TRPC channels contribute to endothelial dysfunction in pulmonary arterial hypertension
Abstract Background- Pulmonary arterial hypertension (PAH) is a rare, fatal, and progressive pulmonary vascular disease. Pulmonary endothelial cell dysfunction is a hallmark of PAH, defined by excessive proliferation and dysregulated angiogenesis, along with imbalanced production and release of vaso...
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| Principais autores: | , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMC
2025-12-01
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| coleção: | Respiratory Research |
| Assuntos: | |
| Acesso em linha: | https://doi.org/10.1186/s12931-025-03376-6 |
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