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Genetic Modifiers of MeCP2 Function in Drosophila
The levels of methyl-CpG–binding protein 2 (MeCP2) are critical for normal post-natal development and function of the nervous system. Loss of function of MeCP2, a transcriptional regulator involved in chromatin remodeling, causes classic Rett syndrome (RTT) as well as other related conditions charac...
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| Hauptverfasser: | , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Public Library of Science
2008
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2518867/ https://ncbi.nlm.nih.gov/pubmed/18773074 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1000179 |
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