| scholarly article | Q13442814 |
| P356 | DOI | 10.1093/HMG/DDW360 |
| P8608 | Fatcat ID | release_hgwzpy3ykvbd7oxbyvqbpu7rli |
| P698 | PubMed publication ID | 27798109 |
| P50 | author | Jozef Gécz | Q16230617 |
| Cheryl Shoubridge | Q37062513 | ||
| Tessa Mattiske | Q57004017 | ||
| P2093 | author name string | Gaelle Friocourt | |
| Kristie Lee | |||
| P2860 | cites work | Mutations of the TWIST gene in the Saethre-Chotzen syndrome | Q24311736 |
| De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies | Q24563008 | ||
| De novo mutations in epileptic encephalopathies | Q24621776 | ||
| Twist-1 regulates the miR-199a/214 cluster during development | Q24652478 | ||
| edgeR: a Bioconductor package for differential expression analysis of digital gene expression data | Q27860819 | ||
| Human ARX gene: genomic characterization and expression | Q28160539 | ||
| Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans | Q28207647 | ||
| ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation | Q28215614 | ||
| High-throughput analysis of promoter occupancy reveals new targets for Arx, a gene mutated in mental retardation and interneuronopathies | Q28506691 | ||
| MEF2C, a transcription factor that facilitates learning and memory by negative regulation of synapse numbers and function | Q28507026 | ||
| Cell-autonomous roles of ARX in cell proliferation and neuronal migration during corticogenesis | Q28571585 | ||
| Inactivation of Arx, the murine ortholog of the X-linked lissencephaly with ambiguous genitalia gene, leads to severe disorganization of the ventral telencephalon with impaired neuronal migration and differentiation | Q28591633 | ||
| HTSeq--a Python framework to work with high-throughput sequencing data | Q29614489 | ||
| 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 | Q30484137 | ||
| Neonatal estradiol stimulation prevents epilepsy in Arx model of X-linked infantile spasms syndrome. | Q30578899 | ||
| Convergence of genes and cellular pathways dysregulated in autism spectrum disorders | Q33794546 | ||
| A de novo convergence of autism genetics and molecular neuroscience | Q33830989 | ||
| Genome-wide Twist1 occupancy in endocardial cushion cells, embryonic limb buds, and peripheral nerve sheath tumor cells | Q34308984 | ||
| DNA methylation analysis of the autistic brain reveals multiple dysregulated biological pathways | Q34370448 | ||
| Molecular convergence of neurodevelopmental disorders | Q34478048 | ||
| Enrichr: interactive and collaborative HTML5 gene list enrichment analysis tool | Q34668270 | ||
| The histone deacetylase HDAC4 regulates long-term memory in Drosophila | Q35071111 | ||
| Unraveling the pathogenesis of ARX polyalanine tract variants using a clinical and molecular interfacing approach | Q35648072 | ||
| Differential effects of a polyalanine tract expansion in Arx on neural development and gene expression | Q35750224 | ||
| Developmental interneuron subtype deficits after targeted loss of Arx | Q36048943 | ||
| Identification of Arx transcriptional targets in the developing basal forebrain | Q36967946 | ||
| ARX spectrum disorders: making inroads into the molecular pathology | Q37761093 | ||
| Targeting the correct HDAC(s) to treat cognitive disorders | Q37803453 | ||
| Treatment of epilepsy in children with developmental disabilities | Q37803574 | ||
| Epithelial plasticity: a common theme in embryonic and cancer cells. | Q38160727 | ||
| ERGDB: Estrogen Responsive Genes Database | Q40403424 | ||
| Identification of estrogen-responsive genes using a genome-wide analysis of promoter elements for transcription factor binding sites | Q40442658 | ||
| Genome-wide identification of high-affinity estrogen response elements in human and mouse | Q40582192 | ||
| Arx acts as a regional key selector gene in the ventral telencephalon mainly through its transcriptional repression activity | Q42457411 | ||
| Reduced polyalanine-expanded Arx mutant protein in developing mouse subpallium alters Lmo1 transcriptional regulation | Q43487904 | ||
| An epilepsy-related ARX polyalanine expansion modifies glutamatergic neurons excitability and morphology without affecting GABAergic neurons development | Q44328224 | ||
| Polyalanine expansion in HOXA13: three new affected families and the molecular consequences in a mouse model | Q45072730 | ||
| Expression of a novel aristaless related homeobox gene 'Arx' in the vertebrate telencephalon, diencephalon and floor plate | Q48047643 | ||
| Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice | Q48521766 | ||
| Identification of Arx targets unveils new candidates for controlling cortical interneuron migration and differentiation | Q58493057 | ||
| P433 | issue | 24 | |
| P921 | main subject | transcriptome | Q252857 |
| P304 | page(s) | 5433-5443 | |
| P577 | publication date | 2016-10-25 | |
| P1433 | published in | Human Molecular Genetics | Q2720965 |
| P1476 | title | Embryonic forebrain transcriptome of mice with polyalanine expansion mutations in the ARX homeobox gene | |
| P478 | volume | 25 |
| Q89600951 | Arx expansion mutation perturbs cortical development by augmenting apoptosis without activating innate immunity in a mouse model of X-Linked Infantile Spasms Syndrome |
| Q61800390 | HDAC4 gene silencing alleviates epilepsy by inhibition of GABA in a rat model |
| Q92794897 | Heterozygous loss of function of IQSEC2/Iqsec2 leads to increased activated Arf6 and severe neurocognitive seizure phenotype in females |
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