An Epilepsy-Related ARX Polyalanine Expansion Modifies Glutamatergic Neurons Excitability and Morphology Without Affecting GABAergic Neurons Development

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

(2011) M. P. Nasrallah et al.   HUMAN MOLECULAR GENETICS

Glutamatergic pre-ictal discharges emerge at the transition to seizure in human epilepsy

(2011) Gilles Huberfeld et al.   NATURE NEUROSCIENCE

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

(2010) Pascale Marcorelles et al.   ACTA NEUROPATHOLOGICA

Generation of interneuron diversity in the mouse cerebral cortex

(2010) Diego M. Gelman et al.   EUROPEAN JOURNAL OF NEUROSCIENCE

ARX spectrum disorders: making inroads into the molecular pathology

(2010) Cheryl Shoubridge et al.   HUMAN MUTATION

Partial Disinhibition Is Required for Transition of Stimulus-Induced Sharp Wave–Ripple Complexes Into Recurrent Epileptiform Discharges in Rat Hippocampal Slices

(2010) Agustin Liotta et al.   JOURNAL OF NEUROPHYSIOLOGY

Epileptic syndromes in infancy and childhood

(2009) Rima Nabbout et al.   CURRENT OPINION IN NEUROLOGY

A novel ARX phenotype: rapid neurodegeneration with Ohtahara syndrome and a dyskinetic movement disorder

(2009) MICHAEL ABSOUD et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

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

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

(2009) M. G. Price et al.   JOURNAL OF NEUROSCIENCE

Abnormal Network Activity in a Targeted Genetic Model of Human Double Cortex

(2009) J. B. Ackman et al.   JOURNAL OF NEUROSCIENCE

Genetics of complex neurological disease: challenges and opportunities for modeling epilepsy in mice and rats

(2009) Wayne N. Frankel   TRENDS IN GENETICS

Aristaless-related homeobox gene disruption leads to abnormal distribution of GABAergic interneurons in human neocortex: evidence based on a case of X-linked lissencephaly with abnormal genitalia (XLAG)

(2008) Shin Okazaki et al.   ACTA NEUROPATHOLOGICA

Cell-Autonomous Roles of ARX in Cell Proliferation and Neuronal Migration during Corticogenesis

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

Neuronal Diversity and Temporal Dynamics: The Unity of Hippocampal Circuit Operations

(2008) T. Klausberger et al.   SCIENCE