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Role of potassium channels KCNK3/TASK-1 and KATP in the pathogenesis of Pulmonary Arterial Hypertension. Rôle des canaux potassiques KCNK3/TASK-1 et KATP dans la pathogenèse de l'hypertension artérielle pulmonaire

Archive ouverte | Le Ribeuz, Hélène | CCSD

Pulmonary arterial hypertension (PAH) is a devastating cause of PH due to a progressive narrowing of the distal pulmonary arteries (<500 µm in diameter) resulting in high pulmonary vascular resistance and right heart failure. To d...

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Archive ouverte | Antigny, Fabrice | CCSD

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Implication of Potassium Channels in the Pathophysiology of Pulmonary Arterial Hypertension

Archive ouverte | Le Ribeuz, Hélène | CCSD

International audience. Pulmonary arterial hypertension (PAH) is a rare and severe cardiopulmonary disease without curative treatments. PAH is a multifactorial disease that involves genetic predisposition, epigeneti...

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