Functional Analysis of TBX5 Missense Mutations Associated with Holt-Oram Syndrome
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference24 articles.
1. T-box genes in development: From hydra to humans
2. Mutations in human cause limb and cardiac malformation in Holt-Oram syndrome
3. Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family
4. Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome
5. The T-box transcription factor gene TBX22 is mutated in X-linked cleft palate and ankyloglossia
Cited by 94 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. Precision Medicine in Congenital Heart Disease, Rheumatic Heart Disease, and Kawasaki Disease of Children: An Overview of Literature;Cardiology in Review;2024-05-02
2. The Role of Genetics in Development of Congenital Heart Disease;Pediatric Cardiology;2024
3. The Role of Genetics in Development of Congenital Heart Disease;Pediatric Cardiology;2023
4. The TH1 cell lineage-determining transcription factor T-bet suppresses TH2 gene expression by redistributing GATA3 away from TH2 genes;Nucleic Acids Research;2022-04-19
5. Two Novel Missense Tbx22 Mutations Frequently Cause Non-Syndromic Cleft Palate in Pakistani Population;Pakistan Journal of Zoology;2022
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