SOX17 in pulmonary arterial hypertension: from development to clinical phenotype

Pulmonary arterial hypertension (PAH) is a severe disease characterised by progressive remodelling and loss of pulmonary microvessels, driven by endothelial cell dysfunction, smooth muscle cell abnormalities, inflammation and immune system dysregulation. Recent research advancements have uncovered p...

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发表在:	European Respiratory Review
Main Authors:	Thomas Lacoste-Palasset, Benoit Aguado, Julien Grynblat, Florence Coulet, Marc Humbert, Fabrice Antigny, David Montani, Grégoire Ruffenach
格式:	文件
语言:	英语
出版:	European Respiratory Society 2025-09-01
在线阅读:	http://err.ersjournals.com/content/34/177/250081.full