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Endothelial HIF signaling regulates pulmonary fibrosis-associated pulmonary hypertension

Pulmonary hypertension (PH) complicating chronic parenchymal lung disease, such as idiopathic pulmonary fibrosis, results in significant morbidity and mortality. Since the hypoxia-inducible factor (HIF) signaling pathway is important for development of pulmonary hypertension in chronic hypoxia, we i...

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Detalhes bibliográficos
Publicado no:Am J Physiol Lung Cell Mol Physiol
Main Authors: Bryant, Andrew J., Carrick, Ryan P., McConaha, Melinda E., Jones, Brittany R., Shay, Sheila D., Moore, Christy S., Blackwell, Thomas R., Gladson, Santhi, Penner, Niki L., Burman, Ankita, Tanjore, Harikrishna, Hemnes, Anna R., Karwandyar, Ayub K., Polosukhin, Vasiliy V., Talati, Megha A., Dong, Hui-Jia, Gleaves, Linda A., Carrier, Erica J., Gaskill, Christa, Scott, Edward W., Majka, Susan M., Fessel, Joshua P., Haase, Volker H., West, James D., Blackwell, Timothy S., Lawson, William E.
Formato: Artigo
Idioma:Inglês
Publicado em: American Physiological Society 2015
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4838140/
https://ncbi.nlm.nih.gov/pubmed/26637636
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajplung.00258.2015
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