Molecular-Genetic Basis of Pulmonary Arterial Hypertension (PAH)

Pulmonary arterial hypertension (PAH) is a progressive, fatal disease of the pulmonary vasculature characterized by obliterative remodeling of small pulmonary arteries, leading to sustained elevation of pulmonary vascular resistance, right ventricular failure, and premature death. The diagnostic gol...

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Autors principals:	Mark Okot, Aneesa Ahmed, Colin W. Wright, Md Talat Nasim
Format:	Artigo
Idioma:	Inglês
Publicat:	MDPI AG 2026-05-01
Col·lecció:	Current Issues in Molecular Biology
Matèries:	pulmonary arterial hypertension BMPR2 heritable PAH genetic predisposition TGF-β signaling SNPs
Accés en línia:	https://www.mdpi.com/1467-3045/48/6/572
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