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Without direct, head-to-head comparisons between GHK-Cu, AHK-Cu, and DHK-Cu, the fields structurefunction understanding is lacking

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Available evidence comes from ingredient studies rather than the complete formulation

We believe these results are due to the nanomolar agonist concentrations applied, which were selected to simulate receptor activation levels similar to those that might occur physiologically, even if not precisely matching actual in vivo concentrations