MeCP2 Mutation Results in Compartment-Specific Reductions in Dendritic Branching and Spine Density in Layer 5 Motor Cortical Neurons of YFP-H Mice
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference91 articles.
1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.;RE Amir;Nat Genet,1999
2. Clinical manifestations and stages of Rett syndrome.;B Hagberg;Ment Retard Dev Disabil Res Rev,2002
3. The story of Rett syndrome: from clinic to neurobiology.;M Chahrour;Neuron,2007
4. Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome.;Y Asaka;Neurobiol Dis,2006
5. MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number.;HT Chao;Neuron,2007
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