. 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
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  • 6. Identification of a patient with atypical MUTYH-associated polyposis through detection of the KRAS c.34G>T mutation in liver metastasis.
    Buisine MP, Cattan S, Wacrenier A, Leclerc J, Lejeune S.
    J Clin Oncol; 2013 Mar 20; 31(9):e125-7. PubMed ID: 23341527
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  • 7. 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 20; 78(4):353-63. PubMed ID: 20618354
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  • 8. Oxidative DNA damage drives carcinogenesis in MUTYH-associated-polyposis by specific mutations of mitochondrial and MAPK genes.
    Venesio T, Balsamo A, Errichiello E, Ranzani GN, Risio M.
    Mod Pathol; 2013 Oct 20; 26(10):1371-81. PubMed ID: 23599153
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  • 11. 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
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  • 12. 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
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  • 14. MUTYH hotspot mutations in unselected colonoscopy patients.
    Casper M, Plotz G, Juengling B, Zeuzem S, Lammert F, Raedle J.
    Colorectal Dis; 2012 May 28; 14(5):e238-44. PubMed ID: 22469480
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  • 18. The first mutations in the MYH gene reported in Moroccan colon cancer patients.
    Laarabi FZ, Cherkaoui Jaouad I, Baert-Desurmont S, Ouldim K, Ibrahimi A, Kanouni N, Frebourg T, Sefiani A.
    Gene; 2012 Mar 15; 496(1):55-8. PubMed ID: 22266422
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