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Implication of Potassium Channels in the Pathophysiology of Pulmonary Arterial Hypertension

1 Sept 2020

Abstract excerpt

Pulmonary arterial hypertension (PAH) is a rare and severe cardiopulmonary disease without curative treatments. PAH is a multifactorial disease that involves genetic predisposition, epigenetic factors, and environmental factors (drugs, toxins, viruses, hypoxia, and inflammation), which contribute to the initiation or development of irreversible remodeling of the pulmonary vessels. The recent identification of...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 32882918
DOI: 10.3390/biom10091261

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