Regulation of mitochondrial fragmentation in microvascular endothelial cells isolated from the SU5416/hypoxia model of pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) is a morbid disease characterized by progressive right ventricle (RV) failure due to elevated pulmonary artery pressures (PAP). In PAH, histologically complex vaso-occlusive lesions in the pulmonary vasculature contribute to elevated PAP. However, the mechanisms...

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Bibliografiska uppgifter
I publikationen:Am J Physiol Lung Cell Mol Physiol
Huvudupphovsmän: Suresh, Karthik, Servinsky, Laura, Jiang, Haiyang, Bigham, Zahna, Zaldumbide, Joel, Huetsch, John C., Kliment, Corrine, Acoba, Michelle G., Kirsch, Brian J., Claypool, Steven M., Le, Anne, Damarla, Mahendra, Shimoda, Larissa A.
Materialtyp: Artigo
Språk:Inglês
Publicerad: American Physiological Society 2019
Ämnen:
Research Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC6879901/
https://ncbi.nlm.nih.gov/pubmed/31461316
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajplung.00396.2018
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