QR Kodea

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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Zoe H Mitchell, Joery den Hoed, Willemijn Claassen, Martina Demurtas, Laura Deelen, Philippe M Campeau, Karen Liu, Simon E Fisher, Marco Trizzino
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: Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!