Loss-of-activity-mutation in the cardiac chloride-bicarbonate exchanger AE3 causes short QT syndrome

Mutations in potassium and calcium channel genes have been associated with cardiac arrhythmias. Here, Jensen et al. show that an anion transporter chloride-bicarbonate exchanger AE3 is also responsible for the genetically-induced mechanism of cardiac arrhythmia, suggesting new therapeutic targets fo...

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Autores principales: Kasper Thorsen, Vibeke S. Dam, Kasper Kjaer-Sorensen, Lisbeth N. Pedersen, V. Arvydas Skeberdis, Jonas Jurevičius, Rimantas Treinys, Ida M. B. S. Petersen, Morten S. Nielsen, Claus Oxvig, J. Preben Morth, Vladimir V. Matchkov, Christian Aalkjær, Henning Bundgaard, Henrik K. Jensen
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/97e6cbf2131e4127b04d04f0aede118d
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spelling oai:doaj.org-article:97e6cbf2131e4127b04d04f0aede118d2021-12-02T14:40:58ZLoss-of-activity-mutation in the cardiac chloride-bicarbonate exchanger AE3 causes short QT syndrome10.1038/s41467-017-01630-02041-1723https://doaj.org/article/97e6cbf2131e4127b04d04f0aede118d2017-11-01T00:00:00Zhttps://doi.org/10.1038/s41467-017-01630-0https://doaj.org/toc/2041-1723Mutations in potassium and calcium channel genes have been associated with cardiac arrhythmias. Here, Jensen et al. show that an anion transporter chloride-bicarbonate exchanger AE3 is also responsible for the genetically-induced mechanism of cardiac arrhythmia, suggesting new therapeutic targets for this diseaseKasper ThorsenVibeke S. DamKasper Kjaer-SorensenLisbeth N. PedersenV. Arvydas SkeberdisJonas JurevičiusRimantas TreinysIda M. B. S. PetersenMorten S. NielsenClaus OxvigJ. Preben MorthVladimir V. MatchkovChristian AalkjærHenning BundgaardHenrik K. JensenNature PortfolioarticleScienceQENNature Communications, Vol 8, Iss 1, Pp 1-10 (2017)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Kasper Thorsen
Vibeke S. Dam
Kasper Kjaer-Sorensen
Lisbeth N. Pedersen
V. Arvydas Skeberdis
Jonas Jurevičius
Rimantas Treinys
Ida M. B. S. Petersen
Morten S. Nielsen
Claus Oxvig
J. Preben Morth
Vladimir V. Matchkov
Christian Aalkjær
Henning Bundgaard
Henrik K. Jensen
Loss-of-activity-mutation in the cardiac chloride-bicarbonate exchanger AE3 causes short QT syndrome
description Mutations in potassium and calcium channel genes have been associated with cardiac arrhythmias. Here, Jensen et al. show that an anion transporter chloride-bicarbonate exchanger AE3 is also responsible for the genetically-induced mechanism of cardiac arrhythmia, suggesting new therapeutic targets for this disease
format article
author Kasper Thorsen
Vibeke S. Dam
Kasper Kjaer-Sorensen
Lisbeth N. Pedersen
V. Arvydas Skeberdis
Jonas Jurevičius
Rimantas Treinys
Ida M. B. S. Petersen
Morten S. Nielsen
Claus Oxvig
J. Preben Morth
Vladimir V. Matchkov
Christian Aalkjær
Henning Bundgaard
Henrik K. Jensen
author_facet Kasper Thorsen
Vibeke S. Dam
Kasper Kjaer-Sorensen
Lisbeth N. Pedersen
V. Arvydas Skeberdis
Jonas Jurevičius
Rimantas Treinys
Ida M. B. S. Petersen
Morten S. Nielsen
Claus Oxvig
J. Preben Morth
Vladimir V. Matchkov
Christian Aalkjær
Henning Bundgaard
Henrik K. Jensen
author_sort Kasper Thorsen
title Loss-of-activity-mutation in the cardiac chloride-bicarbonate exchanger AE3 causes short QT syndrome
title_short Loss-of-activity-mutation in the cardiac chloride-bicarbonate exchanger AE3 causes short QT syndrome
title_full Loss-of-activity-mutation in the cardiac chloride-bicarbonate exchanger AE3 causes short QT syndrome
title_fullStr Loss-of-activity-mutation in the cardiac chloride-bicarbonate exchanger AE3 causes short QT syndrome
title_full_unstemmed Loss-of-activity-mutation in the cardiac chloride-bicarbonate exchanger AE3 causes short QT syndrome
title_sort loss-of-activity-mutation in the cardiac chloride-bicarbonate exchanger ae3 causes short qt syndrome
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/97e6cbf2131e4127b04d04f0aede118d
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