The Role of Nogo and the Mitochondria–Endoplasmic Reticulum Unit in Pulmonary Hypertension

Pulmonary arterial hypertension (PAH) is caused by excessive proliferation of vascular cells, which occlude the lumen of pulmonary arteries (PAs) and lead to right ventricular failure. The cause of the vascular remodeling in PAH remains unknown, and the prognosis of PAH remains poor. Abnormal mitoch...

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Tallennettuna:
Bibliografiset tiedot
Päätekijät: Sutendra, Gopinath, Dromparis, Peter, Wright, Paulette, Bonnet, Sébastien, Haromy, Alois, Hao, Zhengrong, McMurtry, M. Sean, Michalak, Marek, Vance, Jean E., Sessa, William C., Michelakis, Evangelos D.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2011
Aiheet:
Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3744110/
https://ncbi.nlm.nih.gov/pubmed/21697531
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1126/scitranslmed.3002194
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