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The versatile functions of Sox9 in development, stem cells, and human diseases
The transcription factor Sox9 was first discovered in patients with campomelic dysplasia, a haploinsufficiency disorder with skeletal deformities caused by dysregulation of Sox9 expression during chondrogenesis. Since then, its role as a cell fate determiner during embryonic development has been wel...
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| Publicado no: | Genes Dis |
|---|---|
| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Chongqing Medical University
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4326072/ https://ncbi.nlm.nih.gov/pubmed/25685828 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gendis.2014.09.004 |
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