Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions (Q36218243)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19386901 AND SRC:MED&resulttype=core&format=json

26 January 2020

title

Rett syndrome astrocytes are abnormal and spread MeCP2 deficiency through gap junctions (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19386901 AND SRC:MED&resulttype=core&format=json

26 January 2020

0 references

0 references

2

1 reference

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26 January 2020

Janine M. LaSalle

4

1 reference

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26 January 2020

author name string

Izumi Maezawa

1

1 reference

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26 January 2020

Danielle Harvey

3

1 reference

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26 January 2020

Lee-Way Jin

5

1 reference

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26 January 2020

language of work or name

English

0 references

publication date

1 April 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19386901 AND SRC:MED&resulttype=core&format=json

26 January 2020

published in

Journal of Neuroscience

1 reference

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26 January 2020

volume

29

1 reference

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26 January 2020

issue

16

1 reference

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26 January 2020

page(s)

5051-5061

1 reference

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The mystery and magic of glia: a perspective on their roles in health and disease

26 January 2020

cites work

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

1 October 2017

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A transcriptome database for astrocytes, neurons, and oligodendrocytes: a new resource for understanding brain development and function

1 October 2017

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Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes

1 October 2017

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Homeostatic regulation of MeCP2 expression by a CREB-induced microRNA

1 October 2017

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The story of Rett syndrome: from clinic to neurobiology

1 October 2017

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MeCP2 controls excitatory synaptic strength by regulating glutamatergic synapse number

1 October 2017

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Design of an improved set of oligonucleotide primers for genotyping MeCP2tm1.1Bird KO mice by PCR.

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Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation

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Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2.

1 October 2017

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Metabolic fingerprints of altered brain growth, osmoregulation and neurotransmission in a Rett syndrome model

1 October 2017

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MeCP2 dysfunction in Rett syndrome and related disorders

1 October 2017

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Astrocytic purinergic signaling coordinates synaptic networks

1 October 2017

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Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

1 October 2017

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X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/ mouse brain.

1 October 2017

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Expression of MeCP2 in postmitotic neurons rescues Rett syndrome in mice

1 October 2017

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X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett syndrome

1 October 2017

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Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders

1 October 2017

1 reference

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

1 October 2017

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Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

1 October 2017

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Postnatal Neurodevelopmental Disorders: Meeting at the Synapse?

1 October 2017

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

1 October 2017

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Quantitative localization of heterogeneous methyl-CpG-binding protein 2 (MeCP2) expression phenotypes in normal and Rett syndrome brain by laser scanning cytometry

1 October 2017

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

1 October 2017

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

1 October 2017

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Differential neurite growth on astrocyte substrates: interspecies facilitation in green fluorescent protein-transfected rat and human neurons

1 October 2017

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1 October 2017

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1 October 2017

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1 October 2017

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29 June 2018

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Scrape-loading and dye transfer. A rapid and simple technique to study gap junctional intercellular communication

29 June 2018

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Glia are essential for sensory organ function in C. elegans

29 June 2018

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Gap junction-mediated astrocytic networks in the mouse barrel cortex

22 September 2018

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A methyl-CpG-binding protein 2-enhanced green fluorescent protein reporter mouse model provides a new tool for studying the neuronal basis of Rett syndrome

22 September 2018

1 reference

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Targeted delivery of an Mecp2 transgene to forebrain neurons improves the behavior of female Mecp2-deficient mice.

22 September 2018

1 reference

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Cell-specific expression of wild-type MeCP2 in mouse models of Rett syndrome yields insight about pathogenesis

22 September 2018

1 reference

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Tumor necrosis factor-alpha induces neurotoxicity via glutamate release from hemichannels of activated microglia in an autocrine manner.

22 September 2018

1 reference

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

22 September 2018

1 reference

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Endothelins stimulate the expression of neurotrophin-3 in rat brain and rat cultured astrocytes.

22 September 2018

1 reference

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Transgenic mouse model of tau pathology in astrocytes leading to nervous system degeneration.

22 September 2018

1 reference

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Four classes of intercellular channels between glial cells in the CNS.

22 September 2018

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Tau accumulation in astrocytes in progressive supranuclear palsy is a degenerative rather than a reactive process

22 September 2018

1 reference

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MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain.

22 September 2018

1 reference

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Neuropathology of Rett syndrome

22 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19386901

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Gap junctions between cultured astrocytes: immunocytochemical, molecular, and electrophysiological analysis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19386901

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1523/JNEUROSCI.0324-09.2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19386901 AND SRC:MED&resulttype=core&format=json

26 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19386901 AND SRC:MED&resulttype=core&format=json

26 January 2020

PubMed publication ID

19386901

1 reference