Heike Rebholz

This study identifies a CK2α-G3BP1 signaling axis critical for neuronal translation and development, showing its disruption causes OCNDS pathology.

This paper creates a knockin mouse model with a K198R mutation in CK2 kinase, showing ASD-like behaviors and synaptic deficits, validating it as a model for Okur-Chung Neurodevelopmental Syndrome.

This study shows that enhancing sonic hedgehog signaling reduces L-Dopa-induced dyskinesia in Parkinson's models by targeting dopamine neurons and cholinergic interneurons.