(Q51898063)

17 April 2018

title

Patient mutations alter ATRX targeting to PML nuclear bodies. (English)

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17 April 2018

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Nathalie G Bérubé

1

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17 April 2018

Jasmine Healy

2

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17 April 2018

Chantal F Medina

3

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17 April 2018

Shaobo Wu

4

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17 April 2018

Todd Hodgson

5

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17 April 2018

Magdalena Jagla

6

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17 April 2018

David J Picketts

7

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17 April 2018

publication date

24 October 2007

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17 April 2018

European Journal of Human Genetics

published in

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17 April 2018

volume

16

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17 April 2018

issue

2

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17 April 2018

page(s)

192-201

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17 April 2018

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201943

exact match

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cites work

Acquired alpha-thalassemia in association with myelodysplastic syndrome and other hematologic malignancies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

Acquired somatic ATRX mutations in myelodysplastic syndrome associated with α thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

Alpha thalassaemia-mental retardation, X linked

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

Heterochromatin and ND10 are cell-cycle regulated and phosphorylation-dependent alternate nuclear sites of the transcription repressor Daxx and SWI/SNF protein ATRX

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

Localization of a putative transcriptional regulator (ATRX) at pericentromeric heterochromatin and the short arms of acrocentric chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

Specific interaction between the XNP/ATR-X gene product and the SET domain of the human EZH2 protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

A novel transcription regulatory complex containing death domain-associated protein and the ATR-X syndrome protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

Mutations in ATRX, encoding a SWI/SNF-like protein, cause diverse changes in the pattern of DNA methylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

ATR-X mutations cause impaired nuclear location and altered DNA binding properties of the XNP/ATR-X protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

Neurodevelopmental defects resulting from ATRX overexpression in transgenic mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

Large-scale identification of mammalian proteins localized to nuclear sub-compartments

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

PML is critical for ND10 formation and recruits the PML-interacting protein daxx to this nuclear structure when modified by SUMO-1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

Human Daxx regulates Fas-induced apoptosis from nuclear PML oncogenic domains (PODs).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

Syndromes of disordered chromatin remodeling

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

Monogenic causes of X-linked mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

DNA Methylation-Related Chromatin Remodeling in Activity-Dependent Bdnf Gene Regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

Derepression of BDNF Transcription Involves Calcium-Dependent Phosphorylation of MeCP2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

Chromatin acetylation, memory, and LTP are impaired in CBP+/- mice: a model for the cognitive deficit in Rubinstein-Taybi syndrome and its amelioration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

A genetic screen identifies putative targets and binding partners of CREB-binding protein in the developing Drosophila eye.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

A conserved truncated isoform of the ATR-X syndrome protein lacking the SWI/SNF-homology domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

Syndromal mental retardation due to mutations in a regulator of gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

7 January 2021

Molecular-clinical spectrum of the ATR-X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

7 January 2021

Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the α-thalassemia myelodysplasia syndrome (ATMDS)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

7 January 2021

Deletion of the alpha-globin gene cluster as a cause of acquired alpha-thalassemia in myelodysplastic syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

7 January 2021

PML nuclear bodies are highly organised DNA-protein structures with a function in heterochromatin remodelling at the G2 phase.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201943

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201943

1 reference

17 April 2018

1 reference

17 April 2018