טוען...
Rescue of Methyl-CpG Binding Protein 2 Dysfunction-induced Defects in Newborn Neurons by Pentobarbital
Rett syndrome is a neurodevelopmental disorder that usually arises from mutations or deletions in methyl-CpG binding protein 2 (MeCP2), a transcriptional regulator that affects neuronal development and maturation without causing cell loss. Here, we show that silencing of MeCP2 decreased neurite arbo...
שמור ב:
| הוצא לאור ב: | Neurotherapeutics |
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| Main Authors: | , , , , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Springer US
2015
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4404443/ https://ncbi.nlm.nih.gov/pubmed/25753729 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13311-015-0343-0 |
| תגים: |
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