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Additional experiments using isoform-specific inhibitors, eNOS phosphorylation analysis, genetic knockdown, VEGFR2 neutralization, and rescue designs would be needed to define the pathway more precisely

Its stability, mechanisms, and preclinical/clinical evidence position it as a valuable tool in compounding education and practice

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It is engineered with GIP-biased affinity, reflecting the hypothesis that balanced dual activation yields superior metabolic effects compared with GLP-1 activation alone