(Q34200572)

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Cell-autonomous alterations in dendritic arbor morphology and connectivity induced by overexpression of MeCP2 in Xenopus central neurons in vivo

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Europe PubMed Central

PubMed publication ID

31 July 2017

Cell-autonomous alterations in dendritic arbor morphology and connectivity induced by overexpression of MeCP2 in Xenopus central neurons in vivo (English)

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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Sonya Marshak

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Margarita M Meynard

2

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Europe PubMed Central

PubMed publication ID

31 July 2017

Ymkje A De Vries

3

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Europe PubMed Central

PubMed publication ID

31 July 2017

Adhanet H Kidane

4

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Europe PubMed Central

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31 July 2017

Susana Cohen-Cory

5

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Europe PubMed Central

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31 July 2017

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publication date

9 March 2012

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Europe PubMed Central

PubMed publication ID

31 July 2017

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Europe PubMed Central

PubMed publication ID

31 July 2017

7

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Europe PubMed Central

PubMed publication ID

31 July 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

e33153

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Europe PubMed Central

PubMed publication ID

31 July 2017

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Creative Commons Attribution 4.0 International

9 March 2012

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April 2022 Public Data File from Crossref

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Synaptic microcircuit dysfunction in genetic models of neurodevelopmental disorders: focus on Mecp2 and Met.

1 reference

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Exogenous brain-derived neurotrophic factor rescues synaptic dysfunction in Mecp2-null mice

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MeCP2 functions largely cell-autonomously, but also non-cell-autonomously, in neuronal maturation and dendritic arborization of cortical pyramidal neurons

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Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities

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MeCP2 deficiency disrupts axonal guidance, fasciculation, and targeting by altering Semaphorin 3F function.

1 reference

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5 July 2018

Dendritic spine pathologies in hippocampal pyramidal neurons from Rett syndrome brain and after expression of Rett-associated MECP2 mutations

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Mouse models of MeCP2 disorders share gene expression changes in the cerebellum and hypothalamus

1 reference

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Recent advances in MeCP2 structure and function

1 reference

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Non-cell autonomous influence of MeCP2-deficient glia on neuronal dendritic morphology

1 reference

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Bdnf overexpression in hippocampal neurons prevents dendritic atrophy caused by Rett-associated MECP2 mutations

1 reference

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Structural homeostasis: compensatory adjustments of dendritic arbor geometry in response to variations of synaptic input

1 reference

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

1 reference

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The story of Rett syndrome: from clinic to neurobiology

1 reference

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5 July 2018

MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number

1 reference

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5 July 2018

Mecp2 deficiency leads to delayed maturation and altered gene expression in hippocampal neurons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3302857

5 July 2018

Brain-specific phosphorylation of MeCP2 regulates activity-dependent Bdnf transcription, dendritic growth, and spine maturation

1 reference

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5 July 2018

Learning and memory and synaptic plasticity are impaired in a mouse model of Rett syndrome

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Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH.

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Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett syndrome

1 reference

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Hippocampal synaptic plasticity is impaired in the Mecp2-null mouse model of Rett syndrome

1 reference

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Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males

1 reference

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Neurotrophic regulation of retinal ganglion cell synaptic connectivity: from axons and dendrites to synapses

1 reference

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

1 reference

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Live optical imaging of nervous system development

1 reference

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Developmental expression of methyl-CpG binding protein 2 is dynamically regulated in the rodent brain

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DNA Methylation-Related Chromatin Remodeling in Activity-Dependent Bdnf Gene Regulation

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Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

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A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos

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The expression of methyl CpG binding factor MeCP2 correlates with cellular differentiation in the developing rat brain and in cultured cells

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Elevated methyl-CpG-binding protein 2 expression is acquired during postnatal human brain development and is correlated with alternative polyadenylation.

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Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3

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Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

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

1 reference

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Dendritic arbor development and synaptogenesis

1 reference

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1 reference

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1 reference

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Selective dendritic alterations in the cortex of Rett syndrome

1 reference

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1 reference

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The neuropathology of the Rett syndrome

1 reference

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Recurrent infections, hypotonia, and mental retardation caused by duplication of MECP2 and adjacent region in Xq28.

1 reference

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Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males.

1 reference

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Differential expression of the methyl-cytosine binding protein 2 gene in embryonic and adult brain of zebrafish

1 reference

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Expression of MeCP2 in olfactory receptor neurons is developmentally regulated and occurs before synaptogenesis

1 reference

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Mild overexpression of MeCP2 causes a progressive neurological disorder in mice.

1 reference

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

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Increased dendritic complexity and axonal length in cultured mouse cortical neurons overexpressing methyl-CpG-binding protein MeCP2.

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MeCP2-dependent transcriptional repression regulates excitatory neurotransmission

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BDNF increases synapse density in dendrites of developing tectal neurons in vivo

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21 January 2018

Cell-autonomous TrkB signaling in presynaptic retinal ganglion cells mediates axon arbor growth and synapse maturation during the establishment of retinotectal synaptic connectivity

1 reference

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21 January 2018

Activity-dependent matching of excitatory and inhibitory inputs during refinement of visual receptive fields

1 reference

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21 January 2018

Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome: evidence for disruption of neuronal networks

1 reference

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21 January 2018

The disease progression of Mecp2 mutant mice is affected by the level of BDNF expression

1 reference

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Visualizing synapse formation in arborizing optic axons in vivo: dynamics and modulation by BDNF.

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21 January 2018

BDNF stabilizes synapses and maintains the structural complexity of optic axons in vivo

1 reference

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21 January 2018

Evidence for both neuronal cell autonomous and nonautonomous effects of methyl-CpG-binding protein 2 in the cerebral cortex of female mice with Mecp2 mutation

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0033153

21 January 2018

Dynamic morphometrics reveals contributions of dendritic growth cones and filopodia to dendritogenesis in the intact and awake embryonic brain.

1 reference

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Rett syndrome: 3-D confocal microscopy of cortical pyramidal dendrites and afferents.

1 reference

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28 October 2018

Identifiers

10.1371/JOURNAL.PONE.0033153

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

2012PLoSO...733153M

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

ResearchGate publication ID

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