Adenosine Receptors As Drug Targets for Treatment of Pulmonary Arterial Hypertension

Pulmonary arterial hypertension (PAH) is a clinical condition characterized by pulmonary arterial remodeling and vasoconstriction, which promote chronic vessel obstruction and elevation of pulmonary vascular resistance. Long-term right ventricular (RV) overload leads to RV dysfunction and failure, w...

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Dettagli Bibliografici
Pubblicato in:Front Pharmacol
Autori principali: Alencar, Allan K. N., Montes, Guilherme C., Barreiro, Eliezer J., Sudo, Roberto T., Zapata-Sudo, Gisele
Natura: Artigo
Lingua:Inglês
Pubblicazione: Frontiers Media S.A. 2017
Soggetti:
Pharmacology
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5722832/
https://ncbi.nlm.nih.gov/pubmed/29255415
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphar.2017.00858
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