Isabelle Baro
Nantes, France
Last Updated: 09/26/2026
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Found 24 publications
Editorial: Methods and applications in cardiac electrophysiology-application to inherited arrhythmias.
Journal: Frontiers in physiology
Published: February 19, 2024
Long QT syndrome type 3 gain-of-function of Nav1.5 increases ventricular fibroblasts proliferation and pro-fibrotic factors.
Journal: Communications biology
Published: July 05, 2023
SARS-CoV-2 E and 3a Proteins Are Inducers of Pannexin Currents.
Journal: Cells
Published: March 13, 2023
Predicting hERG repolarization power at 37°C from recordings at room temperature.
Journal: Clinical and translational medicine
Published: January 23, 2023
A standardised hERG phenotyping pipeline to evaluate KCNH2 genetic variant pathogenicity.
Journal: Clinical and translational medicine
Published: May 04, 2021
A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype.
Journal: Clinical and translational medicine
Published: January 26, 2021
Modelling sudden cardiac death risks factors in patients with coronavirus disease of 2019: the hydroxychloroquine and azithromycin case.
Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
Published: September 18, 2020
Infanticide vs. inherited cardiac arrhythmias.
Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
Published: August 12, 2020
Computer modeling of whole-cell voltage-clamp analyses to delineate guidelines for good practice of manual and automated patch-clamp.
Journal: Scientific reports
Published: May 08, 2020
Gap-134, a Connexin43 activator, prevents age-related development of ventricular fibrosis in Scn5a+/- mice.
Journal: Pharmacological research
Published: January 22, 2020
Arrhythmias precede cardiomyopathy and remodeling of Ca2+ handling proteins in a novel model of long QT syndrome.
Journal: Journal of molecular and cellular cardiology
Published: March 13, 2018
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome.
Journal: European heart journal
Published: November 08, 2017
Last Updated: 09/26/2026