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Identification of key fatty acid metabolism-related genes in pulmonary arterial hypertension through bioinformatics analysis and experimental studies

2025-11-26

Abstract excerpt

<title>Abstract</title> <p> Background Pulmonary arterial hypertension (PAH) is a clinical illness primarily defined by exertional dyspnea and exhaustion, leading to significant pathophysiological alterations in pulmonary arteries. Several causative factors have been reported, among which dysfunction of fatty acid (FA) metabolism in cardiac and pulmonary vessels has been identified as the cause of structural and...

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Literature Corpus work
79902884-8194-5320-9540-06082751c0df
DOI
10.21203/rs.3.rs-8087755/v1
Open publication

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