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doi: 10.1016/j.semarthrit.2018.08.003
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However, brands should not position GHK-Cu products as a medical treatment
In a bisubstrate-based fluorescence trans-glutamination assay, EA inhibited FXIIIa with a moderate potency ( IC 50 ~ 105 M) and efficacy (Y ~ 66%)
10-12 Although acarbose-induced hepatotoxicity appears to be uncommon, diabetic patients receiving long-term acarbose therapy should be closely monitored for this adverse effect
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