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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Vydáno v:Am J Physiol Lung Cell Mol Physiol
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: American Physiological Society 2016
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On-line přístup: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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