These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

171 related articles for article (PubMed ID: 12210321)

  • 1. Fine mapping of the IBD1 locus did not identify Crohn disease-associated NOD2 variants: implications for complex disease genetics.
    van Heel DA; McGovern DP; Cardon LR; Dechairo BM; Lench NJ; Carey AH; Jewell DP
    Am J Med Genet; 2002 Aug; 111(3):253-9. PubMed ID: 12210321
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Association of NOD2 with Crohn's disease in a homogenous Irish population.
    Bairead E; Harmon DL; Curtis AM; Kelly Y; O'Leary C; Gardner M; Leahy DT; Vaughan P; Keegan D; O'Morain C; O'Donoghue D; Shanahan F; Parfrey NA; Quane KA
    Eur J Hum Genet; 2003 Mar; 11(3):237-44. PubMed ID: 12673278
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. NOD2/CARD15 genotype and phenotype differences between Ashkenazi and Sephardic Jews with Crohn's disease.
    Karban A; Waterman M; Panhuysen CI; Pollak RD; Nesher S; Datta L; Weiss B; Suissa A; Shamir R; Brant SR; Eliakim R
    Am J Gastroenterol; 2004 Jun; 99(6):1134-40. PubMed ID: 15180737
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Variation at NOD2/CARD15 in familial and sporadic cases of Crohn's disease in the Ashkenazi Jewish population.
    Zhou Z; Lin XY; Akolkar PN; Gulwani-Akolkar B; Levine J; Katz S; Silver J
    Am J Gastroenterol; 2002 Dec; 97(12):3095-101. PubMed ID: 12492195
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Significant role of genetics in IBD: the NOD2 gene.
    Cho JH
    Rev Gastroenterol Disord; 2003; 3 Suppl 1():S18-22. PubMed ID: 12684585
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [From gene to disease; 'frame shift'-mutation in the CARD15-gene and Crohn's disease].
    van der Linde K; Kuipers EJ; de Rooij FW; Wilson JH
    Ned Tijdschr Geneeskd; 2002 Dec; 146(52):2539-42. PubMed ID: 12532667
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic variation in DLG5 is associated with inflammatory bowel disease.
    Stoll M; Corneliussen B; Costello CM; Waetzig GH; Mellgard B; Koch WA; Rosenstiel P; Albrecht M; Croucher PJ; Seegert D; Nikolaus S; Hampe J; Lengauer T; Pierrou S; Foelsch UR; Mathew CG; Lagerstrom-Fermer M; Schreiber S
    Nat Genet; 2004 May; 36(5):476-80. PubMed ID: 15107852
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Role of NOD2 variants in spondylarthritis.
    Crane AM; Bradbury L; van Heel DA; McGovern DP; Brophy S; Rubin L; Siminovitch KA; Wordsworth BP; Calin A; Brown MA
    Arthritis Rheum; 2002 Jun; 46(6):1629-33. PubMed ID: 12115195
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Lack of association of ankylosing spondylitis with the most common NOD2 susceptibility alleles to Crohn's disease.
    Ferreirós-Vidal I; Amarelo J; Barros F; Carracedo A; Gómez-Reino JJ; Gonzalez A
    J Rheumatol; 2003 Jan; 30(1):102-4. PubMed ID: 12508397
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 98(11):2479-84. PubMed ID: 14638352
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Progress towards identifying inflammatory bowel disease susceptibility genes.
    Rioux JD
    Novartis Found Symp; 2004; 263():3-11; discussion 11-6, 211-8. PubMed ID: 15669631
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The genetics of inflammatory bowel disease.
    Bonen DK; Cho JH
    Gastroenterology; 2003 Feb; 124(2):521-36. PubMed ID: 12557156
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Characterization of genotype-phenotype relationships and stratification by the CARD15 variant genotype for inflammatory bowel disease susceptibility loci using multiple short tandem repeat genetic markers.
    Crawford NP; Colliver DW; Funke AA; Young MN; Kelley S; Cobbs GA; Petras RE; Galandiuk S
    Hum Mutat; 2005 Feb; 25(2):156-66. PubMed ID: 15643611
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. No evidence for involvement of IL-4R and CD11B from the IBD1 region and STAT6 in the IBD2 region in Crohn's disease.
    de Jong DJ; Franke B; Naber AH; Willemen JJ; Heister AJ; Brunner HG; de Kovel CG; Hol FA
    Eur J Hum Genet; 2003 Nov; 11(11):884-7. PubMed ID: 14571275
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association of interleukin-1 receptor-associated kinase M (IRAK-M) and inflammatory bowel diseases.
    Weersma RK; Oostenbrug LE; Nolte IM; Van Der Steege G; Oosterom E; Van Dullemen HM; Kleibeuker JH; Dijkstra G
    Scand J Gastroenterol; 2007 Jul; 42(7):827-33. PubMed ID: 17558906
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel NOD2/CARD15 haplotype conferring risk for Crohn disease in Ashkenazi Jews.
    Sugimura K; Taylor KD; Lin YC; Hang T; Wang D; Tang YM; Fischel-Ghodsian N; Targan SR; Rotter JI; Yang H
    Am J Hum Genet; 2003 Mar; 72(3):509-18. PubMed ID: 12577202
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.