(Q37422466)

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Genes related to mitochondrial functions, protein degradation, and chromatin folding are differentially expressed in lymphomonocytes of Rett syndrome patients

scientific article published on 12 December 2013

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Europe PubMed Central

PMC publication ID

20 August 2017

Genes related to mitochondrial functions, protein degradation, and chromatin folding are differentially expressed in lymphomonocytes of Rett syndrome patients (English)

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Europe PubMed Central

PMC publication ID

20 August 2017

protein folding

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1 June 2020

Franco Cervellati

3

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1 June 2020

Raffaella Canali

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1 June 2020

Silvia Leoncini

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1 June 2020

Alessio Cortelazzo

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1 June 2020

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1 June 2020

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1 June 2020

Giuseppe Valacchi

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Giuseppe Valacchi

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1 June 2020

Alessandra Pecorelli

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Alessandra Pecorelli

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1 June 2020

Cinzia Signorini

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Cinzia Signorini

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1 June 2020

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Claudio De Felice

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1 June 2020

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12 December 2013

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20 August 2017

Mediators of Inflammation

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1 June 2020

2013

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1 June 2020

137629

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24453408%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

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Creative Commons Attribution 3.0 Unported

1 January 2013

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LIMMA

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Europe PubMed Central

22 June 2022

https://europepmc.org/article/PMC/3876710

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Molecular mechanisms of superoxide production by the mitochondrial respiratory chain.

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The role of MeCP2 in the brain.

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MeCP2: structure and function

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Rett syndrome: revised diagnostic criteria and nomenclature

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23 August 2017

Cell cloning-based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes

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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.

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The sites and topology of mitochondrial superoxide production

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Epigenetic control.

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MeCP2 knockdown reveals DNA methylation-independent gene repression of target genes in living cells and a bias in the cellular location of target gene products.

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

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Investigating genotype-phenotype relationships in Rett syndrome using an international data set.

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The story of Rett syndrome: from clinic to neurobiology

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23 August 2017

Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients

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23 August 2017

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

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Rett syndrome in Australia: a review of the epidemiology.

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23 August 2017

MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression

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Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations

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Systemic oxidative stress in classic Rett syndrome.

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Mitochondrial alterations in Rett syndrome

1 reference

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12 December 2020

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Rett syndrome and mitochondrial enzyme deficiencies

1 reference

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12 December 2020

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inferred from PubMed ID database lookup

Computerized ribosomal RNA secondary structure modeling of mutants found in Rett syndrome patients and their mothers

1 reference

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12 December 2020

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inferred from PubMed ID database lookup

Mutation analysis of 16S rRNA in patients with Rett syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/24453408

12 December 2020

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Rett syndrome: findings suggesting axonopathy and mitochondrial abnormalities

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rett syndrome: the bcl-2 gene--a mediator of neurotrophic mechanisms?

1 reference

https://pubmed.ncbi.nlm.nih.gov/24453408

12 December 2020

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inferred from PubMed ID database lookup

Mutational analysis of mitochondrial DNA of children with Rett syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/24453408

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1155/2013/137629

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24453408%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24453408%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24453408%20AND%20SRC:MED&resulttype=core&format=json

1 June 2020

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