UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 43

Sortiert nach

Mutations in genes related to myocyte contraction and ventricular septum development in non-syndromic tetralogy of Fallot

Frontiers in cardiovascular medicine, 2023-09, Vol.10, p.1249605-1249605

2023

Volltextzugriff (PDF)

Joint analysis of left ventricular expression and circulating plasma levels of Omentin after myocardial ischemia

Cardiovascular diabetology, 2017-07, Vol.16 (1), p.87-87, Article 87

2017

Volltextzugriff (PDF)

Prevention of Ventricular Arrhythmia and Calcium Dysregulation in a Catecholaminergic Polymorphic Ventricular Tachycardia Mouse Model Carrying Calsequestrin-2 Mutation

Journal of cardiovascular electrophysiology, 2011-03, Vol.22 (3), p.316-324

2011

Volltextzugriff (PDF)

Sex differences in gene expression in response to ischemia in the human left ventricular myocardium

Human molecular genetics, 2019-05, Vol.28 (10), p.1682-1693

2019

Volltextzugriff (PDF)

N488I Mutation of the γ2-Subunit Results in Bidirectional Changes in AMP-Activated Protein Kinase Activity

Circulation research, 2005-08, Vol.97 (4), p.323-328

2005

Volltextzugriff (PDF)

Molecular Genetics of Lidocaine-Containing Cardioplegia in the Human Heart During Cardiac Surgery

The Annals of thoracic surgery, 2018-11, Vol.106 (5), p.1379-1387

2018

Volltextzugriff (PDF)

LAMP2 Cardiomyopathy: Consequences of Impaired Autophagy in the Heart

Journal of the American Heart Association, 2021-09, Vol.10 (17), p.e018829-e018829

2021

Volltextzugriff (PDF)

Functional role of AMP-activated protein kinase in the heart during exercise

FEBS letters, 2005-04, Vol.579 (10), p.2045-2050

2005

Volltextzugriff (PDF)

Using Next-generation RNA Sequencing to Examine Ischemic Changes Induced by Cold Blood Cardioplegia on the Human Left Ventricular Myocardium Transcriptome

Anesthesiology (Philadelphia), 2015-03, Vol.122 (3), p.537-550

2015

Volltextzugriff (PDF)

The Long Noncoding RNA Landscape of the Ischemic Human Left Ventricle

Circulation. Cardiovascular genetics, 2017-01, Vol.10 (1)

2017

Volltextzugriff (PDF)

Allele-specific expression in the human heart and its application to postoperative atrial fibrillation and myocardial ischemia

Genome medicine, 2016-12, Vol.8 (1), p.127-127, Article 127

2016

Volltextzugriff (PDF)

Genome-wide identification of mouse congenital heart disease loci

Human molecular genetics, 2010-08, Vol.19 (16), p.3105-3113

2010

Volltextzugriff (PDF)

Single-cell meta-analysis of SARS-CoV-2 entry genes across tissues and demographics

Nature medicine, 2021-03, Vol.27 (3), p.546-559

2021

Volltextzugriff (PDF)

Rare Gene Mutations are a Common Cause of Pediatric Cardiac Hypertrophy

Journal of cardiac failure, 2007, Vol.13 (6), p.S62-S62

2007

Volltextzugriff (PDF)

Hypertrophy, electrical abnormalities, autophagic vacuoles accumulation and cardiac fibrosis in LAMP2 cardiomyopathy mouse model

Progress in pediatric cardiology, 2007-11, Vol.24 (1), p.73-74

2007

Volltextzugriff (PDF)

Abstract 785: Modeling Congenital Heart Disease-Associated Variants in GATA6 Using CRISPR/Cas9 and Human Induced Pluripotent Stem Cells

Circulation research, 2019-08, Vol.125 (Suppl_1)

2019

Volltextzugriff (PDF)

italic toggle="yes">LAMP2 /italic> Cardiomyopathy: Consequences of Impaired Autophagy in the Heart

Journal of the American Heart Association, 2021-09, Vol.10 (17)

2021

Volltextzugriff (PDF)

N488I Mutation of the g2-Subunit Results in Bidirectional Changes in AMP-Activated Protein Kinase Activity

Circulation research, 2005-08, Vol.97 (4), p.323-328

2005

Volltextzugriff (PDF)

