Mitochondrial dysfunction in pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) is characterized by the increased pulmonary vascular resistance due to pulmonary vasoconstriction and vascular remodeling. PAH has high disability, high mortality and poor prognosis, which is becoming a more common global health issue. There is currently no drug...

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Detalles Bibliográficos
Autores principales: Zhang, Weiwei, Liu, Bo, Wang, Yazhou, Zhang, Hengli, He, Lang, Wang, Pan, Dong, Mingqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795033/
https://www.ncbi.nlm.nih.gov/pubmed/36589421
http://dx.doi.org/10.3389/fphys.2022.1079989

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9795033/
https://www.ncbi.nlm.nih.gov/pubmed/36589421
http://dx.doi.org/10.3389/fphys.2022.1079989

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