(Q48690458)

14 February 2018

title

MeCP2: only 100% will do. (English)

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14 February 2018

author

Huda Zoghbi

series ordinal

2

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14 February 2018

author name string

Hsiao-Tuan Chao

series ordinal

1

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14 February 2018

language of work or name

English

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publication date

26 January 2012

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14 February 2018

published in

Nature Neuroscience

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14 February 2018

volume

15

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14 February 2018

issue

2

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14 February 2018

page(s)

176-177

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14 February 2018

https://scigraph.springernature.com/pub.10.1038/nn.3027

exact match

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cites work

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

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

21 January 2018

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

21 January 2018

1 reference

A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Ube3a mRNA and protein expression are not decreased in Mecp2R168X mutant mice

21 January 2018

1 reference

Rett syndrome mutation MeCP2 T158A disrupts DNA binding, protein stability and ERP responses

21 January 2018

1 reference

Enhanced anxiety and stress-induced corticosterone release are associated with increased Crh expression in a mouse model of Rett syndrome

21 January 2018

1 reference

Behavioural and emotional features in Rett syndrome

21 January 2018

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Alterations of cortical and hippocampal EEG activity in MeCP2-deficient mice.

21 January 2018

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Network hyperexcitability in hippocampal slices from Mecp2 mutant mice revealed by voltage-sensitive dye imaging.

21 January 2018

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The MeCP2-null mouse hippocampus displays altered basal inhibitory rhythms and is prone to hyperexcitability.

21 January 2018

1 reference

Reversal of neurological defects in a mouse model of Rett syndrome

21 January 2018

1 reference

Adult neural function requires MeCP2.

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1038/NN.3027

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14 February 2018

release_ynhqinwcojfslibjhv7lhefcbm

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/ynhqinwcojfslibjhv7lhefcbm

mapped directly with Wikidata item

24 November 2022

based on heuristic

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14 February 2018