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Decreased SH3BP2 Inhibits Osteoclast Differentiation and Function
Germline mutations in SH3BP2 gene have been identified in patients with cherubism, a skeletal disorder characterized by excessive osteoclastic bone resorption that is limited to the mandible and maxilla. We previously demonstrated that SH3BP2 overexpression in Raw264.7 cells increased RANKL-induced...
Gorde:
| Egile Nagusiak: | , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2011
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3150609/ https://ncbi.nlm.nih.gov/pubmed/21448930 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jor.21408 |
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