Acquired disorders of mitochondrial metabolism and dynamics in pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) is an orphan disease of the cardiopulmonary unit that reflects an obstructive pulmonary vasculopathy and presents with hypertrophy, inflammation, fibrosis, and ultimately failure of the right ventricle (RVF). Despite treatment using pulmonary hypertension (PH)-t...

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Detalles Bibliográficos
Autores principales: Breault, Nolan M., Wu, Danchen, Dasgupta, Asish, Chen, Kuang-Hueih, Archer, Stephen L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933518/
https://www.ncbi.nlm.nih.gov/pubmed/36819102
http://dx.doi.org/10.3389/fcell.2023.1105565

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9933518/
https://www.ncbi.nlm.nih.gov/pubmed/36819102
http://dx.doi.org/10.3389/fcell.2023.1105565

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