Publications
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Filtres: Author is Chevalier, Philippe [Enlever les filtres]
, « Genetic associations of protein-coding variants in human disease. », Nature, vol. 603, nᵒ 7899, p. 95-102, 2022.
, « Novel G1481V and Q1491H SCN5A Mutations Linked to Long QT Syndrome Destabilize the Nav1.5 Inactivation State. », CJC Open, vol. 3, nᵒ 3, p. 256-266, 2021.
, « Effects of amlodipine and perindoprilate on the structure and function of mitochondria in ventricular cardiomyocytes during ischemia-reperfusion in the pig. », Fundam Clin Pharmacol, vol. 29, nᵒ 1, p. 21-30, 2015.
, « 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.
, « Sudden death of cardiac origin and psychotropic drugs. », Front Pharmacol, vol. 3, p. 76, 2012.
, « 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.
, « A new C-terminal hERG mutation A915fs+47X associated with symptomatic LQT2 and auditory-trigger syncope. », Heart Rhythm, vol. 5, nᵒ 11, p. 1577-86, 2008.
