Kenji Matsuno

The paper identifies loop motifs in Myosin1C that determine cellular and organ chirality by swapping these motifs between Myosin1C and Myosin1D and analyzing their effects.

This study investigates chiral actin filament motion induced by myosin XI in vitro, revealing the formation of stable, rotating actin chiral rings through collective motion.

This study identifies Myo1D and Myo1C as drivers of chiral F-actin flows in Drosophila macrophages, contributing to cell chirality.

The paper investigates how distinct cellular dynamics regulate simultaneous morphogenetic processes in Drosophila hindgut development.

The paper uses live imaging to show that cell motility and invasiveness during epithelial delamination in Drosophila are independently regulated and that motility is not required for invasiveness.

The paper validates that cell chirality determines the LR direction of hindgut rotation in Drosophila through statistical analysis of genetic backgrounds.