UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 165

Sortiert nach

The cardiac sodium channel displays differential distribution in the conduction system and transmural heterogeneity in the murine ventricular myocardium

Basic research in cardiology, 2009-09, Vol.104 (5), p.511-522

2009

Link zum Volltext

Verfügbarkeit prüfen

Mental illness and cardiovascular health: observational and polygenic score analyses in a population-based cohort study

Psychological medicine, 2024-04, Vol.54 (5), p.931-939

2024

Link zum Volltext

Verfügbarkeit prüfen

Unique Cardiac Purkinje Fiber Transient Outward Current β-Subunit Composition: A Potential Molecular Link to Idiopathic Ventricular Fibrillation

Circulation research, 2013-05, Vol.112 (10), p.1310-1322

2013

Link zum Volltext

Verfügbarkeit prüfen

Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity

European journal of human genetics : EJHG, 2008-03, Vol.16 (3), p.350-357

2008

Link zum Volltext

Verfügbarkeit prüfen

Founder mutations in the Netherlands: familial idiopathic ventricular fibrillation and DPP6

Netherlands heart journal, 2011-06, Vol.19 (6), p.290-296

2011

Link zum Volltext

Verfügbarkeit prüfen

Genomic approaches for the elucidation of genes and gene networks underlying cardiovascular traits

Biophysical reviews, 2018-08, Vol.10 (4), p.1053-1060

2018

Link zum Volltext

Verfügbarkeit prüfen

Cardiac sodium channel and inherited arrhythmia syndromes

Cardiovascular research, 2001-02, Vol.49 (2), p.257-271

2001

Link zum Volltext

Verfügbarkeit prüfen

Genotype-phenotype dilemma in a case of sudden cardiac death with the E1053K mutation and a deletion in the SCN5A gene

Forensic science international, 2017-06, Vol.275, p.187-194

2017

Link zum Volltext

Verfügbarkeit prüfen

Cardiac dyssynchrony and response to cardiac resynchronisation therapy in heart failure: can genetic predisposition play a role?

Netherlands heart journal, 2016-01, Vol.24 (1), p.11-15

2016

Link zum Volltext

Verfügbarkeit prüfen

The cardiac sodium channel displays differential distribution in the conduction system and transmural heterogeneity in the murine ventricular myocardium

Basic research in cardiology, 2009-09, Vol.104 (5), p.511-522

2009

Link zum Volltext

Verfügbarkeit prüfen

A Cardiac Sodium Channel Mutation Cosegregates With a Rare Connexin40 Genotype in Familial Atrial Standstill

Circulation research, 2003-01, Vol.92 (1), p.14-22

2003

Link zum Volltext

Verfügbarkeit prüfen

A sodium-channel mutation causes isolated cardiac conduction disease

Nature (London), 2001-02, Vol.409 (6823), p.1043-1047

2001

Link zum Volltext

Verfügbarkeit prüfen

Contribution of Sodium Channel Mutations to Bradycardia and Sinus Node Dysfunction in LQT3 Families

Circulation research, 2003-05, Vol.92 (9), p.976-983

2003

Link zum Volltext

Verfügbarkeit prüfen

Compound Heterozygosity for Mutations (W156X and R225W) in SCN5A Associated With Severe Cardiac Conduction Disturbances and Degenerative Changes in the Conduction System

Circulation research, 2003-02, Vol.92 (2), p.159-168

2003

Link zum Volltext

Verfügbarkeit prüfen

Assessment of multi-trait analysis of GWAS (MTAG) for discovery of novel genetic variants and mechanistic insight in common cardiovascular diseases

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

Link zum Volltext

Verfügbarkeit prüfen

Founder mutations in the Netherlands: SCN5a 1795insD, the first described arrhythmia overlap syndrome and one of the largest and best characterised families worldwide

Netherlands heart journal, 2009-11, Vol.17 (11), p.422-428

2009

Link zum Volltext

Verfügbarkeit prüfen

Diversity in cardiac sodium channel disease phenotype in transgenic mice carrying a single SCN5A mutation

Netherlands heart journal, 2007-06, Vol.15 (6), p.235-238

2007

Link zum Volltext

Verfügbarkeit prüfen

Bradycardia in a long QT type 2 family: coinciding KCNH2 and HCN4 variants

Cardiovascular research, 2024-05, Vol.120 (Supplement_1)

