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doi: 10.1152/ajpendo.1985.249.1.E6 48 YipJGengXShenJDingY

Similar content being viewed by others Introduction Pulmonary Arterial Hypertension (PAH) is a life-threatening disease characterized by vasoconstriction and remodeling of pre-capillary pulmonary arterioles, leading to restriction of blood flow, increases in pulmonary arterial pressure and pulmonary vascular resistance, and eventually right ventricular failure and death 1,2