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Irrespective of L-carnitine supplementation, the proportion of phagocytosing PMN ( Figure 5C ) maintained the initial level for 6 h before peaking significantly at 12 h pi and decreasing to the pre-challenge level until the end of the study

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Mutations in ATP7A and ATP7B can lead to copper metabolism disorders such as Menkes disease and Wilsons disease [41, 42]

These polyphenols also enhance melanocyte pigmentation by promoting TYR activity, a key enzyme in melanin biosynthesis, while simultaneously mitigating UV-induced damage 142

Ann Surg 276: 6673