Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome (Q33826769)

24769161

29 July 2017

title

Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome (English)

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29 July 2017

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4

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Federico Marracino

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Laura Ricceri

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Bianca De Filippis

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Giovanni Laviola

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Stefania Filosa

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Joussef Hayek

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Giuseppe Valacchi

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Alessandra Pecorelli

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Cinzia Signorini

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author name string

Claudio De Felice

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Floriana Della Ragione

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Francesco Scalabrì

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Giuseppe Belmonte

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Thierry Durand

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Jean-Marie Galano

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Camille Oger

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Alexandre Guy

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Valérie Bultel-Poncé

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Jacky Guy

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Maurizio D'Esposito

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1 June 2020

publication date

24 April 2014

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24769161

29 July 2017

number of pages

12

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published in

Neurobiology of Disease

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volume

68

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1 June 2020

page(s)

66-77

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describes a project that uses

1 June 2020

ImageJ

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11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4076513/fullTextXML

inferred from PubMed Central ID database lookup

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Systemic delivery of MeCP2 rescues behavioral and cellular deficits in female mouse models of Rett syndrome

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Morphological and functional reversal of phenotypes in a mouse model of Rett syndrome

4 July 2018

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Partial rescue of Rett syndrome by ω-3 polyunsaturated fatty acids (PUFAs) oil

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Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation

4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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4 July 2018

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

4 July 2018

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4 July 2018

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The story of Rett syndrome: from clinic to neurobiology

4 July 2018

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Reversal of neurological defects in a mouse model of Rett syndrome

4 July 2018

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Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized

4 July 2018

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Rett syndrome: clinical review and genetic update

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Clinical manifestations and stages of Rett syndrome

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Disruption of the glucocorticoid receptor gene in the nervous system results in reduced anxiety

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

On a unusual brain atrophy syndrome in hyperammonemia in childhood

4 July 2018

1 reference

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Cholesterol metabolism and Rett syndrome pathogenesis

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Scavenger receptor B1 post-translational modifications in Rett syndrome.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

MeCP2 deficiency is associated with impaired microtubule stability

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Disease modeling using embryonic stem cells: MeCP2 regulates nuclear size and RNA synthesis in neurons

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Oxidative burden and mitochondrial dysfunction in a mouse model of Rett syndrome

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Non-protein-bound iron and 4-hydroxynonenal protein adducts in classic autism

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Oxidative stress in Rett syndrome: natural history, genotype, and variants.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Increased levels of 4HNE-protein plasma adducts in Rett syndrome.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Unrecognized lung disease in classic Rett syndrome: a physiologic and high-resolution CT imaging study.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Systemic oxidative stress in classic Rett syndrome.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Free iron, total F-isoprostanes and total F-neuroprostanes in a model of neonatal hypoxic-ischemic encephalopathy: neuroprotective effect of melatonin

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Abnormal movements in Rett syndrome are present before the regression period: a case study

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Evidence for abnormal early development in a mouse model of Rett syndrome.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

An altered neonatal behavioral phenotype in Mecp2 mutant mice.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Abnormal general movements in girls with Rett disorder: the first four months of life.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Is the early development of girls with Rett disorder really normal?

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Nurse recognition of early deviation in development in home videos of infants with Rett disorder.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Oxidative stress in Rett syndrome

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4076513

Is the girl with Rett syndrome normal at birth?

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24769161

12 December 2020

inferred from PubMed ID database lookup

Ion trap tandem mass spectrometric determination of F2‐isoprostanes

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24769161

12 December 2020

inferred from PubMed ID database lookup

F4-neuroprostanes mediate neurological severity in Rett syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24769161

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1016/J.NBD.2014.04.006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24769161%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24769161%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

24769161

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24769161%20AND%20SRC:MED&resulttype=core&format=json