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TRPM4 channels in the cardiovascular system: physiology, pathophysiology, and pharmacology.
Abriel H, Syam N, Sottas V, Amarouch MY, Rougier JS. Abriel H, et al. Biochem Pharmacol. 2012 Oct 1;84(7):873-81. doi: 10.1016/j.bcp.2012.06.021. Epub 2012 Jun 27. Biochem Pharmacol. 2012. PMID: 22750058 Review.
Force-controlled patch clamp of beating cardiac cells.
Ossola D, Amarouch MY, Behr P, Vörös J, Abriel H, Zambelli T. Ossola D, et al. Among authors: amarouch my. Nano Lett. 2015 Mar 11;15(3):1743-50. doi: 10.1021/nl504438z. Epub 2015 Feb 6. Nano Lett. 2015. PMID: 25639960
Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I.
Daumy X, Amarouch MY, Lindenbaum P, Bonnaud S, Charpentier E, Bianchi B, Nafzger S, Baron E, Fouchard S, Thollet A, Kyndt F, Barc J, Le Scouarnec S, Makita N, Le Marec H, Dina C, Gourraud JB, Probst V, Abriel H, Redon R, Schott JJ. Daumy X, et al. Among authors: amarouch my. Int J Cardiol. 2016 Mar 15;207:349-58. doi: 10.1016/j.ijcard.2016.01.052. Epub 2016 Jan 11. Int J Cardiol. 2016. PMID: 26820365
Antiarrhythmic Action of Flecainide in Polymorphic Ventricular Arrhythmias Caused by a Gain-of-Function Mutation in the Nav 1.5 Sodium Channel.
Amarouch MY, Swan H, Leinonen J, Marjamaa A, Lahtinen AM, Kontula K, Toivonen L, Widen E, Abriel H. Amarouch MY, et al. Ann Noninvasive Electrocardiol. 2016 Jul;21(4):343-51. doi: 10.1111/anec.12312. Epub 2015 Oct 7. Ann Noninvasive Electrocardiol. 2016. PMID: 26965448 Free PMC article.
Variants of Transient Receptor Potential Melastatin Member 4 in Childhood Atrioventricular Block.
Syam N, Chatel S, Ozhathil LC, Sottas V, Rougier JS, Baruteau A, Baron E, Amarouch MY, Daumy X, Probst V, Schott JJ, Abriel H. Syam N, et al. Among authors: amarouch my. J Am Heart Assoc. 2016 May 20;5(5):e001625. doi: 10.1161/JAHA.114.001625. J Am Heart Assoc. 2016. PMID: 27207958 Free PMC article.
Gain-of-function mutation of the SCN5A gene causes exercise-induced polymorphic ventricular arrhythmias.
Swan H, Amarouch MY, Leinonen J, Marjamaa A, Kucera JP, Laitinen-Forsblom PJ, Lahtinen AM, Palotie A, Kontula K, Toivonen L, Abriel H, Widen E. Swan H, et al. Circ Cardiovasc Genet. 2014 Dec;7(6):771-81. doi: 10.1161/CIRCGENETICS.114.000703. Epub 2014 Sep 10. Circ Cardiovasc Genet. 2014. PMID: 25210054
A long QT mutation substitutes cholesterol for phosphatidylinositol-4,5-bisphosphate in KCNQ1 channel regulation.
Coyan FC, Abderemane-Ali F, Amarouch MY, Piron J, Mordel J, Nicolas CS, Steenman M, Mérot J, Marionneau C, Thomas A, Brasseur R, Baró I, Loussouarn G. Coyan FC, et al. PLoS One. 2014 Mar 28;9(3):e93255. doi: 10.1371/journal.pone.0093255. eCollection 2014. PLoS One. 2014. PMID: 24681627 Free PMC article.
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