Silencing TUFM Inhibits Development of Monocrotaline-Induced Pulmonary Hypertension by Regulating Mitochondrial Autophagy via AMPK/mTOR Signal Pathway

Pulmonary arterial hypertension (PAH) is an extremely malignant cardiovascular disease which mainly involves the uncontrollable proliferation of the pulmonary arterial smooth muscular cells (PASMCs). Recent studies have confirmed that mitochondria play an important role in the pathogenesis of pulmon...

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Detalles Bibliográficos
Autores principales: Wei, Ruyuan, Lv, Xin, Fang, Changcun, Liu, Chuanzhen, Ma, Zengshan, Liu, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9348918/
https://www.ncbi.nlm.nih.gov/pubmed/35936222
http://dx.doi.org/10.1155/2022/4931611

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9348918/
https://www.ncbi.nlm.nih.gov/pubmed/35936222
http://dx.doi.org/10.1155/2022/4931611

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