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Editorial: Methods and applications in cardiac electrophysiology-application to inherited arrhythmias

Frontiers in Physiology, 2024-03, Vol.15, p.1388433-1388433

2024

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In vivo Dominant-Negative Effect of an SCN5A Brugada Syndrome Variant

Frontiers in physiology, 2021-05, Vol.12, p.661413-661413

2021

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Intracardiac electrophysiology to characterize susceptibility to ventricular arrhythmias in murine models

Frontiers in physiology, 2024-01, Vol.15, p.1326663-1326663

2024

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Inter-Regulation of Kv4.3 and Voltage-Gated Sodium Channels Underlies Predisposition to Cardiac and Neuronal Channelopathies

International journal of molecular sciences, 2020-07, Vol.21 (14), p.5057

2020

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Trafficking and Gating Cooperation Between Deficient Nav1.5-mutant Channels to Rescue INa

Frontiers in bioscience (Landmark. Print), 2022-06, Vol.27 (7), p.209-209

2022

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Generation of a heterozygous SCN5A knockout human induced pluripotent stem cell line by CRISPR/Cas9 edition

Stem cell research, 2022-04, Vol.60, p.102680-102680, Article 102680

2022

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A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation

Heart rhythm, 2014-06, Vol.11 (6), p.1015-1023

2014

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Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy

Cardiovascular research, 2008-01, Vol.77 (1), p.118-125

2008

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Desmosomal cadherins are decreased in explanted arrhythmogenic right ventricular dysplasia/cardiomyopathy patient hearts

PloS one, 2013-09, Vol.8 (9), p.e75082-e75082

2013

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A Type 2 Ryanodine Receptor Variant in the Helical Domain 2 Associated with an Impairment of the Adrenergic Response

Journal of personalized medicine, 2021-06, Vol.11 (6), p.579

2021

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A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

Nature genetics, 1997-02, Vol.15 (2), p.186-189

1997

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Isoform-Specific Modulation of Voltage-Gated Na+ Channels by Calmodulin

Circulation research, 2002-03, Vol.90 (4), p.e49-e57

2002

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The anchoring protein SAP97 retains Kv1.5 channels in the plasma membrane of cardiac myocytes

American journal of physiology. Heart and circulatory physiology, 2008-04, Vol.294 (4), p.H1851-H1861

2008

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Characterization of Purkinje-like cardiac cells derived from iPS cells from patients with Purkinje-induced idiopathic ventricular fibrillation

Archives of cardiovascular diseases, 2024-06, Vol.117 (6-7), p.S208-S208

2024

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In vivo Dominant-Negative Effect of an SCN5A Brugada Syndrome Variant

Frontiers in physiology, 2021-05, Vol.12

2021

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In vivo Dominant-Negative Effect of an SCN5A Brugada Syndrome Variant

Frontiers in physiology, 2021-05, Vol.12

2021

Volltextzugriff (PDF)

Inter-Regulation of K v 4.3 and Voltage-Gated Sodium Channels Underlies Predisposition to Cardiac and Neuronal Channelopathies

International journal of molecular sciences, 2020-07, Vol.21 (14)

2020

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A novel gain‐of‐function mutation in SCN5A responsible for multifocal ectopic Purkinje‐related premature contractions

Human mutation, 2020-04, Vol.41 (4), p.850-859

2020

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Dominant-negative effect of SCN5A N-terminal mutations through the interaction of Nav1.5 α-subunits

Cardiovascular research, 2012-10, Vol.96 (1), p.53-63

2012

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Trafficking and Gating Cooperation Between Deficient Nav1.5-mutant Channels to Rescue INa

Frontiers in bioscience (Landmark. Print), 2022-06, Vol.27

2022

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Genetic characterization of KCNQ1 variants improves risk stratification in type 1 long QT syndrome patients

Europace (London, England), 2024-06, Vol.26 (6)

2024

Volltextzugriff (PDF)

Dominant-negative effect of SCN5A N-terminal mutations through the interaction of Na(v)1.5 α-subunits

Cardiovascular research, 2012-10, Vol.96 (1), p.53-63

2012

Volltextzugriff (PDF)

Systematic analysis of SCN5A variants associated with inherited cardiac diseases

Heart rhythm, 2024-08

2024

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MOG1: a new susceptibility gene for Brugada syndrome

Circulation. Cardiovascular genetics, 2011-06, Vol.4 (3), p.261

2011

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Kv4 Potassium Channels Form a Tripartite Complex With the Anchoring Protein SAP97 and CaMKII in Cardiac Myocytes

Circulation research, 2009-03, Vol.104 (6), p.758-769

2009

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Editorial: Methods and applications in cardiac electrophysiology-application to inherited arrhythmias

In vivo Dominant-Negative Effect of an SCN5A Brugada Syndrome Variant

Intracardiac electrophysiology to characterize susceptibility to ventricular arrhythmias in murine models

Inter-Regulation of Kv4.3 and Voltage-Gated Sodium Channels Underlies Predisposition to Cardiac and Neuronal Channelopathies

Trafficking and Gating Cooperation Between Deficient Nav1.5-mutant Channels to Rescue INa

Generation of a heterozygous SCN5A knockout human induced pluripotent stem cell line by CRISPR/Cas9 edition

A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation

Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy

Desmosomal cadherins are decreased in explanted arrhythmogenic right ventricular dysplasia/cardiomyopathy patient hearts

A Type 2 Ryanodine Receptor Variant in the Helical Domain 2 Associated with an Impairment of the Adrenergic Response

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

Isoform-Specific Modulation of Voltage-Gated Na+ Channels by Calmodulin

The anchoring protein SAP97 retains Kv1.5 channels in the plasma membrane of cardiac myocytes

Characterization of Purkinje-like cardiac cells derived from iPS cells from patients with Purkinje-induced idiopathic ventricular fibrillation

In vivo Dominant-Negative Effect of an SCN5A Brugada Syndrome Variant

In vivo Dominant-Negative Effect of an SCN5A Brugada Syndrome Variant

Inter-Regulation of K v 4.3 and Voltage-Gated Sodium Channels Underlies Predisposition to Cardiac and Neuronal Channelopathies

A novel gain‐of‐function mutation in SCN5A responsible for multifocal ectopic Purkinje‐related premature contractions

Dominant-negative effect of SCN5A N-terminal mutations through the interaction of Nav1.5 α-subunits

Trafficking and Gating Cooperation Between Deficient Nav1.5-mutant Channels to Rescue INa

Genetic characterization of KCNQ1 variants improves risk stratification in type 1 long QT syndrome patients

Dominant-negative effect of SCN5A N-terminal mutations through the interaction of Na(v)1.5 α-subunits

Systematic analysis of SCN5A variants associated with inherited cardiac diseases

MOG1: a new susceptibility gene for Brugada syndrome

Kv4 Potassium Channels Form a Tripartite Complex With the Anchoring Protein SAP97 and CaMKII in Cardiac Myocytes

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