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粘附分子及其配体在先天性巨结肠发生中的作用 被引量:1

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摘要 先天性巨结肠(HSCR)是一种常见的胃肠道发育畸形,有遗传倾向,其病理基本变化是病变肠段肌间神经丛和粘膜下神经丛内神经节细胞完全缺如.
作者 周莹 张宪生
出处 《中华小儿外科杂志》 CSCD 北大核心 2003年第5期462-463,共2页 Chinese Journal of Pediatric Surgery
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参考文献14

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同被引文献7

  • 1朱小春,徐本源,邹音,杨文萍,钟华生,冯亮,陶强.先天性巨结肠RET蛋白免疫组化研究[J].临床小儿外科杂志,2002,1(1):1-5. 被引量:4
  • 2Kobayashi H,Li Z,Yamataka A.et al.Overexpression of neural cell adhesion molecule (NCAM) antigens on intestinal smooth muscles in hypoganglionosis:Is hypoganglionosis a disorder of the neuromuscular junction? Pediatr Surg Int,2003,19:190-193.
  • 3Nogueira A,Campos M,Soares-Oliveira M,et al.Histochemical and immunohistochemical study of the intrinsic innervation in colonic dysganglionosis.Pediatr Surg Int,2001,17:144-151.
  • 4McCallion AS,Stames E,Conlon RA.etal.Phenotype variation in two-locus mouse models of Hirschsprung disease:Tissue-specific interaction between Ret and Ednrb.Proc Natl Acad Sci USA,2003,100:1826-1831.
  • 5Fitze G,Appelt H,Konig IR,et al.Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR).Hum Mol Genet,2003,12:3207-3214.
  • 6詹江华,房志勤,谷继卿.先天性巨结肠RET基因转录水平的研究[J].中华小儿外科杂志,1999,20(1):5-6. 被引量:12
  • 7段降龙.先天性巨结肠症的分子遗传学研究进展[J].中华小儿外科杂志,2002,23(4):360-360. 被引量:9

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