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Endothelial Cell Energy Metabolism, Proliferation, and Apoptosis in Pulmonary Hypertension
Pulmonary arterial hypertension (PAH) is a fatal disease characterized by impaired regulation of pulmonary hemodynamics and excessive growth and dysfunction of the endothelial cells that line the arteries in PAH lungs. Establishment of methods for culture of pulmonary artery endothelial cells from P...
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| Publicado no: | Compr Physiol |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6467053/ https://ncbi.nlm.nih.gov/pubmed/23737177 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cphy.c090005 |
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