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Enhanced Cell Death in MeCP2 Null Cerebellar Granule Neurons Exposed to Excitotoxicity and Hypoxia
Rett syndrome (RTT) is associated with mutations in the transcriptional repressor gene MeCP2. Although the clinical and neuropathological signs of RTT suggest disrupted synaptic function, the specific role of MeCP2 in postmitotic neurons remains relatively unknown. We examined whether MeCP2 deficien...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2007
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2227264/ https://ncbi.nlm.nih.gov/pubmed/17997046 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuroscience.2007.09.076 |
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