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Items: 1 to 20 of 108

1.

Conditional Loss of Arx From the Developing Dorsal Telencephalon Results in Behavioral Phenotypes Resembling Mild Human ARX Mutations.

Simonet JC, Sunnen CN, Wu J, Golden JA, Marsh ED.

Cereb Cortex. 2015 Sep;25(9):2939-50. doi: 10.1093/cercor/bhu090. Epub 2014 May 2.

2.

Targeted loss of Arx results in a developmental epilepsy mouse model and recapitulates the human phenotype in heterozygous females.

Marsh E, Fulp C, Gomez E, Nasrallah I, Minarcik J, Sudi J, Christian SL, Mancini G, Labosky P, Dobyns W, Brooks-Kayal A, Golden JA.

Brain. 2009 Jun;132(Pt 6):1563-76. doi: 10.1093/brain/awp107. Epub 2009 May 12.

3.

Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice.

Kitamura K, Itou Y, Yanazawa M, Ohsawa M, Suzuki-Migishima R, Umeki Y, Hohjoh H, Yanagawa Y, Shinba T, Itoh M, Nakamura K, Goto Y.

Hum Mol Genet. 2009 Oct 1;18(19):3708-24. doi: 10.1093/hmg/ddp318. Epub 2009 Jul 15.

PMID:
19605412
4.

Embryonic forebrain transcriptome of mice with polyalanine expansion mutations in the ARX homeobox gene.

Mattiske T, Lee K, Gecz J, Friocourt G, Shoubridge C.

Hum Mol Genet. 2016 Dec 15;25(24):5433-5443. doi: 10.1093/hmg/ddw360.

PMID:
27798109
5.

Reduced polyalanine-expanded Arx mutant protein in developing mouse subpallium alters Lmo1 transcriptional regulation.

Lee K, Mattiske T, Kitamura K, Gecz J, Shoubridge C.

Hum Mol Genet. 2014 Feb 15;23(4):1084-94. doi: 10.1093/hmg/ddt503. Epub 2013 Oct 10.

PMID:
24122442
6.

ARX regulates cortical intermediate progenitor cell expansion and upper layer neuron formation through repression of Cdkn1c.

Colasante G, Simonet JC, Calogero R, Crispi S, Sessa A, Cho G, Golden JA, Broccoli V.

Cereb Cortex. 2015 Feb;25(2):322-35. doi: 10.1093/cercor/bht222. Epub 2013 Aug 22.

7.

A triplet repeat expansion genetic mouse model of infantile spasms syndrome, Arx(GCG)10+7, with interneuronopathy, spasms in infancy, persistent seizures, and adult cognitive and behavioral impairment.

Price MG, Yoo JW, Burgess DL, Deng F, Hrachovy RA, Frost JD Jr, Noebels JL.

J Neurosci. 2009 Jul 8;29(27):8752-63. doi: 10.1523/JNEUROSCI.0915-09.2009.

8.
9.

The vertebrate ortholog of Aristaless is regulated by Dlx genes in the developing forebrain.

Cobos I, Broccoli V, Rubenstein JL.

J Comp Neurol. 2005 Mar 14;483(3):292-303.

PMID:
15682394
11.

Identification of Arx transcriptional targets in the developing basal forebrain.

Fulp CT, Cho G, Marsh ED, Nasrallah IM, Labosky PA, Golden JA.

Hum Mol Genet. 2008 Dec 1;17(23):3740-60. doi: 10.1093/hmg/ddn271. Epub 2008 Sep 16.

12.

An Emerging Female Phenotype with Loss-of-Function Mutations in the Aristaless-Related Homeodomain Transcription Factor ARX.

Mattiske T, Moey C, Vissers LE, Thorne N, Georgeson P, Bakshi M, Shoubridge C.

Hum Mutat. 2017 May;38(5):548-555. doi: 10.1002/humu.23190. Epub 2017 Feb 15.

PMID:
28150386
13.

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

Colasante G, Sessa A, Crispi S, Calogero R, Mansouri A, Collombat P, Broccoli V.

Dev Biol. 2009 Oct 1;334(1):59-71. doi: 10.1016/j.ydbio.2009.07.014. Epub 2009 Jul 21.

14.
15.

Arx is required for specification of the zona incerta and reticular nucleus of the thalamus.

Sunnen CN, Simonet JC, Marsh ED, Golden JA.

J Neuropathol Exp Neurol. 2014 Mar;73(3):253-61. doi: 10.1097/NEN.0000000000000048.

16.

An epilepsy-related ARX polyalanine expansion modifies glutamatergic neurons excitability and morphology without affecting GABAergic neurons development.

Beguin S, Crépel V, Aniksztejn L, Becq H, Pelosi B, Pallesi-Pocachard E, Bouamrane L, Pasqualetti M, Kitamura K, Cardoso C, Represa A.

Cereb Cortex. 2013 Jun;23(6):1484-94. doi: 10.1093/cercor/bhs138. Epub 2012 May 24.

PMID:
22628459
17.

Differential effects of a polyalanine tract expansion in Arx on neural development and gene expression.

Nasrallah MP, Cho G, Simonet JC, Putt ME, Kitamura K, Golden JA.

Hum Mol Genet. 2012 Mar 1;21(5):1090-8. doi: 10.1093/hmg/ddr538. Epub 2011 Nov 22.

18.

Arx together with FoxA2, regulates Shh floor plate expression.

Cho G, Lim Y, Cho IT, Simonet JC, Golden JA.

Dev Biol. 2014 Sep 1;393(1):137-48. doi: 10.1016/j.ydbio.2014.06.012. Epub 2014 Jun 23.

19.

ARX homeodomain mutations abolish DNA binding and lead to a loss of transcriptional repression.

Shoubridge C, Tan MH, Seiboth G, Gécz J.

Hum Mol Genet. 2012 Apr 1;21(7):1639-47. doi: 10.1093/hmg/ddr601. Epub 2011 Dec 21.

PMID:
22194193
20.

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

Bienvenu T, Poirier K, Friocourt G, Bahi N, Beaumont D, Fauchereau F, Ben Jeema L, Zemni R, Vinet MC, Francis F, Couvert P, Gomot M, Moraine C, van Bokhoven H, Kalscheuer V, Frints S, Gecz J, Ohzaki K, Chaabouni H, Fryns JP, Desportes V, Beldjord C, Chelly J.

Hum Mol Genet. 2002 Apr 15;11(8):981-91.

PMID:
11971879

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