Hayate Suzuki

This study uses a Col22a1-EGFP reporter to visualize and analyze the dynamic three-dimensional structure of the myotendinous junction across development and in response to mechanical stress.

The paper introduces a novel method for functional analysis of non-coding regions by inducing random mutations in target genomic regions using CRISPR and transposase in mouse embryonic stem cells.

This study improves transgenic mouse production efficiency using piggyBac, enabling phenotyping in the founder generation and demonstrating application with bacterial artificial chromosome transgenes.