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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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Bibliografske podrobnosti
izdano v:J Cell Mol Med
Main Authors: Zhao, Mei, Chen, Ni, Li, Xuelian, Lin, Ling
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2019
Teme:
Online dostop: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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