R. Wolswinkel

发表

ChannelVPDZ-Domain-Binding Motif Regulates Cardiomyocyte Compartment-Specific

R. Redon, Diana Shy, J. Barc, 2014 .

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

R. Redon, E. Behr, D. Roden, 2013, Nature Genetics.

Intercalated disc abnormalities, reduced Na(+) current density, and conduction slowing in desmoglein-2 mutant mice prior to cardiomyopathic changes.

S. Rizzo, G. Thiene, C. Basso, 2012, Cardiovascular research.

The sodium channel NaV1.5 impacts on early murine embryonic cardiac development, structure and function in a non‐electrogenic manner

A. Verkerk, C. Remme, B. Boukens, 2020, Acta physiologica.

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Dan M Roden, Beverley Balkau, Pierre Lindenbaum, 2013, Nature Genetics.

Production of Resveratrol in Recombinant Microorganisms

J. Beekwilder, A. Bovy, H. Jonker, 2006, Applied and Environmental Microbiology.

PDZ Domain–Binding Motif Regulates Cardiomyocyte Compartment-Specific NaV1.5 Channel Expression and Function

Ludovic C. Gillet, R. Redon, Diana Shy, 2014, Circulation.

Orphan nuclear receptor Nur77 affects cardiomyocyte calcium homeostasis and adverse cardiac remodelling

I. van der Made, E. Creemers, R. D. de Winter, 2015, Scientific Reports.

Systems Genetics Approaches in Rat Identify Novel Genes and Gene Networks Associated With Cardiac Conduction

E. Petretto, M. Pravenec, M. Heinig, 2018, Journal of the American Heart Association.

Functional NaV1.8 Channels in Intracardiac Neurons: The Link Between SCN10A and Cardiac Electrophysiology

B. de Jonge, B. Scicluna, C. Bezzina, 2012, Circulation research.

Integrative Physiology Functional NaV1.8 Channels in Intracardiac Neurons

B. de Jonge, B. Scicluna, C. Bezzina, 2012 .

Integrative Physiology Functional NaV 1 . 8 Channels in Intracardiac Neurons The Link Between SCN 10 A and Cardiac Electrophysiology

B. Jonge, B. Scicluna, C. Bezzina, 2012 .

Genetic variation in GNB5 causes bradycardia by increasing IK,ACh augmenting cholinergic response.

R. Wilders, C. Bezzina, A. Verkerk, 2019, Disease models & mechanisms.

A common co-morbidity modulates disease expression and treatment efficacy in inherited cardiac sodium channelopathy

I. van der Made, E. Creemers, P. Postema, 2018, European heart journal.

Genetic variation in GNB5 causes bradycardia by augmenting the cholinergic response via increased acetylcholine-activated potassium current (IK,ACh)

R. Wilders, C. Bezzina, A. Verkerk, 2019, Disease Models & Mechanisms.

DNA repair in cardiomyocytes is critical for maintaining cardiac function in mice

M. Ghanbari, M. Kavousi, L. Blonden, 2023, Aging cell.

Lysosome mediated Kir2.1 breakdown directly influences inward rectifier current density.

M. Vos, T. V. van Veen, H. V. van Rijen, 2008, Biochemical and biophysical research communications.

PDZ-domain-binding motif regulates cardiomyocyte compartment-specific Na V 1.5 channel expression and function regulation via motif in

R. Redon, Diana Shy, J. Barc, 2014 .

Functional modulation of atrio-ventricular conduction by enhanced late sodium current and calcium-dependent mechanisms in Scn5a1798insD/+ mice

I. van der Made, E. Creemers, G. Thiene, 2020, Europace.

Genetic background determines the severity of age-dependent cardiac structural abnormalities and arrhythmia susceptibility in Scn5a-1798insD mice

T. V. van Veen, C. Remme, M. Rivaud, 2024, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.