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Consequently, balancing phototherapeutic performance with synthetic simplicity and reproducibility remains a critical consideration for advancing CQD-based systems toward clinical translation

Agliardi C, Guerini FR, Saresella M, et al

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Simultaneously, the most abundant circulating GIP fragment GIP(3-42) was identified as a GIP receptor antagonist with the ability to moderate GIP-induced cAMP production and insulin secretion in vitro (65) ( Table 1 )

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