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Journal Abstract Search

217 related items for PubMed ID: 17508420

  • 1. Contribution of the novel inflammatory bowel disease gene IL23R to disease susceptibility and phenotype.
    Cummings JR, Ahmad T, Geremia A, Beckly J, Cooney R, Hancock L, Pathan S, Guo C, Cardon LR, Jewell DP.
    Inflamm Bowel Dis; 2007 Sep; 13(9):1063-8. PubMed ID: 17508420
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  • 2. Confirmation of the role of ATG16L1 as a Crohn's disease susceptibility gene.
    Cummings JR, Cooney R, Pathan S, Anderson CA, Barrett JC, Beckly J, Geremia A, Hancock L, Guo C, Ahmad T, Cardon LR, Jewell DP.
    Inflamm Bowel Dis; 2007 Aug; 13(8):941-6. PubMed ID: 17455206
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  • 4. Association between genetic variants in myosin IXB and Crohn's disease.
    Cooney R, Cummings JR, Pathan S, Beckly J, Geremia A, Hancock L, Guo C, Morris A, Jewell DP.
    Inflamm Bowel Dis; 2009 Jul; 15(7):1014-21. PubMed ID: 19235913
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  • 6. 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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  • 10. Contributions of IBD5, IL23R, ATG16L1, and NOD2 to Crohn's disease risk in a population-based case-control study: evidence of gene-gene interactions.
    Okazaki T, Wang MH, Rawsthorne P, Sargent M, Datta LW, Shugart YY, Bernstein CN, Brant SR.
    Inflamm Bowel Dis; 2008 Nov; 14(11):1528-41. PubMed ID: 18521914
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  • 12. Susceptibility to ulcerative colitis in Hungarian patients determined by gene-gene interactions.
    Sarlos P, Varszegi D, Csongei V, Magyari L, Jaromi L, Nagy L, Melegh B.
    World J Gastroenterol; 2014 Jan 07; 20(1):219-27. PubMed ID: 24415875
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  • 17. Investigation of IL23R, JAK2, and STAT3 gene polymorphisms and gene-gene interactions in Crohn's disease and ulcerative colitis in a Turkish population.
    Can G, Tezel A, Gürkan H, Tozkır H, Ünsal G, Soylu AR, Ümit HC.
    Turk J Gastroenterol; 2016 Nov 07; 27(6):525-536. PubMed ID: 27852544
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  • 18. 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 07; 103(3):682-91. PubMed ID: 18162085
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  • 19. 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 07; 104(3):665-72. PubMed ID: 19262523
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