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...

Molecular genetic framework underlying pulmonary arterial hypertension

Nature reviews cardiology, 2020-02, Vol.17 (2), p.85-95

2020

Volltextzugriff (PDF)

Genetics and Genomics of Pulmonary Arterial Hypertension

Journal of the American College of Cardiology, 2013-12, Vol.62 (25), p.D13-D21

2013

Volltextzugriff (PDF)

Genetics and Genomics of Pulmonary Arterial Hypertension

Journal of the American College of Cardiology, 2009-06, Vol.54 (1), p.S32-S42

2009

Volltextzugriff (PDF)

Elevated levels of inflammatory cytokines predict survival in idiopathic and familial pulmonary arterial hypertension

Circulation (New York, N.Y.), 2010-08, Vol.122 (9), p.920-927

2010

Volltextzugriff (PDF)

Selective enhancement of endothelial BMPR-II with BMP9 reverses pulmonary arterial hypertension

Nature medicine, 2015-07, Vol.21 (7), p.777-785

2015

Volltextzugriff (PDF)

Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects

Human mutation, 2015-12, Vol.36 (12), p.1113-1127

2015

Volltextzugriff (PDF)

Identification of rare sequence variation underlying heritable pulmonary arterial hypertension

Nature communications, 2018-04, Vol.9 (1), p.1416-16, Article 1416

2018

Volltextzugriff (PDF)

Biallelic variants of ATP13A3 cause dose-dependent childhood-onset pulmonary arterial hypertension characterised by extreme morbidity and mortality

Journal of medical genetics, 2022-09, Vol.59 (9), p.906-911

2022

Volltextzugriff (PDF)

Characterization of GDF2 Mutations and Levels of BMP9 and BMP10 in Pulmonary Arterial Hypertension

American journal of respiratory and critical care medicine, 2020-03, Vol.201 (5), p.575-585

2020

Volltextzugriff (PDF)

Pulmonary Arterial Hypertension: A Deeper Evaluation of Genetic Risk in the -Omics Era

Genes, 2021-11, Vol.12 (11), p.1798

2021

Volltextzugriff (PDF)

Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies

American journal of human genetics, 2011-05, Vol.88 (5), p.574-585

2011

Volltextzugriff (PDF)

Molecular genetic characterization of SMAD signaling molecules in pulmonary arterial hypertension

Human mutation, 2011-12, Vol.32 (12), p.1385-1389

2011

Volltextzugriff (PDF)

Defining the clinical validity of genes reported to cause pulmonary arterial hypertension

Genetics in medicine, 2023-11, Vol.25 (11), p.100925, Article 100925

2023

Volltextzugriff (PDF)

Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

Genome medicine, 2021-05, Vol.13 (1), p.80-18, Article 80

2021

Volltextzugriff (PDF)

Impaired Natural Killer Cell Phenotype and Function in Idiopathic and Heritable Pulmonary Arterial Hypertension

Circulation (New York, N.Y.), 2012-08, Vol.126 (9), p.1099-1109

2012

Volltextzugriff (PDF)

Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams-Oliver Syndrome With Variable Cardiac Anomalies

Circulation. Cardiovascular genetics, 2015-08, Vol.8 (4), p.572-581

2015

Volltextzugriff (PDF)

Dymeclin, the gene underlying Dyggve-Melchior-Clausen syndrome, encodes a protein integral to extracellular matrix and golgi organization and is associated with protein secretion pathways critical in bone development

Human mutation, 2011-02, Vol.32 (2), p.231-239

2011

Volltextzugriff (PDF)

BMPR2 Haploinsufficiency as the Inherited Molecular Mechanism for Primary Pulmonary Hypertension

American journal of human genetics, 2001-01, Vol.68 (1), p.92-102

2001

Volltextzugriff (PDF)

Heterozygous germline mutations in BMPR2 , encoding a TGF-β receptor, cause familial primary pulmonary hypertension

Nature genetics, 2000-09, Vol.26 (1), p.81-84

2000

Volltextzugriff (PDF)

Whole Exome Sequence Analysis Provides Novel Insights into the Genetic Framework of Childhood-Onset Pulmonary Arterial Hypertension

Genes, 2020-11, Vol.11 (11), p.1328

2020

Volltextzugriff (PDF)

Clinical and Molecular Genetic Features of Pulmonary Hypertension in Patients with Hereditary Hemorrhagic Telangiectasia

The New England journal of medicine, 2001-08, Vol.345 (5), p.325-334

2001

Volltextzugriff (PDF)

Bayesian Inference Associates Rare KDR Variants with Specific Phenotypes in Pulmonary Arterial Hypertension

Circulation. Genomic and precision medicine, 2021-02, Vol.14 (1), p.e003155-e003155

2021

Volltextzugriff (PDF)

Genetics and Genomics of Pulmonary Arterial Hypertension

2022

Volltextzugriff (PDF)

1 – 25 von 66

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(61)
Mit Volltextzugriff
(55)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Molecular genetic framework underlying pulmonary arterial hypertension

Genetics and Genomics of Pulmonary Arterial Hypertension

Genetics and Genomics of Pulmonary Arterial Hypertension

Elevated levels of inflammatory cytokines predict survival in idiopathic and familial pulmonary arterial hypertension

Selective enhancement of endothelial BMPR-II with BMP9 reverses pulmonary arterial hypertension

Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects

Identification of rare sequence variation underlying heritable pulmonary arterial hypertension

Biallelic variants of ATP13A3 cause dose-dependent childhood-onset pulmonary arterial hypertension characterised by extreme morbidity and mortality

Characterization of GDF2 Mutations and Levels of BMP9 and BMP10 in Pulmonary Arterial Hypertension

Pulmonary Arterial Hypertension: A Deeper Evaluation of Genetic Risk in the -Omics Era

Gain-of-Function Mutations of ARHGAP31, a Cdc42/Rac1 GTPase Regulator, Cause Syndromic Cutis Aplasia and Limb Anomalies

Molecular genetic characterization of SMAD signaling molecules in pulmonary arterial hypertension

Defining the clinical validity of genes reported to cause pulmonary arterial hypertension

Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH

Stress Doppler Echocardiography in Relatives of Patients With Idiopathic and Familial Pulmonary Arterial Hypertension : Results of a Multicenter European Analysis of Pulmonary Artery Pressure Response to Exercise and Hypoxia

Impaired Natural Killer Cell Phenotype and Function in Idiopathic and Heritable Pulmonary Arterial Hypertension

Haploinsufficiency of the NOTCH1 Receptor as a Cause of Adams-Oliver Syndrome With Variable Cardiac Anomalies

Dymeclin, the gene underlying Dyggve-Melchior-Clausen syndrome, encodes a protein integral to extracellular matrix and golgi organization and is associated with protein secretion pathways critical in bone development

Mutations of the TGF-β type II receptor BMPR2 in pulmonary arterial hypertension

BMPR2 Haploinsufficiency as the Inherited Molecular Mechanism for Primary Pulmonary Hypertension

Heterozygous germline mutations in BMPR2 , encoding a TGF-β receptor, cause familial primary pulmonary hypertension

Whole Exome Sequence Analysis Provides Novel Insights into the Genetic Framework of Childhood-Onset Pulmonary Arterial Hypertension

Clinical and Molecular Genetic Features of Pulmonary Hypertension in Patients with Hereditary Hemorrhagic Telangiectasia

Bayesian Inference Associates Rare KDR Variants with Specific Phenotypes in Pulmonary Arterial Hypertension

Genetics and Genomics of Pulmonary Arterial Hypertension

Suchergebnisse filtern