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Molecular Mechanisms of Pulmonary Arterial Remodeling

Pulmonary arterial hypertension (PAH) is characterized by a persistent elevation of pulmonary arterial pressure and pulmonary arterial remodeling with unknown etiology. Current therapeutics available for PAH are primarily directed at reducing the pulmonary blood pressure through their effects on the...

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Podrobná bibliografie
Hlavní autoři: Crosswhite, Patrick, Sun, Zhongjie
Médium: Artigo
Jazyk:Inglês
Vydáno: ScholarOne 2014
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4002851/
https://ncbi.nlm.nih.gov/pubmed/24676136
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2119/molmed.2013.00165
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