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Journal Abstract Search

428 related items for PubMed ID: 18047539

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  • 3. Interleukin 10 (IL-10) gene variants and susceptibility for paediatric onset Crohn's disease.
    Amre DK, Mack DR, Morgan K, Israel D, Lambrette P, Costea I, Krupoves A, Fegury H, Dong J, Grimard G, Deslandres C, Levy E, Seidman EG.
    Aliment Pharmacol Ther; 2009 May 01; 29(9):1025-31. PubMed ID: 19210299
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  • 6. Evaluation of the interleukin-23 receptor gene coding variant R381Q in pediatric and adult Crohn disease.
    Leshinsky-Silver E, Karban A, Dalal I, Eliakim R, Shirin H, Tzofi T, Boaz M, Levine A.
    J Pediatr Gastroenterol Nutr; 2007 Oct 01; 45(4):405-8. PubMed ID: 18030204
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  • 7. 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 01; 103(3):682-91. PubMed ID: 18162085
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  • 9. IL-23 receptor (IL-23R) gene protects against pediatric Crohn's disease.
    Dubinsky MC, Wang D, Picornell Y, Wrobel I, Katzir L, Quiros A, Dutridge D, Wahbeh G, Silber G, Bahar R, Mengesha E, Targan SR, Taylor KD, Rotter JI, Western Regional Research Alliance for Pediatric IBD.
    Inflamm Bowel Dis; 2007 May 01; 13(5):511-5. PubMed ID: 17309073
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  • 10. 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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  • 11. 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 05; 101(6):1354-61. PubMed ID: 16771961
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  • 12. NOD2/CARD15 variants are associated with lower weight at diagnosis in children with Crohn's disease.
    Tomer G, Ceballos C, Concepcion E, Benkov KJ.
    Am J Gastroenterol; 2003 Nov 05; 98(11):2479-84. PubMed ID: 14638352
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  • 13. Tumor necrosis factor receptor gene polymorphisms in Crohn's disease: association with clinical phenotypes.
    Waschke KA, Villani AC, Vermeire S, Dufresne L, Chen TC, Bitton A, Cohen A, Thomson AB, Wild GE.
    Am J Gastroenterol; 2005 May 05; 100(5):1126-33. PubMed ID: 15842589
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  • 16. Association of interleukin 23 receptor variants with psoriatic arthritis.
    Rahman P, Inman RD, Maksymowych WP, Reeve JP, Peddle L, Gladman DD.
    J Rheumatol; 2009 Jan 05; 36(1):137-40. PubMed ID: 19040306
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  • 17. DLG5 R30Q variant is a female-specific protective factor in pediatric onset Crohn's disease.
    Biank V, Friedrichs F, Babusukumar U, Wang T, Stoll M, Broeckel U, Kugathasan S.
    Am J Gastroenterol; 2007 Feb 05; 102(2):391-8. PubMed ID: 17156146
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  • 18. 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
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  • 19. 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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