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Overexpression of Shox2 Leads to Congenital Dysplasia of the Temporomandibular Joint in Mice
Our previous study reported that inactivation of Shox2 led to dysplasia and ankylosis of the temporomandibular joint (TMJ), and that replacing Shox2 with human Shox partially rescued the phenotype with a prematurely worn out articular disc. However, the mechanisms of Shox2 activity in TMJ developmen...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2014
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4159784/ https://www.ncbi.nlm.nih.gov/pubmed/25062348 http://dx.doi.org/10.3390/ijms150813135 |