Tetralogy of Fallot and Other Congenital Heart Defects in Hey2 Mutant Mice
Author:
Publisher
Elsevier BV
Subject
General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology
Reference33 articles.
1. Mutations in the human Jagged1 gene are responsible for Alagille syndrome;Oda;Nat. Genet.,1997
2. Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1;Li;Nat. Genet.,1997
3. Jagged1 mutations in patients ascertained with isolated congenital heart defects;Krantz;Am. J. Med. Genet.,1999
4. Familial Tetralogy of Fallot caused by mutation in the jagged1 gene;Eldadah;Hum. Mol. Genet.,2001
5. Identification and expression of a novel family of bHLH cDNAs related to Drosophila hairy and enhancer of split;Kokubo;Biochem. Biophys. Res. Commun.,1999
Cited by 163 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. Left ventricular hypertrophy and metabolic resetting in the Notch3-deficient adult mouse heart;Scientific Reports;2023-09-12
2. Hey2 enhancer activity defines unipotent progenitors for left ventricular cardiomyocytes in juxta-cardiac field of early mouse embryo;Proceedings of the National Academy of Sciences;2023-09-05
3. Loss of myocardial Hey2/Hrt2 function disrupts rightward shift of atrioventricular cushion tissue and causes tricuspid atresia;Developmental Dynamics;2023-04-25
4. Transcription factors regulating vasculogenesis and angiogenesis;Developmental Dynamics;2023-03-06
5. Activation of the hypoxia response pathway protects against age-induced cardiac hypertrophy;Journal of Molecular and Cellular Cardiology;2022-03
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