Delayed maturation of neuronal architecture and synaptogenesis in cerebral cortex of Mecp2-deficient mice. - Wikidata - wikimedia - TriplyDB

Delayed maturation of neuronal architecture and synaptogenesis in cerebral cortex of Mecp2-deficient mice.

Delayed maturation of neuronal architecture and synaptogenesis in cerebral cortex of Mecp2-deficient mice.

http://www.wikidata.org/entity/Q48835247

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Convulsing toward the pathophysiology of autism Common circuit defect of excitatory-inhibitory balance in mouse models of autism.Role of MicroRNA in Governing Synaptic Plasticity Developmental Dynamics of Rett Syndrome MECP2 disorders: from the clinic to mice and back The impact of MeCP2 loss- or gain-of-function on synaptic plasticity Dendritic spine dysgenesis in autism related disorders Abnormalities of the DNA methylation mark and its machinery: an emerging cause of neurologic dysfunction Behavioral and Neuroanatomical Phenotypes in Mouse Models of Autism Deletion of JMJD2B in neurons leads to defective spine maturation, hyperactive behavior and memory deficits in mouse A Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons.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 Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations Microglia contribute to circuit defects in Mecp2 null mice independent of microglia-specific loss of Mecp2 expression Phosphorylation of MeCP2 at Serine 80 regulates its chromatin association and neurological function.Beyond Widespread Mecp2 Deletions to Model Rett Syndrome: Conditional Spatio-Temporal Knockout, Single-Point Mutations and Transgenic Rescue Mice Synaptic circuit abnormalities of motor-frontal layer 2/3 pyramidal neurons in a mutant mouse model of Rett syndrome Valid statistical approaches for analyzing sholl data: Mixed effects versus simple linear models.Synaptic circuit abnormalities of motor-frontal layer 2/3 pyramidal neurons in an RNA interference model of methyl-CpG-binding protein 2 deficiency.Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation Intrinsic membrane properties of locus coeruleus neurons in Mecp2-null mice.MeCP2 functions largely cell-autonomously, but also non-cell-autonomously, in neuronal maturation and dendritic arborization of cortical pyramidal neurons.Dendritic spine dysgenesis in Rett syndrome.MeCP2 mutation results in compartment-specific reductions in dendritic branching and spine density in layer 5 motor cortical neurons of YFP-H mice.Cell-autonomous alterations in dendritic arbor morphology and connectivity induced by overexpression of MeCP2 in Xenopus central neurons in vivo Acetyl-L-carnitine improves behavior and dendritic morphology in a mouse model of Rett syndrome.Experimental models of Rett syndrome based on Mecp2 dysfunction.Synaptic determinants of rett syndrome.The role of MeCP2 in CNS development and function.Experience-dependent retinogeniculate synapse remodeling is abnormal in MeCP2-deficient mice Neuronal nucleus and cytoplasm volume deficit in children with autism and volume increase in adolescents and adults.Intrauterine inflammation, insufficient to induce parturition, still evokes fetal and neonatal brain injury Beta-actin deficiency with oxidative posttranslational modifications in Rett syndrome erythrocytes: insights into an altered cytoskeletal organization Synaptic microcircuit dysfunction in genetic models of neurodevelopmental disorders: focus on Mecp2 and Met.Genotype-specific effects of Mecp2 loss-of-function on morphology of Layer V pyramidal neurons in heterozygous female Rett syndrome model mice.Network activity-independent coordinated gene expression program for synapse assembly.Brain region-specific expression of Fxyd1, an Mecp2 target gene, is regulated by epigenetic mechanisms.Normal mitral cell dendritic development in the setting of Mecp2 mutation MeCP2 deficiency disrupts axonal guidance, fasciculation, and targeting by altering Semaphorin 3F function.

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Delayed maturation of neuronal architecture and synaptogenesis in cerebral cortex of Mecp2-deficient mice.

http://www.wikidata.org/entity/Q48835247

description

2005 nî lūn-bûn

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name

Delayed maturation of neuronal ...... ortex of Mecp2-deficient mice.

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Delayed maturation of neuronal ...... ortex of Mecp2-deficient mice.

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Delayed maturation of neuronal ...... ortex of Mecp2-deficient mice.

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Delayed maturation of neuronal ...... ortex of Mecp2-deficient mice.

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Journal of Neuropathology & Experimental Neurology

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Delayed maturation of neuronal ...... ortex of Mecp2-deficient mice.

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P2093

Kazuo Washiyama

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Masayuki Itoh

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Tetsuya Fukuda

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Tomio Ichikawa

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Yu-ichi Goto

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P2860

Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2

Dendritic anomalies in disorders associated with mental retardation

Purification, sequence, and cellular localization of a novel chromosomal protein that binds to methylated DNA

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

Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation

MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions

Postnatal development and migration of cholecystokinin-immunoreactive interneurons in rat hippocampus

MeCP2 is a transcriptional repressor with abundant binding sites in genomic chromatin

The transcriptional repressor Mecp2 regulates terminal neuronal differentiation

DNA methylation-related chromatin remodeling in activity-dependent BDNF gene regulation

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6

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64

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2005-06-01T00:00:00Z

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15977646

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