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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...
| Autores principales: | , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2010
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3001432/ https://www.ncbi.nlm.nih.gov/pubmed/21108844 http://dx.doi.org/10.1186/1471-213X-10-116 |