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β-catenin/cyclin D1 mediated development of suture mesenchyme in calvarial morphogenesis
BACKGROUND: Mouse genetic study has demonstrated that Axin2 is essential for calvarial development and disease. Haploid deficiency of β-catenin alleviates the calvarial phenotype caused by Axin2 deficiency. This loss-of-function study provides evidence for the requirement of β-catenin in exerting th...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3001432/ https://ncbi.nlm.nih.gov/pubmed/21108844 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-213X-10-116 |
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