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Items: 1 to 20 of 28

1.

A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype.

Hu D, Barajas-Martinez H, Burashnikov E, Springer M, Wu Y, Varro A, Pfeiffer R, Koopmann TT, Cordeiro JM, Guerchicoff A, Pollevick GD, Antzelevitch C.

Circ Cardiovasc Genet. 2009 Jun;2(3):270-8. doi: 10.1161/CIRCGENETICS.108.829192. Epub 2009 Apr 21.

2.

Scn3b knockout mice exhibit abnormal sino-atrial and cardiac conduction properties.

Hakim P, Brice N, Thresher R, Lawrence J, Zhang Y, Jackson AP, Grace AA, Huang CL.

Acta Physiol (Oxf). 2010 Jan;198(1):47-59. doi: 10.1111/j.1748-1716.2009.02048.x. Epub 2009 Oct 1.

3.

Arrhythmogenic right ventricular cardiomyopathy/dysplasia clinical presentation and diagnostic evaluation: results from the North American Multidisciplinary Study.

Marcus FI, Zareba W, Calkins H, Towbin JA, Basso C, Bluemke DA, Estes NA 3rd, Picard MH, Sanborn D, Thiene G, Wichter T, Cannom D, Wilber DJ, Scheinman M, Duff H, Daubert J, Talajic M, Krahn A, Sweeney M, Garan H, Sakaguchi S, Lerman BB, Kerr C, Kron J, Steinberg JS, Sherrill D, Gear K, Brown M, Severski P, Polonsky S, McNitt S.

Heart Rhythm. 2009 Jul;6(7):984-92. doi: 10.1016/j.hrthm.2009.03.013. Epub 2009 Mar 11.

4.

Electrocardiographic pattern in arrhythmogenic right ventricular cardiomyopathy.

Steriotis AK, Bauce B, Daliento L, Rigato I, Mazzotti E, Folino AF, Marra MP, Brugnaro L, Nava A.

Am J Cardiol. 2009 May 1;103(9):1302-8. doi: 10.1016/j.amjcard.2009.01.017. Epub 2009 Mar 18.

PMID:
19406276
5.

Scn3b knockout mice exhibit abnormal ventricular electrophysiological properties.

Hakim P, Gurung IS, Pedersen TH, Thresher R, Brice N, Lawrence J, Grace AA, Huang CL.

Prog Biophys Mol Biol. 2008 Oct-Nov;98(2-3):251-66. doi: 10.1016/j.pbiomolbio.2009.01.005. Epub 2009 Jan 24.

6.

Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillation.

Alders M, Koopmann TT, Christiaans I, Postema PG, Beekman L, Tanck MW, Zeppenfeld K, Loh P, Koch KT, Demolombe S, Mannens MM, Bezzina CR, Wilde AA.

Am J Hum Genet. 2009 Apr;84(4):468-76. doi: 10.1016/j.ajhg.2009.02.009. Epub 2009 Mar 12.

7.

Ventricular fibrillation with prominent early repolarization associated with a rare variant of KCNJ8/KATP channel.

Haïssaguerre M, Chatel S, Sacher F, Weerasooriya R, Probst V, Loussouarn G, Horlitz M, Liersch R, Schulze-Bahr E, Wilde A, Kääb S, Koster J, Rudy Y, Le Marec H, Schott JJ.

J Cardiovasc Electrophysiol. 2009 Jan;20(1):93-8. doi: 10.1111/j.1540-8167.2008.01326.x.

PMID:
19120683
8.

J-point elevation in survivors of primary ventricular fibrillation and matched control subjects: incidence and clinical significance.

Rosso R, Kogan E, Belhassen B, Rozovski U, Scheinman MM, Zeltser D, Halkin A, Steinvil A, Heller K, Glikson M, Katz A, Viskin S.

J Am Coll Cardiol. 2008 Oct 7;52(15):1231-8. doi: 10.1016/j.jacc.2008.07.010.

9.

Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans.

