Macrophage bone morphogenic protein receptor 2 depletion in idiopathic pulmonary fibrosis and Group III pulmonary hypertension

Idiopathic pulmonary fibrosis (IPF) is a lethal lung disease of unknown etiology. The development of pulmonary hypertension (PH) is considered the single most significant predictor of mortality in patients with chronic lung diseases. The processes that govern the progression and development of fibro...

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Publicado no:Am J Physiol Lung Cell Mol Physiol
Main Authors: Chen, Ning-Yuan, D. Collum, Scott, Luo, Fayong, Weng, Tingting, Le, Thuy-Trahn, M. Hernandez, Adriana, Philip, Kemly, Molina, Jose G., Garcia-Morales, Luis J., Cao, Yanna, Ko, Tien C., Amione-Guerra, Javier, Al-Jabbari, Odeaa, Bunge, Raquel R., Youker, Keith, Bruckner, Brian A., Hamid, Rizwan, Davies, Jonathan, Sinha, Neeraj, Karmouty-Quintana, Harry
Formato: Artigo
Idioma:Inglês
Publicado em: American Physiological Society 2016
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Call for Papers
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6425517/
https://ncbi.nlm.nih.gov/pubmed/27317687
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajplung.00142.2016
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