Publications
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Filtres: Author is Huang, Hai [Enlever les filtres]
, « Mexiletine differentially restores the trafficking defects caused by two brugada syndrome mutations. », Front Pharmacol, vol. 3, p. 62, 2012.
, « A proton leak current through the cardiac sodium channel is linked to mixed arrhythmia and the dilated cardiomyopathy phenotype. », PLoS One, vol. 7, nᵒ 5, p. e38331, 2012.
, « Y1767C, a novel SCN5A mutation, induces a persistent Na+ current and potentiates ranolazine inhibition of Nav1.5 channels. », Am J Physiol Heart Circ Physiol, vol. 300, nᵒ 1, p. H288-99, 2011.
, « Cell membrane expression of cardiac sodium channel Na(v)1.5 is modulated by alpha-actinin-2 interaction. », Biochemistry, vol. 49, nᵒ 1, p. 166-78, 2010.
, « Biophysical characterization of a new SCN5A mutation S1333Y in a SIDS infant linked to long QT syndrome. », FEBS Lett, vol. 583, nᵒ 5, p. 890-6, 2009.
, « Contribution of long-QT syndrome genetic variants in sudden infant death syndrome. », Pediatr Cardiol, vol. 30, nᵒ 4, p. 502-9, 2009.
, « Gain-of-function mutation of Nav1.5 in atrial fibrillation enhances cellular excitability and lowers the threshold for action potential firing. », Biochem Biophys Res Commun, vol. 380, nᵒ 1, p. 132-7, 2009.
, « A novel mutation in the SCN5A gene is associated with Brugada syndrome. », Life Sci, vol. 80, nᵒ 8, p. 716-24, 2007.
, « A novel SCN5A mutation, F1344S, identified in a patient with Brugada syndrome and fever-induced ventricular fibrillation. », Cardiovasc Res, vol. 70, nᵒ 3, p. 521-9, 2006.
