Susceptibility to congenital heart defects associated with a polymorphism in TBX2 3′ untranslated region in the Han Chinese population-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Susceptibility to congenital heart defects associated with a polymorphism in TBX2 3′ untranslated region in the Han Chinese population

Published:2018-09-18 Issue:3 Volume:85 Page:378-383
ISSN:0031-3998
Container-title:Pediatric Research
language:en
Short-container-title:Pediatr Res

Author:

Wang Jie,Zhang Ran-ran,Cai Ke,Yang Qian,Duan Wen-yuan,Zhao Jian-yuan,Gui Yong-hao,Wang Feng

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Link

https://www.nature.com/articles/s41390-018-0181-y.pdf

Reference31 articles.

1. Triedman, J. K. & Newburger, J. W. Trends in congenital heart disease: the next decade. Circulation 133, 2716–2733 (2016).

2. Pradat, P. et al. The epidemiology of cardiovascular defects, part I: a study based on data from three large registries of congenital malformations. Pediatr. Cardiol. 24, 195–221 (2003).

3. Zaidi, S. et al. De novo mutations in histone-modifying genes in congenital heart disease. Nature 498, 220–223 (2013).

4. Christoffels, V. M. et al. Development of the pacemaker tissues of the heart. Circ. Res. 106, 240–254 (2010).

5. Cai, C. L. et al. T-box genes coordinate regional rates of proliferation and regional specification during cardiogenesis. Development 132, 2475–2487 (2005).

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Association between SNP rs59382073 in TBX2 3′ UTR and susceptibility to congenital heart diseases;Gene Reports;2022-06

2. Long non-coding RNA SAP30-2:1 is downregulated in congenital heart disease and regulates cell proliferation by targeting HAND2;Frontiers of Medicine;2020-08-19

3. Hypermethylation‐mediated down‐regulation of lncRNA TBX5‐AS1:2 in Tetralogy of Fallot inhibits cell proliferation by reducingTBX5expression;Journal of Cellular and Molecular Medicine;2020-05-05

4. Insights Figure for ‘‘Susceptibility to congenital heart defects associated with a polymorphism in TBX2 3′ untranslated region in the Han Chinese population’’;Pediatric Research;2018-12-11

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3