(Q50309402)

PubMed publication ID

21888765

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21888765%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

title

Oxidative stress in Rett syndrome: natural history, genotype, and variants (English)

1 reference

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12 May 2020

0 references

1

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12 May 2020

Claudio De Felice

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6837451&resulttype=core&format=json

12 May 2020

Lucia Ciccoli

7

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12 May 2020

Joussef Hayek

8

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6837451&resulttype=core&format=json

12 May 2020

6

Giuseppe Valacchi

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6837451&resulttype=core&format=json

12 May 2020

4

Alessandra Pecorelli

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6837451&resulttype=core&format=json

12 May 2020

3

Cinzia Signorini

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6837451&resulttype=core&format=json

12 May 2020

author name string

Thierry Durand

5

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12 May 2020

publication date

1 January 2011

1 reference

PubMed publication ID

21888765

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21888765%20AND%20SRC:MED&resulttype=core&format=json

12 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6837451&resulttype=core&format=json

12 May 2020

volume

16

1 reference

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12 May 2020

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6837451&resulttype=core&format=json

12 May 2020

page(s)

145-153

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6837451&resulttype=core&format=json

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

12 May 2020

cites work

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The story of Rett syndrome: from clinic to neurobiology

21 January 2018

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CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome

21 January 2018

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FOXG1 is responsible for the congenital variant of Rett syndrome

21 January 2018

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Rett syndrome: revised diagnostic criteria and nomenclature

21 January 2018

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Clinical manifestations and stages of Rett syndrome

21 January 2018

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Understanding omega-3 polyunsaturated fatty acids

21 January 2018

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RettBASE: The IRSA MECP2 variation database-a new mutation database in evolution

21 January 2018

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Italian Rett database and biobank.

21 January 2018

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Docosahexaenoic Acid therapy of experimental ischemic stroke

21 January 2018

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Specific mutations in methyl-CpG-binding protein 2 confer different severity in Rett syndrome.

21 January 2018

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Systemic oxidative stress in classic Rett syndrome.

21 January 2018

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CDKL5 is a brain MeCP2 target gene regulated by DNA methylation

21 January 2018

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Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant).

21 January 2018

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

21 January 2018

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Iron release in erythrocytes and plasma non protein-bound iron in hypoxic and non hypoxic newborns

21 January 2018

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Iron release, superoxide production and binding of autologous IgG to band 3 dimers in newborn and adult erythrocytes exposed to hypoxia and hypoxia-reoxygenation

21 January 2018

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Reversal of neurological defects in a mouse model of Rett syndrome

21 January 2018

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Partial reversal of Rett Syndrome-like symptoms in MeCP2 mutant mice

21 January 2018

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Reversibility of functional deficits in experimental models of Rett syndrome.

21 January 2018

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Fatty acid composition of brain phospholipids in aging and in Alzheimer's disease

21 January 2018

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Chronic administration of docosahexaenoic acid improves reference memory-related learning ability in young rats

21 January 2018

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Docosahexaenoic acid complexed to albumin elicits high-grade ischemic neuroprotection

21 January 2018

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Anti-inflammatory actions of neuroprotectin D1/protectin D1 and its natural stereoisomers: assignments of dihydroxy-containing docosatrienes.

21 January 2018

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Rett syndrome microglia damage dendrites and synapses by the elevated release of glutamate

21 January 2018

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MeCP2 mutant protein is expressed in astrocytes as well as in neurons and localizes in the nucleus.

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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On the track of DNA methylation: an interview with Adrian Bird by Jane Gitschier

21 January 2018

1 reference

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Oxidative damage in Parkinson disease: Measurement using accurate biomarkers.

21 January 2018

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Oxidative stress in Rett syndrome

21 January 2018

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Neuropathology of Rett syndrome: case report with neuronal and mitochondrial abnormalities in the brain

21 January 2018

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Infantile hypotonia as a presentation of Rett syndrome.

21 January 2018

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21 January 2018

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Downstream targets of methyl CpG binding protein 2 and their abnormal expression in the frontal cortex of the human Rett syndrome brain.

21 January 2018

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Gene expression analysis exposes mitochondrial abnormalities in a mouse model of Rett syndrome

21 January 2018

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Neurogenetics: advancing the "next-generation" of brain research

21 January 2018

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Evolutionary aspects of diet: the omega-6/omega-3 ratio and the brain

21 January 2018

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12 December 2020

Rett syndrome and mitochondrial enzyme deficiencies

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12 December 2020

On a unusual brain atrophy syndrome in hyperammonemia in childhood

1 reference

12 December 2020

Effects of eicosapentaenoic acid on asymmetric dimethylarginine in patients in the chronic phase of cerebral infarction: a preliminary study

1 reference

12 December 2020

Rett syndrome: findings suggesting axonopathy and mitochondrial abnormalities

1 reference

12 December 2020

F4-neuroprostanes mediate neurological severity in Rett syndrome

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12 December 2020

Ion trap tandem mass spectrometric determination of F2‐isoprostanes

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12 December 2020

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12 December 2020

Production of superoxide from hemoglobin-bound oxygen under hypoxic conditions

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12 December 2020

Genome-wide expression studies in autism spectrum disorder, Rett syndrome, and Down syndrome

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12 December 2020

Mitochondrial alterations in Rett syndrome

1 reference

12 December 2020

10.1179/1351000211Y.0000000004

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6837451&resulttype=core&format=json

12 May 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6837451&resulttype=core&format=json

12 May 2020

PubMed publication ID

21888765

1 reference