Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Jessica J. Jowais"'
Autor:
Alessia Golluscio, Jodene Eldstrom, Jessica J Jowais, Marta Elena Perez, Kevin Peter Cunningham, Alicia De La Cruz, Xiaoan Wu, Valentina Corradi, D Peter Tieleman, David Fedida, H Peter Larsson
Publikováno v:
eLife, Vol 13 (2024)
In cardiomyocytes, the KCNQ1/KCNE1 channel complex mediates the slow delayed-rectifier current (IKs), pivotal during the repolarization phase of the ventricular action potential. Mutations in IKs cause long QT syndrome (LQTS), a syndrome with a prolo
Externí odkaz:
https://doaj.org/article/3b70b86ed7a5417386c6095c41baafa2
Autor:
Briana M Bohannon, Jessica J Jowais, Leif Nyberg, Vanessa Olivier-Meo, Valentina Corradi, D Peter Tieleman, Sara I Liin, H Peter Larsson
Publikováno v:
eLife, Vol 12 (2023)
Voltage-gated potassium (KV) channels are important regulators of cellular excitability and control action potential repolarization in the heart and brain. KV channel mutations lead to disordered cellular excitability. Loss-of-function mutations, for
Externí odkaz:
https://doaj.org/article/7551a63ea06f42c399ecf18db23a441f
Autor:
Briana M Bohannon, Alicia de la Cruz, Xiaoan Wu, Jessica J Jowais, Marta E Perez, Derek M Dykxhoorn, Sara I Liin, H Peter Larsson
Publikováno v:
eLife, Vol 9 (2020)
Externí odkaz:
https://doaj.org/article/916e39ef8eff457f849713b47ca7bd82
Autor:
Briana M Bohannon, Alicia de la Cruz, Xiaoan Wu, Jessica J Jowais, Marta E Perez, Derek M Dykxhoorn, Sara I Liin, H Peter Larsson
Publikováno v:
eLife, Vol 9 (2020)
The cardiac ventricular action potential depends on several voltage-gated ion channels, including NaV, CaV, and KV channels. Mutations in these channels can cause Long QT Syndrome (LQTS) which increases the risk for ventricular fibrillation and sudde
Externí odkaz:
https://doaj.org/article/e07a4e0605884ed9905949525bae0d17
Voltage-gated potassium (KV) channels are important regulators of cellular excitability and control action potential repolarization in the heart and brain. KVchannel mutations lead to disordered cellular excitability. Loss-of-function mutations, for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03986ba4b524b6f111dc26714b02f583
https://doi.org/10.1101/2023.01.12.523777
https://doi.org/10.1101/2023.01.12.523777
Autor:
Jessica J Jowais, Marina Rieder, Lucilla Giammarino, Katja E. Odening, Michael Brunner, Christoph Bode, Sara I. Liin, Alessandro Castiglione, Manfred Zehender, Stefanie Perez-Feliz, Eike M. Wülfers, Gideon Koren, Hans Peter Larsson, Tibor Hornyik, István Baczkó, Iask Edler, András Varró, Zsuzsanna Bősze
Publikováno v:
Europace
Aim Long QT syndrome (LQTS) is a cardiac channelopathy predisposing to ventricular arrhythmias and sudden cardiac death. Since current therapies often fail to prevent arrhythmic events in certain LQTS subtypes, new therapeutic strategies are needed.
Autor:
Jessica J Jowais, Marta E. Perez, Sara I. Liin, Derek M. Dykxhoorn, Briana M. Bohannon, Alicia de la Cruz, Xiaoan Wu, H. Peter Larsson
Publikováno v:
eLife, Vol 9 (2020)
Autor:
Sara I. Liin, Jessica J Jowais, Derek M. Dykxhoorn, Xiaoan Wu, Marta E. Perez, Briana M. Bohannon, Hans Peter Larsson, Alicia de la Cruz
Publikováno v:
eLife, Vol 9 (2020)
eLife
eLife
The cardiac ventricular action potential depends on several voltage-gated ion channels, including Na-V, Ca-V, and K-V channels. Mutations in these channels can cause Long QT Syndrome (LQTS) which increases the risk for ventricular fibrillation and su