Cargando…
Purinergic Dysfunction in Pulmonary Arterial Hypertension
Pulmonary arterial hypertension (PAH) is a life‐threatening disease characterized by increased pulmonary arterial pressure and pulmonary vascular resistance, which result in an increase in afterload imposed onto the right ventricle, leading to right heart failure. Current therapies are incapable of...
Autores principales: | Cai, Zongye, Tu, Ly, Guignabert, Christophe, Merkus, Daphne, Zhou, Zhichao |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7727004/ https://www.ncbi.nlm.nih.gov/pubmed/32867554 http://dx.doi.org/10.1161/JAHA.120.017404 |
Ejemplares similares
-
Lower Plasma Melatonin Levels Predict Worse Long-Term Survival in Pulmonary Arterial Hypertension
por: Cai, Zongye, et al.
Publicado: (2020) -
The Role of Regulatory T Cells in Pulmonary Arterial Hypertension
por: Qiu, Haihua, et al.
Publicado: (2019) -
Repurposing Medications for Treatment of Pulmonary Arterial Hypertension: What's Old Is New Again
por: Prins, Kurt W., et al.
Publicado: (2018) -
Pulmonary Hypertension in Mitral Regurgitation
por: Patel, Harsh, et al.
Publicado: (2014) -
Kynurenine metabolites predict survival in pulmonary arterial hypertension: A role for IL-6/IL-6Rα
por: Cai, Zongye, et al.
Publicado: (2022)