Pouliot V - Search Results

1

iPSC-derived cardiomyocytes from patients with myotonic dystrophy type 1 have abnormal ion channel functions and slower conduction velocities.

Poulin H, Mercier A, Djemai M, Pouliot V, Deschenes I, Boutjdir M, Puymirat J, Chahine M. Poulin H, et al. Among authors: pouliot v. Sci Rep. 2021 Jan 28;11(1):2500. doi: 10.1038/s41598-021-82007-8. Sci Rep. 2021. PMID: 33510259 Free PMC article.

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: pouliot v. 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

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: pouliot v. Circ Res. 2001 Jun 22;88(12):E78-83. doi: 10.1161/hh1201.093270. Circ Res. 2001. PMID: 11420310

4

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: pouliot v. Can J Physiol Pharmacol. 2003 Feb;81(2):129-34. doi: 10.1139/y02-162. Can J Physiol Pharmacol. 2003. PMID: 12710526

5

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. Among authors: pouliot v. J Membr Biol. 2004 Sep 1;201(1):9-24. doi: 10.1007/s00232-004-0701-z. J Membr Biol. 2004. PMID: 15635808

6

A proton leak current through the cardiac sodium channel is linked to mixed arrhythmia and the dilated cardiomyopathy phenotype.

Gosselin-Badaroudine P, Keller DI, Huang H, Pouliot V, Chatelier A, Osswald S, Brink M, Chahine M. Gosselin-Badaroudine P, et al. Among authors: pouliot v. PLoS One. 2012;7(5):e38331. doi: 10.1371/journal.pone.0038331. Epub 2012 May 31. PLoS One. 2012. PMID: 22675453 Free PMC article.

7

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: pouliot v. Gene. 2014 Feb 25;536(2):348-56. doi: 10.1016/j.gene.2013.11.072. Epub 2013 Dec 12. Gene. 2014. PMID: 24334129 Free article.

8

A204E mutation in Na_v1.4 DIS3 exerts gain- and loss-of-function effects that lead to periodic paralysis combining hyper- with hypo-kalaemic signs.

Kokunai Y, Dalle C, Vicart S, Sternberg D, Pouliot V, Bendahhou S, Fournier E, Chahine M, Fontaine B, Nicole S. Kokunai Y, et al. Among authors: pouliot v. Sci Rep. 2018 Nov 12;8(1):16681. doi: 10.1038/s41598-018-34750-8. Sci Rep. 2018. PMID: 30420713 Free PMC article.

9

Novel G1481V and Q1491H SCN5A Mutations Linked to Long QT Syndrome Destabilize the Nav1.5 Inactivation State.

Plumereau Q, Theriault O, Pouliot V, Moreau A, Morel E, Fressart V, Denjoy I, Delinière A, Bessière F, Chevalier P, Gamal El-Din TM, Chahine M. Plumereau Q, et al. Among authors: pouliot v. CJC Open. 2020 Oct 5;3(3):256-266. doi: 10.1016/j.cjco.2020.09.023. eCollection 2021 Mar. CJC Open. 2020. PMID: 33778442 Free PMC article.

10

Cardiac involvement in patient-specific induced pluripotent stem cells of myotonic dystrophy type 1: unveiling the impact of voltage-gated sodium channels.

Pierre M, Djemai M, Chapotte-Baldacci CA, Pouliot V, Puymirat J, Boutjdir M, Chahine M. Pierre M, et al. Among authors: pouliot v. Front Physiol. 2023 Sep 18;14:1258318. doi: 10.3389/fphys.2023.1258318. eCollection 2023. Front Physiol. 2023. PMID: 37791351 Free PMC article.

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