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(1996) reported the analog was 1.5-2x more potent than equimolar IGF-1 in catabolic rat models, and broader pharmacology literature places it at roughly 3x potency overall
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PMN-MDSCs, on the other hand, facilitate metastasis by restoring the epithelial-to-mesenchymal transition and inducing CSC properties [25]
The FDA has also raised safety concerns around several peptide-related compounding substances
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