SMAD3 regulation contributes to lung vascular remodeling in pulmonary arterial hypertension
European Respiratory Journal, 2015.
Introduction: Pulmonary arterial hypertension (PAH) is a fatal disease characterized by remodelling of pulmonary arteries, smooth muscle cell hyperplasia and hypertrophy. TGF-β, regulating cell proliferation, migration, and cell death, is elevated in PAH, and has been implicated in its pathogenesis based on clinical and experimental data...More
Full Text (Upload PDF)
PPT (Upload PPT)