The Diverse Consequences of FOXC1 Deregulation in Cancer

Forkhead box C1 (FOXC1) is a transcription factor with essential roles in mesenchymal lineage specification and organ development during normal embryogenesis. In keeping with these developmental properties, mutations that impair the activity of FOXC1 result in the heritable Axenfeld-Rieger Syndrome...

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Detalles Bibliográficos
Autores principales: Gilding, L. Niall, Somervaille, Tim C. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406774/
https://www.ncbi.nlm.nih.gov/pubmed/30764547
http://dx.doi.org/10.3390/cancers11020184

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6406774/
https://www.ncbi.nlm.nih.gov/pubmed/30764547
http://dx.doi.org/10.3390/cancers11020184

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