Investigation of Second Genetic Hits at the BMPR2 Locus as a Modulator of Disease Progression in Familial Pulmonary Arterial Hypertension
about
Functional changes in pulmonary arterial endothelial cells associated with BMPR2 mutationsThe molecular genetics and cellular mechanisms underlying pulmonary arterial hypertensionThe genetics of pulmonary arterial hypertensionWhole-exome sequencing reveals TopBP1 as a novel gene in idiopathic pulmonary arterial hypertensionS100A4 and bone morphogenetic protein-2 codependently induce vascular smooth muscle cell migration via phospho-extracellular signal-regulated kinase and chloride intracellular channel 4Heritable forms of pulmonary arterial hypertension.Role of somatic mutations in vascular disease formation.Selective gene expression analysis of muscular and vascular components in hearts using laser microdissection method.Somatic chromosome abnormalities in the lungs of patients with pulmonary arterial hypertension.Epistatic interactions in idiopathic pulmonary arterial hypertension.Pathogenic mechanisms of pulmonary arterial hypertension.Mediators and modulators of pulmonary arterial hypertension.Mutations of TGFbeta signaling molecules in human disease.Genetics and mediators in pulmonary arterial hypertensionDysfunctional intracellular trafficking in the pathobiology of pulmonary arterial hypertension.Pulmonary arterial hypertension: a disease of tethers, SNAREs and SNAPs?Pulmonary Arterial Hypertension-A Deadly Complication of Systemic Sclerosis.Elastin insufficiency predisposes to elevated pulmonary circulatory pressures through changes in elastic artery structureGenetics of pulmonary arterial hypertension.Leads for the treatment of pulmonary hypertension.Molecular pathogenesis and current pathology of pulmonary hypertension.BMPR2 gene therapy for PAH acts via Smad and non-Smad signalling.The role of genetics in pulmonary arterial hypertension.Dysfunction of Golgi tethers, SNAREs, and SNAPs in monocrotaline-induced pulmonary hypertension.Genetic ablation of the BMPR2 gene in pulmonary endothelium is sufficient to predispose to pulmonary arterial hypertension.Waiting in anticipation: the genetics of pulmonary arterial hypertension.Clinical outcomes of pulmonary arterial hypertension in patients carrying an ACVRL1 (ALK1) mutation.Clinical outcomes of pulmonary arterial hypertension in carriers of BMPR2 mutation.Treatment with anti-gremlin 1 antibody ameliorates chronic hypoxia/SU5416-induced pulmonary arterial hypertension in mice.Somatic mutations in pulmonary arterial hypertension: primary or secondary events?BMPR2 mutations and endothelial dysfunction in pulmonary arterial hypertension (2017 Grover Conference Series).
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P2860
Investigation of Second Genetic Hits at the BMPR2 Locus as a Modulator of Disease Progression in Familial Pulmonary Arterial Hypertension
description
im Februar 2005 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 01 February 2005
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в лютому 2005
@uk
name
Investigation of Second Geneti ...... ulmonary Arterial Hypertension
@en
Investigation of Second Geneti ...... ulmonary Arterial Hypertension
@nl
type
label
Investigation of Second Geneti ...... ulmonary Arterial Hypertension
@en
Investigation of Second Geneti ...... ulmonary Arterial Hypertension
@nl
prefLabel
Investigation of Second Geneti ...... ulmonary Arterial Hypertension
@en
Investigation of Second Geneti ...... ulmonary Arterial Hypertension
@nl
P2093
P50
P1433
P1476
Investigation of second geneti ...... ulmonary arterial hypertension
@en
P2093
Carl Atkinson
Micheala A Aldred
Rachel E Harrison
Susan Stewart
P304
P356
10.1161/01.CIR.0000154543.07679.08
P407
P577
2005-02-01T00:00:00Z