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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Detalles Bibliográficos
Autores principales: Wu, Zhenhua, Geng, Jie, Qi, Yujuan, Li, Jian, Bai, Yaobang, Guo, Zhigang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Original Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734527/
https://www.ncbi.nlm.nih.gov/pubmed/33354317
http://dx.doi.org/10.1177/2045894020974919

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734527/
https://www.ncbi.nlm.nih.gov/pubmed/33354317
http://dx.doi.org/10.1177/2045894020974919

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