Llwytho...
Temporal and regional alterations in NMDA receptor expression in Mecp2-null mice
Our previous postmortem study of girls with Rett Syndrome (RTT), a development disorder caused by MECP2 mutations, found increases in the density of NMDA receptors in the prefrontal cortex of 2–8 year-old girls, while girls older than 10 years had reductions in NMDA receptors compared to age matched...
Wedi'i Gadw mewn:
| Prif Awduron: | , , , , , , |
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| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
2011
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4122218/ https://ncbi.nlm.nih.gov/pubmed/21901842 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ar.21380 |
| Tagiau: |
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