N488I mutation of the gamma2-subunit results in bidirectional changes in AMP-activated protein kinase activity

Circulation research, 2005-08, Vol.97 (4), p.323-328

2005

Volltextzugriff (PDF)

Transcription of Mouse κ Chain Genes: Implications for Allelic Exclusion

Proceedings of the National Academy of Sciences - PNAS, 1980-04, Vol.77 (4), p.1937-1941

1980

Volltextzugriff (PDF)

T-cell receptor gene rearrangement and expression in human natural killer cells: natural killer activity is not dependent on the rearrangement and expression of T-cell receptor α, β, or γ genes

Immunogenetics (New York), 1988, Vol.27 (4), p.231-238

1988

Volltextzugriff (PDF)

A comparison of two cloned mouse β-globin genes and their surrounding and intervening sequences

Cell, 1978-06, Vol.14 (2), p.237-245

1978

Volltextzugriff (PDF)

T-cell receptor gene rearrangement and expression in human natural killer cells: natural killer activity is not dependent on the rearrangement and expression of T-cell receptor ?, ?, or ? genes

Immunogenetics (New York), 1988-04, Vol.27 (4), p.231-238

1988

Volltextzugriff (PDF)

1 – 25 von 43

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(43)
Mit Volltextzugriff
(40)

Publikationsform

Artikel
(43)

Sprache

Englisch
(43)
Japanisch
(7)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Mutations in genes related to myocyte contraction and ventricular septum development in non-syndromic tetralogy of Fallot

Joint analysis of left ventricular expression and circulating plasma levels of Omentin after myocardial ischemia

Prevention of Ventricular Arrhythmia and Calcium Dysregulation in a Catecholaminergic Polymorphic Ventricular Tachycardia Mouse Model Carrying Calsequestrin-2 Mutation

Sex differences in gene expression in response to ischemia in the human left ventricular myocardium

N488I Mutation of the γ2-Subunit Results in Bidirectional Changes in AMP-Activated Protein Kinase Activity

Molecular Genetics of Lidocaine-Containing Cardioplegia in the Human Heart During Cardiac Surgery

LAMP2 Cardiomyopathy: Consequences of Impaired Autophagy in the Heart

Functional role of AMP-activated protein kinase in the heart during exercise

Using Next-generation RNA Sequencing to Examine Ischemic Changes Induced by Cold Blood Cardioplegia on the Human Left Ventricular Myocardium Transcriptome

The Long Noncoding RNA Landscape of the Ischemic Human Left Ventricle

Allele-specific expression in the human heart and its application to postoperative atrial fibrillation and myocardial ischemia

Genome-wide identification of mouse congenital heart disease loci

Single-cell meta-analysis of SARS-CoV-2 entry genes across tissues and demographics

Rare Gene Mutations are a Common Cause of Pediatric Cardiac Hypertrophy

Hypertrophy, electrical abnormalities, autophagic vacuoles accumulation and cardiac fibrosis in LAMP2 cardiomyopathy mouse model

Abstract 785: Modeling Congenital Heart Disease-Associated Variants in GATA6 Using CRISPR/Cas9 and Human Induced Pluripotent Stem Cells

Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndrome

italic toggle="yes">LAMP2 /italic> Cardiomyopathy: Consequences of Impaired Autophagy in the Heart

Loss-of-Function Mutations in PTPN11 Cause Metachondromatosis, but Not Ollier Disease or Maffucci Syndrome: e1002050

N488I Mutation of the g2-Subunit Results in Bidirectional Changes in AMP-Activated Protein Kinase Activity

N488I mutation of the gamma2-subunit results in bidirectional changes in AMP-activated protein kinase activity

Transcription of Mouse κ Chain Genes: Implications for Allelic Exclusion

T-cell receptor gene rearrangement and expression in human natural killer cells: natural killer activity is not dependent on the rearrangement and expression of T-cell receptor α, β, or γ genes

A comparison of two cloned mouse β-globin genes and their surrounding and intervening sequences

T-cell receptor gene rearrangement and expression in human natural killer cells: natural killer activity is not dependent on the rearrangement and expression of T-cell receptor ?, ?, or ? genes

Suchergebnisse filtern