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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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Russell, Juliet C., Blue, Mary E., Johnston, Michael V., Naidu, Sakkubai, Hossain, Mir Ahamed
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2007
Gaiak:
Sarrera elektronikoa: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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