Rook MB - Search Results

1

Human SCN5A gene mutations alter cardiac sodium channel kinetics and are associated with the Brugada syndrome.

Rook MB, Bezzina Alshinawi C, Groenewegen WA, van Gelder IC, van Ginneken AC, Jongsma HJ, Mannens MM, Wilde AA. Rook MB, et al. Cardiovasc Res. 1999 Dec;44(3):507-17. doi: 10.1016/s0008-6363(99)00350-8. Cardiovasc Res. 1999. PMID: 10690282

2

A cardiac sodium channel mutation cosegregates with a rare connexin40 genotype in familial atrial standstill.

Groenewegen WA, Firouzi M, Bezzina CR, Vliex S, van Langen IM, Sandkuijl L, Smits JP, Hulsbeek M, Rook MB, Jongsma HJ, Wilde AA. Groenewegen WA, et al. Among authors: rook mb. Circ Res. 2003 Jan 10;92(1):14-22. doi: 10.1161/01.res.0000050585.07097.d7. Circ Res. 2003. PMID: 12522116

3

Compound heterozygosity for mutations (W156X and R225W) in SCN5A associated with severe cardiac conduction disturbances and degenerative changes in the conduction system.

Bezzina CR, Rook MB, Groenewegen WA, Herfst LJ, van der Wal AC, Lam J, Jongsma HJ, Wilde AA, Mannens MM. Bezzina CR, et al. Among authors: rook mb. Circ Res. 2003 Feb 7;92(2):159-68. doi: 10.1161/01.res.0000052672.97759.36. Circ Res. 2003. PMID: 12574143

4

A novel LQT3 mutation implicates the human cardiac sodium channel domain IVS6 in inactivation kinetics.

Groenewegen WA, Bezzina CR, van Tintelen JP, Hoorntje TM, Mannens MM, Wilde AA, Jongsma HJ, Rook MB. Groenewegen WA, et al. Among authors: rook mb. Cardiovasc Res. 2003 Mar 15;57(4):1072-8. doi: 10.1016/s0008-6363(02)00838-6. Cardiovasc Res. 2003. PMID: 12650885

5

P19 embryonal carcinoma cells: a suitable model system for cardiac electrophysiological differentiation at the molecular and functional level.

van der Heyden MA, van Kempen MJ, Tsuji Y, Rook MB, Jongsma HJ, Opthof T. van der Heyden MA, et al. Among authors: rook mb. Cardiovasc Res. 2003 May 1;58(2):410-22. doi: 10.1016/s0008-6363(03)00247-5. Cardiovasc Res. 2003. PMID: 12757875

6

Trafficking and functional expression of cardiac Na+ channels.

Herfst LJ, Rook MB, Jongsma HJ. Herfst LJ, et al. Among authors: rook mb. J Mol Cell Cardiol. 2004 Feb;36(2):185-93. doi: 10.1016/j.yjmcc.2003.11.014. J Mol Cell Cardiol. 2004. PMID: 14871545 Review.

7

Cardiac sodium channel and inherited arrhythmia syndromes.

Bezzina CR, Rook MB, Wilde AA. Bezzina CR, et al. Among authors: rook mb. Cardiovasc Res. 2001 Feb 1;49(2):257-71. doi: 10.1016/s0008-6363(00)00272-8. Cardiovasc Res. 2001. PMID: 11164836 Review. No abstract available.

8

A single Na(+) channel mutation causing both long-QT and Brugada syndromes.

Bezzina C, Veldkamp MW, van Den Berg MP, Postma AV, Rook MB, Viersma JW, van Langen IM, Tan-Sindhunata G, Bink-Boelkens MT, van Der Hout AH, Mannens MM, Wilde AA. Bezzina C, et al. Among authors: rook mb. Circ Res. 1999 Dec 3-17;85(12):1206-13. doi: 10.1161/01.res.85.12.1206. Circ Res. 1999. PMID: 10590249

9

Na+ channel mutation leading to loss of function and non-progressive cardiac conduction defects.

Herfst LJ, Potet F, Bezzina CR, Groenewegen WA, Le Marec H, Hoorntje TM, Demolombe S, Baró I, Escande D, Jongsma HJ, Wilde AA, Rook MB. Herfst LJ, et al. Among authors: rook mb. J Mol Cell Cardiol. 2003 May;35(5):549-57. doi: 10.1016/s0022-2828(03)00078-6. J Mol Cell Cardiol. 2003. PMID: 12738236

10

Biology of cardiac sodium channel Nav1.5 expression.

Rook MB, Evers MM, Vos MA, Bierhuizen MF. Rook MB, et al. Cardiovasc Res. 2012 Jan 1;93(1):12-23. doi: 10.1093/cvr/cvr252. Epub 2011 Sep 21. Cardiovasc Res. 2012. PMID: 21937582 Review.

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