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Full UPF3B function is critical for neuronal differentiation of neural stem cells
BACKGROUND: Mutation in the UPF3B gene on chromosome X is implicated in neurodevelopmental disorders including X-linked intellectual disability, autism and schizophrenia. The protein UPF3B is involved in the nonsense-mediated mRNA decay pathway (NMD) that controls mRNA stability and functions in the...
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| Publicado no: | Mol Brain |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4445987/ https://ncbi.nlm.nih.gov/pubmed/26012578 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13041-015-0122-1 |
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