Therapeutic Approaches for Treating Pulmonary Arterial Hypertension by Correcting Imbalanced TGF-β Superfamily Signaling

Pulmonary arterial hypertension (PAH) is a rare disease characterized by high blood pressure in the pulmonary circulation driven by pathological remodeling of distal pulmonary arteries, leading typically to death by right ventricular failure. Available treatments improve physical activity and slow d...

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Detalles Bibliográficos
Autores principales: Andre, Patrick, Joshi, Sachindra R., Briscoe, Steven D., Alexander, Mark J., Li, Gang, Kumar, Ravindra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8818880/
https://www.ncbi.nlm.nih.gov/pubmed/35141256
http://dx.doi.org/10.3389/fmed.2021.814222

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8818880/
https://www.ncbi.nlm.nih.gov/pubmed/35141256
http://dx.doi.org/10.3389/fmed.2021.814222

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