Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized
about
Loss of FOXA1/2 is essential for the epithelial-to-mesenchymal transition in pancreatic cancerTrisomy-21 gene dosage over-expression of miRNAs results in the haploinsufficiency of specific target proteinsBalanced gene regulation by an embryonic brain ncRNA is critical for adult hippocampal GABA circuitryDLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiencySYNGAP1: Mind the GapPotential Role of Selenoenzymes and Antioxidant Metabolism in relation to Autism Etiology and PathologyTargeted pharmacological treatment of autism spectrum disorders: fragile X and Rett syndromesEpigenetic mechanisms of chronic painSynaptic maturation at cortical projections to the lateral amygdala in a mouse model of Rett syndromeRett syndrome - biological pathways leading from MECP2 to disorder phenotypesEpigenetics of Renal Development and DiseaseUsing mouse models of autism spectrum disorders to study the neurotoxicology of gene-environment interactionsMecp2 deficiency leads to delayed maturation and altered gene expression in hippocampal neuronsDisturbance of cardiac gene expression and cardiomyocyte structure predisposes Mecp2-null mice to arrhythmiasBdnf overexpression in hippocampal neurons prevents dendritic atrophy caused by Rett-associated MECP2 mutationsBrain-specific phosphorylation of MeCP2 regulates activity-dependent Bdnf transcription, dendritic growth, and spine maturationMild expression differences of MECP2 influencing aggressive social behavior.A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome.Rett syndrome mutation MeCP2 T158A disrupts DNA binding, protein stability and ERP responsesAltered microtubule dynamics and vesicular transport in mouse and human MeCP2-deficient astrocytes.Early-life stress links 5-hydroxymethylcytosine to anxiety-related behaviorsMecp2-null mice provide new neuronal targets for Rett syndrome.Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardationChromosome 21-derived microRNAs provide an etiological basis for aberrant protein expression in human Down syndrome brains.Development of a Novel AAV Gene Therapy Cassette with Improved Safety Features and Efficacy in a Mouse Model of Rett SyndromePersistent Unresolved Inflammation in the Mecp2-308 Female Mutated Mouse Model of Rett SyndromeMeCP2 functions largely cell-autonomously, but also non-cell-autonomously, in neuronal maturation and dendritic arborization of cortical pyramidal neurons.Human-specific epigenetic variation in the immunological Leukotriene B4 Receptor (LTB4R/BLT1) implicated in common inflammatory diseasesCross talk between microRNA and epigenetic regulation in adult neurogenesis.MeCP2 regulates Tet1-catalyzed demethylation, CTCF binding, and learning-dependent alternative splicing of the BDNF gene in Turtle.Oxidative brain damage in Mecp2-mutant murine models of Rett syndromeMeCP2 repression of G9a in regulation of pain and morphine reward.Respiratory phenotypes are distinctly affected in mice with common Rett syndrome mutations MeCP2 T158A and R168X.Neuronal activity-regulated gene transcription in synapse development and cognitive function.Alterations of gene expression and glutamate clearance in astrocytes derived from an MeCP2-null mouse model of Rett syndromeA selective histone deacetylase-6 inhibitor improves BDNF trafficking in hippocampal neurons from Mecp2 knockout mice: implications for Rett syndrome.MeCP2 dependent heterochromatin reorganization during neural differentiation of a novel Mecp2-deficient embryonic stem cell reporter line.Acetyl-L-carnitine improves behavior and dendritic morphology in a mouse model of Rett syndrome.Disrupted microRNA expression caused by Mecp2 loss in a mouse model of Rett syndromeSynaptic signaling and aberrant RNA splicing in autism spectrum disorders
P2860
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P2860
Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized
description
2006 nî lūn-bûn
@nan
2006 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized
@ast
Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized
@en
Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized
@nl
type
label
Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized
@ast
Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized
@en
Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized
@nl
prefLabel
Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized
@ast
Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized
@en
Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized
@nl
P3181
P356
P1476
Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized
@en
P2093
Thierry Bienvenu
P2888
P304
P3181
P356
10.1038/NRG1878
P407
P50
P577
2006-06-01T00:00:00Z
P5875
P6179
1038502340