Cargando…
Atrial arrhythmogenicity of KCNJ2 mutations in short QT syndrome: Insights from virtual human atria
Gain-of-function mutations in KCNJ2-encoded Kir2.1 channels underlie variant 3 (SQT3) of the short QT syndrome, which is associated with atrial fibrillation (AF). Using biophysically-detailed human atria computer models, this study investigated the mechanistic link between SQT3 mutations and atrial...
Autores principales: | Whittaker, Dominic G., Ni, Haibo, El Harchi, Aziza, Hancox, Jules C., Zhang, Henggui |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487071/ https://www.ncbi.nlm.nih.gov/pubmed/28609477 http://dx.doi.org/10.1371/journal.pcbi.1005593 |
Ejemplares similares
-
Correction: Atrial arrhythmogenicity of KCNJ2 mutations in short QT syndrome: Insights from virtual human atria
Publicado: (2019) -
In silico investigation of a KCNQ1 mutation associated with short QT syndrome
por: Adeniran, Ismail, et al.
Publicado: (2017) -
Human Atrial Arrhythmogenesis and Sinus Bradycardia in KCNQ1-Linked Short QT Syndrome: Insights From Computational Modelling
por: Whittaker, Dominic G., et al.
Publicado: (2018) -
Pro-arrhythmogenic effects of atrial fibrillation-induced electrical remodelling: insights from the three-dimensional virtual human atria
por: Colman, Michael A, et al.
Publicado: (2013) -
In silico Assessment of Pharmacotherapy for Human Atrial Patho-Electrophysiology Associated With hERG-Linked Short QT Syndrome
por: Whittaker, Dominic G., et al.
Publicado: (2019)