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...

Mutations in Ribonucleic Acid Binding Protein Gene Cause Familial Dilated Cardiomyopathy

Journal of the American College of Cardiology, 2009-09, Vol.54 (10), p.930-941

2009

Volltextzugriff (PDF)

Human KATP channelopathies: diseases of metabolic homeostasis

Pflügers Archiv, 2010-07, Vol.460 (2), p.295-306

2010

Volltextzugriff (PDF)

RG flows in d dimensions, the dilaton effective action, and the a-theorem

The journal of high energy physics, 2013-03, Vol.2013 (3), p.1-30, Article 34

2013

Volltextzugriff (PDF)

Regenerative therapy for hypoplastic left heart syndrome: First report of intraoperative intramyocardial injection of autologous umbilical-cord blood–derived cells

The Journal of thoracic and cardiovascular surgery, 2015-03, Vol.149 (3), p.e35-e37

2015

Volltextzugriff (PDF)

Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation

Human molecular genetics, 2006-07, Vol.15 (14), p.2185-2191

2006

Volltextzugriff (PDF)

Idiopathic Restrictive Cardiomyopathy in Children and Young Adults

The American journal of cardiology, 2018-05, Vol.121 (10), p.1266-1270

2018

Volltextzugriff (PDF)

Cardiac transcriptome and dilated cardiomyopathy genes in zebrafish

Circulation. Cardiovascular genetics, 2015-04, Vol.8 (2), p.261-269

2015

Volltextzugriff (PDF)

Atrial Natriuretic Peptide Frameshift Mutation in Familial Atrial Fibrillation

The New England journal of medicine, 2008-07, Vol.359 (2), p.158-165

2008

Volltextzugriff (PDF)

Rbm20-deficient cardiogenesis reveals early disruption of RNA processing and sarcomere remodeling establishing a developmental etiology for dilated cardiomyopathy

Human molecular genetics, 2014-07, Vol.23 (14), p.3779-3791

2014

Volltextzugriff (PDF)

Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

JAMA : the journal of the American Medical Association, 2005-01, Vol.293 (4), p.447

2005

Volltextzugriff (PDF)

Mitochondrial MICOS complex genes, implicated in hypoplastic left heart syndrome, maintain cardiac contractility and actomyosin integrity

eLife, 2023-07, Vol.12

2023

Volltextzugriff (PDF)

Transcriptional atlas of cardiogenesis maps congenital heart disease interactome

Physiological genomics, 2014-07, Vol.46 (13), p.482-495

2014

Volltextzugriff (PDF)

A Genetic Variant of the Atrial Natriuretic Peptide Gene Is Associated With Cardiometabolic Protection in the General Community

Journal of the American College of Cardiology, 2011-08, Vol.58 (6), p.629-636

2011

Volltextzugriff (PDF)

Whole Genome Sequencing in Hypoplastic Left Heart Syndrome

Journal of cardiovascular development and disease, 2022-04, Vol.9 (4), p.117

2022

Volltextzugriff (PDF)

TFEB Overexpression, Not mTOR Inhibition, Ameliorates RagCS75Y Cardiomyopathy

International journal of molecular sciences, 2021-05, Vol.22 (11), p.5494

2021

Volltextzugriff (PDF)

Diagnostic Yield of Whole Exome Sequencing in Pediatric Dilated Cardiomyopathy

Journal of cardiovascular development and disease, 2017-08, Vol.4 (3), p.11

2017

Volltextzugriff (PDF)

Familial Incidence of Cardiovascular Malformations in Hypoplastic Left Heart Syndrome

The American journal of cardiology, 2015-12, Vol.116 (11), p.1762-1766

2015

Volltextzugriff (PDF)

TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy

Human molecular genetics, 2014-11, Vol.23 (21), p.5793-5804

2014

Volltextzugriff (PDF)

ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating

Nature genetics, 2004-04, Vol.36 (4), p.382-387

2004

Volltextzugriff (PDF)

