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MiR‐629 regulates hypoxic pulmonary vascular remodelling by targeting FOXO3 and PERP
Pulmonary arterial hypertension (PAH) is featured by the increase in pulmonary vascular resistance and pulmonary arterial pressure. Despite that abnormal proliferation and phenotypic changes in human pulmonary artery smooth muscle cells (HPASMCs) contributing to the pathophysiology of PAH, the under...
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| Publicado no: | J Cell Mol Med |
|---|---|
| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6653446/ https://ncbi.nlm.nih.gov/pubmed/31240850 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcmm.14385 |
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