(Q34013518)

30 July 2017

title

The MeCP2/YY1 interaction regulates ANT1 expression at 4q35: novel hints for Rett syndrome pathogenesis. (English)

1 reference

Charlotte Kilstrup-Nielsen

30 July 2017

0 references

Charlotte Kilstrup-Nielsen

7

0 references

Greta Forlani

Greta Forlani

1

0 references

Ugo Ala

Ugo Ala

3

0 references

Rossella Tupler

Rossella Tupler

6

0 references

Ferdinando Di Cunto

Ferdinando Di Cunto

4

0 references

Nicoletta Landsberger

Nicoletta Landsberger

8

0 references

author name string

Elisa Giarda

2

1 reference

30 July 2017

Monica Salani

5

1 reference

30 July 2017

language of work or name

1 reference

26 May 2010

1 reference

30 July 2017

published in

Human Molecular Genetics

1 reference

30 July 2017

volume

19

1 reference

30 July 2017

issue

16

1 reference

30 July 2017

page(s)

3114-3123

1 reference

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

30 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

Differential CpG island methylation of murine adenine nucleotide translocase genes

5 July 2018

1 reference

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Mouse models of Rett syndrome: from behavioural phenotyping to preclinical evaluation of new therapeutic approaches

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

Prediction of human disease genes by human-mouse conserved coexpression analysis

5 July 2018

1 reference

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The story of Rett syndrome: from clinic to neurobiology

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

Intrinsic disorder and autonomous domain function in the multifunctional nuclear protein, MeCP2.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

Interaction between chromatin proteins MECP2 and ATRX is disrupted by mutations that cause inherited mental retardation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

Reversal of neurological defects in a mouse model of Rett syndrome

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

Polycomb recruitment to DNA in vivo by the YY1 REPO domain.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

Functional consequences of mutations in CDKL5, an X-linked gene involved in infantile spasms and mental retardation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

The adenine nucleotide translocase type 1 (ANT1): a new factor in mitochondrial disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

CLOE: identification of putative functional relationships among genes by comparison of expression profiles between two species

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

Molecular basis of facioscapulohumeral muscular dystrophy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

The DNA methyltransferases associate with HP1 and the SUV39H1 histone methyltransferase

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

MethPrimer: designing primers for methylation PCRs

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

Inappropriate Gene Activation in FSHD

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

Regulation of transcription factor YY1 by acetylation and deacetylation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

Functional consequences of Rett syndrome mutations on human MeCP2.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

Role of adenine nucleotide translocator 1 in mtDNA maintenance

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

Adenine nucleotide translocase-1, a component of the permeability transition pore, can dominantly induce apoptosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

Unlocking the mechanisms of transcription factor YY1: are chromatin modifying enzymes the key?

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

A third locus predisposing to multiple deletions of mtDNA in autosomal dominant progressive external ophthalmoplegia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2908467

Molecular biology. MeCP2 repression goes nonglobal

5 July 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ214

Infantile hypotonia as a presentation of Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ214

Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome: evidence for disruption of neuronal networks

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ214

Expression and sequence analysis of the mouse adenine nucleotide translocase 1 and 2 genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ214

Yin Yang 1 expression in the adult rodent brain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ214

The transcription factor Yin Yang 1 is essential for oligodendrocyte progenitor differentiation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ214

The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDQ214

A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20504995

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Facioscapulohumeral muscular dystrophy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20504995

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

MeCP2-chromatin interactions include the formation of chromatosome-like structures and are altered in mutations causing Rett syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20504995

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDQ214

1 reference

30 July 2017

1 reference

30 July 2017

1 reference