VPA alleviates neurological deficits and restores gene expression in a mouse model of Rett syndrome (Q28540049)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24968028%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

title

VPA alleviates neurological deficits and restores gene expression in a mouse model of Rett syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24968028%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

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Weixiang Guo

1

1 reference

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21 March 2020

Maky Otsuka I

3

1 reference

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21 March 2020

Koichiro Irie

4

1 reference

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21 March 2020

Katsuhide Igarashi

5

1 reference

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21 March 2020

Xinyu Zhao

7

1 reference

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21 March 2020

language of work or name

English

0 references

publication date

26 June 2014

1 reference

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21 March 2020

1 reference

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21 March 2020

volume

9

1 reference

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21 March 2020

issue

6

1 reference

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21 March 2020

page(s)

e100215

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Creative Commons Attribution 4.0 International

21 March 2020

copyright license

start time

26 June 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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

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

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

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

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Reversal of neurological defects in a mouse model of Rett syndrome

19 March 2017

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

7 April 2017

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

7 April 2017

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Loss of MeCP2 function is associated with distinct gene expression changes in the striatum

7 April 2017

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Intragenic DNA methylation modulates alternative splicing by recruiting MeCP2 to promote exon recognition

29 September 2017

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Increased gene expression of FOXP1 in patients with autism spectrum disorders

29 September 2017

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The relationship of Rett syndrome and MECP2 disorders to autism.

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Age-dependent expression of MeCP2 in a heterozygous mosaic mouse model

29 September 2017

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Cross talk between microRNA and epigenetic regulation in adult neurogenesis

29 September 2017

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MeCP2 deficiency downregulates specific nuclear proteins that could be partially recovered by valproic acid in vitro

29 September 2017

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

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29 September 2017

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Valproate and risk of fracture in Rett syndrome

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21 January 2018

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10.1371/JOURNAL.PONE.0100215

27 November 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24968028%20AND%20SRC:MED&resulttype=core&format=json

21 March 2020

0 references

1 reference

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21 March 2020

PubMed publication ID

24968028

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24968028%20AND%20SRC:MED&resulttype=core&format=json