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MiR-193-3p attenuates the vascular remodeling in pulmonary arterial hypertension by targeting PAK4
Pulmonary arterial hypertension (PAH) is a progressive pulmonary vascular disease associated with dysfunction of pulmonary artery endothelial cells and pulmonary artery smooth muscle cells (PASMCs). To explore the potential mechanism of miR-193-3p in pulmonary arterial hypertension, human PASMCs and...
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| Publicat a: | Pulm Circ |
|---|---|
| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
SAGE Publications
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7734527/ https://ncbi.nlm.nih.gov/pubmed/33354317 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2045894020974919 |
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