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Items: 1 to 20 of 33

1.

[General Data Protection Regulation and medical research: friend or foe?]

Groenewegen WA, van de Putte EM.

Ned Tijdschr Geneeskd. 2018 Oct 12;162. pii: D3308. Dutch.

PMID:
30379505
2.

Heterogeneous Connexin43 distribution in heart failure is associated with dispersed conduction and enhanced susceptibility to ventricular arrhythmias.

Boulaksil M, Winckels SK, Engelen MA, Stein M, van Veen TA, Jansen JA, Linnenbank AC, Bierhuizen MF, Groenewegen WA, van Oosterhout MF, Kirkels JH, de Jonge N, VarrĂ³ A, Vos MA, de Bakker JM, van Rijen HV.

Eur J Heart Fail. 2010 Sep;12(9):913-21. doi: 10.1093/eurjhf/hfq092. Epub 2010 Jun 9.

3.

Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions.

Volkers L, Rook MB, Das JH, Verbeek NE, Groenewegen WA, van Kempen MJ, Lindhout D, Koeleman BP.

Neurosci Lett. 2009 Oct 2;462(1):24-9. doi: 10.1016/j.neulet.2009.06.064. Epub 2009 Jun 25.

PMID:
19559753
4.

The human Cx40 promoter polymorphism -44G-->A differentially affects transcriptional regulation by Sp1 and GATA4.

Firouzi M, Bierhuizen MF, Kok B, Teunissen BE, Jansen AT, Jongsma HJ, Groenewegen WA.

Biochim Biophys Acta. 2006 Oct;1759(10):491-6. Epub 2006 Sep 16.

PMID:
17050003
5.

Cx40 polymorphism in human atrial fibrillation.

Hauer RNW, Groenewegen WA, Firouzi M, Ramanna H, Jongsma HJ.

Adv Cardiol. 2006;42:284-291. doi: 10.1159/000092579.

PMID:
16646598
6.

Polymorphisms in human connexin40 gene promoter are associated with increased risk of hypertension in men.

Firouzi M, Kok B, Spiering W, Busjahn A, Bezzina CR, Ruijter JM, Koeleman BP, Schipper M, Groenewegen WA, Jongsma HJ, de Leeuw PW.

J Hypertens. 2006 Feb;24(2):325-30.

PMID:
16508580
7.

Congenital atrial standstill associated with coinheritance of a novel SCN5A mutation and connexin 40 polymorphisms.

Makita N, Sasaki K, Groenewegen WA, Yokota T, Yokoshiki H, Murakami T, Tsutsui H.

Heart Rhythm. 2005 Oct;2(10):1128-34.

8.

Letter regarding article by McNair et al, "SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia".

Groenewegen WA, Wilde AA.

Circulation. 2005 Jul 5;112(1):e9; author reply e9-10. No abstract available.

PMID:
15998690
9.

Association of human connexin40 gene polymorphisms with atrial vulnerability as a risk factor for idiopathic atrial fibrillation.

Firouzi M, Ramanna H, Kok B, Jongsma HJ, Koeleman BP, Doevendans PA, Groenewegen WA, Hauer RN.

Circ Res. 2004 Aug 20;95(4):e29-33. Epub 2004 Aug 5.

PMID:
15297374
10.

Gene polymorphisms and cardiac arrhythmias.

Firouzi M, Groenewegen WA.

Europace. 2003 Jul;5(3):235-42. Review. No abstract available.

PMID:
12842634
11.

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, BarĂ³ I, Escande D, Jongsma HJ, Wilde AA, Rook MB.

J Mol Cell Cardiol. 2003 May;35(5):549-57.

PMID:
12738236
12.

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.

Cardiovasc Res. 2003 Mar 15;57(4):1072-8.

PMID:
12650885
13.

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.

Circ Res. 2003 Feb 7;92(2):159-68.

PMID:
12574143
14.

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.

Circ Res. 2003 Jan 10;92(1):14-22.

PMID:
12522116
15.

Characterization of the rat connexin40 promoter: two Sp1/Sp3 binding sites contribute to transcriptional activation.

Bierhuizen MF, van Amersfoorth SC, Groenewegen WA, Vliex S, Jongsma HJ.

Cardiovasc Res. 2000 Jun;46(3):511-22.

PMID:
10912461
16.

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.

Cardiovasc Res. 1999 Dec;44(3):507-17.

PMID:
10690282
17.

Genomic organization of the rat connexin40 gene: identical transcription start sites in heart and lung.

Groenewegen WA, van Veen TA, van der Velden HM, Jongsma HJ.

Cardiovasc Res. 1998 May;38(2):463-71.

PMID:
9709407
18.

Altered pattern of connexin40 distribution in persistent atrial fibrillation in the goat.

van der Velden HM, van Kempen MJ, Wijffels MC, van Zijverden M, Groenewegen WA, Allessie MA, Jongsma HJ.

J Cardiovasc Electrophysiol. 1998 Jun;9(6):596-607.

PMID:
9654224
19.

Dysbetalipoproteinemia in a kindred with hypobetalipoproteinemia due to mutations in the genes for ApoB (ApoB-70.5) and ApoE (ApoE2).

Groenewegen WA, Krul ES, Averna MR, Pulai J, Schonfeld G.

Arterioscler Thromb. 1994 Nov;14(11):1695-704.

PMID:
7947592
20.

Apolipoprotein B-38.9 does not associate with apo[a] and forms two distinct HDL density particle populations that are larger than HDL.

Groenewegen WA, Averna MR, Pulai J, Krul ES, Schonfeld G.

J Lipid Res. 1994 Jun;35(6):1012-25.

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