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To confirm that the stimulant effect of TAT-DAT NT was due to its disruptive actions on D2R-DAT protein complexes, we performed co-immunoprecipitation using striatal brain tissues from SD rats that received the treatments

The fluorescent imaging data obtained were consistent with the induction of Met phosphorylation at the Y1234/1235 site, indicating that the dimeric macrocycles actively promoted the initial hallmark phosphorylation

Both require once-weekly injections

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