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Retatrutide went a step further, activating GLP-1, GIP, and glucagon receptors simultaneously, creating what researchers describe as a triple agonist with complementary and additive mechanisms

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The current understanding of p53 dysfunction has significantly promoted the development of therapeutic strategies targeting p53

Besides, the relationship between FGFR1 and androgen has been reported in studies of the transition of hormone-naive to castrate-resistant prostate cancer 43

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