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...

Manipulation of Strawberry Fruit Softening by Antisense Expression of a Pectate Lyase Gene

Plant physiology (Bethesda), 2002-02, Vol.128 (2), p.751-759

2002

Volltextzugriff (PDF)

convenient protocol for extraction and purification of DNA from Fragaria

In vitro cellular & developmental biology. Plant, 1999-03, Vol.35 (2), p.152-153

1999

Volltextzugriff (PDF)

Assessment of in vitro growth of apical stem sections and adventitious organogenesis to evaluate salinity tolerance in cultivated tomato

Plant cell, tissue and organ culture, 2000, Vol.62 (2), p.101-106

2000

Volltextzugriff (PDF)

Agrobacterium cells as microprojectile coating: a novel approach to enhance stable transformation rates in strawberry

Functional plant biology : FPB, 2000, Vol.27 (12), p.1093

2000

Volltextzugriff (PDF)

Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia

Circulation (New York, N.Y.), 2018-04, Vol.137 (15), p.1595-1610

2018

Volltextzugriff (PDF)

A rare presentation of infective endocarditis: Phase 4 block of the left bundle branch as key for the diagnosis. A case report

Journal of electrocardiology, 2024-07, Vol.85, p.72-74

2024

Volltextzugriff (PDF)

Giant biventricular aneurysms: a novel cardiac phenotype in myotubular/centronuclear myopathy

European heart journal, 2018-12, Vol.39 (48), p.4289-4290

2018

Volltextzugriff (PDF)

The Kir2.1E299V mutation increases atrial fibrillation vulnerability while protecting the ventricles against arrhythmias in a mouse model of short QT syndrome type 3

Cardiovascular research, 2024-04, Vol.120 (5), p.490-505

2024

Volltextzugriff (PDF)

Myocardial fibrosis in arrhythmogenic cardiomyopathy: a genotype–phenotype correlation study

European heart journal cardiovascular imaging, 2020-04, Vol.21 (4), p.378-386

2020

Volltextzugriff (PDF)

Prevalence and clinical outcomes of dystrophin‐associated dilated cardiomyopathy without severe skeletal myopathy

European journal of heart failure, 2021-08, Vol.23 (8), p.1276-1286

2021

Volltextzugriff (PDF)

Association of Left Ventricular Systolic Dysfunction Among Carriers of Truncating Variants in Filamin C With Frequent Ventricular Arrhythmia and End-stage Heart Failure

JAMA cardiology, 2021-08, Vol.6 (8), p.891

2021

Volltextzugriff (PDF)

Phenotype and Clinical Outcomes in Desmin-Related Arrhythmogenic Cardiomyopathy

JACC. Clinical electrophysiology, 2024-06, Vol.10 (6), p.1178-1190

2024

Volltextzugriff (PDF)

Fallen and Lost into the Abyss? A Mesolithic Human Skull from Sima Hedionda IV (Casares, Málaga, Iberian Peninsula)

Open archaeology (Berlin, Germany), 2022-11, Vol.8 (1), p.892-904

2022

Volltextzugriff (PDF)

ROD2 domain filamin C missense mutations exhibit a distinctive cardiac phenotype with restrictive/hypertrophic cardiomyopathy and saw-tooth myocardium

Revista española de cardiología (English ed.), 2023-05, Vol.76 (5), p.301-311

2023

Volltextzugriff (PDF)

Genotype, Family History, and Outcomes in Noncompaction Cardiomyopathy

Journal of the American College of Cardiology, 2018-06, Vol.71 (24), p.2864-2864

2018

Volltextzugriff (PDF)

Fruit yield and quality of strawberry plants transformed with a fruit specific strawberry pectate lyase gene

Scientia horticulturae, 2009, Vol.119 (2), p.120-125

2009

Volltextzugriff (PDF)

Unraveling the links between genetics and electrophysiological phenotype of sustained monomorphic ventricular tachycardias in left and biventricular arrhythmogenic cardiomyopathy

Europace (London, England), 2024-05, Vol.26 (Supplement_1)

2024

Volltextzugriff (PDF)

Atrial-specific reduction of Kir2.1 channel pore diameter in addition to loss of inward-going rectification underlies inducible atrial fibrillation in a mouse model of short QT syndrome type 3

European heart journal, 2022-10, Vol.43 (Supplement_2)

2022

Volltextzugriff (PDF)

Abstract 14479: Compound Heterozygosity With Two Novel Mutations in MYBPC3 as a Cause of Severe and Early-Onset Hypertrophic Cardiomyopathy

Circulation (New York, N.Y.), 2023-11, Vol.148 (Suppl_1)

2023

Volltextzugriff (PDF)

Lactococcus garvieae endocarditis in a native valve identified by MALDI-TOF MS and PCR-based 16s rRNA in Spain: A case report

New microbes and new infections, 2015-05, Vol.5 (C), p.13-15

2015

Volltextzugriff (PDF)

Atypical left-ventricular hypertrophy with apical aneurysm in leopard syndrome

The international journal of cardiovascular imaging, 2024-08, Vol.40 (8), p.1809-1811

