Microrna-486-5P Regulates Human Pulmonary Artery Smooth Muscle Cell Migration via Endothelin-1

Pulmonary arterial hypertension (PAH) is a fatal or life-threatening disorder characterized by elevated pulmonary arterial pressure and pulmonary vascular resistance. Abnormal vascular remodeling, including the proliferation and phenotypic modulation of pulmonary artery smooth muscle cells (PASMCs),...

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Detalles Bibliográficos
Autores principales: Yen, Ting-An, Huang, Hsin-Chung, Wu, En-Ting, Chou, Heng-Wen, Chou, Hung-Chieh, Chen, Chien-Yi, Huang, Shu-Chien, Chen, Yih-Sharng, Lu, Frank, Wu, Mei-Hwan, Tsao, Po-Nien, Wang, Ching-Chia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9499400/
https://www.ncbi.nlm.nih.gov/pubmed/36142307
http://dx.doi.org/10.3390/ijms231810400

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9499400/
https://www.ncbi.nlm.nih.gov/pubmed/36142307
http://dx.doi.org/10.3390/ijms231810400

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