The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis (Q24557516)

ORCID Public Data File 2021

GOA release 2020-03-11

Marie Mangelsdorf

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author name string

Nathalie G Bérubé

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Magdalena Jagla

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Jackie Vanderluit

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David Garrick

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Richard J Gibbons

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Douglas R Higgs

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Ruth S Slack

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David J Picketts

Journal of Clinical Investigation

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language of work or name

English

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publication date

February 2005

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published in

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volume

115

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issue

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page(s)

258-67

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cites work

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

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

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

24 March 2017

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27 September 2017

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27 September 2017

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30 May 2018

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30 May 2018

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Pax6 controls radial glia differentiation in the cerebral cortex

30 May 2018

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30 May 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=544602

Comparison of the human and murine ATRX gene identifies highly conserved, functionally important domains

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=544602

A critical temporal requirement for the retinoblastoma protein family during neuronal determination

30 May 2018

1 reference

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30 May 2018

1 reference

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30 May 2018

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Elevated apoptosis in pre-mature neurons differentiated from mouse ES cells containing a single human chromosome 21.

30 May 2018

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Expanding phenotype of XNP mutations: mild to moderate mental retardation.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=544602

Neurodevelopmental defects resulting from ATRX overexpression in transgenic mice.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=544602

Evidence for apoptosis in the fetal Down syndrome brain

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=544602

A nonsense mutation of the ATRX gene causing mild mental retardation and epilepsy.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=544602

Mutation of the XNP/ATR-X gene in a family with severe mental retardation, spastic paraplegia and skewed pattern of X inactivation: demonstration that the mutation is involved in the inactivation bias

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=544602

Neuronal apoptosis in mouse trisomy 16: mediation by caspases.

28 November 2018

1 reference

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Widespread programmed cell death in proliferative and postmitotic regions of the fetal cerebral cortex.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=544602

Identification of a mutation in the XNP/ATR-X gene in a family reported as Smith-Fineman-Myers syndrome

28 November 2018

1 reference

12 December 2020

Carpenter-Waziri syndrome results from a mutation in XNP

1 reference

12 December 2020

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

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12 December 2020

Nestin mRNA expression correlates with the central nervous system progenitor cell state in many, but not all, regions of developing central nervous system

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12 December 2020

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12 December 2020

Identifiers

DOI

10.1172/JCI22329

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1 reference

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PubMed publication ID

15668733

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