The effect of the cleidocranial dysplasia-related novel 1116_1119insC mutation in the RUNX2 gene on the biological function of mesenchymal cells. [electronic resource]
Producer: 20130917Description: 180-7 p. digitalISSN:- 1878-0849
- Adult
- Cell Differentiation -- genetics
- Cell Proliferation
- Cleidocranial Dysplasia -- diagnosis
- Core Binding Factor Alpha 1 Subunit -- genetics
- Frameshift Mutation
- Humans
- Male
- Mesenchymal Stem Cells -- cytology
- Mutagenesis, Insertional
- Osteoblasts -- cytology
- Osteogenesis -- genetics
- Wnt Signaling Pathway
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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