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Fig. 2 | Orphanet Journal of Rare Diseases

Fig. 2

From: Pathogenic mechanisms of osteogenesis imperfecta, evidence for classification

Fig. 2

Bone mineralization disorders & osteoblastic differentiation and functional defects

OASIS: old astrocyte-specific inducible substance; S1P, S2P: endopeptidases on the Golgi apparatus that together form the Regulatory Intramembrane Protein Hydrolysis System (RIP); WNT1: a secreted ligand; LRP5/6: low-density lipoprotein receptor-related protein 5/6; Frizzled: receptor on the cell membrane, a seventh transmembrane protein; BMP: bone morphogenetic protein.

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