SMAD3 regulation contributes to lung vascular remodeling in pulmonary arterial hypertension

    European Respiratory Journal, 2015.

    Cited by: 0|Bibtex|Views0|

    Abstract:

    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

    Code:

    Data:

    Your rating :
    0

     

    Tags
    Comments