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Expression of Wnt9b and activation of canonical Wnt signaling during midfacial morphogenesis in mice
Cleft lip with or without cleft palate (CLP) is the most common craniofacial birth defect in humans. Recently, mutations in the WNT3 and Wnt9b genes, encoding two members of the Wnt family of signaling molecules, were found associated with CLP in human and mice, respectively. To investigate whether...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2559872/ https://ncbi.nlm.nih.gov/pubmed/16496313 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/dvdy.20723 |
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