Pathogenic mechanism of a catecholaminergic polymorphic ventricular tachycardia causing-mutation in cardiac calcium release channel RyR2-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Pathogenic mechanism of a catecholaminergic polymorphic ventricular tachycardia causing-mutation in cardiac calcium release channel RyR2

Published:2018-04 Issue: Volume:117 Page:26-35
ISSN:0022-2828
Container-title:Journal of Molecular and Cellular Cardiology
language:en
Short-container-title:Journal of Molecular and Cellular Cardiology

Author:

Xiong Jing,Liu Xijun,Gong Yunyun,Zhang Peng^ORCID,Qiang Sujing,Zhao Qian,Guo Rong,Qian Yunyun,Wang Lipeng,Zhu Li,Wang Ruiwu,Hao Zhiyuan,Wen Han,Zhang Jingying,Tang Kai,Zang Wang-Fu,Yuchi Zhiguang,Chen Haijun,Chen S.R. Wayne,Zheng Wenjun,Wang Shi-Qiang,Xu Ya-Wei,Liu Zheng^ORCID

Funder

National Natural Science Foundation of China

Science and Technology Commission of Shanghai Municipality

National Key Research and Development

American Heart Association

National Science Foundation

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine,Molecular Biology

Reference48 articles.

1. Polymorphic ventricular tachyarrhythmias in the absence of organic heart disease: classification, differential diagnosis, and implications for therapy;Viskin;Prog. Cardiovasc. Dis.,1998

2. Targeted mutational analysis of the RyR2-encoded cardiac ryanodine receptor in sudden unexplained death: a molecular autopsy of 49 medical examiner/coroner's cases;Tester;Mayo Clin. Proc.,2004

3. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia;Priori;Circulation,2001

4. A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in bedouin families from Israel;Lahat;Am. J. Hum. Genet.,2001

5. Clinical phenotype and functional characterization of CASQ2 mutations associated with catecholaminergic polymorphic ventricular tachycardia;di Barletta;Circulation,2006

Cited by 21 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. The Dysfunction of Ca2+ Channels in Hereditary and Chronic Human Heart Diseases and Experimental Animal Models;International Journal of Molecular Sciences;2023-10-27

2. Arrhythmogenic mechanism of a novel ryanodine receptor mutation underlying sudden cardiac death;Europace;2023-07

3. HIV-Tat Exacerbates the Actions of Atazanavir, Efavirenz, and Ritonavir on Cardiac Ryanodine Receptor (RyR2);International Journal of Molecular Sciences;2022-12-23

4. Correction: “Ryanopathies” and RyR2 dysfunctions: can we further decipher them using in vitro human disease models?;Cell Death & Disease;2022-11-30

5. A novel mutation in ryanodine receptor 2 (RYR2) genes at c.12670G>T associated with focal epilepsy in a 3-year-old child;Frontiers in Pediatrics;2022-10-19

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