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This analysis supports the hypothesis that nausea suppression by GIPR agonism (57, 65, 69) contributes to the better tolerability profile of tirzepatide (15 mg) at doses 6.25x higher than semaglutide (2.4 mg)
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Induccin de hTERT y elongacin de telmeros del sinttico AEDG en fibroblastos fetales humanos en cultivo (in vitro, N0)
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