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Journal Abstract Search

294 related items for PubMed ID: 11586304

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  • 2. 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
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  • 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
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  • 6. 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
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  • 8. Gene-based single nucleotide polymorphisms and linkage disequilibrium patterns of 29 asthma candidate genes in the chromosome 5q31-33 region in Koreans.
    Ryu HJ, Jung HY, Park JS, Ryu GM, Heo JY, Kim JJ, Moon SM, Kim HT, Lee JY, Koh I, Kim JW, Rho JK, Han BG, Kim H, Park CS, Oh B, Park C, Lee JK, Kimm K.
    Int Arch Allergy Immunol; 2006 May; 139(3):209-16. PubMed ID: 16446543
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  • 12. 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
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  • 14. Haplotype tagging for the identification of common disease genes.
    Johnson GC, Esposito L, Barratt BJ, Smith AN, Heward J, Di Genova G, Ueda H, Cordell HJ, Eaves IA, Dudbridge F, Twells RC, Payne F, Hughes W, Nutland S, Stevens H, Carr P, Tuomilehto-Wolf E, Tuomilehto J, Gough SC, Clayton DG, Todd JA.
    Nat Genet; 2001 Oct; 29(2):233-7. PubMed ID: 11586306
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  • 20. ABCB1/MDR1 gene determines susceptibility and phenotype in ulcerative colitis: discrimination of critical variants using a gene-wide haplotype tagging approach.
    Ho GT, Soranzo N, Nimmo ER, Tenesa A, Goldstein DB, Satsangi J.
    Hum Mol Genet; 2006 Mar 01; 15(5):797-805. PubMed ID: 16434479
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