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Items: 1 to 20 of 101

1.

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.

2.

Arx polyalanine expansion in mice leads to reduced pancreatic α-cell specification and increased α-cell death.

Wilcox CL, Terry NA, May CL.

PLoS One. 2013 Nov 13;8(11):e78741. doi: 10.1371/journal.pone.0078741. eCollection 2013.

3.

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
4.

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
5.

Dlx transcription factors regulate differentiation of dopaminergic neurons of the ventral thalamus.

Andrews GL, Yun K, Rubenstein JL, Mastick GS.

Mol Cell Neurosci. 2003 May;23(1):107-20.

PMID:
12799141
6.

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
7.

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
8.

Aristaless-related homeobox plays a key role in hyperplasia of the pancreas islet α-like cells in mice deficient in proglucagon-derived peptides.

Xu S, Hayashi Y, Takagishi Y, Itoh M, Murata Y.

PLoS One. 2013 May 9;8(5):e64415. doi: 10.1371/journal.pone.0064415. Print 2013.

9.

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.

10.

Aristaless-related homeobox gene, the gene responsible for West syndrome and related disorders, is a Groucho/transducin-like enhancer of split dependent transcriptional repressor.

McKenzie O, Ponte I, Mangelsdorf M, Finnis M, Colasante G, Shoubridge C, Stifani S, Gécz J, Broccoli V.

Neuroscience. 2007 Apr 25;146(1):236-47. Epub 2007 Feb 27.

PMID:
17331656
11.

Arx homeobox gene is essential for development of mouse olfactory system.

Yoshihara S, Omichi K, Yanazawa M, Kitamura K, Yoshihara Y.

Development. 2005 Feb;132(4):751-62.

12.

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
13.

Dysgenesis of enteroendocrine cells in Aristaless-Related Homeobox polyalanine expansion mutations.

Terry NA, Lee RA, Walp ER, Kaestner KH, Lee May C.

J Pediatr Gastroenterol Nutr. 2015 Feb;60(2):192-9. doi: 10.1097/MPG.0000000000000542.

14.

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.

15.

Lhx6 directly regulates Arx and CXCR7 to determine cortical interneuron fate and laminar position.

Vogt D, Hunt RF, Mandal S, Sandberg M, Silberberg SN, Nagasawa T, Yang Z, Baraban SC, Rubenstein JL.

Neuron. 2014 Apr 16;82(2):350-64. doi: 10.1016/j.neuron.2014.02.030.

16.

Molecular pathology of expanded polyalanine tract mutations in the Aristaless-related homeobox gene.

Shoubridge C, Cloosterman D, Parkinson-Lawerence E, Brooks D, Gécz J.

Genomics. 2007 Jul;90(1):59-71. Epub 2007 May 9.

17.

Connections of the zona incerta to the reticular nucleus of the thalamus in the rat.

Cavdar S, Onat F, Cakmak YO, Saka E, Yananli HR, Aker R.

J Anat. 2006 Aug;209(2):251-8.

18.

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

Quillé ML, Carat S, Quéméner-Redon S, Hirchaud E, Baron D, Benech C, Guihot J, Placet M, Mignen O, Férec C, Houlgatte R, Friocourt G.

PLoS One. 2011;6(9):e25181. doi: 10.1371/journal.pone.0025181. Epub 2011 Sep 22.

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 gene for all seasons.

Gécz J, Cloosterman D, Partington M.

Curr Opin Genet Dev. 2006 Jun;16(3):308-16. Epub 2006 May 2. Review.

PMID:
16650978

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