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Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalitiesMeCP2 post-translational modifications: a mechanism to control its involvement in synaptic plasticity and homeostasis?BDNF deregulation in Rett syndromeMeCP2 Affects Skeletal Muscle Growth and Morphology through Non Cell-Autonomous MechanismsMeCP2 deficiency results in robust Rett-like behavioural and motor deficits in male and female ratsDendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutationsBdnf overexpression in hippocampal neurons prevents dendritic atrophy caused by Rett-associated MECP2 mutationsNetwork hyperexcitability in hippocampal slices from Mecp2 mutant mice revealed by voltage-sensitive dye imaging.Developmental delay in Rett syndrome: data from the natural history study.A selective histone deacetylase-6 inhibitor improves BDNF trafficking in hippocampal neurons from Mecp2 knockout mice: implications for Rett syndrome.Genetic controls balancing excitatory and inhibitory synaptogenesis in neurodevelopmental disorder models.Emerging themes in GABAergic synapse developmentLong-lasting beneficial effects of central serotonin receptor 7 stimulation in female mice modeling Rett syndromeLinking epigenetics to human disease and Rett syndrome: the emerging novel and challenging concepts in MeCP2 research.Hippocampal CA1 pyramidal neurons of Mecp2 mutant mice show a dendritic spine phenotype only in the presymptomatic stage.Modeling Rett syndrome with stem cells.Transient receptor potential channels as novel effectors of brain-derived neurotrophic factor signaling: potential implications for Rett syndrome.Evaluation of current pharmacological treatment options in the management of Rett syndrome: from the present to future therapeutic alternatives.Epigenetics and Neural developmental disorders: Washington DC, September 18 and 19, 2006Longevity in Rett syndrome: analysis of the North American Database.Lack of IL-1R8 in neurons causes hyperactivation of IL-1 receptor pathway and induces MECP2-dependent synaptic defectsRett syndrome: North American database.The BDNF val-66-met Polymorphism Affects Neuronal Morphology and Synaptic Transmission in Cultured Hippocampal Neurons from Rett Syndrome Mice.RNA sequencing and proteomics approaches reveal novel deficits in the cortex of Mecp2-deficient mice, a model for Rett syndrome.Betaine enhances antidepressant-like, but blocks psychotomimetic effects of ketamine in mice.EEA1 restores homeostatic synaptic plasticity in hippocampal neurons from Rett syndrome mice.MeCP2, A Modulator of Neuronal Chromatin Organization Involved in Rett Syndrome.Detection of rarely identified multiple mutations in MECP2 gene do not contribute to enhanced severity in Rett syndrome.
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh
2005年學術文章
@zh-hant
name
Rett syndrome: model of neurodevelopmental disorders.
@ast
Rett syndrome: model of neurodevelopmental disorders.
@en
type
label
Rett syndrome: model of neurodevelopmental disorders.
@ast
Rett syndrome: model of neurodevelopmental disorders.
@en
prefLabel
Rett syndrome: model of neurodevelopmental disorders.
@ast
Rett syndrome: model of neurodevelopmental disorders.
@en
P2860
P1476
Rett syndrome: model of neurodevelopmental disorders.
@en
P2093
Alan K Percy
Jane B Lane
P2860
P304
P356
10.1177/08830738050200090301
P577
2005-09-01T00:00:00Z