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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Gepubliceerd in:Am J Physiol Lung Cell Mol Physiol
Hoofdauteurs: 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
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: American Physiological Society 2016
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Online toegang: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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