Epigenetics in the mature mammalian brain: Effects on behavior and synaptic transmission
Keywords: HDAC; DNA methylation; MeCP2; Neurotransmission; Synaptic plasticity
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F4-neuroprostanes mediate neurological severity in Rett syndrome
Keywords: Rett syndrome; MeCP2; CDKL5; Neuroprostanes; Autism spectrum disorders; Ï-3 polyunsaturated fatty acids;
Synaptic plasticity deficits in an experimental model of rett syndrome: long-term potentiation saturation and its pharmacological reversal
Keywords: MECP2; Rett syndrome; memantine; LTP; plasticityfEPSPs, field excitatory postsynaptic potentials; HFS, high frequency stimulation; LTP, long-term potentiation; MeCP2, methyl-CpG-binding protein 2; PPF, paired-pulse facilitation; PTP, posttetanic potentiat
Rett Syndrome: From Bed to Bench
Keywords: animal model; MECP2; Rett Syndrome
Zinc-finger protein 90 negatively regulates neuron-restrictive silencer factor-mediated transcriptional repression of fetal cardiac genes
Keywords: NRSE; neuron-restrictive silencer element; NRSF; neuron-restrictive silencer factor; Zfp; zinc finger protein; DBD; DNA-binding domain; CHF; chronic heart failure; ANP; atrial natriuretic peptide; BNP; brain natriuretic peptide; MeCP2; methyl CpG-binding
Genomic and transcriptomic analyses distinguish classic Rett and Rett-like syndrome and reveals shared altered pathways
Keywords: Rett; Rett-like; RTT; MECP2; NTNG1; CDKL5; MBD2; FOXG1; Mutation analysis; mtDNA sequencing; Copy number; Microarray; Genome-wide gene expression profiling; Functional pathway analysis; Genes related to Rett phenotype
What the nose knows, what the eyes see, how we feel, how we learn, how we understand motor acts, why “YY” is essential for ion transport, how epigenetics meet neurobiology in Rett syndrome: seven topics at the 2010 Kavli Prize Symposium on Neuroscience
Keywords: FHM2; familial hemiplegic migraine 2; LIP; lateral intraparietal area; MD; monocular deprivation; MeCP2; methyl-CpG-binding protein 2; NKA; Na+K+ATPase; SM; an anonymous patient;
MeCP2 is required for global heterochromatic and nucleolar changes during activity-dependent neuronal maturation
Keywords: MeCP2; methyl-CpG binding protein 2; MeCP2e1; isoform of MeCP2; MBD; methyl-binding domain; RTT; Rett syndrome; DIV; days in vitro; rDNA; ribosomal DNA; MeCP2; DNA methylation; Maturation; Chromatin; Nucleoli; Neuronal; Epigenetic; Neurodevelopmental; Ret
Longevity in Rett Syndrome: Analysis of the North American Database
Keywords: IRSA; International Rett Syndrome Association; MECP2; Methyl-CpG-binding protein 2 gene; RTT; Rett syndrome;
Altered bone matrix mineralization in a patient with Rett syndrome
Keywords: Bone matrix; Mineralization; Rett syndrome; MECP2; Scoliosis
Identification and characterization of novel sequence variations in MECP2 gene in Rett syndrome patients
Keywords: MECP2; Rett syndrome; Mutation screening; X-linked dominant disease
Synaptic circuit abnormalities of motor-frontal layer 2/3 pyramidal neurons in a mutant mouse model of Rett syndrome
Keywords: MeCP2; Rett syndrome; Cortical circuits; Circuitopathy; Laser scanning photostimulation; Glutamate uncaging
Expression analysis and mutation detection of DLX5 and DLX6 in autism
Keywords: Autism; MECP2; DLX5; DLX6; PEG10; Imprinting; 7q; Mutation
MeCP2 functions largely cell-autonomously, but also non-cell-autonomously, in neuronal maturation and dendritic arborization of cortical pyramidal neurons
Keywords: MeCP2; Rett syndrome; Mecp2-null mice; Neuronal maturation; Physical chimeras; Dendritic complexity; Callosal projection neurons
Early abnormalities of post-sigh breathing in a mouse model of Rett syndrome
