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Volumn 18, Issue 2, 2012, Pages 393-394

Homozygosity for the NOD2 p.Leu1007fsX1008 variant is the main genetic predictor for fibrostenotic Crohn's disease

Author keywords

[No Author keywords available]

Indexed keywords

CROHN DISEASE; FIBROSIS; GENE; GENE MUTATION; GENETIC VARIABILITY; HOMOZYGOSITY; HUMAN; INTESTINE FISTULA; INTESTINE STENOSIS; LETTER; NOD2 GENE; PHENOTYPE; PREDICTIVE VALUE; PRIORITY JOURNAL; RISK FACTOR; SENSITIVITY AND SPECIFICITY;

EID: 84855665333     PISSN: 10780998     EISSN: 15364844     Source Type: Journal    
DOI: 10.1002/ibd.21914     Document Type: Letter
Times cited : (6)

References (8)
  • 1
    • 80051548464 scopus 로고    scopus 로고
    • Predictors of fibrostenotic Crohn's disease
    • Rieder F, Lawrance IC, Leite A, et al. Predictors of fibrostenotic Crohn's disease. Inflamm Bowel Dis. 2011; 17: 2000-2007.
    • (2011) Inflamm Bowel Dis , vol.17 , pp. 2000-2007
    • Rieder, F.1    Lawrance, I.C.2    Leite, A.3
  • 2
    • 80051544183 scopus 로고    scopus 로고
    • Genetic factors conferring an increased susceptibility to develop Crohn's disease also influence disease phenotype, but do not predict it. Results from the IBDChip European Project
    • Figueroa CD, Cleynen I, Franke A, et al. Genetic factors conferring an increased susceptibility to develop Crohn's disease also influence disease phenotype, but do not predict it. Results from the IBDChip European Project. Gastroenterology. 2010; 138:(suppl 1): S677.
    • (2010) Gastroenterology , vol.138 , Issue.SUPPL. 1
    • Figueroa, C.D.1    Cleynen, I.2    Franke, A.3
  • 3
    • 79953771887 scopus 로고    scopus 로고
    • The prognostic power of the NOD2 genotype for complicated Crohn's disease: A meta-analysis
    • Adler J, Rangwalla SC, Dwamena BA, et al. The prognostic power of the NOD2 genotype for complicated Crohn's disease: a meta-analysis. Am J Gastroenterol. 2011; 106: 699-712.
    • (2011) Am J Gastroenterol , vol.106 , pp. 699-712
    • Adler, J.1    Rangwalla, S.C.2    Dwamena, B.A.3
  • 4
    • 78651239059 scopus 로고    scopus 로고
    • The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants
    • Glas J, Seiderer J, Tillack C, et al. The NOD2 single nucleotide polymorphisms rs2066843 and rs2076756 are novel and common Crohn's disease susceptibility gene variants. PLoS One. 2010; 5: e14466.
    • (2010) PLoS One , vol.5
    • Glas, J.1    Seiderer, J.2    Tillack, C.3
  • 5
    • 33645457756 scopus 로고    scopus 로고
    • Eight novel CARD15 variants detected by DNA sequence analysis of the CARD15 gene in 111 patients with inflammatory bowel disease
    • Schnitzler F, Brand S, Staudinger T, et al. Eight novel CARD15 variants detected by DNA sequence analysis of the CARD15 gene in 111 patients with inflammatory bowel disease. Immunogenetics. 2006; 58: 99-106.
    • (2006) Immunogenetics , vol.58 , pp. 99-106
    • Schnitzler, F.1    Brand, S.2    Staudinger, T.3
  • 8
    • 77955664679 scopus 로고    scopus 로고
    • The presence of fistulas and NOD2 homozygosity strongly predict intestinal stenosis in Crohn's disease independent of the IL23R genotype
    • Jürgens M, Brand S, Laubender RP, et al. The presence of fistulas and NOD2 homozygosity strongly predict intestinal stenosis in Crohn's disease independent of the IL23R genotype. J Gastroenterol. 2010; 45: 721-731.
    • (2010) J Gastroenterol , vol.45 , pp. 721-731
    • Jürgens, M.1    Brand, S.2    Laubender, R.P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.