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Pulmonary Artery Hypertension (PAH) PAH is characterized by elevated pulmonary artery pressure and increased pulmonary vascular resistance, which can lead to maladaptive right ventricular remodeling, heart failure, and even death [105,106]

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DTP cells enter a diapause state, leading to the emergence of more generalized and broad-spectrum drug resistance phenomena in terms of drug response, rather than the specific drug resistance reactions seen in drug resistant cancer cells

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