Publications
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Filtres: Author is Poulin, Hugo [Enlever les filtres]
, « De novo Y1460C missense variant in Na1.1 impedes the pore region and results in epileptic encephalopathy. », Sci Rep, vol. 12, nᵒ 1, p. 17182, 2022.
, « -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.
, « Na1.5 knockout in iPSCs: a novel approach to study Na1.5 variants in a human cardiomyocyte environment. », Sci Rep, vol. 11, nᵒ 1, p. 17168, 2021.
, « R1617Q epilepsy mutation slows Na 1.6 sodium channel inactivation and increases the persistent current and neuronal firing. », J Physiol, vol. 599, nᵒ 5, p. 1651-1664, 2021.
, « 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.
