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Pathogenesis of the Novel Autoimmune-Associated Long-QT Syndrome. Circulation. 2015;132(4):230-40.
Unmasked Brugada pattern by ajmaline challenge in patients with myotonic dystrophy type 1. Ann Noninvasive Electrocardiol. 2015;20(1):28-36.
Biophysics, pathophysiology, and pharmacology of ion channel gating pores. Front Pharmacol. 2014;5:53.
Correlation of the electrophysiological profiles and sodium channel transcripts of individual rat dorsal root ganglia neurons. Front Cell Neurosci. 2014;8:285.
Fluoxetine blocks Nav1.5 channels via a mechanism similar to that of class 1 antiarrhythmics. Mol Pharmacol. 2014;86(4):378-89.
Modulation of peripheral Na(+) channels and neuronal firing by n-butyl-p-aminobenzoate. Eur J Pharmacol. 2014;727:158-66.
Molecular biology and biophysical properties of ion channel gating pores. Q Rev Biophys. 2014;47(4):364-88.
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.
Nav 1.5 mutations linked to dilated cardiomyopathy phenotypes: Is the gating pore current the missing link? Channels (Austin). 2014;8(1):90-4.
Pyrethroids differentially alter voltage-gated sodium channels from the honeybee central olfactory neurons. PLoS ONE. 2014;9(11):e112194.
Pyridoxal-5'-phosphate (MC-1), a vitamin B6 derivative, inhibits expressed P2X receptors. Can J Physiol Pharmacol. 2014;92(3):189-96.
Regulation/modulation of sensory neuron sodium channels. Handb Exp Pharmacol. 2014;221:111-35.
Characterization of the first honeybee Ca²⁺ channel subunit reveals two novel species- and splicing-specific modes of regulation of channel inactivation. Pflugers Arch. 2013;465(7):985-96.
Novel SCN5A mutations in two families with "Brugada-like" ST elevation in the inferior leads and conduction disturbances. J Interv Card Electrophysiol. 2013;37(2):131-40.
Recent advances in voltage-gated sodium channels, their pharmacology, and related diseases. Front Pharmacol. 2013;4:52.
Sodium overload due to a persistent current that attenuates the arrhythmogenic potential of a novel LQT3 mutation. Front Pharmacol. 2013;4:126.
Biophysical characterization of M1476I, a sodium channel founder mutation associated with cold-induced myotonia in French Canadians. J Physiol (Lond). 2012;590(11):2629-44.
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. 2012;131(8):1295-304.
Differential expression of sodium channel β subunits in dorsal root ganglion sensory neurons. J Biol Chem. 2012;287(18):15044-53.
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.
Gating pore currents and the resting state of Nav1.4 voltage sensor domains. Proc Natl Acad Sci USA. 2012;109(47):19250-5.
Mexiletine differentially restores the trafficking defects caused by two brugada syndrome mutations. Front Pharmacol. 2012;3:62.
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.
Sudden death of cardiac origin and psychotropic drugs. Front Pharmacol. 2012;3:76.