Publications | Centre de recherche CERVO

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Filtres: Author is Keller, Dagmar I [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, et al. 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.

2012

Moreau A, Keller DI, Huang H, Fressart V, Schmied C, Timour Q, et al. Mexiletine differentially restores the trafficking defects caused by two brugada syndrome mutations. Front Pharmacol. 2012;3:62.

Gosselin-Badaroudine P, Keller DI, Huang H, Pouliot V, Chatelier A, Osswald S, et al. A proton leak current through the cardiac sodium channel is linked to mixed arrhythmia and the dilated cardiomyopathy phenotype. PLoS ONE. 2012;7(5):e38331.

2009

Keller DI, Grenier J, Christé G, Dubouloz F, Osswald S, Brink M, et al. Characterization of novel KCNH2 mutations in type 2 long QT syndrome manifesting as seizures. Can J Cardiol. 2009;25(8):455-62.

2006

Keller DI, Huang H, Zhao J, Frank R, Suarez V, Delacrétaz E, et al. A novel SCN5A mutation, F1344S, identified in a patient with Brugada syndrome and fever-induced ventricular fibrillation. Cardiovasc Res. 2006;70(3):521-9.

2005

Keller DI, Barrane F-, Gouas L, Martin J, Pilote S, Suarez V, et al. A novel nonsense mutation in the SCN5A gene leads to Brugada syndrome and a silent gene mutation carrier state. Can J Cardiol. 2005;21(11):925-31.

2003

Keller DI, Acharfi S, Delacrétaz E, Benammar N, Rotter M, Pfammatter JP, et al. A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation. J Mol Cell Cardiol. 2003;35(12):1513-21.

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