Escande D - Search Results

1

14-3-3 is a regulator of the cardiac voltage-gated sodium channel Nav1.5.

Allouis M, Le Bouffant F, Wilders R, Péroz D, Schott JJ, Noireaud J, Le Marec H, Mérot J, Escande D, Baró I. Allouis M, et al. Among authors: escande d. Circ Res. 2006 Jun 23;98(12):1538-46. doi: 10.1161/01.RES.0000229244.97497.2c. Epub 2006 May 25. Circ Res. 2006. PMID: 16728661

2

Impaired KCNQ1-KCNE1 and phosphatidylinositol-4,5-bisphosphate interaction underlies the long QT syndrome.

Park KH, Piron J, Dahimene S, Mérot J, Baró I, Escande D, Loussouarn G. Park KH, et al. Among authors: escande d. Circ Res. 2005 Apr 15;96(7):730-9. doi: 10.1161/01.RES.0000161451.04649.a8. Epub 2005 Mar 3. Circ Res. 2005. PMID: 15746441

3

KCNQ1 K+ channel-mediated cardiac channelopathies.

Loussouarn G, Baró I, Escande D. Loussouarn G, et al. Among authors: escande d. Methods Mol Biol. 2006;337:167-83. doi: 10.1385/1-59745-095-2:167. Methods Mol Biol. 2006. PMID: 16929947

4

The N-terminal juxtamembranous domain of KCNQ1 is critical for channel surface expression: implications in the Romano-Ward LQT1 syndrome.

Dahimène S, Alcoléa S, Naud P, Jourdon P, Escande D, Brasseur R, Thomas A, Baró I, Mérot J. Dahimène S, et al. Among authors: escande d. Circ Res. 2006 Nov 10;99(10):1076-83. doi: 10.1161/01.RES.0000250262.12219.95. Epub 2006 Oct 19. Circ Res. 2006. PMID: 17053194

5

IKs response to protein kinase A-dependent KCNQ1 phosphorylation requires direct interaction with microtubules.

Nicolas CS, Park KH, El Harchi A, Camonis J, Kass RS, Escande D, Mérot J, Loussouarn G, Le Bouffant F, Baró I. Nicolas CS, et al. Among authors: escande d. Cardiovasc Res. 2008 Aug 1;79(3):427-35. doi: 10.1093/cvr/cvn085. Epub 2008 Apr 5. Cardiovasc Res. 2008. PMID: 18390900 Free PMC article.

6

Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family.

Kyndt F, Probst V, Potet F, Demolombe S, Chevallier JC, Baro I, Moisan JP, Boisseau P, Schott JJ, Escande D, Le Marec H. Kyndt F, et al. Among authors: escande d. Circulation. 2001 Dec 18;104(25):3081-6. doi: 10.1161/hc5001.100834. Circulation. 2001. PMID: 11748104

7

Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease.

Probst V, Kyndt F, Potet F, Trochu JN, Mialet G, Demolombe S, Schott JJ, Baró I, Escande D, Le Marec H. Probst V, et al. Among authors: escande d. J Am Coll Cardiol. 2003 Feb 19;41(4):643-52. doi: 10.1016/s0735-1097(02)02864-4. J Am Coll Cardiol. 2003. PMID: 12598077 Free article.

8

Novel brugada SCN5A mutation leading to ST segment elevation in the inferior or the right precordial leads.

Potet F, Mabo P, Le Coq G, Probst V, Schott JJ, Airaud F, Guihard G, Daubert JC, Escande D, Le Marec H. Potet F, et al. Among authors: escande d. J Cardiovasc Electrophysiol. 2003 Feb;14(2):200-3. doi: 10.1046/j.1540-8167.2003.02382.x. J Cardiovasc Electrophysiol. 2003. PMID: 12693506

9

Mutation in the KCNQ1 gene leading to the short QT-interval syndrome.

Bellocq C, van Ginneken AC, Bezzina CR, Alders M, Escande D, Mannens MM, Baró I, Wilde AA. Bellocq C, et al. Among authors: escande d. Circulation. 2004 May 25;109(20):2394-7. doi: 10.1161/01.CIR.0000130409.72142.FE. Circulation. 2004. PMID: 15159330

10

A common antitussive drug, clobutinol, precipitates the long QT syndrome 2.

Bellocq C, Wilders R, Schott JJ, Louérat-Oriou B, Boisseau P, Le Marec H, Escande D, Baró I. Bellocq C, et al. Among authors: escande d. Mol Pharmacol. 2004 Nov;66(5):1093-102. doi: 10.1124/mol.104.001065. Epub 2004 Jul 27. Mol Pharmacol. 2004. PMID: 15280442

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