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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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Dades bibliogràfiques
Publicat a:J Cell Mol Med
Autors principals: Zhao, Mei, Chen, Ni, Li, Xuelian, Lin, Ling
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2019
Matèries:
Accés en línia: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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