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Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology
The neurodevelopmental disorder Rett Syndrome (RTT) is caused by sporadic mutations in the transcriptional factor methyl-CpG binding protein 2 (MeCP2). Although it is thought that the primary cause of RTT is cell autonomous due to lack of functional MeCP2 in neurons, whether non-cell autonomous fact...
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| Hlavní autoři: | , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2009
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3134296/ https://ncbi.nlm.nih.gov/pubmed/19234456 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nn.2275 |
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