Potassium Channels as Therapeutic Targets in Pulmonary Arterial Hypertension

Pulmonary arterial hypertension (PAH) is a devastating disease with high morbidity and mortality. Deleterious remodeling in the pulmonary arterial system leads to irreversible arterial constriction and elevated pulmonary arterial pressures, right heart failure, and eventually death. The difficulty i...

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Detalles Bibliográficos
Autores principales: Redel-Traub, Gabriel, Sampson, Kevin J., Kass, Robert S., Bohnen, Michael S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599705/
https://www.ncbi.nlm.nih.gov/pubmed/36291551
http://dx.doi.org/10.3390/biom12101341

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599705/
https://www.ncbi.nlm.nih.gov/pubmed/36291551
http://dx.doi.org/10.3390/biom12101341

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