Publications
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Filters: Author is Keller, Dagmar I [Clear All Filters]
, “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, pp. 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, pp. 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, pp. 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, pp. 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, pp. 1513-21, 2003.
