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Methyl-CpG-binding protein 2 binding disruption during neuronal maturation
PubMed Full text in PMC Similar studies GEO Profiles Analyze DataSet
Identifying targets of MeCP2 during neuronal maturational differentiation
PubMed Full text in PMC Similar studies Analyze with GEO2R
MeCP2 binds to mCH as neurons mature, influencing transcription and onset of Rett syndrome
PubMed Full text in PMC Similar studies
MeCP2 binds to mCH as neurons mature, influencing transcription and onset of Rett syndrome [mRNA-Seq]
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MeCP2 binds to mCH as neurons mature, influencing transcription and onset of Rett syndrome [Mnase-Seq]
MeCP2 binds to mCH as neurons mature, influencing transcription and onset of Rett syndrome [ChIP-Seq]
Gene expression profiles of wild type and Mecp2-null mice in three different regions of the brain
Expression in Superior Frontal Gyrus of normal individuals or females of different ages affected by Rett syndrome
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Rett syndrome: brain frontal cortex
PubMed Similar studies GEO Profiles Analyze DataSet
Cerebellar gene expression profiles of mouse models for Rett Syndrome reveal MeCP2 targets
Activity-dependent aberrations in gene expression and alternative splicing in a mouse model of Rett syndrome
Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes
RNA-Sequencing and proteomics approaches reveal multi-cellular deficits in the cortex of Rett syndrome mice
Vitamin D modulates cortical transcriptome in an Mecp2 heterozygous Rett syndrome mouse model
Genome-wide Analysis Reveals Mecp2-dependent Regulation of MicroRNAs in a Mouse Model of Rett Syndrome
Genome-wide Analysis Reveals Mecp2-dependent Regulation of MicroRNAs in a Mouse Model of Rett Syndrome (high-throughput sequencing)
Genome-wide Analysis Reveals Mecp2-dependent Regulation of MicroRNAs in a Mouse Model of Rett Syndrome (mm8 promoter arrays)
Genome-wide Analysis Reveals Mecp2-dependent Regulation of MicroRNAs in a Mouse Model of Rett Syndrome (mm8 tiling array)
Length-dependent gene misregulation in Rett syndrome (RNA-Seq)
Length-dependent gene misregulation in Rett syndrome (ChIP-Seq 2)
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