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Mesoderm-specific Stat3 deletion affects expression of Sox9 yielding Sox9-dependent phenotypes
To date, mutations within the coding region and translocations around the SOX9 gene both constitute the majority of genetic lesions underpinning human campomelic dysplasia (CD). While pathological coding-region mutations typically result in a non-functional SOX9 protein, little is known about what m...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Public Library of Science
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319801/ https://www.ncbi.nlm.nih.gov/pubmed/28166224 http://dx.doi.org/10.1371/journal.pgen.1006610 |