UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex

Proceedings of the National Academy of Sciences - PNAS, 2008-07, Vol.105 (27), p.9355-9360

2008

Volltextzugriff (PDF)

Editorial commentary: Genetic testing for congenital heart disease: The future is now

Trends in cardiovascular medicine, 2022-07, Vol.32 (5), p.320-321

Vatta, Matteo

2022

Volltextzugriff (PDF)

Telethonin variants found in Brugada syndrome, J‐wave pattern ECG, and ARVC reduce peak Nav1.5 currents in HEK‐293 cells

Pacing and clinical electrophysiology, 2020-08, Vol.43 (8), p.838-846

2020

Volltextzugriff (PDF)

ANKRD1 , the Gene Encoding Cardiac Ankyrin Repeat Protein, Is a Novel Dilated Cardiomyopathy Gene

Journal of the American College of Cardiology, 2009-07, Vol.54 (4), p.325-333

2009

Volltextzugriff (PDF)

Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy

Journal of the American College of Cardiology, 2010-02, Vol.55 (6), p.587-597

2010

Volltextzugriff (PDF)

ZASP interacts with the mechanosensing protein Ankrd2 and p53 in the signalling network of striated muscle

PloS one, 2014-03, Vol.9 (3), p.e92259-e92259

2014

Volltextzugriff (PDF)

Clinical characteristics and 12-month outcomes of patients with valvular and non-valvular atrial fibrillation in Kenya

PloS one, 2017-09, Vol.12 (9), p.e0185204-e0185204

2017

Volltextzugriff (PDF)

Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis

Journal of the American College of Cardiology, 2010-10, Vol.56 (18), p.1493-1502

2010

Volltextzugriff (PDF)

Ionic Mechanisms Responsible for the Electrocardiographic Phenotype of the Brugada Syndrome Are Temperature Dependent

Circulation research, 1999-10, Vol.85 (9), p.803-809

1999

Volltextzugriff (PDF)

Evaluation of the Genetic Basis of Familial Aggregation of Pacemaker Implantation by a Large Next Generation Sequencing Panel

PloS one, 2015-12, Vol.10 (12), p.e0143588-e0143588

2015

Volltextzugriff (PDF)

Myocardial alternative RNA splicing and gene expression profiling in early stage hypoplastic left heart syndrome

PloS one, 2012-01, Vol.7 (1), p.e29784-e29784

2012

Volltextzugriff (PDF)

Genetic mutations in African patients with atrial fibrillation: Rationale and design of the Study of Genetics of Atrial Fibrillation in an African Population (SIGNAL)

The American heart journal, 2015-09, Vol.170 (3), p.455-464.e5

2015

Volltextzugriff (PDF)

A ZASP Missense Mutation, S196L, Leads to Cytoskeletal and Electrical Abnormalities in a Mouse Model of Cardiomyopathy

Circulation. Arrhythmia and electrophysiology, 2010-12, Vol.3 (6), p.646-656

2010

Volltextzugriff (PDF)

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome

Human molecular genetics, 2002-02, Vol.11 (3), p.337-345

2002

Volltextzugriff (PDF)

Mutations in Cypher/ZASP in patients with Dilated cardiomyopathy and left ventricular non-compaction

Journal of the American College of Cardiology, 2003-12, Vol.42 (11), p.2014-2027

2003

Volltextzugriff (PDF)

Genetic analyses in a bonobo (Pan paniscus) with arrhythmogenic right ventricular cardiomyopathy

Scientific reports, 2018-03, Vol.8 (1), p.4350-9, Article 4350

2018

Volltextzugriff (PDF)

Ondansetron blocks wild-type and p.F503L variant small-conductance Ca^sup 2+^-activated K^sup +^ channels

American journal of physiology. Heart and circulatory physiology, 2018-08, Vol.315 (2), p.H375

2018

Volltextzugriff (PDF)

Impaired binding of ZASP/Cypher with phosphoglucomutase 1 is associated with dilated cardiomyopathy

Cardiovascular research, 2009-07, Vol.83 (1), p.80-88

2009

Volltextzugriff (PDF)

The Contribution of Known Familial Cardiovascular Disease Genes to Sudden Cardiac Death in Patients Undergoing Hemodialysis

Cardiorenal medicine, 2021-08, Vol.11 (4), p.174-183

2021

Volltextzugriff (PDF)

APOL1 G3 Variant Is Associated with Cardiovascular Mortality and Sudden Cardiac Death in Patients Receiving Maintenance Hemodialysis of European Ancestry

