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...

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Detalles Bibliográficos
Autores principales: Hall, Michael D., Murray, Caroline A., Valdez, Michael J., Perantoni, Alan O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
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

Internet

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

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