Daichi Kamiyama

The paper examines postsynaptic morphogenetic strategies in Drosophila embryonic muscles during neuromuscular junction formation, revealing distinct myopodial organization across different muscle types.

The paper demonstrates 2D nonlinear structured illumination microscopy (NSIM) using rsEGFP2 to achieve sub-80 nm resolution for live-cell actin imaging.

The paper presents a method to label endogenous proteins in a cell-type-specific manner using the split GFP system in Drosophila, demonstrating its application with the Ten-m gene.

This study identifies the Vap33/Eph/Vav/Cdc42 complex as a temporal regulator of primary dendrite outgrowth in Drosophila neurons by integrating signals from multiple pathways.