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Chatelier A, Dahllund L, Eriksson A, Krupp J, Chahine M. Biophysical properties of human Na v1.7 splice variants and their regulation by protein kinase A. J Neurophysiol. 2008;99(5):2241-50.
Christé G, Chahine M, Chevalier P, Pásek M. Changes in action potentials and intracellular ionic homeostasis in a ventricular cell model related to a persistent sodium current in SCN5A mutations underlying LQT3. Prog Biophys Mol Biol. 2008;96(1-3):281-93.
Hossain MI, Iwasaki H, Okochi Y, Chahine M, Higashijima S, Nagayama K, et al. Enzyme domain affects the movement of the voltage sensor in ascidian and zebrafish voltage-sensing phosphatases. J Biol Chem. 2008;283(26):18248-59.
Lin M-, Wu M-, Chang C-, Chiu S-, Thériault O, Huang H, et al. 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. 2008;5(11):1567-74.
Christé G, Thériault O, Chahine M, Millat G, Rodriguez-Lafrasse C, Rousson R, et al. A new C-terminal hERG mutation A915fs+47X associated with symptomatic LQT2 and auditory-trigger syncope. Heart Rhythm. 2008;5(11):1577-86.
Six I, Hermida J-, Huang H, Gouas L, Fressart V, Benammar N, et al. The occurrence of Brugada syndrome and isolated cardiac conductive disease in the same family could be due to a single SCN5A mutation or to the accidental association of both diseases. Europace. 2008;10(1):79-85.
Chahine M, Qu Y, Mancarella S, Boutjdir M. Protein kinase C activation inhibits alpha1D L-type Ca channel: a single-channel analysis. Pflugers Arch. 2008;455(5):913-9.
Chahine M, Chatelier A, Babich O, Krupp JJ. Voltage-gated sodium channels in neurological disorders. CNS Neurol Disord Drug Targets. 2008;7(2):144-58.

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