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Journal Abstract Search

317 related items for PubMed ID: 15955786

  • 1. Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn's disease.
    Török HP, Glas J, Tonenchi L, Lohse P, Müller-Myhsok B, Limbersky O, Neugebauer C, Schnitzler F, Seiderer J, Tillack C, Brand S, Brünnler G, Jagiello P, Epplen JT, Griga T, Klein W, Schiemann U, Folwaczny M, Ochsenkühn T, Folwaczny C.
    Gut; 2005 Oct; 54(10):1421-7. PubMed ID: 15955786
    [Abstract] [Full Text] [Related]

  • 2. Evidence for association of OCTN genes and IBD5 with ulcerative colitis.
    Waller S, Tremelling M, Bredin F, Godfrey L, Howson J, Parkes M.
    Gut; 2006 Jun; 55(6):809-14. PubMed ID: 16361305
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  • 3. Association of organic cation transporter risk haplotype with perianal penetrating Crohn's disease but not with susceptibility to IBD.
    Vermeire S, Pierik M, Hlavaty T, Claessens G, van Schuerbeeck N, Joossens S, Ferrante M, Henckaerts L, Bueno de Mesquita M, Vlietinck R, Rutgeerts P.
    Gastroenterology; 2005 Dec; 129(6):1845-53. PubMed ID: 16344053
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  • 4. Contribution of OCTN variants within the IBD5 locus to pediatric onset Crohn's disease.
    Babusukumar U, Wang T, McGuire E, Broeckel U, Kugathasan S.
    Am J Gastroenterol; 2006 Jun; 101(6):1354-61. PubMed ID: 16771961
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  • 5. The contribution of OCTN1/2 variants within the IBD5 locus to disease susceptibility and severity in Crohn's disease.
    Noble CL, Nimmo ER, Drummond H, Ho GT, Tenesa A, Smith L, Anderson N, Arnott ID, Satsangi J.
    Gastroenterology; 2005 Dec; 129(6):1854-64. PubMed ID: 16344054
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  • 7. 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]

  • 8. DLG5 variants in inflammatory bowel disease.
    Büning C, Geerdts L, Fiedler T, Gentz E, Pitre G, Reuter W, Luck W, Buhner S, Molnar T, Nagy F, Lonovics J, Dignass A, Landt O, Nickel R, Genschel J, Lochs H, Schmidt HH, Witt H.
    Am J Gastroenterol; 2006 Apr 28; 101(4):786-92. PubMed ID: 16494592
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  • 9. Relationship between CARD15, SLC22A4/5, and DLG5 polymorphisms and early-onset inflammatory bowel diseases: an Italian multicentric study.
    Ferraris A, Torres B, Knafelz D, Barabino A, Lionetti P, de Angelis GL, Iacono G, Papadatou B, D'Amato G, Di Ciommo V, Dallapiccola B, Castro M.
    Inflamm Bowel Dis; 2006 May 28; 12(5):355-61. PubMed ID: 16670523
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  • 10. Identification of DLG5 and SLC22A5 gene polymorphisms in Malaysian patients with Crohn's disease.
    Chua KH, Lian LH, Kee BP, Thum CM, Lee WS, Hilmi I, Goh KL.
    J Dig Dis; 2011 Dec 28; 12(6):459-66. PubMed ID: 22118696
    [Abstract] [Full Text] [Related]

  • 11. Analysis of the influence of OCTN1/2 variants within the IBD5 locus on disease susceptibility and growth indices in early onset inflammatory bowel disease.
    Russell RK, Drummond HE, Nimmo ER, Anderson NH, Noble CL, Wilson DC, Gillett PM, McGrogan P, Hassan K, Weaver LT, Bisset WM, Mahdi G, Satsangi J.
    Gut; 2006 Aug 28; 55(8):1114-23. PubMed ID: 16469794
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  • 15. Genetic variation in DLG5 is associated with inflammatory bowel disease.
    Stoll M, Corneliussen B, Costello CM, Waetzig GH, Mellgard B, Koch WA, Rosenstiel P, Albrecht M, Croucher PJ, Seegert D, Nikolaus S, Hampe J, Lengauer T, Pierrou S, Foelsch UR, Mathew CG, Lagerstrom-Fermer M, Schreiber S.
    Nat Genet; 2004 May 28; 36(5):476-80. PubMed ID: 15107852
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  • 17. Functional variants of OCTN cation transporter genes are associated with Crohn disease.
    Peltekova VD, Wintle RF, Rubin LA, Amos CI, Huang Q, Gu X, Newman B, Van Oene M, Cescon D, Greenberg G, Griffiths AM, St George-Hyslop PH, Siminovitch KA.
    Nat Genet; 2004 May 28; 36(5):471-5. PubMed ID: 15107849
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  • 18. 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
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  • 19. 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 05; 14(2):222-6. PubMed ID: 16333318
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  • 20. The association of MYO9B gene in Italian patients with inflammatory bowel diseases.
    Latiano A, Palmieri O, Valvano MR, D'Incà R, Caprilli R, Cucchiara S, Sturniolo GC, Bossa F, Andriulli A, Annese V.
    Aliment Pharmacol Ther; 2008 Feb 01; 27(3):241-8. PubMed ID: 17944996
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