BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

201 related articles for article (PubMed ID: 16724073)

  • 1. Sequence variation, linkage disequilibrium and association with Crohn's disease on chromosome 5q31.
    Onnie C; Fisher SA; King K; Mirza M; Roberts R; Forbes A; Sanderson J; Lewis CM; Mathew CG
    Genes Immun; 2006 Jul; 7(5):359-65. PubMed ID: 16724073
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

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

  • 7. Haplotype variation at the IBD5/SLC22A4 locus (5q31) in coeliac disease in the Irish population.
    Ryan AW; Thornton JM; Brophy K; Daly JS; O'Morain C; McLoughlin RM; Kennedy NP; Abuzakouk M; Stevens FM; Feighery C; Kelleher D; McManus R
    Tissue Antigens; 2004 Aug; 64(2):195-8. PubMed ID: 15245375
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Functional variants of OCTN cation transporter genes are associated with Crohn disease.
    Peltekova VD; Wintle RF; Rubin LA; Amos CI; Huang Q; Gu X; Newman B; Van Oene M; Cescon D; Greenberg G; Griffiths AM; St George-Hyslop PH; Siminovitch KA
    Nat Genet; 2004 May; 36(5):471-5. PubMed ID: 15107849
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease.
    Rioux JD; Daly MJ; Silverberg MS; Lindblad K; Steinhart H; Cohen Z; Delmonte T; Kocher K; Miller K; Guschwan S; Kulbokas EJ; O'Leary S; Winchester E; Dewar K; Green T; Stone V; Chow C; Cohen A; Langelier D; Lapointe G; Gaudet D; Faith J; Branco N; Bull SB; McLeod RS; Griffiths AM; Bitton A; Greenberg GR; Lander ES; Siminovitch KA; Hudson TJ
    Nat Genet; 2001 Oct; 29(2):223-8. PubMed ID: 11586304
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 41(1):48-53. PubMed ID: 16373276
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Evidence for the association of the SLC22A4 and SLC22A5 genes with type 1 diabetes: a case control study.
    Santiago JL; Martínez A; de la Calle H; Fernández-Arquero M; Figueredo MA; de la Concha EG; Urcelay E
    BMC Med Genet; 2006 Jun; 7():54. PubMed ID: 16796743
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis.
    Tokuhiro S; Yamada R; Chang X; Suzuki A; Kochi Y; Sawada T; Suzuki M; Nagasaki M; Ohtsuki M; Ono M; Furukawa H; Nagashima M; Yoshino S; Mabuchi A; Sekine A; Saito S; Takahashi A; Tsunoda T; Nakamura Y; Yamamoto K
    Nat Genet; 2003 Dec; 35(4):341-8. PubMed ID: 14608356
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Epitope shared by functional variant of organic cation/carnitine transporter, OCTN1, Campylobacter jejuni and Mycobacterium paratuberculosis may underlie susceptibility to Crohn's disease at 5q31.
    Lamhonwah AM; Ackerley C; Onizuka R; Tilups A; Lamhonwah D; Chung C; Tao KS; Tellier R; Tein I
    Biochem Biophys Res Commun; 2005 Dec; 337(4):1165-75. PubMed ID: 16246312
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Investigation of reported associations between the 20q13 and 21q22 loci and pediatric-onset Crohn's disease in Canadian children.
    Amre DK; Mack DR; Morgan K; Fujiwara M; Israel D; Deslandres C; Seidman EG; Lambrette P; Costea I; Krupoves A; Fegury H; Dong J; Grimard G; Levy E
    Am J Gastroenterol; 2009 Nov; 104(11):2824-8. PubMed ID: 19623168
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 104(3):665-72. PubMed ID: 19262523
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The IBD6 Crohn's disease locus demonstrates complex interactions with CARD15 and IBD5 disease-associated variants.
    van Heel DA; Dechairo BM; Dawson G; McGovern DP; Negoro K; Carey AH; Cardon LR; Mackay I; Jewell DP; Lench NJ
    Hum Mol Genet; 2003 Oct; 12(20):2569-75. PubMed ID: 12928481
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism.
    Nurmi EL; Amin T; Olson LM; Jacobs MM; McCauley JL; Lam AY; Organ EL; Folstein SE; Haines JL; Sutcliffe JS
    Mol Psychiatry; 2003 Jun; 8(6):624-34, 570. PubMed ID: 12851639
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.