Int J Physiol Pathophysiol Pharmacol
November 2017
[This corrects the article on p. 112 in vol. 9, PMID: 28951773.
View Article and Find Full Text PDFInt J Physiol Pathophysiol Pharmacol
September 2017
Background: Pulmonary Arterial Hypertension (PAH) is a deadly and disabling disease for which there is no marketed drug that addresses the underlying disease mechanism and targets to cure patients. The lack of understanding of the disease mechanism represents the main challenges in developing curative therapies. We here report, for the first time, that mice lacking natriuretic peptides clearance receptor develop PAH.
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