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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Publicat a:Am J Physiol Lung Cell Mol Physiol
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: American Physiological Society 2016
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Call for Papers
Accés en línia: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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