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Loss of MeCP2 in immature neurons leads to impaired network integration
Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutations or deletions in Methyl-CpG-binding Protein 2 (MeCP2), a brain-enriched transcriptional regulator. MeCP2 is highly expressed during neuronal maturation and its deficiency results in impaired dendritic morphogenesis and reduced d...
Tallennettuna:
| Julkaisussa: | Hum Mol Genet |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Oxford University Press
2019
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6322069/ https://ncbi.nlm.nih.gov/pubmed/30277526 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy338 |
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