Literature DB >> 26940926

Gene-Specific Therapy for Congenital Long QT Syndrome: Are We There Yet?

Elena Arbelo1, Georgia Sarquella-Brugada2, Josep Brugada3.   

Abstract

Entities:  

Keywords:  arrhythmia; mutation; sodium-channel blocker; sudden cardiac death

Mesh：

Substances：

Year:  2016        PMID： 26940926     DOI： 10.1016/j.jacc.2015.12.030

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN： 0735-1097            Impact factor:   24.094


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  4 in total

Review 1.  Cardiac Organoids: A 3D Technology for Modeling Heart Development and Disease.

Authors:  Liyuan Zhu; Kui Liu; Qi Feng; Yingnan Liao
Journal:  Stem Cell Rev Rep       Date:  2022-05-08       Impact factor: 5.739

2.  Gating Properties of Mutant Sodium Channels and Responses to Sodium Current Inhibitors Predict Mexiletine-Sensitive Mutations of Long QT Syndrome 3.

Authors:  Gang Li; Ryan L Woltz; Cheng-Yu Wang; Lu Ren; Pei-Xin He; Shan-Dong Yu; Xue-Qin Liu; Vladimir Yarov-Yarovoy; Dan Hu; Nipavan Chiamvimonvat; Lin Wu
Journal:  Front Pharmacol       Date:  2020-08-04       Impact factor: 5.810

3.  A novel mutation in KCNH2 yields loss-of-function of hERG potassium channel in long QT syndrome 2.

Authors:  Kai Gu; Duoduo Qian; Huiyuan Qin; Chang Cui; W C Hewith A Fernando; Daowu Wang; Juejin Wang; Kejiang Cao; Minglong Chen
Journal:  Pflugers Arch       Date:  2021-01-15       Impact factor: 3.657

Review 4.  Voltage-Gated Ca2+-Channel α1-Subunit de novo Missense Mutations: Gain or Loss of Function - Implications for Potential Therapies.

Authors:  Jörg Striessnig
Journal:  Front Synaptic Neurosci       Date:  2021-03-03
  4 in total

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