Publications by authors named "Isabelle Baro"

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Long QT syndrome type 3 gain-of-function of Na1.5 increases ventricular fibroblasts proliferation and pro-fibrotic factors.
Claire Castro, Justine Patin, Cyrielle Jajkiewicz, Franck Chizelle, Cynthia Ore Cerpa

Commun Biol· February 2025

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Editorial: Methods and applications in cardiac electrophysiology-application to inherited arrhythmias.
Nathalie Neyroud, Isabelle Baró, Ange Maguy

Front Physiol· March 2024

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Predicting hERG repolarization power at 37°C from recordings at room temperature.
Barbara B R Oliveira-Mendes, Malak Alameh, Jérôme Montnach, Béatrice Ollivier, Solène Gibaud

Clin Transl Med· May 2023

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SARS-CoV-2 E and 3a Proteins Are Inducers of Pannexin Currents.
Barbara B R Oliveira-Mendes, Malak Alameh, Béatrice Ollivier, Jérôme Montnach, Nicolas Bidère

Cells· May 2023

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A standardised hERG phenotyping pipeline to evaluate KCNH2 genetic variant pathogenicity.
Barbara Oliveira-Mendes, Sylvain Feliciangeli, Mélissa Ménard, Frank Chatelain, Malak Alameh

Clin Transl Med· November 2021

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Modelling sudden cardiac death risks factors in patients with coronavirus disease of 2019: the hydroxychloroquine and azithromycin case.
Jérôme Montnach, Isabelle Baró, Flavien Charpentier, Michel De Waard, Gildas Loussouarn

Europace· July 2021

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A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype.
Zeina R Al Sayed, Mariam Jouni, Jean-Baptiste Gourraud, Nadjet Belbachir, Julien Barc

Clin Transl Med· June 2021

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Infanticide vs. inherited cardiac arrhythmias.
Malene Brohus, Todor Arsov, David A Wallace, Helene Halkjær Jensen, Mette Nyegaard

Europace· March 2021

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Computer modeling of whole-cell voltage-clamp analyses to delineate guidelines for good practice of manual and automated patch-clamp.
Jérôme Montnach, Maxime Lorenzini, Adrien Lesage, Isabelle Simon, Sébastien Nicolas

Sci Rep· February 2021

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Gap-134, a Connexin43 activator, prevents age-related development of ventricular fibrosis in Scn5a mice.
Justine Patin, Claire Castro, Marja Steenman, Agnès Hivonnait, Agnès Carcouët

Pharmacol Res· September 2020

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RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome.
Nadjet Belbachir, Vincent Portero, Zeina R Al Sayed, Jean-Baptiste Gourraud, Florian Dilasser

Eur Heart J· October 2019

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Arrhythmias precede cardiomyopathy and remodeling of Ca handling proteins in a novel model of long QT syndrome.
Jérôme Montnach, Franck F Chizelle, Nadjet Belbachir, Claire Castro, Linwei Li

J Mol Cell Cardiol· October 2018

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Transforming growth factor β receptor inhibition prevents ventricular fibrosis in a mouse model of progressive cardiac conduction disease.
Mickael Derangeon, Jérôme Montnach, Cynthia Ore Cerpa, Benoit Jagu, Justine Patin

Cardiovasc Res· April 2017

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HIV-Tat induces a decrease in I and Ivia reduction in phosphatidylinositol-(4,5)-bisphosphate availability.
Zeineb Es-Salah-Lamoureux, Mariam Jouni, Olfat A Malak, Nadjet Belbachir, Zeina Reda Al Sayed

J Mol Cell Cardiol· October 2016

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Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome.
Vincent Portero, Solena Le Scouarnec, Zeineb Es-Salah-Lamoureux, Sophie Burel, Jean-Baptiste Gourraud, Estelle Baron

J Am Heart Assoc· June 2016

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Physiological and Pathophysiological Insights of Nav1.4 and Nav1.5 Comparison.
Gildas Loussouarn, Damien Sternberg, Sophie Nicole, Céline Marionneau, Francoise Le Bouffant

Front Pharmacol· February 2016

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Toward Personalized Medicine: Using Cardiomyocytes Differentiated From Urine-Derived Pluripotent Stem Cells to Recapitulate Electrophysiological Characteristics of Type 2 Long QT Syndrome.
Mariam Jouni, Karim Si-Tayeb, Zeineb Es-Salah-Lamoureux, Xenia Latypova, Benoite Champon

J Am Heart Assoc· September 2015

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A long QT mutation substitutes cholesterol for phosphatidylinositol-4,5-bisphosphate in KCNQ1 channel regulation.
Fabien C Coyan, Fayal Abderemane-Ali, Mohamed Yassine Amarouch, Julien Piron, Jérôme Mordel

PLoS One· June 2015

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Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations.
Delphine M Béziau, Julien Barc, Thomas O'Hara, Laurianne Le Gloan, Mohamed Yassine Amarouch

Basic Res Cardiol· May 2015

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Marine n-3 PUFAs modulate IKs gating, channel expression, and location in membrane microdomains.
Cristina Moreno, Alicia de la Cruz, Anna Oliveras, Sanjay R Kharche, Miriam Guizy

Cardiovasc Res· February 2015

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Mouse Models of SCN5A-Related Cardiac Arrhythmias.
Mickael Derangeon, Jérôme Montnach, Isabelle Baró, Flavien Charpentier

Front Physiol· October 2012

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Opposite Effects of the S4-S5 Linker and PIP(2) on Voltage-Gated Channel Function: KCNQ1/KCNE1 and Other Channels.
Frank S Choveau, Fayal Abderemane-Ali, Fabien C Coyan, Zeineb Es-Salah-Lamoureux, Isabelle Baró

Front Pharmacol· October 2012

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Dual effect of phosphatidylinositol (4,5)-bisphosphate PIP(2) on Shaker K(+) [corrected] channels.
Fayal Abderemane-Ali, Zeineb Es-Salah-Lamoureux, Lucie Delemotte, Marina A Kasimova, Alain J Labro

J Biol Chem· October 2012

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Multifocal ectopic Purkinje-related premature contractions: a new SCN5A-related cardiac channelopathy.
Gabriel Laurent, Samuel Saal, Mohamed Yassine Amarouch, Delphine M Béziau, Roos F J Marsman, Estelle Baron

J Am Coll Cardiol· July 2012

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KCNQ1 channels voltage dependence through a voltage-dependent binding of the S4-S5 linker to the pore domain.
Frank S Choveau, Nicolas Rodriguez, Fayal Abderemane Ali, Alain J Labro, Thierry Rose

J Biol Chem· January 2011

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