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Molecular Studies on the Roles of Runx2 and Twist1 in Regulating FGF signaling
BACKGROUND: Supernumerary teeth are often observed in patients suffering from cleidocranial dysplasia due to a mutation in Runx2 that results in haploinsufficiencty. However, the underlying molecular mechanisms are poorly defined. In this study, we assessed the roles of Runx2 and its functional anta...
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| Autori principali: | , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2012
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4153435/ https://ncbi.nlm.nih.gov/pubmed/22972545 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/dvdy.23858 |
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