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Article

MicroRNA networks in pulmonary arterial hypertension

14 Nov 2015

Abstract excerpt

PURPOSE OF REVIEW: Pulmonary arterial hypertension (PAH) is a rare disease with poor prognosis and no therapeutics. PAH is characterized by severe remodeling of precapillary pulmonary arteries, leading to increased vascular resistance, pulmonary hypertension compensatory right ventricular hypertrophy, then heart failure and death. PAH pathogenesis shares similarities with carcinogenesis such as excessive cell...

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Share to Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
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Share to Pulmonary Hypertension Research and Treatments

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PMID: 26569423
DOI: 10.1097/cco.0000000000000253

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