Watanabe H, Koopmann TT, Le Scouarnec S, Yang T, Ingram CR, Schott JJ, Demolombe S, Probst V, Anselme F, Escande D, Wiesfeld AC, Pfeufer A, Kääb S, Wichmann HE, Hasdemir C, Aizawa Y, Wilde AA, Roden DM, Bezzina CR.

J Clin Invest. 2008 Jun;118(6):2260-8. doi: 10.1172/JCI33891.

10.

Sudden cardiac arrest associated with early repolarization.

Haïssaguerre M, Derval N, Sacher F, Jesel L, Deisenhofer I, de Roy L, Pasquié JL, Nogami A, Babuty D, Yli-Mayry S, De Chillou C, Scanu P, Mabo P, Matsuo S, Probst V, Le Scouarnec S, Defaye P, Schlaepfer J, Rostock T, Lacroix D, Lamaison D, Lavergne T, Aizawa Y, Englund A, Anselme F, O'Neill M, Hocini M, Lim KT, Knecht S, Veenhuyzen GD, Bordachar P, Chauvin M, Jais P, Coureau G, Chene G, Klein GJ, Clémenty J.

N Engl J Med. 2008 May 8;358(19):2016-23. doi: 10.1056/NEJMoa071968.

11.

Prevalence of abnormal electrocardiograms in a large, unselected population undergoing pre-participation cardiovascular screening.

Pelliccia A, Culasso F, Di Paolo FM, Accettura D, Cantore R, Castagna W, Ciacciarelli A, Costini G, Cuffari B, Drago E, Federici V, Gribaudo CG, Iacovelli G, Landolfi L, Menichetti G, Atzeni UO, Parisi A, Pizzi AR, Rosa M, Santelli F, Santilio F, Vagnini A, Casasco M, Di Luigi L.

Eur Heart J. 2007 Aug;28(16):2006-10. Epub 2007 Jul 10.

12.

SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndrome.

Medeiros-Domingo A, Kaku T, Tester DJ, Iturralde-Torres P, Itty A, Ye B, Valdivia C, Ueda K, Canizales-Quinteros S, Tusié-Luna MT, Makielski JC, Ackerman MJ.

Circulation. 2007 Jul 10;116(2):134-42. Epub 2007 Jun 25.

13.
14.

Distinct domains of the sodium channel beta3-subunit modulate channel-gating kinetics and subcellular location.

Yu EJ, Ko SH, Lenkowski PW, Pance A, Patel MK, Jackson AP.

Biochem J. 2005 Dec 15;392(Pt 3):519-26.

15.

Modulation of Na(v)1.5 by beta1-- and beta3-subunit co-expression in mammalian cells.

Ko SH, Lenkowski PW, Lee HC, Mounsey JP, Patel MK.

Pflugers Arch. 2005 Jan;449(4):403-12. Epub 2004 Sep 28.

PMID:
15455233
16.

Role of auxiliary beta1-, beta2-, and beta3-subunits and their interaction with Na(v)1.8 voltage-gated sodium channel.

Vijayaragavan K, Powell AJ, Kinghorn IJ, Chahine M.

Biochem Biophys Res Commun. 2004 Jun 25;319(2):531-40.

PMID:
15178439
17.

Cortisol influences the ontogeny of both alpha- and beta-subunits of the cardiac sodium channel in fetal sheep.

Fahmi AI, Forhead AJ, Fowden AL, Vandenberg JI.

J Endocrinol. 2004 Mar;180(3):449-55.

18.
19.

A novel SCN5A arrhythmia mutation, M1766L, with expression defect rescued by mexiletine.

Valdivia CR, Ackerman MJ, Tester DJ, Wada T, McCormack J, Ye B, Makielski JC.

Cardiovasc Res. 2002 Aug 1;55(2):279-89.

20.

Slowed conduction and ventricular tachycardia after targeted disruption of the cardiac sodium channel gene Scn5a.

Papadatos GA, Wallerstein PM, Head CE, Ratcliff R, Brady PA, Benndorf K, Saumarez RC, Trezise AE, Huang CL, Vandenberg JI, Colledge WH, Grace AA.

Proc Natl Acad Sci U S A. 2002 Apr 30;99(9):6210-5. Epub 2002 Apr 23.

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