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This property enables the targeted release of encapsulated polyphenolic compounds, facilitating site-specific delivery (70)

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When [ 13 C 5 ]KIV was used as substrate, the TCA cycle intermediates were now clearly labeled, but MMA hepatocytes had significantly lower incorporation of 13 C into these intermediates under all experimental conditions compared with healthy hepatocytes (Figure 4, BE)

Non-alcoholic fatty liver disease as a cause and a consequence of metabolic syndrome

Results vary by dose, route, baseline pigmentation, and cofactors like vitamin C

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