期刊文献+

先天性脊柱侧弯遗传及环境病因学研究进展 被引量:6

Progress in genetic and environmental etiology of congenital scoliosis
原文传递
导出
摘要 先天性脊柱侧弯(congenital scoliosis, CS)是由于胚胎期椎体的形成障碍或分节不良所引起的一种以纵向和旋转不平衡为特征的畸形,前者所致的半椎体畸形是导致先天性脊柱侧弯的主要原因。引起CS的病因极其复杂,目前尚不清楚,近年来,关于CS的病因相关研究较多,大多研究认为遗传与环境是CS重要致病因素。本文就CS发病原因中的遗传因素与环境因素的研究进展作一综述,以期为该病的诊疗提供新思路。 Congenital scoliosis(CS)is a deformity characterized by longitudinal and rotational imbalance caused by formation disorder and malsegmentation of embryonic vertebral bodies.Hemivertebra deformity caused by the former is the main type of congenital scoliosis.The etiology of CS is relatively complex and unclear.In recent years,there have been many researches on the etiology of CS,most of which agree that heredity and environment are the main pathogenesis factors.Advances in genetic and environmental factors related to the pathogenesis of CS are reviewed in this article.
作者 杨涛 赵继荣 马同 寄婧 陈祁青 张天龙 蔡毅 李玮农 张立存 YANG Tao;ZHAO Ji-rong;MA Tong;JI Jing;CHEN Qi-qing;ZHANG Tian-long;CAI Yi;LI Wei-nong;ZHANG Li-cun(Gansu University of Traditional Chinese Medicine,Lanzhou 730030;Gansu Provincial Hospital of Traditional Chinese Medicine,Lanzhou 730050,China)
出处 《中国矫形外科杂志》 CAS CSCD 北大核心 2020年第15期1399-1403,共5页 Orthopedic Journal of China
基金 国家自然科学基金项目(编号:81760877) 卫生部医药卫生科技发展研究中心科研基金项目(编号:W2014ZT210) 国家中医药管理局国家中医临床研究基地业务建设科研专项课题(编号:JDZX2015039) 兰州市创新人才项目(编号:2018-RC-99) 兰州市创新人才项目(编号:2018-RC-94) 甘肃省自然科学基金项目(编号:17JR5RA051) 甘肃中医药大学研究生创新基金项目(编号:CX2018-10)。
关键词 先天性脊柱侧弯 病因 基因 环境 缺氧 维生素 congenital scoliosis etiology gene environment hypoxia vitamin
  • 相关文献

参考文献10

二级参考文献204

  • 1于海泉,沈建雄.脊柱侧凸后路矫形融合术后深部感染的治疗[J].中国骨与关节外科,2013,6(S1):39-43. 被引量:3
  • 2Davis RL, Turner DL. Vertebrate hairy and Enhancer of split related proteins: transcriptional repressors regulating cellular differentiation and embryonic patterning [J]. Oncogene,2001,20(58):8342-8357.
  • 3Zhou M, Yan J, Ma Z, et al. Comparative and Evolutionary Analysis of the HES/HEY Gene Family Reveal Exon/Intron Loss and Teleost Specific Duplication Events [J]. PLoS One,2012,7(7):e40649.
  • 4Ishibashi M, Sasai Y, Nakanishi S, et al. Molecular characterization of HES-2, a mammalian helix-loop-helix factor structurally related to Drosophila hairy and Enhancer of split [J]. Eur J Biochem,1993,215 (3):645-652.
  • 5Sakagami T, Sakurada K, Sakai Y, et al. Structure and chromosomal locus of the mouse gene encoding a cerebellar Purkinje cell-specific helix-loop-helix factor Hes-3[J]. Biochem Biophys Res Commun,199 4,203(1):594-601.
  • 6Takebayashi K, Sasai Y, Sakai Y, et al. Structure, chromosomal locus, and promoter analysis of the gene encoding the mouse helix-loop-helix factor HES-1. Negative autoregulation through the multiple N box elements [J]. J Biol Chem,1994,269(7):5150-5156.
  • 7Takebayashi K, Akazawa C, Nakanishi S, et al. Structure and promoter analysis of the gene encoding the mouse helix-loop-helix factor HES-5. Identification of the neural precursor cell-specific promoter element [J]. J Biol Chem, 1995,270(3): 1342- 1349.
  • 8Nishimura M, Isaka F, Ishibashi M, et al. Structure, chromosomal locus, and promoter of mouse Hes2 gene, a homologue of Drosophila hairy and Enhancer of split [J]. Genomics, 1998,49( 1 ):69-75.
  • 9Vasiliauskas D, Stem CD. Expression of mouse HES-6, a new member of the Hairy/Enhancer of split family of bHLH transcription factors [J]. Mech Dev,2000,98(1-2): 133 - 137.
  • 10Liu J, Sun YH, Wang N, et al. Cloning, characterization and promoter analysis of common carp hairy/Enhancer-of-split-related gene, her6 [J]. J Genet,2006,85(3): 171-178.

共引文献52

同被引文献44

引证文献6

二级引证文献7

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