Zheng Fu

This study shows that Katnip deletion in mice causes hydrocephalus by increasing ciliogenesis and reducing neuroprogenitor cell proliferation.

This study shows that a CILK1 variant linked to epilepsy impairs primary cilia and Hedgehog signaling by disrupting KATNIP regulation in mouse cells.

The paper shows that mutating KIF3A's phosphorylation site T674 to Ala in mice does not reproduce the severe ciliopathy defects seen with CILK1 loss of function.

This study investigates the role of ICK in skeletal development using a mouse model, showing that ICK deficiency leads to skeletal abnormalities by impairing chondrocyte proliferation and maturation.