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Severe cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2

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Extracellular Signal-Regulated Kinase 1 (ERK1) and ERK2 Play Essential Roles in Osteoblast Differentiation and in Supporting Osteoclastogenesis

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Transcriptional Control of Skeletogenesis

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Expression and function of Dlx genes in the osteoblast lineage

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A Runx2 threshold for the cleidocranial dysplasia phenotype

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Prevention of Trabecular Bone Loss Induced by Estrogen Deficiency by a Selective p38α Inhibitor

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