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Other relevant examples, such as SG1 and HMRef-gal, have been reported to detect -gal expressing cells in vivo, although not limited to cellular senescence 69,72

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Because appetite signaling, fat-mass regulation, and metabolic control are tightly linked, cagrilintide has become a useful research tool for studying how long-acting amylin agonism may influence weight-related biology and adipose-tissue function across integrated experimental systems [1][3][4]

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