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It should be emphasized that the detailed pharmacokinetics of subcutaneous GHK-Cu absorption rate from the subcutaneous depot, plasma concentrationtime curves, tissue distribution, metabolic fate of the peptide backbone, and dose-linearity have not been characterized in controlled human studies
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The key molecules associated with the former include xCT, GSH, GPX4, intracellular labile iron, and ferroptosis-inhibitory pathways
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