MeCP2-Dependent Transcriptional Repression Regulates Excitatory Neurotransmission
- 1 April 2006
- journal article
- other
- Published by Elsevier in Current Biology
- Vol. 16 (7) , 710-716
- https://doi.org/10.1016/j.cub.2006.02.062
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndromeNeurobiology of Disease, 2006
- Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett SyndromeProceedings of the National Academy of Sciences, 2005
- Limited numbers of recycling vesicles in small CNS nerve terminals: implications for neural signaling and vesicular cyclingTrends in Neurosciences, 2001
- Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients.Human Molecular Genetics, 2000
- MECP2 mutations account for most cases of typical forms of Rett syndromeHuman Molecular Genetics, 2000
- Candidate gene analysis in Rett syndrome and the identification of 21 SNPs in XqAmerican Journal of Medical Genetics, 2000
- Rett Syndrome and Beyond: Recurrent Spontaneous and Familial MECP2 Mutations at CpG HotspotsAmerican Journal of Human Genetics, 1999
- Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2Nature Genetics, 1999
- Imaging exocytosis and endocytosisCurrent Opinion in Neurobiology, 1996
- Definition of the Readily Releasable Pool of Vesicles at Hippocampal SynapsesNeuron, 1996