Publications
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Filtres: Author is Thériault, Olivier [Enlever les filtres]
, « -related epilepsy of infancy with migrating focal seizures: report of a variant with apparent gain- and loss-of-function effects. », J Neurophysiol, vol. 127, nᵒ 5, p. 1388-1397, 2022.
, « Novel G1481V and Q1491H SCN5A Mutations Linked to Long QT Syndrome Destabilize the Nav1.5 Inactivation State. », CJC Open, vol. 3, nᵒ 3, p. 256-266, 2021.
, « 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.
, « Differential modulation of Nav1.7 and Nav1.8 channels by antidepressant drugs. », Eur J Pharmacol, vol. 764, p. 395-403, 2015.
, « Correlation of the electrophysiological profiles and sodium channel transcripts of individual rat dorsal root ganglia neurons. », Front Cell Neurosci, vol. 8, p. 285, 2014.
, « Fluoxetine blocks Nav1.5 channels via a mechanism similar to that of class 1 antiarrhythmics. », Mol Pharmacol, vol. 86, nᵒ 4, p. 378-89, 2014.
, « Modulation of peripheral Na(+) channels and neuronal firing by n-butyl-p-aminobenzoate. », Eur J Pharmacol, vol. 727, p. 158-66, 2014.
, « Pyridoxal-5'-phosphate (MC-1), a vitamin B6 derivative, inhibits expressed P2X receptors. », Can J Physiol Pharmacol, vol. 92, nᵒ 3, p. 189-96, 2014.
, « Coexisting mutations/polymorphisms of the long QT syndrome genes in patients with repaired Tetralogy of Fallot are associated with the risks of life-threatening events. », Hum Genet, vol. 131, nᵒ 8, p. 1295-304, 2012.
, « A distinct de novo expression of Nav1.5 sodium channels in human atrial fibroblasts differentiated into myofibroblasts. », J Physiol, vol. 590, nᵒ 17, p. 4307-19, 2012.
, « In utero onset of long QT syndrome with atrioventricular block and spontaneous or lidocaine-induced ventricular tachycardia: compound effects of hERG pore region mutation and SCN5A N-terminus variant. », Heart Rhythm, vol. 5, nᵒ 11, p. 1567-74, 2008.
, « A new C-terminal hERG mutation A915fs+47X associated with symptomatic LQT2 and auditory-trigger syncope. », Heart Rhythm, vol. 5, nᵒ 11, p. 1577-86, 2008.
