Publications
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Filters: Author is Baroudi, Ghayath [Clear All Filters]
, “Phosphorylation of the consensus sites of protein kinase A on alpha1D L-type calcium channel.”, J Biol Chem, vol. 284, no. 8, pp. 5042-9, 2009.
, “Protein kinase C activation inhibits Cav1.3 calcium channel at NH2-terminal serine 81 phosphorylation site.”, Am J Physiol Heart Circ Physiol, vol. 291, no. 4, pp. H1614-22, 2006.
, “Loss of function associated with novel mutations of the SCN5A gene in patients with Brugada syndrome.”, Can J Cardiol, vol. 20, no. 4, pp. 425-30, 2004.
, “A newly characterized SCN5A mutation underlying Brugada syndrome unmasked by hyperthermia.”, J Cardiovasc Electrophysiol, vol. 14, no. 4, pp. 407-11, 2003.
, “Expression and intracellular localization of an SCN5A double mutant R1232W/T1620M implicated in Brugada syndrome.”, Circ Res, vol. 90, no. 1, pp. E11-6, 2002.
