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Journal Abstract Search

170 related items for PubMed ID: 21674708

  • 1. Two independent genetic factors responsible for the associations of the IBD5 locus with Crohn's disease in the Czech population.
    Hradsky O, Dusatkova P, Lenicek M, Bronsky J, Duricova D, Nevoral J, Vitek L, Lukas M, Cinek O.
    Inflamm Bowel Dis; 2011 Jul; 17(7):1523-9. PubMed ID: 21674708
    [Abstract] [Full Text] [Related]

  • 2. Contribution of the IBD5 locus to Crohn's disease in the Swedish population.
    Törkvist L, Noble CL, Lördal M, Sjöqvist U, Lindforss U, Nimmo ER, Löfberg R, Russell RK, Satsangi J.
    Scand J Gastroenterol; 2007 Feb; 42(2):200-6. PubMed ID: 17340776
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. Haplotype in the IBD5 region is associated with refractory Crohn's disease in Slovenian patients and modulates expression of the SLC22A5 gene.
    Repnik K, Potočnik U.
    J Gastroenterol; 2011 Sep; 46(9):1081-91. PubMed ID: 21695374
    [Abstract] [Full Text] [Related]

  • 5. 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; 55(8):1114-23. PubMed ID: 16469794
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn disease.
    Fisher SA, Hampe J, Onnie CM, Daly MJ, Curley C, Purcell S, Sanderson J, Mansfield J, Annese V, Forbes A, Lewis CM, Schreiber S, Rioux JD, Mathew CG.
    Hum Mutat; 2006 Aug; 27(8):778-85. PubMed ID: 16835882
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Polymorphisms in the IBD5 locus are associated with Crohn disease in pediatric Ashkenazi Jewish patients.
    Tomer G, Wetzler G, Keddache M, Denson LA.
    J Pediatr Gastroenterol Nutr; 2009 May; 48(5):531-7. PubMed ID: 19412005
    [Abstract] [Full Text] [Related]

  • 10. Runt-related transcription factor 3 is associated with ulcerative colitis and shows epistasis with solute carrier family 22, members 4 and 5.
    Weersma RK, Zhou L, Nolte IM, van der Steege G, van Dullemen HM, Oosterom E, Bok L, Peppelenbosch MP, Faber KN, Kleibeuker JH, Dijkstra G.
    Inflamm Bowel Dis; 2008 Dec; 14(12):1615-22. PubMed ID: 18668679
    [Abstract] [Full Text] [Related]

  • 11. 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; 14(2):222-6. PubMed ID: 16333318
    [Abstract] [Full Text] [Related]

  • 12. A risk haplotype in the Solute Carrier Family 22A4/22A5 gene cluster influences phenotypic expression of Crohn's disease.
    Newman B, Gu X, Wintle R, Cescon D, Yazdanpanah M, Liu X, Peltekova V, Van Oene M, Amos CI, Siminovitch KA.
    Gastroenterology; 2005 Feb; 128(2):260-9. PubMed ID: 15685536
    [Abstract] [Full Text] [Related]

  • 13. Evidence for common genetic control in pathways of inflammation for Crohn's disease and psoriatic arthritis.
    Ho P, Bruce IN, Silman A, Symmons D, Newman B, Young H, Griffiths CE, John S, Worthington J, Barton A.
    Arthritis Rheum; 2005 Nov; 52(11):3596-602. PubMed ID: 16255050
    [Abstract] [Full Text] [Related]

  • 14. 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
    [Abstract] [Full Text] [Related]

  • 15. Refined genomic localization and ethnic differences observed for the IBD5 association with Crohn's disease.
    Silverberg MS, Duerr RH, Brant SR, Bromfield G, Datta LW, Jani N, Kane SV, Rotter JI, Philip Schumm L, Hillary Steinhart A, Taylor KD, Yang H, Cho JH, Rioux JD, Daly MJ, NIDDK IBD Genetics Consortium.
    Eur J Hum Genet; 2007 Mar 07; 15(3):328-35. PubMed ID: 17213842
    [Abstract] [Full Text] [Related]

  • 16. 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 07; 54(10):1421-7. PubMed ID: 15955786
    [Abstract] [Full Text] [Related]

  • 17. OCTNs: will the real IBD5 gene please stand up?
    Silverberg MS.
    World J Gastroenterol; 2006 Jun 21; 12(23):3678-81. PubMed ID: 16773684
    [Abstract] [Full Text] [Related]

  • 18. Lack of association between IBD5 and Crohn's disease in Japanese patients demonstrates population-specific differences in inflammatory bowel disease.
    Tosa M, Negoro K, Kinouchi Y, Abe H, Nomura E, Takagi S, Aihara H, Oomori S, Sugimura M, Takahashi K, Hiwatashi N, Takahashi S, Shimosegawa T.
    Scand J Gastroenterol; 2006 Jan 21; 41(1):48-53. PubMed ID: 16373276
    [Abstract] [Full Text] [Related]

  • 19. Crohn's disease and genetic hitchhiking at IBD5.
    Huff CD, Witherspoon DJ, Zhang Y, Gatenbee C, Denson LA, Kugathasan S, Hakonarson H, Whiting A, Davis CT, Wu W, Xing J, Watkins WS, Bamshad MJ, Bradfield JP, Bulayeva K, Simonson TS, Jorde LB, Guthery SL.
    Mol Biol Evol; 2012 Jan 21; 29(1):101-11. PubMed ID: 21816865
    [Abstract] [Full Text] [Related]

  • 20. Variants of OCTN1-2 cation transporter genes are associated with both Crohn's disease and ulcerative colitis.
    Palmieri O, Latiano A, Valvano R, D'Incà R, Vecchi M, Sturniolo GC, Saibeni S, Peyvandi F, Bossa F, Zagaria C, Andriulli A, Devoto M, Annese V.
    Aliment Pharmacol Ther; 2006 Feb 15; 23(4):497-506. PubMed ID: 16441470
    [Abstract] [Full Text] [Related]

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