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pro vyhledávání: '"Huating Xie"'
Autor:
Xinyu Li, Hui Li, Bo Feng, Xiaoyan Chen, Ting Chen, Jiafei Lu, Huating Xie, Nana Su, Houlin Chen, Chenghao Lou, Runxin Zhuang, Xi Chen, Shengwei Jin, Yu Hao
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 177, Iss , Pp 117023- (2024)
Pulmonary hypertension (PH) is a life-threatening disease characterized by pulmonary vascular remodeling. Endothelial-to-mesenchymal transition (EndMT) is an important manifestation and mechanism of pulmonary vascular remodeling. Resolvin D1 (RvD1) i
Externí odkaz:
https://doaj.org/article/7358180d236a483ca7f8c4e21e9deb68
Publikováno v:
Toxicology and Applied Pharmacology. 457:116319
Pulmonary hypertension (PH) is a serious cardiovascular disease with a poor prognosis and high mortality. The pathogenesis of PH is complex, and the main pathological changes in PH are abnormal hypertrophy and vessel stiffness. Cysteine and glycine r