期刊文献+

核因子-κB通路在溃疡性结肠炎治疗中的应用 被引量:2

下载PDF
导出
摘要 溃疡性结肠炎(UC)的病因和发病机制目前尚未完全明确,但肠黏膜免疫功能异常为公认的重要发病机制之一。核因子-κB(NF-κB)是一类细胞核转录调节因子,在炎性反应中起到枢纽作用。近年来有关NF-κB通路与UC之间关系的研究备受关注,在通路各环节进行阻断时,该病的动物模型可获得明显的疗效。该文就NF-κB通路在UC治疗中的应用作一综述。
出处 《国际消化病杂志》 CAS 2015年第4期241-243,共3页 International Journal of Digestive Diseases
  • 相关文献

参考文献2

二级参考文献134

  • 1[1]Podolsky DK.Inflammatory bowel disease.N Engl J Med 2002; 347:417-429
  • 2[2]Satsangi J,Morecroft J,Shah NB,Nimmo E.Genetics of inflammatory bowel disease:scientific and clinical implications.Best Pract Res Clin Gastroenterol 2003; 17:3-18
  • 3[3]Hugot JP,Laurent-Puig P,Gower-Rousseau C,Olson JM,Lee JC,Beaugerie L,Naom I,Dupas JL,Van Gossum A,Orholm M,Bonaiti-Pellie C,Weissenbach J,Mathew CG,LennardJones JE,Cortot A,Colombel JF,Thomas G.Mapping of a susceptibility locus for Crohn's disease on chromosome 16.Nature 1996; 379:821-823
  • 4[4]Hampe J,Schreiber S,Shaw SH,Lau KF,Bridger S,Macpherson AJ,Cardon LR,Sakul H,Harris TJ,Buckler A,Hall J,Stokkers P,van Deventer SJ,Nurnberg P,Mirza MM,Lee JC,Lennard-Jones JE,Mathew CG,Curran ME.A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort.Ant J Hum Genet 1999; 64:808-816
  • 5[5]Williams CN,Kocher K,Lander ES,Daly MJ,Rioux JD.Using a genome-wide scan and meta-analysis to identify a novel IBD locus and confirm previously identified IBD loci.Inflamm Bowel Dis 2002; 8:375-381
  • 6[6]Barmada MM,Brant SR,Nicolae DL,Achkar JP,Panhuysen CI,Bayless TM,Cho JH,Duerr RH.A genome scan in 260 inflammatory bowel disease-affected relative pairs.Inflamm Bowel Dis 2004; 10:15-22
  • 7[7]Ogura Y,Bonen DK,Inohara N,Nicolae DL,Chen FF,Ramos R,Britton H,Moran T,Karaliuskas R,Duerr RH,Achkar JP,Brant SR,Bayless TM,Kirschner BS,Hanauer SB,Nunez G,Cho JH.A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease.Nature 2001; 411:603-606
  • 8[8]Hugot JP,Chamaillard M,Zouali H,Lesage S,Cezard JP,Belaiche J,Aimer S,Tysk C,O'Morain CA,Gassull M,Binder V,Finkel Y,Cortot A,Modigliani R,Laurent-Puig P,GowerRousseau C,Macry J,Colombel JF,Sahbatou M,Thomas G.Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease.Nature 2001; 411:599-603
  • 9[9]Hampe J,Cuthbert A,Croucher PJ,Mirza MM,Mascheretti S,Fisher S,Frenzel H,King K,Hasselmeyer A,MacFtierson AJ,Bridger S,van Deventer S,Forbes A,Nikolaus S,LennardJones JE,Foelsch UR,Krawczak M,Lewis C,Schreiber S,Mathew CG.Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations.Lancet 2001; 357:1925-1928
  • 10[10]Hampe J,Frenzel H,Mirza MM,Croucher PJ,Cuthbert A,Mascheretti S,Huse K,Platzer M,Bridger S,Meyer B,Nurnberg P,Stokkers P,Krawczak M,Mathew CG,Curran M,Schreiber S.Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p.Proc Natl Acad Sci USA 2002; 99:321-326

共引文献8

同被引文献21

引证文献2

二级引证文献16

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部