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CORC

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Dysfunctional Nav1.5 channels due to SCN5A mutations 期刊论文
EXPERIMENTAL BIOLOGY AND MEDICINE, 2018, 卷号: 243, 页码: 852-863
作者:  Han, Dan;  Tan, Hui;  Sun, Chaofeng;  Li, Guoliang
收藏  |  浏览/下载：3/0  |  提交时间：2019/11/26
Readthrough of SCN5A Nonsense Mutations p.R1623X and p.S1812X Questions Gene-therapy in Brugada Syndrome 期刊论文
2017, 卷号: 7, 期号: 1, 页码: 50-58
作者:  Teng Siyong;  Huang Jian;  Gao Zhan;  Hao Jie;  Yang Yuejin
收藏  |  浏览/下载：12/0  |  提交时间：2020/01/04
A Brugada syndrome proband with compound heterozygote SCN5A mutations identified from a Chinese family in Singapore 期刊论文
EUROPACE, 2016, 卷号: 18, 期号: 6
作者:  Tan, Boon Yew;  Yong, Rita Yu Yin;  Barajas-Martinez, Hector;  Dumaine, Robert;  Chew, Ying Xia
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/05
A novel mutation in the SCN5A gene contributes to arrhythmogenic characteristics of early repolarization syndrome 期刊论文
2016, 卷号: 37, 期号: 3, 页码: 727-733
作者:  Guo, Qi;  Ren, Lan;  Chen, Xuhua;  Hou, Cuihong;  Chu, Jianmin
收藏  |  浏览/下载：2/0  |  提交时间：2020/01/04
The SCN5A Mutation A1180V is Associated With Electrocardiographic Features of LQT3 期刊论文
PEDIATRIC CARDIOLOGY, 2014, 卷号: 35, 期号: [db:dc_citation_issue], 页码: 295-300
作者:  Zhang, Yanmin;  Wang, Juanli;  Chang, Suer;  Zhou, Nan;  Xing, Haijian
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/03
Isoprenaline: A Potential Contributor in Sick Sinus Syndrome-Insights from a Mathematical Model of the Rabbit Sinoatrial Node 期刊论文
http://dx.doi.org/10.1155/2014/540496, 2014
Li, Xiang; Zhang, Ji-qian; Shuai, Jian-wei; 帅建伟
收藏  |  浏览/下载：9/0  |  提交时间：2015/07/22
Electrophysiological Characteristics of a SCN5A Voltage Sensors Mutation R1629Q Associated With Brugada Syndrome 期刊论文
http://dx.doi.org/10.1371/journal.pone.0078382, 2013
Zeng, Zhipeng; Zhou, Jieqiong; Hou, Yuxi; Liang, Xiaojing; Zhang, Ziguan; Xu, Xuejing; Xie, Qiang; Li, Weihua; Huang, Zhengrong; 周洁琼; 梁晓静; 谢强; 李卫华; 黄峥嵘
收藏  |  浏览/下载：3/0  |  提交时间：2015/07/22
Altered Cardiac Sodium Channel Function Due to Voltage-Sensor Mutation in Dilated Cardiomyopathy Patients with SCN5A Mutations 会议论文
作者:  Aijun Sun;  Lei Xu;  Shaochun Wang;  Kai Hu;  Chunyu Zhang
收藏  |  浏览/下载：4/0  |  提交时间：2019/12/19
Digenic inheritance novel mutations in SCN5a and SNTA1 increase late I-Na contributing to LQT syndrome 期刊论文
2013, 卷号: 304, 期号: 7, 页码: H994-H1001
作者:  Hu, Rou-Mu;  Tan, Bi-Hua;  Orland, Kate M.;  Valdivia, Carmen R.;  Peterson, Amber
收藏  |  浏览/下载：2/0  |  提交时间：2020/01/13
Altered Cardiac Sodium Channel Function Due to Voltage-Sensor Mutation in Dilated Cardiomyopathy Patients with SCN5A Mutations 会议论文
中华医学会第十五次全国心血管病学大会
作者:  Aijun Sun;  Lei Xu;  Shaochun Wang;  Kai Hu;  Chunyu Zhang
收藏  |  浏览/下载：2/0  |  提交时间：2019/12/31

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