Murine models of sickle cell disease and beta‐thalassemia demonstrate pulmonary hypertension with distinctive features

Sickle cell anemia and β‐thalassemia intermedia are very different genetically determined hemoglobinopathies predisposing to pulmonary hypertension. The etiologies responsible for the associated development of pulmonary hypertension in both diseases are multi‐factorial with extensive mechanistic con...

Full description

Bibliographic Details

Published in:	Pulmonary Circulation
Main Authors:	Paul W. Buehler, Delaney Swindle, David I. Pak, Mehdi A. Fini, Kathryn Hassell, Rachelle Nuss, Rebecca B. Wilkerson, Angelo D’Alessandro, David C. Irwin
Format:	Article
Language:	English
Published:	Wiley 2021-10-01
Subjects:	lung heart metabolomics pulmonary vascular disease hemaglobinopathies
Online Access:	https://doi.org/10.1177/20458940211055996