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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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Pubblicato in:Int J Mol Sci
Autori principali: Leopold, Jane A., Maron, Bradley A.
Natura: Artigo
Lingua:Inglês
Pubblicazione: MDPI 2016
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Accesso online: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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