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Molecular Mechanisms of Pulmonary Vascular Remodeling in Pulmonary Arterial Hypertension
Pulmonary arterial hypertension (PAH) is a devastating disease that is precipitated by hypertrophic pulmonary vascular remodeling of distal arterioles to increase pulmonary artery pressure and pulmonary vascular resistance in the absence of left heart, lung parenchymal, or thromboembolic disease. De...
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| Publicado no: | Int J Mol Sci |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4881582/ https://ncbi.nlm.nih.gov/pubmed/27213345 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms17050761 |
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