Rett syndrome: a prototypical neurodevelopmental disorder
about
Childhood developmental disorders: an academic and clinical convergence point for psychiatry, neurology, psychology and pediatricsMeCP2 post-translational modifications: a mechanism to control its involvement in synaptic plasticity and homeostasis?Dendritic spine dysgenesis in autism related disordersGenetic modifiers of MeCP2 function in Drosophila.MeCP2: the chromatin connection and beyondA partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndromeSex bias in copy number variation of olfactory receptor gene family depends on ethnicityLoss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome.Network hyperexcitability in hippocampal slices from Mecp2 mutant mice revealed by voltage-sensitive dye imaging.Improvement of the Rett syndrome phenotype in a MeCP2 mouse model upon treatment with levodopa and a dopa-decarboxylase inhibitorSleep, plasticity and the pathophysiology of neurodevelopmental disorders: the potential roles of protein synthesis and other cellular processes.High levels of MeCP2 depress MHC class I expression in neuronal cells.Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardationAutism and other neuropsychiatric symptoms are prevalent in individuals with MeCP2 duplication syndrome.Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.Dendritic spine dysgenesis in Rett syndrome.Disrupted microRNA expression caused by Mecp2 loss in a mouse model of Rett syndromeGestational hypoxia and epigenetic programming of brain development disorders.Cure therapeutics and strategic prevention: raising the bar for mental health research.15q11.2-13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain.Structural, Dynamical, and Energetical Consequences of Rett Syndrome Mutation R133C in MeCP2.Early life stress inhibits expression of a novel innate immune pathway in the developing hippocampus.Cerebellar associative sensory learning defects in five mouse autism models.Heightened Delta Power during Slow-Wave-Sleep in Patients with Rett Syndrome Associated with Poor Sleep Efficiency.Hippocampal CA1 pyramidal neurons of Mecp2 mutant mice show a dendritic spine phenotype only in the presymptomatic stage.The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders.Newborn screening and prenatal diagnosis for Rett syndrome: implications for therapy.The relationship of Rett syndrome and MECP2 disorders to autism.Transient receptor potential channels as novel effectors of brain-derived neurotrophic factor signaling: potential implications for Rett syndrome.X-linked mental retardation and epigenetics.Layered hydrogels accelerate iPSC-derived neuronal maturation and reveal migration defects caused by MeCP2 dysfunction.Molecular basis of genetic neuropsychiatric disordersSpecific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.Respiratory circuits: function, mechanisms, topology, and pathology.Brief report: MECP2 mutations in people without Rett syndrome.Mitochondrial Dysfunction in the Pathogenesis of Rett Syndrome: Implications for Mitochondria-Targeted Therapies.MeCP2 and Rett syndrome: reversibility and potential avenues for therapy.Rett syndrome and MeCP2.Brief report: systematic review of Rett syndrome in males.MeCP2-regulated miRNAs control early human neurogenesis through differential effects on ERK and AKT signaling.
P2860
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P2860
Rett syndrome: a prototypical neurodevelopmental disorder
description
2004 nî lūn-bûn
@nan
2004 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Rett syndrome: a prototypical neurodevelopmental disorder
@ast
Rett syndrome: a prototypical neurodevelopmental disorder
@en
Rett syndrome: a prototypical neurodevelopmental disorder
@nl
type
label
Rett syndrome: a prototypical neurodevelopmental disorder
@ast
Rett syndrome: a prototypical neurodevelopmental disorder
@en
Rett syndrome: a prototypical neurodevelopmental disorder
@nl
prefLabel
Rett syndrome: a prototypical neurodevelopmental disorder
@ast
Rett syndrome: a prototypical neurodevelopmental disorder
@en
Rett syndrome: a prototypical neurodevelopmental disorder
@nl
P2860
P3181
P356
P1433
P1476
Rett syndrome: a prototypical neurodevelopmental disorder
@en
P2860
P304
P3181
P356
10.1177/1073858403260995
P407
P577
2004-04-01T00:00:00Z