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FMRP Stalls Ribosomal Translocation on mRNAs Linked to Synaptic Function and Autism

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Genomic insights into MeCP2 function: A role for the maintenance of chromatin architecture

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The Role of MeCP2 in Regulating Synaptic Plasticity in the Context of Stress and Depression

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Epigenetic Factors that Control Pericentric Heterochromatin Organization in Mammals

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MeCP2 Deficiency Leads to Loss of Glial Kir4.1

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MeCP2 Levels Regulate the 3D Structure of Heterochromatic Foci in Mouse Neurons

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Differential roles of epigenetic regulators in the survival and differentiation of oligodendrocyte precursor cells

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A mutation-led search for novel functional domains in MeCP2

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Long genes linked to autism spectrum disorders harbor broad enhancer-like chromatin domainsPreprint

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Exploring the complexity of MECP2 function in Rett syndrome

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Importin α5 Regulates Anxiety through MeCP2 and Sphingosine Kinase 1

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MeCP2 Promotes Colorectal Cancer Metastasis by Modulating ZEB1 Transcription

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Emerging Insights into the Distinctive Neuronal Methylome

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An all-to-all approach to the identification of sequence-specific readers for epigenetic DNA modifications on cytosine

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U1 snRNP Telescripting Roles in Transcription and Its MechanismPreprint

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Dnmt3a knockout in excitatory neurons impairs postnatal synapse maturation and increases the repressive histone modification H3K27me3

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MeCP2 binds to methylated DNA independently of phase separation and heterochromatin organisation

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Transcriptomic Analysis of Mecp2 Mutant Mice Reveals Differentially Expressed Genes and Altered Mechanisms in Both Blood and Brain

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A powerful conditional gene-based association approach implicated functionally important genes for schizophrenia

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The distinct methylation landscape of maturing neurons and its role in Rett syndrome pathogenesis

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Brain phosphorylation of MeCP2 at serine 164 is developmentally regulated and globally alters its chromatin association

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It is a complex issue: emerging connections between epigenetic regulators in drug addiction

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Reciprocal control of translation and transcription in autism spectrum disorder

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Distinctive Klf4 mutants determine preference for DNA methylation status

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Integrated Transcriptome Analyses Revealed Key Target Genes in Mouse Models of Autism

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Quantitative proteomic analysis of Rett iPSC-derived neuronal progenitors

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Transcriptomic Studies in Mouse Models of Rett Syndrome: A Review

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Developmental remodelling of non-CG methylation at satellite DNA repeats

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RNA and neuronal function: the importance of post-transcriptional regulation

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Neurodevelopmental deficits and cell-type-specific transcriptomic perturbations in a mouse model of HNRNPU haploinsufficiency

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Genome-wide redistribution of MeCP2 in dorsal root ganglia after peripheral nerve injury

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Lateralized Expression of Cortical Perineuronal Nets during Maternal Experience is Dependent on MECP2

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Vitamin D Supplementation Rescues Aberrant NF-κB Pathway Activation and Partially Ameliorates Rett Syndrome Phenotypes inMecp2Mutant Mice

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Gene expression and epigenetics reveal species-specific mechanisms acting upon common molecular pathways in the evolution of task division in bees

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Topoisomerase-Mediated DNA Damage in Neurological Disorders

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Examining non-LTR retrotransposons in the context of the evolving primate brain

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Differential dynamics specify MeCP2 function at nucleosomes and methylated DNA

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Acute MeCP2 loss in adult mice reveals transcriptional and chromatin changes that precede neurological dysfunction and inform pathogenesis

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Meta-analysis of classical swine fever prevalence in pigs in India: A 5-year study

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Sex disparate gut microbiome and metabolome perturbations precede disease progression in a mouse model of Rett syndrome

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