Chahine M - Search Results

1

The variant hERG/R148W associated with LQTS is a mutation that reduces current density on co-expression with the WT.

Mechakra A, Vincent Y, Chevalier P, Millat G, Ficker E, Jastrzebski M, Poulin H, Pouliot V, Chahine M, Christé G. Mechakra A, et al. Among authors: chahine m. Gene. 2014 Feb 25;536(2):348-56. doi: 10.1016/j.gene.2013.11.072. Epub 2013 Dec 12. Gene. 2014. PMID: 24334129

2

SCN5A mutation (T1620M) causing Brugada syndrome exhibits different phenotypes when expressed in Xenopus oocytes and mammalian cells.

Baroudi G, Carbonneau E, Pouliot V, Chahine M. Baroudi G, et al. Among authors: chahine m. FEBS Lett. 2000 Feb 4;467(1):12-6. doi: 10.1016/s0014-5793(00)01099-1. FEBS Lett. 2000. PMID: 10664447 Free article.

3

The distinct HERG missense mutation L564P causes long QT syndrome in one French Canadian family.

St-Pierre J, Roy N, Blier L, Plante E, Cote JM, Gilbert M, Chahine M. St-Pierre J, et al. Among authors: chahine m. Can J Cardiol. 2000 Mar;16(3):307-12. Can J Cardiol. 2000. PMID: 10744792

4

Novel mechanism for Brugada syndrome: defective surface localization of an SCN5A mutant (R1432G).

Baroudi G, Pouliot V, Denjoy I, Guicheney P, Shrier A, Chahine M. Baroudi G, et al. Among authors: chahine m. Circ Res. 2001 Jun 22;88(12):E78-83. doi: 10.1161/hh1201.093270. Circ Res. 2001. PMID: 11420310

5

Biophysical characteristics of a new mutation on the KCNQ1 potassium channel (L251P) causing long QT syndrome.

Deschênes D, Acharfi S, Pouliot V, Hegele R, Krahn A, Daleau P, Chahine M. Deschênes D, et al. Among authors: chahine m. Can J Physiol Pharmacol. 2003 Feb;81(2):129-34. doi: 10.1139/y02-162. Can J Physiol Pharmacol. 2003. PMID: 12710526

6

Role of arginine residues on the S4 segment of the Bacillus halodurans Na+ channel in voltage-sensing.

Chahine M, Pilote S, Pouliot V, Takami H, Sato C. Chahine M, et al. J Membr Biol. 2004 Sep 1;201(1):9-24. doi: 10.1007/s00232-004-0701-z. J Membr Biol. 2004. PMID: 15635808

7

Changes in action potentials and intracellular ionic homeostasis in a ventricular cell model related to a persistent sodium current in SCN5A mutations underlying LQT3.

Christé G, Chahine M, Chevalier P, Pásek M. Christé G, et al. Among authors: chahine m. Prog Biophys Mol Biol. 2008 Jan-Apr;96(1-3):281-93. doi: 10.1016/j.pbiomolbio.2007.07.023. Epub 2007 Aug 11. Prog Biophys Mol Biol. 2008. PMID: 17892895 Free article. Review.

8

In utero onset of long QT syndrome with atrioventricular block and spontaneous or lidocaine-induced ventricular tachycardia: compound effects of hERG pore region mutation and SCN5A N-terminus variant.

Lin MT, Wu MH, Chang CC, Chiu SN, Thériault O, Huang H, Christé G, Ficker E, Chahine M. Lin MT, et al. Among authors: chahine m. Heart Rhythm. 2008 Nov;5(11):1567-74. doi: 10.1016/j.hrthm.2008.08.010. Epub 2008 Aug 17. Heart Rhythm. 2008. PMID: 18848812 Free article.

9

A new C-terminal hERG mutation A915fs+47X associated with symptomatic LQT2 and auditory-trigger syncope.

Christé G, Thériault O, Chahine M, Millat G, Rodriguez-Lafrasse C, Rousson R, Deschênes I, Ficker E, Chevalier P. Christé G, et al. Among authors: chahine m. Heart Rhythm. 2008 Nov;5(11):1577-86. doi: 10.1016/j.hrthm.2008.08.031. Epub 2008 Aug 31. Heart Rhythm. 2008. PMID: 18984536 Free PMC article.

10

Biophysical characterization of a new SCN5A mutation S1333Y in a SIDS infant linked to long QT syndrome.

Huang H, Millat G, Rodriguez-Lafrasse C, Rousson R, Kugener B, Chevalier P, Chahine M. Huang H, et al. Among authors: chahine m. FEBS Lett. 2009 Mar 4;583(5):890-6. doi: 10.1016/j.febslet.2009.02.007. Epub 2009 Feb 10. FEBS Lett. 2009. PMID: 19302788 Free article.

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