recent investigation involving mutated RUNX 2 in Cleido Cranial Dysplasia associated mouse model clearly demonstrated that the de novo repression or activation of this gene might be used to stimulate new tooth formation in the mouse.
recent investigation involving mutated RUNX 2 in Cleido Cranial Dysplasia associated mouse model clearly demonstrated that the de novo repression or activation of this gene might be used to stimulate new tooth formation in the mouse.