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Pulmonary Hypertension (PH) is a vascular disease characterized by persistently elevated pulmonary arterial pressure. Common modeling methods include single-dose SU5416 combined with hypoxia exposure, chronic hypoxia, and monocrotaline (MCT) induction. These models are widely used to investigate vascular remodeling, right heart failure, and the mechanisms of action of anti-PH therapies.
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