Chi‐chung Hui

This study shows that Irx3/5 genes are critical for patterning vestibular and cochlear sensory domains in the mammalian inner ear, with their deletion causing structural and cellular abnormalities in the cochlea.

This study investigates the dose-dependent cooperative roles of Irx1 and Irx2 in mouse development, revealing distinct phenotypic outcomes from their genetic ablation.

This study shows that Irx5 deficiency in mice leads to reduced body mass and resistance to diet-induced obesity through increased metabolic rate and decreased adiposity.