Keywords: MeCP2; Breathing symptoms; Sigh; Post-sigh apnoea; Bradypnoea
CDKL5 is a brain MeCP2 target gene regulated by DNA methylation
Keywords: Rett syndrome; Neurodevelopmental disorders; Drug of abuse; Epigenetics; DNA methylation; Chromatin remodeling; MeCP2
MeCP2 Controls an Epigenetic Pathway That Promotes Myofibroblast Transdifferentiation and Fibrosis
Keywords: BDL; bile duct ligation; CCl4; carbon tetrachloride; ChIP; chromatin immunoprecipitation; CREB; adenosine 3â²,5â²-cyclic monophosphate response element-binding protein; HSC; hepatic stellate cell; MeCP2; methyl-CpG binding protein 2; PPARγ; peroxisome
Monoamine deficits in the brain of methyl-CpG binding protein 2 null mice suggest the involvement of the cerebral cortex in early stages of Rett syndrome
Keywords: RTT; neurodevelopment; autism; mental retardation; norepinephrine; serotonin; Adrα2a; adrenergic receptor α2a; Adrβ2; adrenergic receptor β2; ANOVA; analysis of variance; BSA; bovine serum albumin; CSF; cerebrospinal fluid; DA; dopamine; DAB; diaminob
Altered expression of Autism-associated genes in the brain of Fragile X mouse model
Keywords: Autism; Fragile X; WNT2; MECP2; FMR1; Mutagegesis; Real-time PCR
Evidence for both neuronal cell autonomous and nonautonomous effects of methyl-CpG-binding protein 2 in the cerebral cortex of female mice with Mecp2 mutation
Keywords: Rett syndrome; MeCP2; Mouse models; Brain; Motor cortex; Spines; Morphometry
Breathing disorders in Rett syndrome: Progressive neurochemical dysfunction in the respiratory network after birth
Keywords: Rett syndrome (RTT); Respiratory dysfunction; Breathing disorders; MeCP2; Brain derived neurotrophic factor; Norepinephrine
Neuronal differentiation of neural precursor cells is promoted by the methyl-CpG-binding protein MeCP2
Keywords: MeCP2; Rett syndrome; Epigenetics; Differentiation; Neural stem cells; Cytokine; Transplantation
Interaction between the inner nuclear membrane lamin B receptor and the heterochromatic methyl binding protein, MeCP2
Keywords: MeCP2; LBR; Heterochromatin; Nuclear membrane
Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant)
Keywords: Rett syndrome; Preserved speech variant; Zappella variant; Diagnostic criteria; Statistical analysis; MECP2
Distinct HIC1-SIRT1-p53 Loop Deregulation in Lung Squamous Carcinoma and Adenocarcinoma Patients
Keywords: 5-aza-dC; 5-aza-2â²-deoxycytidine; AD; adenocarcinoma; DBC1; deleted in breast cancer 1; H3K9me; histone H3 methylated at Lys9; H3K9ac; histone H3 acetylated at Lys9; HIC1; hypermethylation in cancer 1; MeCP2; methyl CpG binding protein 2; NSCLC; non-sma
Early breathing defects after moderate hypoxia or hypercapnia in a mouse model of Rett syndrome
Keywords: Hypoxia; Hypercapnia; Mecp2; Rett syndrome; Tidal volume
Bdnf overexpression in hippocampal neurons prevents dendritic atrophy caused by Rett-associated MECP2 mutations
Keywords: MeCP2; Rett; Dendrite; Axon; Pyramidal neuron; BDNF; Hippocampus;
InterRett, a model for international data collection in a rare genetic disorder
Keywords: RTT, Rett syndrome; MECP2, methyl CpG binding protein 2; ARSD, Australian Rett syndrome databaseRett syndrome; International database; Rare disorder; MECP2; Phenotype
Activity-dependent NR2B expression is mediated by MeCP2-dependent epigenetic regulation
Keywords: NMDA receptor; NR2B; MeCP2; Epigenetic regulation; DNA methylation; Synaptic plasticity
MeCP2 preferentially binds to methylated linker DNA in the absence of the terminal tail of histone H3 and independently of histone acetylation
Keywords: MeCP2; Chromatin; Nucleosome; DNA methylation; Histones; Acetylation
Epigenetic regulation of the estrogen receptor alpha promoter in the cerebral cortex following ischemia in male and female rats
