Potential therapeutic targets for hypoxia-induced pulmonary artery hypertension

BACKGROUND: Hypoxic pulmonary artery hypertension (PAH) as a severe pulmonary disease is characterized by changes of pulmonary vascular reconstruction. Mitochondrial ATP-sensitive potassium channel (mitoK(ATP)) was considered as one of factors responsible for the proliferation of hypoxic pulmonary a...

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Detalles Bibliográficos
Autores principales: Dong, Li, Li, Yuping, Hu, HongLing, Shi, Lin, Chen, Junjie, Wang, Beibei, Chen, Chaolei, Zhu, Haiping, Li, Yunlei, Li, Qiu, Zhang, Liping, Chen, Chengshui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946029/
https://www.ncbi.nlm.nih.gov/pubmed/24507703
http://dx.doi.org/10.1186/1479-5876-12-39

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946029/
https://www.ncbi.nlm.nih.gov/pubmed/24507703
http://dx.doi.org/10.1186/1479-5876-12-39

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