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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Detalhes bibliográficos
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 em: 2009
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Article
Acesso em linha: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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