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Apoptosis-based therapy to treat pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) is rare, but patients who are diagnosed with this disease still suffer from a lack of satisfactory treatment strategies to prolong survival. While currently approved drugs for PAH have some benefits, these vasodilators only have limited efficacy for eliminating...

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Detalles Bibliográficos
Autores principales: Suzuki, Yuichiro J., Ibrahim, Yasmine F., Shults, Nataliia V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5094193/
https://www.ncbi.nlm.nih.gov/pubmed/27819072