snRNA-seq analysis in multinucleated myogenic FSHD cells identifies heterogeneous FSHD transcriptome signatures associated with embryonic-like program activation and oxidative stress-induced apoptosis.
Hum Mol Genet
; 33(3): 284-298, 2024 Jan 20.
Article
in En
| MEDLINE
| ID: mdl-37934801
Key words
Full text:
1
Database:
MEDLINE
Main subject:
Muscular Dystrophy, Facioscapulohumeral
Limits:
Humans
Language:
En
Journal:
Hum Mol Genet
Journal subject:
BIOLOGIA MOLECULAR
/
GENETICA MEDICA
Year:
2024
Type:
Article
Affiliation country:
Netherlands