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Journal Abstract Search

332 related items for PubMed ID: 16344053

  • 21. Genetic polymorphisms associated with inflammatory bowel disease do not confer risk for primary sclerosing cholangitis.
    Karlsen TH, Hampe J, Wiencke K, Schrumpf E, Thorsby E, Lie BA, Broomé U, Schreiber S, Boberg KM.
    Am J Gastroenterol; 2007 Jan; 102(1):115-21. PubMed ID: 17100974
    [Abstract] [Full Text] [Related]

  • 22. The ATG16L1 gene variants rs2241879 and rs2241880 (T300A) are strongly associated with susceptibility to Crohn's disease in the German population.
    Glas J, Konrad A, Schmechel S, Dambacher J, Seiderer J, Schroff F, Wetzke M, Roeske D, Török HP, Tonenchi L, Pfennig S, Haller D, Griga T, Klein W, Epplen JT, Folwaczny C, Lohse P, Göke B, Ochsenkühn T, Mussack T, Folwaczny M, Müller-Myhsok B, Brand S.
    Am J Gastroenterol; 2008 Mar; 103(3):682-91. PubMed ID: 18162085
    [Abstract] [Full Text] [Related]

  • 23. Homozygosity for the CARD15 frameshift mutation 1007fs is predictive of early onset of Crohn's disease with ileal stenosis, entero-enteral fistulas, and frequent need for surgical intervention with high risk of re-stenosis.
    Seiderer J, Schnitzler F, Brand S, Staudinger T, Pfennig S, Herrmann K, Hofbauer K, Dambacher J, Tillack C, Sackmann M, Göke B, Lohse P, Ochsenkühn T.
    Scand J Gastroenterol; 2006 Dec; 41(12):1421-32. PubMed ID: 17101573
    [Abstract] [Full Text] [Related]

  • 24. New serological markers for inflammatory bowel disease are associated with earlier age at onset, complicated disease behavior, risk for surgery, and NOD2/CARD15 genotype in a Hungarian IBD cohort.
    Papp M, Altorjay I, Dotan N, Palatka K, Foldi I, Tumpek J, Sipka S, Udvardy M, Dinya T, Lakatos L, Kovacs A, Molnar T, Tulassay Z, Miheller P, Norman GL, Szamosi T, Papp J, Hungarian IBD Study Group, Lakatos PL.
    Am J Gastroenterol; 2008 Mar; 103(3):665-81. PubMed ID: 18047543
    [Abstract] [Full Text] [Related]

  • 25. Association of the organic cation transporter OCTN genes with Crohn's disease in the Spanish population.
    Martínez A, Martín MC, Mendoza JL, Taxonera C, Díaz-Rubio M, de la Concha EG, Urcelay E.
    Eur J Hum Genet; 2006 Feb; 14(2):222-6. PubMed ID: 16333318
    [Abstract] [Full Text] [Related]

  • 26. Investigation of NOD1/CARD4 variation in inflammatory bowel disease using a haplotype-tagging strategy.
    Van Limbergen J, Nimmo ER, Russell RK, Drummond HE, Smith L, Anderson NH, Davies G, Arnott ID, Wilson DC, Satsangi J.
    Hum Mol Genet; 2007 Sep 15; 16(18):2175-86. PubMed ID: 17613538
    [Abstract] [Full Text] [Related]

  • 27. ABCB1/MDR1 gene determines susceptibility and phenotype in ulcerative colitis: discrimination of critical variants using a gene-wide haplotype tagging approach.
    Ho GT, Soranzo N, Nimmo ER, Tenesa A, Goldstein DB, Satsangi J.
    Hum Mol Genet; 2006 Mar 01; 15(5):797-805. PubMed ID: 16434479
    [Abstract] [Full Text] [Related]

  • 28. Variants of CARD15 are associated with an aggressive clinical course of Crohn's disease--an IG-IBD study.
    Annese V, Lombardi G, Perri F, D'Incà R, Ardizzone S, Riegler G, Giaccari S, Vecchi M, Castiglione F, Gionchetti P, Cocchiara E, Vigneri S, Latiano A, Palmieri O, Andriulli A.
    Am J Gastroenterol; 2005 Jan 01; 100(1):84-92. PubMed ID: 15654786
    [Abstract] [Full Text] [Related]

  • 29. Role of CARD15, DLG5 and OCTN genes polymorphisms in children with inflammatory bowel diseases.
    Cucchiara S, Latiano A, Palmieri O, Staiano AM, D'Incà R, Guariso G, Vieni G, Rutigliano V, Borrelli O, Valvano MR, Annese V.
    World J Gastroenterol; 2007 Feb 28; 13(8):1221-9. PubMed ID: 17451203
    [Abstract] [Full Text] [Related]

  • 30. Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn disease.
    Fisher SA, Hampe J, Onnie CM, Daly MJ, Curley C, Purcell S, Sanderson J, Mansfield J, Annese V, Forbes A, Lewis CM, Schreiber S, Rioux JD, Mathew CG.
    Hum Mutat; 2006 Aug 28; 27(8):778-85. PubMed ID: 16835882
    [Abstract] [Full Text] [Related]

