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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Detalles Bibliográficos
Autores principales: Jo, Alice, Denduluri, Sahitya, Zhang, Bosi, Wang, Zhongliang, Yin, Liangjun, Yan, Zhengjian, Kang, Richard, Shi, Lewis L., Mok, James, Lee, Michael J., Haydon, Rex C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chongqing Medical University 2014
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4326072/
https://www.ncbi.nlm.nih.gov/pubmed/25685828
http://dx.doi.org/10.1016/j.gendis.2014.09.004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4326072/
https://www.ncbi.nlm.nih.gov/pubmed/25685828
http://dx.doi.org/10.1016/j.gendis.2014.09.004

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