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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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Publicat a:Compr Physiol
Autors principals: Xu, Weiling, Erzurum, Serpil C.
Format: Artigo
Idioma:Inglês
Publicat: 2011
Matèries:
Accés en línia: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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