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Figure 3 3.2.2 Pulmonary arterial hypertension Pulmonary arterial hypertension (PAH) is a multifactorial, chronic disease process that results in pulmonary arterial endothelial dysfunction and smooth muscular hypertrophy, leading to right ventricular failure and even death (Humbert et al., 2023

Negi V, Singh P, Singh L, Pandey RK, Kumar S (2024) A comprehensive review on molecular mechanism involved in arsenic trioxide mediated cerebral neurodegenerative and infectious diseases

Scientists took it, tweaked the amino acid sequence, and made it hit harder and last longer in your system

Then, N , N '-dicyclohexylcarbodiimide (DCC) (2.27 g, 11 mmol) was added and stirring was continued at room temperature overnight

Imran, A.A