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Reduced neuronal size and mTOR pathway activity in the Mecp2 A140V Rett syndrome mouse model
Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutation in the X-linked MECP2 gene, encoding methyl-CpG-binding protein 2. We have created a mouse model ( Mecp2 A140V “knock-in” mutant) expressing the recurrent human MECP2 A140V mutation linked to an X-linked mental retardation/Rett...
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| Izdano u: | F1000Res |
|---|---|
| Glavni autori: | , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
F1000Research
2016
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5040159/ https://ncbi.nlm.nih.gov/pubmed/27781091 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.8156.1 |
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