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Consistent with these in vitro findings, co-immunoprecipitation assays in G2-synchronized HeLa cells revealed that Myc-tagged Pds5B associated with wild-type Sororin-GFP, but not with the phospho-mimetic Sororin-S145E-GFP mutant (Supplementary Fig

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Current research reveals several critical limitations: insufficient investigation into the material basis of Mongolian drugs, a lack of systematic pharmacological studies, unclear pharmacokinetic properties, ambiguous compatibility principles in formulation, and slow progress in the development of new Mongolian medicines (Song et al., 2021)