Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets.
about
DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiencyDevelopmental Dynamics of Rett SyndromeIn Sickness and in Health: Perineuronal Nets and Synaptic Plasticity in Psychiatric DisordersBDNF deregulation in Rett syndromeGenetic modifiers of MeCP2 function in Drosophila.Microglia as a critical player in both developmental and late-life CNS pathologies.Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function.Induced chromosome deletion in a Williams-Beuren syndrome mouse model causes cardiovascular abnormalities.Mecp2-null mice provide new neuronal targets for Rett syndrome.Neonatal maternal deprivation response and developmental changes in gene expression revealed by hypothalamic gene expression profiling in mice.Improved MECP2 Gene Therapy Extends the Survival of MeCP2-Null Mice without Apparent Toxicity after Intracisternal Delivery.Global transcriptional and translational repression in human-embryonic-stem-cell-derived Rett syndrome neurons.MeCP2 mutation results in compartment-specific reductions in dendritic branching and spine density in layer 5 motor cortical neurons of YFP-H mice.GluD1 is a common altered player in neuronal differentiation from both MECP2-mutated and CDKL5-mutated iPS cells.Phospholemman: a novel cardiac stress protein.Disruption of DNA-methylation-dependent long gene repression in Rett syndrome.Setdb1-mediated histone H3K9 hypermethylation in neurons worsens the neurological phenotype of Mecp2-deficient mice.Fetal alcohol exposure alters proopiomelanocortin gene expression and hypothalamic-pituitary-adrenal axis function via increasing MeCP2 expression in the hypothalamus.The role of MeCP2 in CNS development and function.Complexities of Rett syndrome and MeCP2Neuronal MeCP2 is expressed at near histone-octamer levels and globally alters the chromatin state.The protocadherins, PCDHB1 and PCDH7, are regulated by MeCP2 in neuronal cells and brain tissues: implication for pathogenesis of Rett syndrome.Brain region-specific expression of Fxyd1, an Mecp2 target gene, is regulated by epigenetic mechanisms.Synaptic dysfunction in neurodevelopmental disorders associated with autism and intellectual disabilities.MECP2 Is a Frequently Amplified Oncogene with a Novel Epigenetic Mechanism That Mimics the Role of Activated RAS in MalignancyLinking epigenetics to human disease and Rett syndrome: the emerging novel and challenging concepts in MeCP2 research.Effects of Mecp2 loss of function in embryonic cortical neurons: a bioinformatics strategy to sort out non-neuronal cells variability from transcriptome profiling.Depression in pregnancy, infant birth weight and DNA methylation of imprint regulatory elementsCorrecting deregulated Fxyd1 expression ameliorates a behavioral impairment in a mouse model of Rett syndrome.MeCP2 modulates gene expression pathways in astrocytesImpaired in vivo binding of MeCP2 to chromatin in the absence of its DNA methyl-binding domainMECP2 genomic structure and function: insights from ENCODEBreathing dysfunction in Rett syndrome: understanding epigenetic regulation of the respiratory networkMouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus.Cell cloning-based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes.DNA methylation and methyl-CpG binding proteins: developmental requirements and function.MECP2 promotes the growth of gastric cancer cells by suppressing miR-338-mediated antiproliferative effect.Enhanced dense core granule function and adrenal hypersecretion in a mouse model of Rett syndrome.Negative Allosteric Modulation of mGluR5 Partially Corrects Pathophysiology in a Mouse Model of Rett Syndrome.Promoter-like sequences regulating transcriptional activity in neurexin and neuroligin genes
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P2860
Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets.
description
2007 nî lūn-bûn
@nan
2007 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Cerebellar gene expression pro ...... me reveal novel MeCP2 targets.
@ast
Cerebellar gene expression pro ...... me reveal novel MeCP2 targets.
@en
type
label
Cerebellar gene expression pro ...... me reveal novel MeCP2 targets.
@ast
Cerebellar gene expression pro ...... me reveal novel MeCP2 targets.
@en
prefLabel
Cerebellar gene expression pro ...... me reveal novel MeCP2 targets.
@ast
Cerebellar gene expression pro ...... me reveal novel MeCP2 targets.
@en
P2093
P2860
P356
P1433
P1476
Cerebellar gene expression pro ...... me reveal novel MeCP2 targets.
@en
P2093
ChaRandle Jordan
Helen C Kwan
Hong Hua Li
Uta Francke
P2860
P2888
P356
10.1186/1471-2350-8-36
P577
2007-06-20T00:00:00Z
P5875
P6179
1014153384