Cardiorenal medicine, 2022-01, Vol.12 (5-6), p.229-235

2022

Volltextzugriff (PDF)

α1-Syntrophin Mutations Identified in Sudden Infant Death Syndrome Cause an Increase in Late Cardiac Sodium Current

Circulation. Arrhythmia and electrophysiology, 2009-12, Vol.2 (6), p.667-676

2009

Volltextzugriff (PDF)

Coffin–Lowry syndrome and left ventricular noncompaction cardiomyopathy with a restrictive pattern

American journal of medical genetics. Part A, 2011-12, Vol.155 (12), p.3030-3034

2011

Volltextzugriff (PDF)

Molecular remodelling of dystrophin in patients with end-stage cardiomyopathies and reversal in patients on assistance-device therapy

The Lancet (British edition), 2002-03, Vol.359 (9310), p.936-941

2002

Volltextzugriff (PDF)

β2-adrenergic receptor genetic variants and risk of sudden cardiac death

Circulation (New York, N.Y.), 2006-04, Vol.113 (15), p.1842-1848

2006

Volltextzugriff (PDF)

Familial dilated cardiomyopathy : Evidence for genetic and phenotypic heterogeneity

Journal of the American College of Cardiology, 1999-07, Vol.34 (1), p.181-190

1999

Volltextzugriff (PDF)

1 – 25 von 37

Suche als RSS-Feed

Aktive Filter

ThemaHeart

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(37)
Mit Volltextzugriff
(37)

Publikationsform

Artikel
(37)

Sprache

Englisch
(37)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex

Editorial commentary: Genetic testing for congenital heart disease: The future is now

Telethonin variants found in Brugada syndrome, J‐wave pattern ECG, and ARVC reduce peak Nav1.5 currents in HEK‐293 cells

ANKRD1 , the Gene Encoding Cardiac Ankyrin Repeat Protein, Is a Novel Dilated Cardiomyopathy Gene

Compound and Digenic Heterozygosity Contributes to Arrhythmogenic Right Ventricular Cardiomyopathy

ZASP interacts with the mechanosensing protein Ankrd2 and p53 in the signalling network of striated muscle

Clinical characteristics and 12-month outcomes of patients with valvular and non-valvular atrial fibrillation in Kenya

Nebulette Mutations Are Associated With Dilated Cardiomyopathy and Endocardial Fibroelastosis

Ionic Mechanisms Responsible for the Electrocardiographic Phenotype of the Brugada Syndrome Are Temperature Dependent

Evaluation of the Genetic Basis of Familial Aggregation of Pacemaker Implantation by a Large Next Generation Sequencing Panel

Myocardial alternative RNA splicing and gene expression profiling in early stage hypoplastic left heart syndrome

Genetic mutations in African patients with atrial fibrillation: Rationale and design of the Study of Genetics of Atrial Fibrillation in an African Population (SIGNAL)

A ZASP Missense Mutation, S196L, Leads to Cytoskeletal and Electrical Abnormalities in a Mouse Model of Cardiomyopathy

Genetic and biophysical basis of sudden unexplained nocturnal death syndrome (SUNDS), a disease allelic to Brugada syndrome

Mutations in Cypher/ZASP in patients with Dilated cardiomyopathy and left ventricular non-compaction

Genetic analyses in a bonobo (Pan paniscus) with arrhythmogenic right ventricular cardiomyopathy

Ondansetron blocks wild-type and p.F503L variant small-conductance Ca^sup 2+^-activated K^sup +^ channels

Impaired binding of ZASP/Cypher with phosphoglucomutase 1 is associated with dilated cardiomyopathy

The Contribution of Known Familial Cardiovascular Disease Genes to Sudden Cardiac Death in Patients Undergoing Hemodialysis

APOL1 G3 Variant Is Associated with Cardiovascular Mortality and Sudden Cardiac Death in Patients Receiving Maintenance Hemodialysis of European Ancestry

α1-Syntrophin Mutations Identified in Sudden Infant Death Syndrome Cause an Increase in Late Cardiac Sodium Current

Coffin–Lowry syndrome and left ventricular noncompaction cardiomyopathy with a restrictive pattern

Molecular remodelling of dystrophin in patients with end-stage cardiomyopathies and reversal in patients on assistance-device therapy

β2-adrenergic receptor genetic variants and risk of sudden cardiac death

Familial dilated cardiomyopathy : Evidence for genetic and phenotypic heterogeneity

Aktive Filter

Suchergebnisse filtern