Publications
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Filtres: Author is Keller, Dagmar I [Enlever les filtres]
, « A leaky voltage sensor domain of cardiac sodium channels causes arrhythmias associated with dilated cardiomyopathy. », Sci Rep, vol. 8, nᵒ 1, p. 13804, 2018.
, « Biophysical, Molecular, and Pharmacological Characterization of Voltage-Dependent Sodium Channels From Induced Pluripotent Stem Cell-Derived Cardiomyocytes. », Can J Cardiol, vol. 33, nᵒ 2, p. 269-278, 2017.
, « Mexiletine differentially restores the trafficking defects caused by two brugada syndrome mutations. », Front Pharmacol, vol. 3, p. 62, 2012.
, « A proton leak current through the cardiac sodium channel is linked to mixed arrhythmia and the dilated cardiomyopathy phenotype. », PLoS One, vol. 7, nᵒ 5, p. e38331, 2012.
, « Characterization of novel KCNH2 mutations in type 2 long QT syndrome manifesting as seizures. », Can J Cardiol, vol. 25, nᵒ 8, p. 455-62, 2009.
, « A novel SCN5A mutation, F1344S, identified in a patient with Brugada syndrome and fever-induced ventricular fibrillation. », Cardiovasc Res, vol. 70, nᵒ 3, p. 521-9, 2006.
, « A novel nonsense mutation in the SCN5A gene leads to Brugada syndrome and a silent gene mutation carrier state. », Can J Cardiol, vol. 21, nᵒ 11, p. 925-31, 2005.
, « A novel mutation in SCN5A, delQKP 1507-1509, causing long QT syndrome: role of Q1507 residue in sodium channel inactivation. », J Mol Cell Cardiol, vol. 35, nᵒ 12, p. 1513-21, 2003.
