Stephanie I. Miller

The paper evaluates and combines four epitope-based labeling systems for live-imaging of endogenous proteins in C. elegans, showing their effectiveness and advantages over direct labeling.

This study uses single-molecule imaging in C. elegans embryos to show that P granules concentrate mRNAs but do not directly promote translation.

This study shows PLK-1 phosphorylation regulates MEX-1 polarization in C. elegans zygotes, similar to its role in POS-1 segregation.

The paper adapts the SapTrap method to efficiently assemble MosSCI targeting vectors in C. elegans containing promoters, 3UTR, and gene fragments.