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Hoxa2 Inhibits Bone Morphogenetic Protein Signaling during Osteogenic Differentiation of the Palatal Mesenchyme
Cleft palate is one of the most common congenital birth defects worldwide. The homeobox (Hox) family of genes are key regulators of embryogenesis, with Hoxa2 having a direct role in secondary palate development. Hoxa2(−/−) mice exhibit cleft palate; however, the cellular and molecular mechanisms lea...
Tallennettuna:
| Julkaisussa: | Front Physiol |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Frontiers Media S.A.
2017
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5694536/ https://ncbi.nlm.nih.gov/pubmed/29184513 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2017.00929 |
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