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Journal Abstract Search

340 related items for PubMed ID: 15289769

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  • 22. CARD15 in inflammatory bowel disease and Crohn's disease phenotypes: an association study and pooled analysis.
    Oostenbrug LE, Nolte IM, Oosterom E, van der Steege G, te Meerman GJ, van Dullemen HM, Drenth JP, de Jong DJ, van der Linde K, Jansen PL, Kleibeuker JH.
    Dig Liver Dis; 2006 Nov; 38(11):834-45. PubMed ID: 16920047
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  • 23. Diverse effects of the CARD15 and IBD5 loci on clinical phenotype in 630 patients with Crohn's disease.
    Onnie CM, Fisher SA, Prescott NJ, Mirza MM, Green P, Sanderson J, Forbes A, Lewis CM, Mathew CG.
    Eur J Gastroenterol Hepatol; 2008 Jan; 20(1):37-45. PubMed ID: 18090989
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  • 30. [Does smoking influence the course of Crohn's disease in patients with the presence of gene NOD2/CARD15 mutation?].
    Dobrowolska-Zachwieja A, Kaczmarek M, Hoppe-Gołebiewska J, Kalak R, Słomski R, Linke K.
    Pol Merkur Lekarski; 2005 May; 18(107):560-5. PubMed ID: 16161956
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  • 31. CARD15 variants in patients with sporadic Parkinson's disease.
    Bialecka M, Kurzawski M, Klodowska-Duda G, Opala G, Juzwiak S, Kurzawski G, Tan EK, Drozdzik M.
    Neurosci Res; 2007 Mar; 57(3):473-6. PubMed ID: 17174426
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  • 32. NOD2/CARD15 gene polymorphisms in Crohn's disease: a genotype- phenotype analysis.
    Heresbach D, Gicquel-Douabin V, Birebent B, D'halluin PN, Heresbach-Le Berre N, Dreano S, Siproudhis L, Dabadie A, Gosselin M, Mosser J, Semana G, Bretagne JF, Yaouanq J.
    Eur J Gastroenterol Hepatol; 2004 Jan; 16(1):55-62. PubMed ID: 15095853
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  • 37. NOD2/CARD15 gene mutation is not associated with susceptibility to Wegener's granulomatosis.
    Newman B, Rubin LA, Siminovitch KA.
    J Rheumatol; 2003 Feb; 30(2):305-7. PubMed ID: 12563685
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  • 38. NOD1 gene E266K polymorphism is associated with disease susceptibility but not with disease phenotype or NOD2/CARD15 in Hungarian patients with Crohn's disease.
    Molnar T, Hofner P, Nagy F, Lakatos PL, Fischer S, Lakatos L, Kovacs A, Altorjay I, Papp M, Palatka K, Demeter P, Tulassay Z, Nyari T, Miheller P, Papp J, Mandi Y, Lonovics J, Hungarian IBD Study Group.
    Dig Liver Dis; 2007 Dec; 39(12):1064-70. PubMed ID: 17964870
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  • 39. 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
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