Publications
Export 9 results:
Filtres: Author is Chatelier, Aurélien [Enlever les filtres]
, « Unmasked Brugada pattern by ajmaline challenge in patients with myotonic dystrophy type 1. », Ann Noninvasive Electrocardiol, vol. 20, nᵒ 1, p. 28-36, 2015.
, « Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1.5 sodium channel loss-of-function mutation. », Heart Rhythm, vol. 11, nᵒ 8, p. 1393-400, 2014.
, « A distinct de novo expression of Nav1.5 sodium channels in human atrial fibroblasts differentiated into myofibroblasts. », J Physiol, vol. 590, nᵒ 17, p. 4307-19, 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.
, « The β1-subunit of Na(v)1.5 cardiac sodium channel is required for a dominant negative effect through α-α interaction. », PLoS One, vol. 7, nᵒ 11, p. e48690, 2012.
, « Biophysical characterisation of the persistent sodium current of the Nav1.6 neuronal sodium channel: a single-channel analysis. », Pflugers Arch, vol. 460, nᵒ 1, p. 77-86, 2010.
, « Biophysical properties of human Na v1.7 splice variants and their regulation by protein kinase A. », J Neurophysiol, vol. 99, nᵒ 5, p. 2241-50, 2008.
, « Voltage-gated sodium channels in neurological disorders. », CNS Neurol Disord Drug Targets, vol. 7, nᵒ 2, p. 144-58, 2008.
, « Lidocaine promotes the trafficking and functional expression of Na(v)1.8 sodium channels in mammalian cells. », J Neurophysiol, vol. 98, nᵒ 1, p. 467-77, 2007.