Identification of Rare Genetic Variants in Familial Spontaneous Coronary Artery Dissection and Evidence for Shared Biological Pathways

Journal of cardiovascular development and disease, 2023-09, Vol.10 (9), p.393

2023

Volltextzugriff (PDF)

Gene mutations in apical hypertrophic cardiomyopathy

Circulation (New York, N.Y.), 2005-11, Vol.112 (18), p.2805-2811

2005

Volltextzugriff (PDF)

Late Outcomes for Surgical Repair of Supravalvar Aortic Stenosis

The Annals of thoracic surgery, 2012-09, Vol.94 (3), p.854-859

2012

Volltextzugriff (PDF)

Exome Sequencing Identifies Pathogenic and Modifier Mutations in a Child With Sporadic Dilated Cardiomyopathy

Journal of the American Heart Association, 2015-12, Vol.4 (12), p.n/a

2015

Volltextzugriff (PDF)

Metavinculin mutations alter actin interaction in dilated cardiomyopathy

Circulation (New York, N.Y.), 2002-01, Vol.105 (4), p.431-437

2002

Volltextzugriff (PDF)

1 – 25 von 783

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(728)
Mit Volltextzugriff
(673)

Publikationsform

3 weitere anzeigen...

Weniger anzeigen...

Sprache

Englisch
(782)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Blood
(29)
Journal Of The American College Of Cardiology
(19)
Chest
(16)
Edis
(16)
Circulation
(14)
Biology Of Blood And Marrow Transplantation
(11)
Plos One
(11)
The New England Journal Of Medicine
(11)
Arthritis & Rheumatology
(9)
Human Genetics
(9)

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(3)
... seit 90 Tagen
(6)

Menü

Weitere Dienste

Einstellungen

Mutations in Ribonucleic Acid Binding Protein Gene Cause Familial Dilated Cardiomyopathy

Human KATP channelopathies: diseases of metabolic homeostasis

RG flows in d dimensions, the dilaton effective action, and the a-theorem

Regenerative therapy for hypoplastic left heart syndrome: First report of intraoperative intramyocardial injection of autologous umbilical-cord blood–derived cells

Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation

Idiopathic Restrictive Cardiomyopathy in Children and Young Adults

Cardiac transcriptome and dilated cardiomyopathy genes in zebrafish

Atrial Natriuretic Peptide Frameshift Mutation in Familial Atrial Fibrillation

Patient-specific genomics and cross-species functional analysis implicate LRP2 in hypoplastic left heart syndrome

Rbm20-deficient cardiogenesis reveals early disruption of RNA processing and sarcomere remodeling establishing a developmental etiology for dilated cardiomyopathy

Sodium channel mutations and susceptibility to heart failure and atrial fibrillation

Mitochondrial MICOS complex genes, implicated in hypoplastic left heart syndrome, maintain cardiac contractility and actomyosin integrity

Transcriptional atlas of cardiogenesis maps congenital heart disease interactome

A Genetic Variant of the Atrial Natriuretic Peptide Gene Is Associated With Cardiometabolic Protection in the General Community

Whole Genome Sequencing in Hypoplastic Left Heart Syndrome

TFEB Overexpression, Not mTOR Inhibition, Ameliorates RagCS75Y Cardiomyopathy

Diagnostic Yield of Whole Exome Sequencing in Pediatric Dilated Cardiomyopathy

Familial Incidence of Cardiovascular Malformations in Hypoplastic Left Heart Syndrome

TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy

ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating

Identification of Rare Genetic Variants in Familial Spontaneous Coronary Artery Dissection and Evidence for Shared Biological Pathways

Gene mutations in apical hypertrophic cardiomyopathy

Late Outcomes for Surgical Repair of Supravalvar Aortic Stenosis

Exome Sequencing Identifies Pathogenic and Modifier Mutations in a Child With Sporadic Dilated Cardiomyopathy

Metavinculin mutations alter actin interaction in dilated cardiomyopathy

Suchergebnisse filtern