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Journal Abstract Search

212 related items for PubMed ID: 16493449

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  • 2. 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; 101(4):786-92. PubMed ID: 16494592
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  • 4. 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; 36(5):476-80. PubMed ID: 15107852
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  • 5. Association of interleukin-1 receptor-associated kinase M (IRAK-M) and inflammatory bowel diseases.
    Weersma RK, Oostenbrug LE, Nolte IM, Van Der Steege G, Oosterom E, Van Dullemen HM, Kleibeuker JH, Dijkstra G.
    Scand J Gastroenterol; 2007 Jul; 42(7):827-33. PubMed ID: 17558906
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  • 7. 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; 100(1):84-92. PubMed ID: 15654786
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  • 8. Epistasis between Toll-like receptor-9 polymorphisms and variants in NOD2 and IL23R modulates susceptibility to Crohn's disease.
    Török HP, Glas J, Endres I, Tonenchi L, Teshome MY, Wetzke M, Klein W, Lohse P, Ochsenkühn T, Folwaczny M, Göke B, Folwaczny C, Müller-Myhsok B, Brand S.
    Am J Gastroenterol; 2009 Jul; 104(7):1723-33. PubMed ID: 19455129
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  • 9. 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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  • 15. 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
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  • 16. Variants of CARD15, TNFA and PTPN22 and susceptibility to Crohn's disease in the Czech population: high frequency of the CARD15 1007fs.
    Hradsky O, Lenicek M, Dusatkova P, Bronsky J, Nevoral J, Valtrova V, Kotalova R, Szitanyi P, Petro R, Starzykova V, Bortlik M, Vitek L, Lukas M, Cinek O.
    Tissue Antigens; 2008 Jun; 71(6):538-47. PubMed ID: 18489434
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  • 18. Analysis of the CARD15 variants R702W, G908R and L1007fs in Italian IBD patients.
    Giachino D, van Duist MM, Regazzoni S, Gregori D, Bardessono M, Salacone P, Scaglione N, Sostegni R, Sapone N, Bresso F, Sambataro A, Gaia E, Pera A, Astegiano M, De Marchi M.
    Eur J Hum Genet; 2004 Mar; 12(3):206-12. PubMed ID: 14747834
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  • 19. 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
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