Thapsigargin Selectively Rescues the Trafficking Defective LQT2 Channels G601S and F805C
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference28 articles.
1. HERG Channel Dysfunction in Human Long QT Syndrome
2. Novel Mechanism Associated With an Inherited Cardiac Arrhythmia
3. Correction of Defective Protein Trafficking of a Mutant HERG Potassium Channel in Human Long QT Syndrome
4. Long QT Syndrome: Cellular Basis and Arrhythmia Mechanism in LQT2
5. The Binding Site for Channel Blockers That Rescue Misprocessed Human Long QT Syndrome Type 2 ether-a-gogo-related Gene (HERG) Mutations
Cited by 91 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. Rescue of expression and function of long QT syndrome-causing mutant hERG channels by enhancing channel stability in the plasma membrane;Journal of Biological Chemistry;2024-08
2. Ligand-based virtual-screening identified a novel CFTR ligand which improves the defective cell surface expression of misfolded ABC transporters;Frontiers in Pharmacology;2024-04-11
3. Detecting organelle-specific activity of potassium channels with a DNA nanodevice;Nature Biotechnology;2023-09-21
4. Differential Effects of Remdesivir and Lumacaftor on Homomeric and Heteromeric hERG Channels;Molecular Pharmacology;2023-07-07
5. Modeling long QT syndrome type 2 on-a-chip via in-depth assessment of isogenic gene-edited 3D cardiac tissues;Science Advances;2022-12-16
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