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

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

Identification of Arx transcriptional targets in the developing basal forebrain

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

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

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

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

Reversing Neurodevelopmental Disorders in Adults

(2008) Dan Ehninger et al.   NEURON

Satb2 Is a Postmitotic Determinant for Upper-Layer Neuron Specification in the Neocortex

(2008) Olga Britanova et al.   NEURON

Repeated blockade of GABAA receptors in the medial septal region induces epileptiform activity in the hippocampus

(2008) Maria V. Butuzova et al.   NEUROSCIENCE LETTERS