Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation - Wikidata - wikimedia - TriplyDB

Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation

Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation

http://www.wikidata.org/entity/Q33531946

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Recent advances in understanding synaptic abnormalities in Rett syndrome Daily rhythmic behaviors and thermoregulatory patterns are disrupted in adult female MeCP2-deficient mice Rett syndrome: disruption of epigenetic control of postnatal neurological functions A new synaptic player leading to autism risk: Met receptor tyrosine kinase Essential Roles for ARID1B in Dendritic Arborization and Spine Morphology of Developing Pyramidal Neurons MeCP2 deficiency results in robust Rett-like behavioural and motor deficits in male and female rats Stem cells and modeling of autism spectrum disorders.Female Mecp2(+/-) mice display robust behavioral deficits on two different genetic backgrounds providing a framework for pre-clinical studies.Beyond Widespread Mecp2 Deletions to Model Rett Syndrome: Conditional Spatio-Temporal Knockout, Single-Point Mutations and Transgenic Rescue Mice Rett syndrome mutation MeCP2 T158A disrupts DNA binding, protein stability and ERP responses Morphological and functional reversal of phenotypes in a mouse model of Rett syndrome.Preclinical research in Rett syndrome: setting the foundation for translational success.Twenty-four hour quantitative-EEG and in-vivo glutamate biosensor detects activity and circadian rhythm dependent biomarkers of pathogenesis in Mecp2 null mice.Transcriptome analysis of microglia in a mouse model of Rett syndrome: differential expression of genes associated with microglia/macrophage activation and cellular stress Temporal and regional alterations in NMDA receptor expression in Mecp2-null mice.Drosophila as a model for MECP2 gain of function in neurons.MeCP2 mutation results in compartment-specific reductions in dendritic branching and spine density in layer 5 motor cortical neurons of YFP-H mice.Experimental models of Rett syndrome based on Mecp2 dysfunction.Complexities of Rett syndrome and MeCP2 Aberrant dendritic excitability: a common pathophysiology in CNS disorders affecting memory?Neuronal morphology in MeCP2 mouse models is intrinsically variable and depends on age, cell type, and Mecp2 mutation.Apoptotic Activity of MeCP2 Is Enhanced by C-Terminal Truncating Mutations.A/T Run Geometry of B-form DNA Is Independent of Bound Methyl-CpG Binding Domain, Cytosine Methylation and Flanking Sequence.MicroRNA function is required for neurite outgrowth of mature neurons in the mouse postnatal cerebral cortex.Epigenetics, autism spectrum, and neurodevelopmental disorders.Reduced neuronal size and mTOR pathway activity in the Mecp2 A140V Rett syndrome mouse model Loss of MeCP2 disrupts cell autonomous and autocrine BDNF signaling in mouse glutamatergic neurons MeCP2-Related Diseases and Animal Models.Genetic diseases: congenital central hypoventilation, Rett, and Prader-Willi syndromes.Translating human genetics into mouse: the impact of ultra-rapid in vivo genome editing.Rett syndrome and MeCP2.Genetic alterations of DNA methylation machinery in human diseases.Temporal- and Location-Specific Alterations of the GABA Recycling System in Mecp2 KO Mouse Brains.Autism spectrum disorder: neuropathology and animal models.MECP2 impairs neuronal structure by regulating KIBRA.RNA sequencing and proteomics approaches reveal novel deficits in the cortex of Mecp2-deficient mice, a model for Rett syndrome.Adolescent onset cognitive regression and neuropsychiatric symptoms associated with the A140V MECP2 mutation.[Epigenetic regulation in neuronal differentiation and brain function].Early motor phenotype detection in a female mouse model of Rett syndrome is improved by cross-fostering.ANKRD11 associated with intellectual disability and autism regulates dendrite differentiation via the BDNF/TrkB signaling pathway.

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Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation

http://www.wikidata.org/entity/Q33531946

description

2010 nî lūn-bûn

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2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2010 թվականի փետրվարին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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Abnormalities of cell packing ...... me/X-linked mental retardation

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Abnormalities of cell packing ...... me/X-linked mental retardation

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Abnormalities of cell packing ...... me/X-linked mental retardation

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Abnormalities of cell packing ...... me/X-linked mental retardation

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BMC Neuroscience

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Abnormalities of cell packing ...... me/X-linked mental retardation

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Garilyn M Jentarra

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Mary Blue

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Nishit Srivastava

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Sakkubai Naidu

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Shannon L Olfers

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Stephen G Rice

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P2860

Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

Solution structure of the methyl-CpG binding domain of human MBD1 in complex with methylated DNA

Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation

The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis

MeCP2, a key contributor to neurological disease, activates and represses transcription

Dendritic anomalies in disorders associated with mental retardation

Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized

Rett syndrome: a prototypical neurodevelopmental disorder

Altered visual function and interneuron survival in Atrx knockout mice: inference for the human syndrome

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

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