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Endothelial Nox1 oxidase assembly in human pulmonary arterial hypertension; driver of Gremlin1-mediated proliferation

Pulmonary arterial hypertension (PAH) is a rapidly degenerating and devastating disease of increased pulmonary vessel resistance leading to right heart failure. Palliative modalities remain limited despite recent endeavors to investigate the mechanisms underlying increased pulmonary vascular resista...

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Bibliografske podrobnosti
izdano v:Clin Sci (Lond)
Main Authors: Al Ghouleh, Imad, Sahoo, Sanghamitra, Meijles, Daniel N., Amaral, Jefferson H., de Jesus, Daniel S., Sembrat, John, Rojas, Mauricio, Goncharov, Dmitry A., Goncharova, Elena A., Pagano, Patrick J.
Format: Artigo
Jezik:Inglês
Izdano: 2017
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5705051/
https://ncbi.nlm.nih.gov/pubmed/28522681
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/CS20160812
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