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

Mechanisms of Regulation of the <i>CHRDL1</i> 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 (<i>CHRDL1</i>) gene is up-regulated in dermal fibroblasts from thr...

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Bibliographic Details
Main Authors: José J. Casasnovas-Nieves, Yacidzohara Rodríguez, Hector L. Franco, Carmen L. Cadilla
Format: Article
Language:English
Published: MDPI AG 2023-08-01
Series:Genes
Subjects:
Setleis syndrome
TWIST transcription factors
bHLH
SREBP1c
ADD1
CHRDL1
Online Access:https://www.mdpi.com/2073-4425/14/9/1733

Internet

https://www.mdpi.com/2073-4425/14/9/1733

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