Fig. 1
From: The role of proteoglycan form of DMP1 in cranial repair
Construction of the cranial defect model. A Graphic representation of the cranial defect model. B DMP1-PG was highly expressed in the defect sites of the model mice, scale bars = 100 µm. C RT‒qPCR quantification of Dmp1 in the defect sites of the WT mice. *p < 0.05, n = 4. D Strategy for the DMP1-PG point mutation in the mouse model. E The expression of DMP1-PG protein (high molecular weight smear) was significantly decreased in the bone matrix in the S89G-DMP1 mice