Phosphoproteomic analysis of lung tissue from patients with pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) is a rare disorder associated with high morbidity and mortality despite currently available treatments. We compared the phosphoproteome of lung tissue from subjects with idiopathic PAH (iPAH) obtained at the time of lung transplant with control lung tissue. The...

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Bibliographic Details
Main Authors: Ravikumar Sitapara, TuKiet T. Lam, Aneta Gandjeva, Rubin M. Tuder, Lawrence S. Zisman
Format: Article
Language:English
Published: Wiley 2021-07-01
Series:Pulmonary Circulation
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Online Access:https://doi.org/10.1177/20458940211031109
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