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NOD2基因突变与克罗恩病易感性及临床表型的关系 被引量:2

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作者 郑家驹
出处 《中华消化杂志》 CAS CSCD 北大核心 2004年第7期443-444,共2页 Chinese Journal of Digestion
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参考文献10

  • 1Duerr RH. The genetics of inflammatory bowel disease. Gastroenterol Clin North Am,2002,31:63-76. 被引量:2
  • 2Ahmad T, Armuzzi A, Bunce M, et al. The molecular classification of the clinical manifestations of Crohn's disease. Gastroenterology, 2002,122: 854-866. 被引量:1
  • 3Cuthbert AP, Fisher SA, Mirza MM, et al. The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease. Gastroenterology, 2002,122:867-874. 被引量:1
  • 4Hugot JP, Laurent-Puig P, Gower-Roussean C, et al. Mapping of a susceptibility locus for Crohn's disease on chromosome 16. Nature, 1996,379:821-823. 被引量:1
  • 5Hugot JP, Chamaillard M, Zouali H, et al. Association of NOD2 leucine-rich repeat variants with susceptibility of Crohn's disease. Nature, 2001,411: 599-603. 被引量:1
  • 6Ogura Y, Bonen DK, Inohara N, et al. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature,2001,411:603-606. 被引量:1
  • 7Hampe J, Cuthbert A, Croucher PJ, et al. Association between inertion mutation in NOD2 gene and Crohn's disease in German and British populations. Lancet ,2001,357: 1925-1928. 被引量:1
  • 8Cavanaugh J, IBD International Genetics Consortium. International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set:Crohn's disease and ehromose 16. Am J Hum Genet, 2001,68:1165-1171. 被引量:1
  • 9Chang EB. Predicting patterns of Crohn's disease through genetic markers. Gastroenterology, 2002,122: 847-848. 被引量:1
  • 10Abreu MT, Taylor KD, Lin YC, et al. Mutations in NOD2 are associated with fibrostenosing disease in patients with Crohn's dis ease. Gastroenterology, 2002,123:679-688. 被引量:1

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同被引文献41

  • 1高敏,曹倩,罗灵和,吴敏良,胡伟玲,姒健敏.NOD2/CARD15基因多态性与克罗恩病患者相关性研究[J].中华内科杂志,2005,44(3):210-212. 被引量:22
  • 2张以洋,智发朝,周殿元,姜泊,赖卓胜,张迎春,钟长青,龙靖华,徐迪辉,张奕.克罗恩病CARD15/NOD2基因突变的研究[J].中华消化杂志,2006,26(7):456-459. 被引量:15
  • 3Halme L,Turunen U,Paavola-Sakki P,et al.CARD15 frameshift mutation in patients with CROHN disease is associated with immune dysregulation[J].Scand J Gastroenterol,2004,39(12):1243 -1249 被引量:1
  • 4Sugimura K,Taylor KD,Lin YC,et al.A novel NOD2/CARD15 haplotype conferring risk for Crohn disease in Ashkenazi Jews[J].Am J Hum Genet,2003,72(3):509-518 被引量:1
  • 5Lombardi Maria Luisa,Pirozzi Giuseppe,Luongo Vincenza,et al.Crohn disease:susceptibility and disease heterogeneity revealed by HLA genotyping[J].Human Immunology,2001,62(7):701-704 被引量:1
  • 6Pierik M,De Hertogh G,Vermeire S,et al.Epithelioid granulomas,pattern recognition receptors,and phenotypes of Crohn' s disease[J].Gut,2005,54(2):223-227 被引量:1
  • 7Idestrom M,Rubio C,Granath F,et al.CARD15 mutations are rare in Swedish pediatric Crohn disease[J].J Pediatr Gastroenterol Nutr,2005,40(4):456-460 被引量:1
  • 8Halme L,Turunen U,Paavola-Sakki P,et al.CARD15 frameshift mutation in patients with CROHN disease is associated with immune dysregulation[J].Scand J Gastroenterol,2004,39(12):1243 -1249 被引量:1
  • 9Akagi S,Hiyama E,Imamura Y,et al.Hollenbach E,Vieth M,Roessner A,Interleukin-10 expression in intestine of Crohn disease[J].Int J Mol Med,2000,5(4):389-395 被引量:1
  • 10Denis MA,Louis R,Malaise M,et al.Increased response of blood eosinophils to various chemotactic agents in quiescent Crohn disease[J].Scand J Gastroenterol,2001,36(2):190-195 被引量:1

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