SMAD4 loss-of-function mutation predisposes to congenital heart disease
Author:
Funder
Fudan University
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference50 articles.
1. A novel KLF13 mutation underlying congenital patent ductus arteriosus and ventricular septal defect, as well as bicuspid aortic valve;Abhinav;Exp. Ther. Med.,2022
2. Biallelic loss-of-function variants of GFRA1 cause lethal bilateral renal agenesis;Al-Shamsi;Eur. J. Med. Genet.,2022
3. SMAD4 mutation segregating in a family with juvenile polyposis, aortopathy, and mitral valve dysfunction;Andrabi;Am. J. Med. Genet. A.,2011
4. Myocardial deletion of Smad4 using a novel alpha skeletal muscle actin Cre recombinase transgenic mouse causes misalignment of the cardiac outflow tract;Azhar;Int. J. Biol. Sci.,2010
5. The smads;Attisano;Genome Biol.,2001
Cited by 7 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. Deamidation enables pathogenic SMAD6 variants to activate the BMP signaling pathway;Science China Life Sciences;2024-06-21
2. Somatic GATA4 mutation contributes to tetralogy of Fallot;Experimental and Therapeutic Medicine;2024-01-08
3. Discovery and functional investigation of BMP4 as a new causative gene for human congenital heart disease;American Journal of Translational Research;2024
4. Discovery of BMP10 as a new gene underpinning congenital heart defects;American Journal of Translational Research;2024
5. Role of Stimulated by Retinoic Acid 6 In 46 Children of Coarctation Of the Aorta;2024
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