The NuRD component CHD3 promotes BMP signalling during cranial neural crest cell specification
Abstract Pathogenic genetic variants in the NuRD component CHD3 cause Snijders Blok–Campeau Syndrome, a neurodevelopmental disorder manifesting with intellectual disability and craniofacial anomalies. To investigate the role of CHD3 in craniofacial development, we differentiated control and CHD3-dep...
Gorde:
| Egile Nagusiak: | , , , , , , , , |
|---|---|
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Springer Nature
2025-08-01
|
| Saila: | EMBO Reports |
| Gaiak: | |
| Sarrera elektronikoa: | https://doi.org/10.1038/s44319-025-00555-w |
| Etiketak: |
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!
|
