Cellular and Molecular Basis of Pulmonary Arterial Hypertension

Pulmonary arterial hypertension (PAH) is caused by functional and structural changes in the pulmonary vasculature, leading to increased pulmonary vascular resistance. The process of pulmonary vascular remodeling is accompanied by endothelial dysfunction, activation of fibroblasts and smooth muscle c...

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Main Authors: Morrell, Nicholas W., Adnot, Serge, Archer, Stephen L., Dupuis, Jocelyn, Jones, Peter Lloyd, MacLean, Margaret R., McMurtry, Ivan F., Stenmark, Kurt R., Thistlethwaite, Patricia A., Weissmann, Norbert, Yuan, Jason X.-J., Weir, E. Kenneth
Formato: Artigo
Idioma:Inglês
Publicado: 2009
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC2790324/
https://ncbi.nlm.nih.gov/pubmed/19555855
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jacc.2009.04.018
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