Keywords: stroke; methylation; methyl binding proteins; estrogen; âAb; âantibody; BDNF; brain-derived neurotrophic factor; ChIP; chromatin immunoprecipitation; ERα; estrogen receptor alpha; ERβ; estrogen receptor beta; IHC; immunohistochemistry; IR; immunorea
MeCP2 mutation causes distinguishable phases of acute and chronic defects in synaptogenesis and maintenance, respectively
Keywords: MeCP2; Rett syndrome; Olfactory system; Olfactory sensory neurons; Neurodevelopment; Regeneration; Process outgrowth; Synaptogenesis
MECP2 mutant allele in a boy with Rett syndrome and his unaffected heterozygous mother
Keywords: MECP2; Rett syndrome; Mental retardation; X-linked disease
Low significance of MECP2 mutations as a cause of mental retardation in Brazilian males
Keywords: MECP2; Mental retardation; Male patients; XLMR
Postnatal dietary choline supplementation alters behavior in a mouse model of Rett syndrome
Keywords: Mecp2; Acetylcholine; Rotor-rod
Sleep problems in Rett syndrome
Keywords: MECP2; Rett syndrome; Sleep problems
Mutation screening of the MECP2 gene in a large cohort of 613 fragile-X negative patients with mental retardation
Keywords: Mental retardation; MECP2; Mutation; Polymorphism; Molecular screening
Mecp2 deficiency leads to delayed maturation and altered gene expression in hippocampal neurons
Keywords: Neuronal maturation; Mecp2; Synaptogenesis; Dendritic spines; Rett Syndrome; Hippocampus
MECP2 mutations are an infrequent cause of mental retardation associated with neurological problems in male patients
Keywords: Male patients; MECP2; Rett variant; Unexplained mental retardation
Brain magnetic resonance study of Mecp2 deletion effects on anatomy and metabolism
Keywords: Rett syndrome; Mecp2; Mental retardation; Brain imaging; Brain magnetic resonance spectroscopy; Metabolism; Neurons; Astrocytes
Predictors of seizure onset in Rett syndrome
Keywords: CDKL5; Cyclin-dependent kinase-like 5; HC; Head circumference; HR; Hazard ratio; IQR; Interquartile range; MECP2; Methyl-CpG binding protein 2; NLS; Nuclear localization signal; RTT; Rett syndrome; STK9; Serine threonine kinase 9; TRD; Transcription repre
Postnatal Loss of Methyl-CpG Binding Protein 2 in the Forebrain is Sufficient to Mediate Behavioral Aspects of Rett Syndrome in Mice
Keywords: MeCP2; Rett syndrome; knockout; behavior; animal model
Spectrum and distribution of MECP2 mutations in 424 Rett syndrome patients: a molecular update
Keywords: MECP2; Rett syndrome; Mutations
Classic Rett syndrome in a boy with R133C mutation of MECP2
Keywords: Male Rett syndrome; MECP2; Preserved speech variant; R133C;
A transcriptional repressor MeCP2 causing Rett syndrome is expressed in embryonic non-neuronal cells and controls their growth
Keywords: Development and regeneration; Glia and other non-neuronal cells; Astrocyte; MeCP2; DNA methylation; Epigenetic; Rett Syndrome; Microcephaly;
Defect in normal developmental increase of the brain biogenic amine concentrations in the mecp2-null mouse
Keywords: Mecp2; Rett syndrome; Biogenic amines; Neurotransmitters;
The A140V mutation in the MECP2 gene is not a common etiological factor among Brazilian mentally retarded males
Keywords: MECP2; Methylation; Chromatin remodeling; Mental retardation; MBP;
Mutation analysis of methyl-CpG binding protein family genes in autistic patients
Keywords: Autism; Methyl-CpG binding protein genes; MECP2; MBD1;
Histone modifications in Rett syndrome lymphocytes: a preliminary evaluation
Keywords: Rett syndrome; MeCP2; Histone; Acetylation; Neurologic impairment;
Genotype and early development in Rett syndrome: The value of international data
Keywords: Rett syndrome; MECP2; Phenotype; Early development; International; Internet; Database;