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Journal Abstract Search

169 related items for PubMed ID: 17113749

  • 1. Host susceptibility to tuberculosis: CARD15 polymorphisms in a South African population.
    Möller M, Nebel A, Kwiatkowski R, van Helden PD, Hoal EG, Schreiber S.
    Mol Cell Probes; 2007 Apr; 21(2):148-51. PubMed ID: 17113749
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  • 3. Association between CARD15/NOD2 gene polymorphisms and paratuberculosis infection in cattle.
    Pinedo PJ, Buergelt CD, Donovan GA, Melendez P, Morel L, Wu R, Langaee TY, Rae DO.
    Vet Microbiol; 2009 Mar 02; 134(3-4):346-52. PubMed ID: 18926647
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  • 4. Variants of CARD15, TNFA and PTPN22 and susceptibility to Crohn's disease in the Czech population: high frequency of the CARD15 1007fs.
    Hradsky O, Lenicek M, Dusatkova P, Bronsky J, Nevoral J, Valtrova V, Kotalova R, Szitanyi P, Petro R, Starzykova V, Bortlik M, Vitek L, Lukas M, Cinek O.
    Tissue Antigens; 2008 Jun 02; 71(6):538-47. PubMed ID: 18489434
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  • 5. Clinical applications of NOD2/CARD15 mutations in Crohn's disease.
    Barreiro-de Acosta M, Peña AS.
    Acta Gastroenterol Latinoam; 2007 Mar 02; 37(1):49-54. PubMed ID: 17486745
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  • 7. Polymorphism in NOD2, Crohn's disease, and susceptibility to pulmonary tuberculosis.
    Stockton JC, Howson JM, Awomoyi AA, McAdam KP, Blackwell JM, Newport MJ.
    FEMS Immunol Med Microbiol; 2004 Jun 01; 41(2):157-60. PubMed ID: 15145460
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  • 9. Association of NOD2/CARD15 mutations on Crohn's disease phenotype in an Italian population.
    Bianchi V, Maconi G, Ardizzone S, Colombo E, Ferrara E, Russo A, Tenchini ML, Porro GB.
    Eur J Gastroenterol Hepatol; 2007 Mar 01; 19(3):217-23. PubMed ID: 17301648
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  • 10. NOD2/CARD15 polymorphisms impair innate immunity and increase susceptibility to gastric cancer in an Italian population.
    Angeletti S, Galluzzo S, Santini D, Ruzzo A, Vincenzi B, Ferraro E, Spoto C, Lorino G, Graziano N, Calvieri A, Magnani M, Graziano F, Pantano F, Tonini G, Dicuonzo G.
    Hum Immunol; 2009 Sep 01; 70(9):729-32. PubMed ID: 19397946
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  • 11. Identification of NOD2/CARD15 mutations in Malaysian patients with Crohn's disease.
    Chua KH, Hilmi I, Ng CC, Eng TL, Palaniappan S, Lee WS, Goh KL.
    J Dig Dis; 2009 May 01; 10(2):124-30. PubMed ID: 19426395
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  • 12. CARD15 single nucleotide polymorphisms 8, 12 and 13 are not increased in ethnic Danes with sarcoidosis.
    Milman N, Nielsen OH, Hviid TV, Fenger K.
    Respiration; 2007 May 01; 74(1):76-9. PubMed ID: 16397396
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  • 13. Mutations in CARD15 and smoking confer susceptibility to Crohn's disease in the Danish population.
    Ernst A, Jacobsen B, Østergaard M, Okkels H, Andersen V, Dagiliene E, Pedersen IS, Thorsgaard N, Drewes AM, Krarup HB.
    Scand J Gastroenterol; 2007 Dec 01; 42(12):1445-51. PubMed ID: 17852840
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  • 14. Impact of NOD2/CARD15 haplotypes on the outcome after kidney transplantation.
    Krüger B, Böger CA, Schröppel B, Obed A, Hoffmann U, Murphy BT, Fischereder M, Holler E, Banas B, Krämer BK.
    Transpl Int; 2007 Jul 01; 20(7):600-7. PubMed ID: 17498224
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  • 15. Analysis of CARD15 polymorphisms in Korean patients with ankylosing spondylitis reveals absence of common variants seen in western populations.
    Kim TH, Rahman P, Jun JB, Lee HS, Park YW, Im HJ, Snelgrove T, Peddle L, Hallett D, Inman RD.
    J Rheumatol; 2004 Oct 01; 31(10):1959-61. PubMed ID: 15468360
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  • 16. Granulomatous rosacea and Crohn's disease in a patient homozygous for the Crohn-associated NOD2/CARD15 polymorphism R702W.
    van Steensel MA, Badeloe S, Winnepenninckx V, Vreeburg M, Steijlen PM, van Geel M.
    Exp Dermatol; 2008 Dec 01; 17(12):1057-8. PubMed ID: 18616576
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  • 17. The V249I polymorphism of the CX3CR1 gene is associated with fibrostenotic disease behavior in patients with Crohn's disease.
    Sabate JM, Ameziane N, Lamoril J, Jouet P, Farmachidi JP, Soulé JC, Harnois F, Sobhani I, Jian R, Deybach JC, de Prost D, Coffin B.
    Eur J Gastroenterol Hepatol; 2008 Aug 01; 20(8):748-55. PubMed ID: 18617779
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  • 19. CARD15 gene variants in aggressive periodontitis.
    Noack B, Görgens H, Hoffmann T, Schackert HK.
    J Clin Periodontol; 2006 Nov 01; 33(11):779-83. PubMed ID: 16965521
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