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Conditional Loss of Arx From the Developing Dorsal Telencephalon Results in Behavioral Phenotypes Resembling Mild Human ARX Mutations.Common transcriptional mechanisms for visual photoreceptor cell differentiation among PancrustaceansHigh-throughput analysis of promoter occupancy reveals new targets for Arx, a gene mutated in mental retardation and interneuronopathiesA 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 impairmentArx is required for specification of the zona incerta and reticular nucleus of the thalamus.Mutations in ARX Result in Several Defects Involving GABAergic Neurons.Candidate gene screen in the red flour beetle Tribolium reveals six3 as ancient regulator of anterior median head and central complex development.The genetic basis of non-syndromic intellectual disability: a reviewRole of cytoskeletal abnormalities in the neuropathology and pathophysiology of type I lissencephalyAltered GABA signaling in early life epilepsies.ARX regulates cortical intermediate progenitor cell expansion and upper layer neuron formation through repression of Cdkn1c.Genetics and function of neocortical GABAergic interneurons in neurodevelopmental disordersCharacterization of homeobox genes reveals sophisticated regionalization of the central nervous system in the European cuttlefish Sepia officinalis.Epilepsy as a neurodevelopmental disorder.Transcription factor modularity in a gene-centered C. elegans core neuronal protein-DNA interaction network.Karyopherins in nuclear transport of homeodomain proteins during development.Mutation screening of the ARX gene in patients with autismArx polyalanine expansion in mice leads to reduced pancreatic α-cell specification and increased α-cell death.Involvement of cortical fast-spiking parvalbumin-positive basket cells in epilepsy.Molecules and mechanisms involved in the generation and migration of cortical interneuronsDevelopmental mechanisms for the generation of telencephalic interneurons.The role of GABAergic system in neurodevelopmental disorders: a focus on autism and epilepsy.Interneuron, interrupted: molecular pathogenesis of ARX mutations and X-linked infantile spasms.Axon guidance mechanisms for establishment of callosal connections.Nuclear import of aristaless-related homeobox protein via its NLS1 regulates its transcriptional function.Copy number variants in patients with intellectual disability affect the regulation of ARX transcription factor gene.The terminal nerve plays a prominent role in GnRH-1 neuronal migration independent from proper olfactory and vomeronasal connections to the olfactory bulbs.A novel mutation in the aristaless domain of the ARX gene leads to Ohtahara syndrome, global developmental delay, and ambiguous genitalia in males and neuropsychiatric disorders in females.A new mouse model of ARX dup24 recapitulates the patients' behavioural and fine motor alterations.Basal ganglia involvement in ARX patients: The reason for ARX patients very specific grasping?Identification of Arx targets unveils new candidates for controlling cortical interneuron migration and differentiation
P2860
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P2860
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh
2006年學術文章
@zh-hant
name
The role of ARX in cortical development.
@ast
The role of ARX in cortical development.
@en
type
label
The role of ARX in cortical development.
@ast
The role of ARX in cortical development.
@en
prefLabel
The role of ARX in cortical development.
@ast
The role of ARX in cortical development.
@en
P2093
P1476
The role of ARX in cortical development.
@en
P2093
Gaëlle Friocourt
Jamel Chelly
John G Parnavelas
Sonja Rakić
P2860
P304
P356
10.1111/J.1460-9568.2006.04629.X
P407
P577
2006-02-01T00:00:00Z