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

Corpus callosum agenesis, severe mental retardation, epilepsy, and dyskinetic quadriparesis due to a novel mutation in the homeodomain of ARX

(2011) Valerio Conti et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Screening and cell-based assessment of mutations in the Aristaless-related homeobox (ARX) gene

(2011) T Fullston et al.   CLINICAL GENETICS

Genome-wide mapping of ZNF652 promoter binding sites in breast cancer cells

(2011) Raman Kumar et al.   JOURNAL OF CELLULAR BIOCHEMISTRY

ARX spectrum disorders: making inroads into the molecular pathology

(2010) Cheryl Shoubridge et al.   HUMAN MUTATION

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

(2009) Eric Marsh et al.   BRAIN

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

(2009) Kunio Kitamura et al.   HUMAN MOLECULAR GENETICS

The Roles of Multiple Importins for Nuclear Import of Murine Aristaless-related Homeobox Protein

(2009) Wenbo Lin et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

The genetic landscape of intellectual disability arising from chromosome X

(2009) Jozef Gécz et al.   TRENDS IN GENETICS

Identification of Arx transcriptional targets in the developing basal forebrain

(2008) Carl T. Fulp et al.   HUMAN MOLECULAR GENETICS

Arx Is a Direct Target of Dlx2 and Thereby Contributes to the Tangential Migration of GABAergic Interneurons

(2008) G. Colasante et al.   JOURNAL OF NEUROSCIENCE