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Filtres: Author is Mercier, Aurélie [Enlever les filtres]

2018

Moreau A, Gosselin-Badaroudine P, Mercier A, Burger B, Keller DI, Chahine M. A leaky voltage sensor domain of cardiac sodium channels causes arrhythmias associated with dilated cardiomyopathy. Sci Rep. 2018;8(1):13804.

2017

Moreau A, Mercier A, Thériault O, Boutjdir M, Burger B, Keller DI, Chahine M. Biophysical, Molecular, and Pharmacological Characterization of Voltage-Dependent Sodium Channels From Induced Pluripotent Stem Cell-Derived Cardiomyocytes. Can J Cardiol. 2017;33(2):269-278.

2015

Pambrun T, Bortone A, Bois P, Degand B, Patri S, Mercier A, Chahine M, Chatelier A, Coisne D, Amiel A. Unmasked Brugada pattern by ajmaline challenge in patients with myotonic dystrophy type 1. Ann Noninvasive Electrocardiol. 2015;20(1):28-36.

2014

Pambrun T, Mercier A, Chatelier A, Patri S, Schott J-J, Le Scouarnec S, Chahine M, Degand B, Bois P. Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1.5 sodium channel loss-of-function mutation. Heart Rhythm. 2014;11(8):1393-400.

2012

Chatelier A, Mercier A, Tremblier B, Thériault O, Moubarak M, Benamer N, Corbi P, Bois P, Chahine M, Faivre JFr. A distinct de novo expression of Nav1.5 sodium channels in human atrial fibroblasts differentiated into myofibroblasts. J Physiol (Lond). 2012;590(17):4307-19.

Mercier A, Clément R, Harnois T, Bourmeyster N, Faivre J-F, Findlay I, Chahine M, Bois P, Chatelier A. The β1-subunit of Na(v)1.5 cardiac sodium channel is required for a dominant negative effect through α-α interaction. PLoS ONE. 2012;7(11):e48690.

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