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Stem/Progenitor Cells and Pulmonary Arterial Hypertension.

Arteriosclerosis, thrombosis, and vascular biology - 1 Jan 2021

Pu Xiangyuan, Du Luping, Hu Yanhua, Fan Ye, Xu Qingbo

Abstract excerpt

Pulmonary arterial hypertension (PAH) is a progressive disease characterized by endothelial dysfunction and vascular remodeling. Despite significant advancement in our understanding of the pathogenesis of PAH in recent years, treatment options for PAH are limited and their prognosis remains poor. PAH is now seen as a severe pulmonary arterial vasculopathy with structural changes driven by excessive vascular...

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Arterial Pressure
Endothelial Progenitor Cells
Endothelium, Vascular
Induced Pluripotent Stem Cells
Mesenchymal Stem Cell Transplantation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Pulmonary Arterial Hypertension

Pulmonary Artery

Vascular Remodeling

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Identifiers

PMID: 33028095
DOI: 10.1161/ATVBAHA.120.315052

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

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