2024

Volltextzugriff (PDF)

Abstract 13516: Natural History, Penotypes and Clinical Outcomes in Desmin Related Arrhythmogenic Cardiomyopathy

Circulation (New York, N.Y.), 2022-11, Vol.146 (Suppl_1)

2022

Volltextzugriff (PDF)

Three dimensional modelling of mutant Kir2.1 channel PIP2 interactions help stratify arrhythmia severity in Andersen Tawil syndrome type 1

European heart journal, 2022-10, Vol.43 (Supplement_2)

2022

Volltextzugriff (PDF)

Clinical Risk Score to Predict Pathogenic Genotypes in Patients With Dilated Cardiomyopathy

Journal of the American College of Cardiology, 2022-09, Vol.80 (12), p.1115-1126

2022

Volltextzugriff (PDF)

Myocardial deformation techniques as potential tools to detect arrhythmogenic cardiomyopathy in early stages of the disease

European heart journal, 2021-10, Vol.42 (Supplement_1)

2021

Volltextzugriff (PDF)

1 – 25 von 103

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(87)
Mit Volltextzugriff
(92)

Publikationsform

Artikel
(102)
Berichte
(1)

Sprache

Englisch
(100)
Spanisch
(4)

Erscheinungsjahr

n.n

Thema

Science & Technology
(47)
Life Sciences & Biomedicine
(40)
Humans
(33)
Cardiac & Cardiovascular Systems
(25)
Cardiovascular System & Cardiology
(25)
Male
(19)
Female
(17)
Middle Aged
(15)
Electrocardiography
(13)
Mutation
(13)
Adult
(11)
Phenotype
(10)
Genetics
(8)
Young Adult
(8)
Biological And Medical Sciences
(7)
Fundamental And Applied Biological Sciences. Psychology
(7)
Transgenic Plants
(7)
Adolescent
(6)
Aged
(6)
Cardiomyopathy
(6)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Manipulation of Strawberry Fruit Softening by Antisense Expression of a Pectate Lyase Gene

convenient protocol for extraction and purification of DNA from Fragaria

Assessment of in vitro growth of apical stem sections and adventitious organogenesis to evaluate salinity tolerance in cultivated tomato

Agrobacterium cells as microprojectile coating: a novel approach to enhance stable transformation rates in strawberry

Novel Desmin Mutation p.Glu401Asp Impairs Filament Formation, Disrupts Cell Membrane Integrity, and Causes Severe Arrhythmogenic Left Ventricular Cardiomyopathy/Dysplasia

A rare presentation of infective endocarditis: Phase 4 block of the left bundle branch as key for the diagnosis. A case report

Giant biventricular aneurysms: a novel cardiac phenotype in myotubular/centronuclear myopathy

The Kir2.1E299V mutation increases atrial fibrillation vulnerability while protecting the ventricles against arrhythmias in a mouse model of short QT syndrome type 3

Myocardial fibrosis in arrhythmogenic cardiomyopathy: a genotype–phenotype correlation study

Prevalence and clinical outcomes of dystrophin‐associated dilated cardiomyopathy without severe skeletal myopathy

Association of Left Ventricular Systolic Dysfunction Among Carriers of Truncating Variants in Filamin C With Frequent Ventricular Arrhythmia and End-stage Heart Failure

Phenotype and Clinical Outcomes in Desmin-Related Arrhythmogenic Cardiomyopathy

Fallen and Lost into the Abyss? A Mesolithic Human Skull from Sima Hedionda IV (Casares, Málaga, Iberian Peninsula)

ROD2 domain filamin C missense mutations exhibit a distinctive cardiac phenotype with restrictive/hypertrophic cardiomyopathy and saw-tooth myocardium

Genotype, Family History, and Outcomes in Noncompaction Cardiomyopathy

Fruit yield and quality of strawberry plants transformed with a fruit specific strawberry pectate lyase gene

Unraveling the links between genetics and electrophysiological phenotype of sustained monomorphic ventricular tachycardias in left and biventricular arrhythmogenic cardiomyopathy

Atrial-specific reduction of Kir2.1 channel pore diameter in addition to loss of inward-going rectification underlies inducible atrial fibrillation in a mouse model of short QT syndrome type 3

Abstract 14479: Compound Heterozygosity With Two Novel Mutations in MYBPC3 as a Cause of Severe and Early-Onset Hypertrophic Cardiomyopathy

Lactococcus garvieae endocarditis in a native valve identified by MALDI-TOF MS and PCR-based 16s rRNA in Spain: A case report

Atypical left-ventricular hypertrophy with apical aneurysm in leopard syndrome

Abstract 13516: Natural History, Penotypes and Clinical Outcomes in Desmin Related Arrhythmogenic Cardiomyopathy

Three dimensional modelling of mutant Kir2.1 channel PIP2 interactions help stratify arrhythmia severity in Andersen Tawil syndrome type 1

Clinical Risk Score to Predict Pathogenic Genotypes in Patients With Dilated Cardiomyopathy

Myocardial deformation techniques as potential tools to detect arrhythmogenic cardiomyopathy in early stages of the disease

Suchergebnisse filtern