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J Pain Res (2018) 11:312940

Recurrence is seen in all patients

This medication potently inhibits the URAT1 transporter to a lesser extent, which also affects ABCG2, OAT1, and OAT3

Secondary structure predictions with BeStSel 51 revealed almost identical content of -sheets and -turns, and absence of -helices, between recombinant and synthetic l-/d-DAM27 versions (Table S6)