  • 31. CARD15 mutations in Dutch familial and sporadic inflammatory bowel disease and an overview of European studies.
    van der Linde K, Boor PP, Houwing-Duistermaat JJ, Crusius BJ, Wilson PJ, Kuipers EJ, de Rooij FW.
    Eur J Gastroenterol Hepatol; 2007 Jun 28; 19(6):449-59. PubMed ID: 17489054
    [Abstract] [Full Text] [Related]

  • 32. DLG5 variants do not influence susceptibility to inflammatory bowel disease in the Scottish population.
    Noble CL, Nimmo ER, Drummond H, Smith L, Arnott ID, Satsangi J.
    Gut; 2005 Oct 28; 54(10):1416-20. PubMed ID: 15843420
    [Abstract] [Full Text] [Related]

  • 33. Characterization of genotype-phenotype relationships and stratification by the CARD15 variant genotype for inflammatory bowel disease susceptibility loci using multiple short tandem repeat genetic markers.
    Crawford NP, Colliver DW, Funke AA, Young MN, Kelley S, Cobbs GA, Petras RE, Galandiuk S.
    Hum Mutat; 2005 Feb 28; 25(2):156-66. PubMed ID: 15643611
    [Abstract] [Full Text] [Related]

  • 34. rs224136 on chromosome 10q21.1 and variants in PHOX2B, NCF4, and FAM92B are not major genetic risk factors for susceptibility to Crohn's disease in the German population.
    Glas J, Seiderer J, Pasciuto G, Tillack C, Diegelmann J, Pfennig S, Konrad A, Schmechel S, Wetzke M, Török HP, Stallhofer J, Jürgens M, Griga T, Klein W, Epplen JT, Schiemann U, Mussack T, Lohse P, Göke B, Ochsenkühn T, Folwaczny M, Müller-Myhsok B, Brand S.
    Am J Gastroenterol; 2009 Mar 28; 104(3):665-72. PubMed ID: 19262523
    [Abstract] [Full Text] [Related]

  • 35. Evidence of allelic heterogeneity for associations between the NOD2/CARD15 gene and ulcerative colitis among North Indians.
    Juyal G, Amre D, Midha V, Sood A, Seidman E, Thelma BK.
    Aliment Pharmacol Ther; 2007 Nov 15; 26(10):1325-32. PubMed ID: 17892524
    [Abstract] [Full Text] [Related]

  • 36. Mannan-binding lectin (MBL) gene polymorphisms in ulcerative colitis and Crohn's disease.
    Rector A, Lemey P, Laffut W, Keyaerts E, Struyf F, Wollants E, Vermeire S, Rutgeerts P, Van Ranst M.
    Genes Immun; 2001 Oct 15; 2(6):323-8. PubMed ID: 11607788
    [Abstract] [Full Text] [Related]

  • 37. Risk factors for perianal Crohn's disease: the role of genotype, phenotype, and ethnicity.
    Karban A, Itay M, Davidovich O, Leshinsky-Silver E, Kimmel G, Fidder H, Shamir R, Waterman M, Eliakim R, Levine A.
    Am J Gastroenterol; 2007 Aug 15; 102(8):1702-8. PubMed ID: 17509030
    [Abstract] [Full Text] [Related]

  • 38. rs1004819 is the main disease-associated IL23R variant in German Crohn's disease patients: combined analysis of IL23R, CARD15, and OCTN1/2 variants.
    Glas J, Seiderer J, Wetzke M, Konrad A, Török HP, Schmechel S, Tonenchi L, Grassl C, Dambacher J, Pfennig S, Maier K, Griga T, Klein W, Epplen JT, Schiemann U, Folwaczny C, Lohse P, Göke B, Ochsenkühn T, Müller-Myhsok B, Folwaczny M, Mussack T, Brand S.
    PLoS One; 2007 Sep 05; 2(9):e819. PubMed ID: 17786191
    [Abstract] [Full Text] [Related]

  • 39. The contribution of the DLG5 113A variant in early-onset inflammatory bowel disease.
    Russell RK, Drummond HE, Nimmo ER, Anderson N, Wilson DC, Gillett PM, McGrogan P, Hassan K, Weaver LT, Bisset WM, Mahdi G, Satsangi J.
    J Pediatr; 2007 Mar 05; 150(3):268-73. PubMed ID: 17307543
    [Abstract] [Full Text] [Related]

  • 40. Haplotypes of PADI4 susceptible to rheumatoid arthritis are also associated with ulcerative colitis in the Japanese population.
    Chen CC, Isomoto H, Narumi Y, Sato K, Oishi Y, Kobayashi T, Yanagihara K, Mizuta Y, Kohno S, Tsukamoto K.
    Clin Immunol; 2008 Feb 05; 126(2):165-71. PubMed ID: 17980669
    [Abstract] [Full Text] [Related]

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