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Results: 1 to 20 of 187

1.

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.

Circ Res. 2001 Jun 22;88(12):E78-83.

PMID:
11420310
[PubMed - indexed for MEDLINE]
Free Article
2.

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

Baroudi G, Acharfi S, Larouche C, Chahine M.

Circ Res. 2002 Jan 11;90(1):E11-6.

PMID:
11786529
[PubMed - indexed for MEDLINE]
Free Article
3.

Enhanced Na(+) channel intermediate inactivation in Brugada syndrome.

Wang DW, Makita N, Kitabatake A, Balser JR, George AL Jr.

Circ Res. 2000 Oct 13;87(8):E37-43.

PMID:
11029409
[PubMed - indexed for MEDLINE]
Free Article
4.

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.

FEBS Lett. 2000 Feb 4;467(1):12-6.

PMID:
10664447
[PubMed - indexed for MEDLINE]
Free Article
5.

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.

Can J Cardiol. 2004 Mar 15;20(4):425-30.

PMID:
15057319
[PubMed - indexed for MEDLINE]
6.

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

Baroudi G, Chahine M.

FEBS Lett. 2000 Dec 29;487(2):224-8.

PMID:
11150514
[PubMed - indexed for MEDLINE]
Free Article
7.

Novel Brugada syndrome-causing mutation in ion-conducting pore of cardiac Na+ channel does not affect ion selectivity properties.

Amin AS, Verkerk AO, Bhuiyan ZA, Wilde AA, Tan HL.

Acta Physiol Scand. 2005 Dec;185(4):291-301.

PMID:
16266370
[PubMed - indexed for MEDLINE]
8.

Cardiac Na(+) channel dysfunction in Brugada syndrome is aggravated by beta(1)-subunit.

Makita N, Shirai N, Wang DW, Sasaki K, George AL Jr, Kanno M, Kitabatake A.

Circulation. 2000 Jan 4-11;101(1):54-60.

PMID:
10618304
[PubMed - indexed for MEDLINE]
Free Article
9.

Functional suppression of sodium channels by beta(1)-subunits as a molecular mechanism of idiopathic ventricular fibrillation.

Wan X, Wang Q, Kirsch GE.

J Mol Cell Cardiol. 2000 Oct;32(10):1873-84.

PMID:
11013131
[PubMed - indexed for MEDLINE]
10.

A novel mutation in the SCN5A gene is associated with Brugada syndrome.

Shin DJ, Kim E, Park SB, Jang WC, Bae Y, Han J, Jang Y, Joung B, Lee MH, Kim SS, Huang H, Chahine M, Yoon SK.

Life Sci. 2007 Jan 30;80(8):716-24. Epub 2006 Dec 1.

PMID:
17141278
[PubMed - indexed for MEDLINE]
11.

A novel missense mutation in the SCN5A gene associated with Brugada syndrome bidirectionally affecting blocking actions of antiarrhythmic drugs.

Itoh H, Shimizu M, Takata S, Mabuchi H, Imoto K.

J Cardiovasc Electrophysiol. 2005 May;16(5):486-93.

PMID:
15877619
[PubMed - indexed for MEDLINE]
12.

Clinical and electrophysiological characteristics of Brugada syndrome caused by a missense mutation in the S5-pore site of SCN5A.

Itoh H, Shimizu M, Mabuchi H, Imoto K.

J Cardiovasc Electrophysiol. 2005 Apr;16(4):378-83.

PMID:
15828879
[PubMed - indexed for MEDLINE]
13.

Distinct functional defect of three novel Brugada syndrome related cardiac sodium channel mutations.

Hsueh CH, Chen WP, Lin JL, Tsai CT, Liu YB, Juang JM, Tsao HM, Su MJ, Lai LP.

J Biomed Sci. 2009 Feb 20;16:23. doi: 10.1186/1423-0127-16-23.

PMID:
19272188
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

A novel SCN5A mutation, F1344S, identified in a patient with Brugada syndrome and fever-induced ventricular fibrillation.

Keller DI, Huang H, Zhao J, Frank R, Suarez V, Delacrétaz E, Brink M, Osswald S, Schwick N, Chahine M.

Cardiovasc Res. 2006 Jun 1;70(3):521-9. Epub 2006 Mar 3.

PMID:
16616735
[PubMed - indexed for MEDLINE]
Free Article
15.

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome.

Vatta M, Dumaine R, Varghese G, Richard TA, Shimizu W, Aihara N, Nademanee K, Brugada R, Brugada J, Veerakul G, Li H, Bowles NE, Brugada P, Antzelevitch C, Towbin JA.

Hum Mol Genet. 2002 Feb 1;11(3):337-45.

PMID:
11823453
[PubMed - indexed for MEDLINE]
Free Article
16.

Electrocardiographic characteristics and SCN5A mutations in idiopathic ventricular fibrillation associated with early repolarization.

Watanabe H, Nogami A, Ohkubo K, Kawata H, Hayashi Y, Ishikawa T, Makiyama T, Nagao S, Yagihara N, Takehara N, Kawamura Y, Sato A, Okamura K, Hosaka Y, Sato M, Fukae S, Chinushi M, Oda H, Okabe M, Kimura A, Maemura K, Watanabe I, Kamakura S, Horie M, Aizawa Y, Shimizu W, Makita N.

Circ Arrhythm Electrophysiol. 2011 Dec;4(6):874-81. doi: 10.1161/CIRCEP.111.963983. Epub 2011 Oct 25.

PMID:
22028457
[PubMed - indexed for MEDLINE]
Free Article
17.

Genetic analysis of the cardiac sodium channel gene SCN5A in Koreans with Brugada syndrome.

Shin DJ, Jang Y, Park HY, Lee JE, Yang K, Kim E, Bae Y, Kim J, Kim J, Kim SS, Lee MH, Chahine M, Yoon SK.

J Hum Genet. 2004;49(10):573-8. Epub 2004 Aug 26.

PMID:
15338453
[PubMed - indexed for MEDLINE]
18.

Characterization of a novel Nav1.5 channel mutation, A551T, associated with Brugada syndrome.

Chiang KC, Lai LP, Shieh RC.

J Biomed Sci. 2009 Aug 25;16:76. doi: 10.1186/1423-0127-16-76.

PMID:
19706159
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Molecular mechanism for an inherited cardiac arrhythmia.

Bennett PB, Yazawa K, Makita N, George AL Jr.

Nature. 1995 Aug 24;376(6542):683-5.

PMID:
7651517
[PubMed - indexed for MEDLINE]
20.

Novel mutations in domain I of SCN5A cause Brugada syndrome.

Vatta M, Dumaine R, Antzelevitch C, Brugada R, Li H, Bowles NE, Nademanee K, Brugada J, Brugada P, Towbin JA.

Mol Genet Metab. 2002 Apr;75(4):317-24.

PMID:
12051963
[PubMed - indexed for MEDLINE]

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