Regulation of sh3px1 by dnedd4-long at the drosophila neuromuscular junction

HIGHLIGHTS

• who: Samantha S. Wasserman from the Fly stocks All fly strains and crosses are depicted in Table S The UASGal, system was used to drive tissue-specific overexpression of dNedd, isoforms or mutants in all transgenic lines. SH , mutant larvae, kindly provided by Dr. K. O'Connor-Giles (Wisconsin University), were generated using CRISPR-mediated homology-directed repair to replace a portion of the coding sequence from the SH , locus with a, ⫻P3-DsRed marker (25). All flies were maintained at room temperature on standard food and all experiments were performed at , °C. The dNedd, null mutant . . .
  

   

  

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