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"The results demonstrated that the interaction between IGF2BP3 and USP16 could be abolished by ribonuclease (RNase) treatment ( Fig. 5 F) and MNX1-AS1 silencing ( Fig. 5 G)."

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"Therefore, we explored whether MNX1-AS1 was required for the interaction between IGF2BP3 and USP16."

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"Overall, these results illustrated that MNX1-AS1 functioned as a scaffold platform for IGF2BP3/USP16 interaction, thereby protecting IGF2BP3 from being degraded by the ubiquitin/proteasome system.To d[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

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"The specific interaction of IGF2BP3 and USP16 was confirmed by Co-IP followed by western blotting ( Fig. 5 B), and the results of RNA-pull-down and RIP assays demonstrated that there was an interactio[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"