Baroudi G - Search Results

1

Localization and modulation of {alpha}1D (Cav1.3) L-type Ca channel by protein kinase A.

Qu Y, Baroudi G, Yue Y, El-Sherif N, Boutjdir M. Qu Y, et al. Among authors: baroudi g. Am J Physiol Heart Circ Physiol. 2005 May;288(5):H2123-30. doi: 10.1152/ajpheart.01023.2004. Epub 2004 Dec 22. Am J Physiol Heart Circ Physiol. 2005. PMID: 15615842 Free article.

2

Protein kinase C activation inhibits Cav1.3 calcium channel at NH2-terminal serine 81 phosphorylation site.

Baroudi G, Qu Y, Ramadan O, Chahine M, Boutjdir M. Baroudi G, et al. Am J Physiol Heart Circ Physiol. 2006 Oct;291(4):H1614-22. doi: 10.1152/ajpheart.00095.2006. Am J Physiol Heart Circ Physiol. 2006. PMID: 16973824 Free article.

3

Phosphorylation of the consensus sites of protein kinase A on alpha1D L-type calcium channel.

Ramadan O, Qu Y, Wadgaonkar R, Baroudi G, Karnabi E, Chahine M, Boutjdir M. Ramadan O, et al. Among authors: baroudi g. J Biol Chem. 2009 Feb 20;284(8):5042-9. doi: 10.1074/jbc.M809132200. Epub 2008 Dec 11. J Biol Chem. 2009. PMID: 19074150 Free PMC article.

4

Novel molecular mechanism involving alpha1D (Cav1.3) L-type calcium channel in autoimmune-associated sinus bradycardia.

Qu Y, Baroudi G, Yue Y, Boutjdir M. Qu Y, et al. Among authors: baroudi g. Circulation. 2005 Jun 14;111(23):3034-41. doi: 10.1161/CIRCULATIONAHA.104.517326. Epub 2005 Jun 6. Circulation. 2005. PMID: 15939813

5

Atrial fibrillation: molecular biology has yet to impact management.

El-Sherif N, Baroudi G. El-Sherif N, et al. Among authors: baroudi g. J Cardiovasc Electrophysiol. 2004 Feb;15(2):224-5. doi: 10.1046/j.1540-8167.2004.03618.x. J Cardiovasc Electrophysiol. 2004. PMID: 15028054 No abstract available.

6

Biophysical phenotypes of SCN5A mutations causing long QT and Brugada syndromes.

Baroudi G, Chahine M. Baroudi G, et al. FEBS Lett. 2000 Dec 29;487(2):224-8. doi: 10.1016/s0014-5793(00)02360-7. FEBS Lett. 2000. PMID: 11150514 Free article.

7

Expression and intracellular localization of an SCN5A double mutant R1232W/T1620M implicated in Brugada syndrome.

Baroudi G, Acharfi S, Larouche C, Chahine M. Baroudi G, et al. Circ Res. 2002 Jan 11;90(1):E11-6. Circ Res. 2002. PMID: 11786529

8

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

9

Loss of function associated with novel mutations of the SCN5A gene in patients with Brugada syndrome.

Baroudi G, Napolitano C, Priori SG, Del Bufalo A, Chahine M. Baroudi G, et al. Can J Cardiol. 2004 Mar 15;20(4):425-30. Can J Cardiol. 2004. PMID: 15057319

10

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. FEBS Lett. 2000 Feb 4;467(1):12-6. doi: 10.1016/s0014-5793(00)01099-1. FEBS Lett. 2000. PMID: 10664447 Free article.

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