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Cellular mechanosignaling in pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) is a vasculopathy characterized by sustained elevated pulmonary arterial pressures in which the pulmonary vasculature undergoes significant structural and functional remodeling. To better understand disease mechanisms, in this review article we highlight recent...

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Detalles Bibliográficos
Autores principales:	Wang, Ariel, Valdez-Jasso, Daniela
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer Berlin Heidelberg 2021
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8555029/ https://www.ncbi.nlm.nih.gov/pubmed/34765048 http://dx.doi.org/10.1007/s12551-021-00828-3

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