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Chromatin context and ncRNA highlight targets of MeCP2 in brain
The discovery that Rett syndrome (RTT) is caused by mutation of the methyl-CpG-binding-protein MeCP2 provided a major breakthrough in understanding the neurodevelopmental disorder and accelerated MeCP2 research. However, gene regulation by MeCP2 is complicated. The current consensus for MeCP2 remain...
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| Hauptverfasser: | , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Landes Bioscience
2013
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3907483/ https://ncbi.nlm.nih.gov/pubmed/24270455 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/rna.26921 |
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