Mechanisms of Regulation of the CHRDL1 Gene by the TWIST2 and ADD1/SREBP1c Transcription Factors

Setleis syndrome (SS) is a rare focal facial dermal dysplasia caused by recessive mutations in the basic helix-loop-helix (bHLH) transcription factor, TWIST2. Expression microarray analysis showed that the chordin-like 1 (CHRDL1) gene is up-regulated in dermal fibroblasts from three SS patients with...

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Detalles Bibliográficos
Autores principales: Casasnovas-Nieves, José J., Rodríguez, Yacidzohara, Franco, Hector L., Cadilla, Carmen L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10530651/
https://www.ncbi.nlm.nih.gov/pubmed/37761873
http://dx.doi.org/10.3390/genes14091733

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10530651/
https://www.ncbi.nlm.nih.gov/pubmed/37761873
http://dx.doi.org/10.3390/genes14091733

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