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Journal Abstract Search

1262 related items for PubMed ID: 26446593

  • 21. 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]

  • 22. Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects.
    Stekrova J, Sulova M, Kebrdlova V, Zidkova K, Kotlas J, Ilencikova D, Vesela K, Kohoutova M.
    BMC Med Genet; 2007 Apr 05; 8():16. PubMed ID: 17411426
    [Abstract] [Full Text] [Related]

  • 23. Germline hypermethylation of the APC promoter is not a frequent cause of familial adenomatous polyposis in APC/MUTYH mutation negative families.
    Romero-Giménez J, Dopeso H, Blanco I, Guerra-Moreno A, Gonzalez S, Vogt S, Aretz S, Schwartz S, Capella G, Arango D.
    Int J Cancer; 2008 Mar 15; 122(6):1422-5. PubMed ID: 18027849
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  • 25. 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 15; 9(12):836-41. PubMed ID: 18091433
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  • 26. Molecular basis of familial adenomatous polyposis in the southeast of Brazil: identification of six novel mutations.
    Araujo LF, Molfetta GA, Vincenzi OC, Huber J, Teixeira LA, Ferraz VE, Silva WA.
    Int J Biol Markers; 2019 Mar 15; 34(1):80-89. PubMed ID: 30852976
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  • 28. 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 15; 12(3):555-62. PubMed ID: 23460355
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  • 29. Two Chinese pedigrees for adenomatous polyposis coli: new mutations at codon 1309 and predisposition to phenotypic variations.
    Liao DX, Li B, Du XM, Yu JH, Chang H, Wu ZQ, Hao HJ, Wang YX, Han WD, Cheng SJ, Luo CH.
    Fam Cancer; 2014 Sep 15; 13(3):361-8. PubMed ID: 24664542
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  • 30. Spectrum of APC and MUTYH germ-line mutations in Russian patients with colorectal malignancies.
    Yanus GA, Akhapkina TA, Ivantsov AO, Preobrazhenskaya EV, Aleksakhina SN, Bizin IV, Sokolenko AP, Mitiushkina NV, Kuligina ES, Suspitsin EN, Venina AR, Holmatov MM, Zaitseva OA, Yatsuk OS, Pashkov DV, Belyaev AM, Togo AV, Imyanitov EN, Iyevleva AG.
    Clin Genet; 2018 May 15; 93(5):1015-1021. PubMed ID: 29406563
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  • 31. Mutation analysis of MUTYH in Japanese colorectal adenomatous polyposis patients.
    Taki K, Sato Y, Nomura S, Ashihara Y, Kita M, Tajima I, Sugano K, Arai M.
    Fam Cancer; 2016 Apr 15; 15(2):261-5. PubMed ID: 26684191
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  • 32. 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 Apr 15; 208(7-8):390-5. PubMed ID: 26056087
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  • 33. Mutation spectrum of the APC gene in 83 Korean FAP families.
    Kim DW, Kim IJ, Kang HC, Park HW, Shin Y, Park JH, Jang SG, Yoo BC, Lee MR, Hong CW, Park KJ, Oh NG, Kim NK, Sung MK, Lee BW, Kim YJ, Lee H, Park JG.
    Hum Mutat; 2005 Sep 15; 26(3):281. PubMed ID: 16088911
    [Abstract] [Full Text] [Related]

  • 34. c.1227_1228dupGG (p.Glu410Glyfs), a frequent variant in Tunisian patients with MUTYH associated polyposis.
    Kdissa A, Brusgaard K, Ksiaa M, Golli L, Hallara O, Ousager LB, Manoubi W, Seghaier RB, Adala L, Halleb Y, Saad A, Hmila F, Gribaa M.
    Cancer Genet; 2020 Jan 15; 240():45-53. PubMed ID: 31739127
    [Abstract] [Full Text] [Related]

  • 35. Presence of c.3956delC mutation in familial adenomatous polyposis patients from Brazil.
    Moreira-Nunes CA, Alcântara Dd, Lima-Júnior SF, Cavalléro SR, Rey JA, Pinto GR, de Assumpção PP, Burbano RR.
    World J Gastroenterol; 2015 Aug 21; 21(31):9413-9. PubMed ID: 26309368
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  • 36. Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families.
    Kanter-Smoler G, Fritzell K, Rohlin A, Engwall Y, Hallberg B, Bergman A, Meuller J, Grönberg H, Karlsson P, Björk J, Nordling M.
    BMC Med; 2008 Apr 24; 6():10. PubMed ID: 18433509
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  • 38. A novel pathogenic splice acceptor site germline mutation in intron 14 of the APC gene in a Chinese family with familial adenomatous polyposis.
    Wang D, Liang S, Zhang Z, Zhao G, Hu Y, Liang S, Zhang X, Banerjee S.
    Oncotarget; 2017 Mar 28; 8(13):21327-21335. PubMed ID: 28423518
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  • 39. Characterization of two novel adenomatous polyposis coli (APC) gene mutations in patients with familial adenomatous polyposis (FAP).
    Bapat B, Berk T, Mitri A, Cohen Z, Gallinger S, Stern H.
    Hum Mutat; 1994 Mar 28; 4(4):253-6. PubMed ID: 7866403
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  • 40. MutYH-associated polyposis.
    Toboeva MK, Shelygin YA, Frolov SA, Kuzminov MA, Tsukanov AS.
    Ter Arkh; 2019 Mar 18; 91(2):97-100. PubMed ID: 31094179
    [Abstract] [Full Text] [Related]

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