2024

Link zum Volltext

Verfügbarkeit prüfen

Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

Link zum Volltext

Verfügbarkeit prüfen

New risk predictor of arrhythmias in patients with congenital Long-QT Syndrome

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

Link zum Volltext

Verfügbarkeit prüfen

Polygenic risk score for hypertrophic cardiomyopathy predicts population disease risk, penetrance in sarcomeric rare variant carriers and survival in cases

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

Link zum Volltext

Verfügbarkeit prüfen

Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

Link zum Volltext

Verfügbarkeit prüfen

Population-specific and cross-ancestry genome-wide association study identifies shared genetic architecture and 6 new risk loci including CAMK2D associated for Brugada syndrome

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

Link zum Volltext

Verfügbarkeit prüfen

Large-scale genetic and multi-omics analyses identify molecular pathways underlying dilated cardiomyopathy

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

Link zum Volltext

Verfügbarkeit prüfen

Gating-dependent mechanisms for flecainide action in SCN5A-linked arrhythmia syndromes

Circulation (New York, N.Y.), 2001-09, Vol.104 (10), p.1200-1205

2001

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 165

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(155)
Mit Volltextzugriff
(157)

Publikationsform

Artikel
(165)

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(97)
Life Sciences & Biomedicine
(91)
Humans
(86)
Cardiovascular System & Cardiology
(65)
Cardiac & Cardiovascular Systems
(64)
Male
(49)
Female
(44)
Mutation
(38)
Adult
(33)
Biological And Medical Sciences
(33)
Heart
(33)
Medical Sciences
(32)
Electrocardiography
(30)
Cardiology. Vascular System
(29)
Animals
(28)
Sodium Channels - Genetics
(27)
Middle Aged
(25)
Arrhythmia
(21)
Cardiology And Cardiovascular Medicine
(21)
Arrhythmias, Cardiac - Genetics
(20)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

European Heart Journal
(23)
Cardiovascular Research
(20)
Circulation
(12)
Circulation Research
(11)
Europace
(8)
Netherlands Heart Journal
(8)
Journal Of The American College Of Cardiology
(7)
Atherosclerosis
(6)
Heart Rhythm
(5)
Nature Genetics
(4)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

The cardiac sodium channel displays differential distribution in the conduction system and transmural heterogeneity in the murine ventricular myocardium

Mental illness and cardiovascular health: observational and polygenic score analyses in a population-based cohort study

Unique Cardiac Purkinje Fiber Transient Outward Current β-Subunit Composition: A Potential Molecular Link to Idiopathic Ventricular Fibrillation

Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity

Founder mutations in the Netherlands: familial idiopathic ventricular fibrillation and DPP6

Genomic approaches for the elucidation of genes and gene networks underlying cardiovascular traits

Cardiac sodium channel and inherited arrhythmia syndromes

Genotype-phenotype dilemma in a case of sudden cardiac death with the E1053K mutation and a deletion in the SCN5A gene

Cardiac dyssynchrony and response to cardiac resynchronisation therapy in heart failure: can genetic predisposition play a role?

The cardiac sodium channel displays differential distribution in the conduction system and transmural heterogeneity in the murine ventricular myocardium

A Cardiac Sodium Channel Mutation Cosegregates With a Rare Connexin40 Genotype in Familial Atrial Standstill

A sodium-channel mutation causes isolated cardiac conduction disease

Contribution of Sodium Channel Mutations to Bradycardia and Sinus Node Dysfunction in LQT3 Families

Compound Heterozygosity for Mutations (W156X and R225W) in SCN5A Associated With Severe Cardiac Conduction Disturbances and Degenerative Changes in the Conduction System

Assessment of multi-trait analysis of GWAS (MTAG) for discovery of novel genetic variants and mechanistic insight in common cardiovascular diseases

Founder mutations in the Netherlands: SCN5a 1795insD, the first described arrhythmia overlap syndrome and one of the largest and best characterised families worldwide

Diversity in cardiac sodium channel disease phenotype in transgenic mice carrying a single SCN5A mutation

Bradycardia in a long QT type 2 family: coinciding KCNH2 and HCN4 variants

Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies

New risk predictor of arrhythmias in patients with congenital Long-QT Syndrome

Polygenic risk score for hypertrophic cardiomyopathy predicts population disease risk, penetrance in sarcomeric rare variant carriers and survival in cases

Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

Population-specific and cross-ancestry genome-wide association study identifies shared genetic architecture and 6 new risk loci including CAMK2D associated for Brugada syndrome

Large-scale genetic and multi-omics analyses identify molecular pathways underlying dilated cardiomyopathy

Gating-dependent mechanisms for flecainide action in SCN5A-linked arrhythmia syndromes

Suchergebnisse filtern