High-throughput analysis of promoter occupancy reveals new targets for Arx, a gene mutated in mental retardation and interneuronopathies (Q28506691)

24 January 2017

title

High-throughput analysis of promoter occupancy reveals new targets for Arx, a gene mutated in mental retardation and interneuronopathies (English)

1 reference

Aristaless related homeobox

24 January 2017

main subject

1 reference

GOA release 2020-03-11

9

Olivier Mignen

1 reference

24 January 2017

11

Rémi Houlgatte

1 reference

24 January 2017

Marie-Lise Quillé

1

1 reference

24 January 2017

Solenne Carat

2

1 reference

24 January 2017

Sylvia Quéméner-Redon

3

1 reference

24 January 2017

Edouard Hirchaud

4

1 reference

24 January 2017

Daniel Baron

5

1 reference

24 January 2017

Caroline Benech

6

1 reference

24 January 2017

Jeanne Guihot

7

1 reference

24 January 2017

Morgane Placet

8

1 reference

24 January 2017

Claude Férec

10

1 reference

24 January 2017

Gaëlle Friocourt

12

1 reference

24 January 2017

language of work or name

English

0 references

publication date

1 January 2011

1 reference

24 January 2017

1 reference

24 January 2017

volume

6

1 reference

24 January 2017

issue

9

1 reference

24 January 2017

page(s)

e25181

1 reference

Creative Commons Attribution 4.0 International

24 January 2017

copyright license

start time

22 September 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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19 March 2017

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A longer polyalanine expansion mutation in the ARX gene causes early infantile epileptic encephalopathy with suppression-burst pattern (Ohtahara syndrome)

19 March 2017

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Inactivation of Arx, the murine ortholog of the X-linked lissencephaly with ambiguous genitalia gene, leads to severe disorganization of the ventral telencephalon with impaired neuronal migration and differentiation

19 March 2017

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19 March 2017

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Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans

19 March 2017

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X-linked myoclonic epilepsy with spasticity and intellectual disability: mutation in the homeobox gene ARX

19 March 2017

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Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX

19 March 2017

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ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation

19 March 2017

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7 April 2017

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29 September 2017

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29 September 2017

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29 September 2017

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29 September 2017

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Identification of Arx transcriptional targets in the developing basal forebrain

29 September 2017

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29 September 2017

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The homeobox gene Arx is a novel positive regulator of embryonic myogenesis.

29 September 2017

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29 September 2017

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29 September 2017

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Mouse orthologue of ARX, a gene mutated in several X-linked forms of mental retardation and epilepsy, is a marker of adult neural stem cells and forebrain GABAergic neurons

29 September 2017

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Opposing actions of Arx and Pax4 in endocrine pancreas development

29 September 2017

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29 September 2017

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Evidence for tangential migration disturbances in human lissencephaly resulting from a defect in LIS1, DCX and ARX genes

29 September 2017

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Arx acts as a regional key selector gene in the ventral telencephalon mainly through its transcriptional repression activity

2 June 2018

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2 June 2018

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Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation

2 June 2018

1 reference

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Expansion of the first PolyA tract of ARX causes infantile spasms and status dystonicus

2 June 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0025181

Expression of a novel aristaless related homeobox gene 'Arx' in the vertebrate telencephalon, diencephalon and floor plate

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0025181

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0025181

The function of the Aristaless-related homeobox (Arx) gene product as a transcriptional repressor is diminished by mutations associated with X-linked mental retardation (XLMR).

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0025181

A parallel scheme for comparing transcription factor binding sites matrices.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0025181

Xenopus aristaless-related homeobox (xARX) gene product functions as both a transcriptional activator and repressor in forebrain development

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0025181

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0025181

Polyalanine expansion of ARX associated with cryptogenic West syndrome

21 January 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/21966449

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0025181

0 references

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1 reference