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Role of Biomarkers in the Diagnosis, Risk Assessment, and Management of Pulmonary HypertensionMolecular Background of miRNA Role in Asthma and COPD: An Updated InsightBMPR2 spruces up the endothelium in pulmonary hypertensionPulmonary capillary hemangiomatosis: a focus on the EIF2AK4 mutation in onset and pathogenesisEpigenetic modulation as a therapeutic approach for pulmonary arterial hypertensionDiffuse lung disease of infancy: a pattern-based, algorithmic approach to histological diagnosisPulmonary Hypertension in Children.World Health Organization Group I Pulmonary Hypertension: Epidemiology and Pathophysiology.Functional prostacyclin synthase promoter polymorphisms. Impact in pulmonary arterial hypertension.Serum endostatin is a genetically determined predictor of survival in pulmonary arterial hypertension.Role of innate immunity-triggered pathways in the pathogenesis of Sickle Cell Disease: a meta-analysis of gene expression studiesHigh Frequency of Pulmonary Hypertension-Causing Gene Mutation in Chinese Patients with Chronic Thromboembolic Pulmonary HypertensionAccurate genetic diagnosis of Finnish pulmonary arterial hypertension patients using oligonucleotide-selective sequencing.1α,25-Dihydroxyvitamin D3 prevents the differentiation of human lung fibroblasts via microRNA-27b targeting the vitamin D receptor.A burden of rare variants in BMPR2 and KCNK3 contributes to a risk of familial pulmonary arterial hypertension.The serotonin transporter promotes a pathological estrogen metabolic pathway in pulmonary hypertension via cytochrome P450 1B1Plasma Metabolomics Implicates Modified Transfer RNAs and Altered Bioenergetics in the Outcomes of Pulmonary Arterial Hypertension.Inhibition of heat shock protein 90 improves pulmonary arteriole remodeling in pulmonary arterial hypertension.Implication of overexpression of dishevelled-associated activator of morphogenesis 1 (Daam-1) for the pathogenesis of human Idiopathic Pulmonary Arterial Hypertension (IPAH).The role of BMPs in endothelial cell function and dysfunction.Pulmonary vascular development goes awry in congenital lung abnormalities.Lung Circulation.The role of genetics in pulmonary arterial hypertension.Pulmonary arterial hypertension - progress in understanding the disease and prioritizing strategies for drug development.The genomic complexity underlying pulmonary arterial hypertension: from mendel to networks.Transforming growth factor-β plays divergent roles in modulating vascular remodeling, inflammation, and pulmonary fibrosis in a murine model of scleroderma.Diagnosis, Evaluation and Treatment of Pulmonary Arterial Hypertension in Children.Importance and usage of chromosomal microarray analysis in diagnosing intellectual disability, global developmental delay, and autism; and discovering new loci for these disordersExome data clouds the pathogenicity of genetic variants in Pulmonary Arterial Hypertension
P2860
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P2860
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
The genetic basis of pulmonary arterial hypertension.
@en
type
label
The genetic basis of pulmonary arterial hypertension.
@en
prefLabel
The genetic basis of pulmonary arterial hypertension.
@en
P2860
P1433
P1476
The genetic basis of pulmonary arterial hypertension.
@en
P2093
Lijiang Ma
Wendy K Chung
P2860
P2888
P304
P356
10.1007/S00439-014-1419-3
P577
2014-01-21T00:00:00Z
P6179
1015955969