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[PubMed] [Google Scholar] Chen Y., Mestek A., Liu J., Yu L
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They provide a phenolic hydroxyl group that reacts with free radicals, thereby inhibiting oxidative mechanisms that contribute to degenerative diseases
10.1242/dev.092882 88 RiccomagnoM
The stronger pharmacokinetic and metabolic stability of icFSP1 renders it suitable for use in vivo (103), making it a promising candidate for targeting FSP1-dependent phase separation in anticancer therapy
doi: 10.1007/s11926-013-0400-9
