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...

Descrizione completa

Dettagli Bibliografici

Autori principali:	Zoe H Mitchell, Joery den Hoed, Willemijn Claassen, Martina Demurtas, Laura Deelen, Philippe M Campeau, Karen Liu, Simon E Fisher, Marco Trizzino
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Springer Nature 2025-08-01
Serie:	EMBO Reports
Soggetti:	NuRD CHD3 Cranial Neural Crest Snijders Blok–Campeau Syndrome BMP
Accesso online:	https://doi.org/10.1038/s44319-025-00555-w
Tags:	Aggiungi Tag Nessun Tag, puoi essere il primo ad aggiungerne!!