Publications
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Filtres: Author is Poulin, Hugo [Enlever les filtres]
« A recessive Nav1.4 mutation underlies congenital myasthenic syndrome with periodic paralysis. », Neurology, vol. 86, nᵒ 2, p. 161-9, 2016.
, « Differential modulation of Nav1.7 and Nav1.8 channels by antidepressant drugs. », Eur J Pharmacol, vol. 764, p. 395-403, 2015.
, « 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.
, « The variant hERG/R148W associated with LQTS is a mutation that reduces current density on co-expression with the WT. », Gene, vol. 536, nᵒ 2, p. 348-56, 2014.
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