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Inflammatory Bowel Diseases
Volumn 16, Issue 11, 2010, Pages 1819-1820
Lack of correlation between IL-10R1 S138G loss-of-function allele and IBD in the Lebanese population
Author keywords

[No Author keywords available]
Indexed keywords

CASPASE RECRUITMENT DOMAIN PROTEIN 15; INTERLEUKIN 10 RECEPTOR; INTERLEUKIN 10 RECEPTOR 1; INTERLEUKIN 10 RECEPTOR 2; INTERLEUKIN 10 RECEPTOR ALPHA; INTERLEUKIN 10 RECEPTOR BETA; STAT3 PROTEIN; UNCLASSIFIED DRUG;
EID: 78249280625     PISSN: 10780998     EISSN: 15364844     Source Type: Journal    
DOI: 10.1002/ibd.21230     Document Type: Letter
Times cited : (3)
References (8)
  • 1
    • 70449479014 scopus 로고    scopus 로고
    • The genetic basis of inflammatory bowel disease
    • Cooney R, Jewell D,. The genetic basis of inflammatory bowel disease. Dig Dis. 2009; 27: 428-442.
    • (2009) Dig Dis. , vol.27 , pp. 428-442
    • Cooney, R.1    Jewell, D.2
  • 2
    • 34848850085 scopus 로고    scopus 로고
    • The genetics of inflammatory bowel disease
    • Cho JH, Weaver CT,. The genetics of inflammatory bowel disease. Gastroenterology. 2007; 133: 1327-1339.
    • (2007) Gastroenterology. , vol.133 , pp. 1327-1339
    • Cho, J.H.1    Weaver, C.T.2
  • 3
    • 22044432709 scopus 로고    scopus 로고
    • The role of Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms and CARD15/NOD2 mutations in the susceptibility and phenotype of Crohns disease
    • Brand S, Staudinger T, Schnitzler F, et al. The role of Toll-like receptor 4 Asp299Gly and Thr399Ile polymorphisms and CARD15/NOD2 mutations in the susceptibility and phenotype of Crohns disease. Inflamm Bowel Dis. 2005; 11: 645-652.
    • (2005) Inflamm Bowel Dis. , vol.11 , pp. 645-652
    • Brand, S.1    Staudinger, T.2    Schnitzler, F.3
  • 4
    • 0035978651 scopus 로고    scopus 로고
    • Association of NOD2 leucine-rich repeat variants with susceptibility to Crohns disease
    • Hugot JP, Chamaillard M, Zouali H, et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohns disease. Nature. 2001; 411: 599-603.
    • (2001) Nature. , vol.411 , pp. 599-603
    • Hugot, J.P.1    Chamaillard, M.2    Zouali, H.3
  • 5
    • 2442585704 scopus 로고    scopus 로고
    • Functional variants of OCTN cation transporter genes are associated with Crohn disease
    • Peltekova VD, Wintle RF, Rubin LA, et al. Functional variants of OCTN cation transporter genes are associated with Crohn disease. Nat Genet. 2004; 36: 471-475.
    • (2004) Nat Genet. , vol.36 , pp. 471-475
    • Peltekova, V.D.1    Wintle, R.F.2    Rubin, L.A.3
  • 6
    • 65449141343 scopus 로고    scopus 로고
    • MEP1A allele for meprin A metalloprotease is a susceptibility gene for inflammatory bowel disease
    • Banerjee S, Oneda B, Yap LM, et al. MEP1A allele for meprin A metalloprotease is a susceptibility gene for inflammatory bowel disease. Mucosal Immunol. 2009; 2: 220-231.
    • (2009) Mucosal Immunol. , vol.2 , pp. 220-231
    • Banerjee, S.1    Oneda, B.2    Yap, L.M.3
  • 7
    • 70949087383 scopus 로고    scopus 로고
    • Inflammatory bowel disease and mutations affecting the interleukin-10 receptor
    • Glocker EO, Kotlarz D, Boztug K, et al. Inflammatory bowel disease and mutations affecting the interleukin-10 receptor. N Engl J Med. 2009; 361: 2033-2045.
    • (2009) N Engl J Med. , vol.361 , pp. 2033-2045
    • Glocker, E.O.1    Kotlarz, D.2    Boztug, K.3
  • 8
    • 59149088183 scopus 로고    scopus 로고
    • The IL-10R1 S138G loss-of-function allele and ulcerative colitis
    • Grundtner P, Gruber S, Murray SS, et al. The IL-10R1 S138G loss-of-function allele and ulcerative colitis. Genes Immun. 2009; 10: 84-92.
    • (2009) Genes Immun. , vol.10 , pp. 84-92
    • Grundtner, P.1    Gruber, S.2    Murray, S.S.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.