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In vivo investigations on mice indicated no discernible poisonousness throughout HPs60 therapy, as demonstrated by the lack of substantial changes in body weight across the groups (488)

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Investment in peptide drug development by pharmaceutical companies continues to increase, reflecting confidence in the therapeutic potential and commercial viability of this drug class

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KD activates peroxisome proliferator-activated receptor gamma to inhibit cyclooxygenase-2-dependent pathways and thereby suppress neuroinflammation in the mouse model of epilepsy (148)