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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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Am J Physiol Lung Cell Mol Physiol
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: American Physiological Society 2016
Pynciau:
Call for Papers
Mynediad Ar-lein: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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