Pages that link to "Q28207647"

The following pages link to Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans (Q28207647):

Displaying 50 items.

• lissencephaly (Q1544416) (← links)
• Aristaless related homeobox (Q15319745) (← links)
• Deletion of ultraconserved elements yields viable mice (Q21092753) (← links)
• X-linked disorders with cerebellar dysgenesis (Q21202871) (← links)
• Analysis of four DLX homeobox genes in autistic probands (Q21283791) (← links)
• Childhood autism and associated comorbidities (Q22252337) (← links)
• Disruption of the serine/threonine kinase 9 gene causes severe X-linked infantile spasms and mental retardation (Q24532056) (← links)
• Seizures and X-linked intellectual disability (Q24594966) (← links)
• Regulatory long non-coding RNAs and neuronal disorders (Q24632237) (← links)
• Dlx5 and Dlx6 regulate the development of parvalbumin-expressing cortical interneurons (Q24633275) (← links)
• Male sex determination: insights into molecular mechanisms (Q24633383) (← links)
• A longer polyalanine expansion mutation in the ARX gene causes early infantile epileptic encephalopathy with suppression-burst pattern (Ohtahara syndrome) (Q24678062) (← links)
• Genes and brain malformations associated with abnormal neuron positioning (Q26779045) (← links)
• Cellullar insights into cerebral cortical development: focusing on the locomotion mode of neuronal migration (Q26779317) (← links)
• TALE transcription factors during early development of the vertebrate brain and eye (Q26825693) (← links)
• Fragile X and X-linked intellectual disability: four decades of discovery (Q27027343) (← links)
• Conditional Loss of Arx From the Developing Dorsal Telencephalon Results in Behavioral Phenotypes Resembling Mild Human ARX Mutations (Q27302983) (← links)
• The Transcriptional Activator Krüppel-like Factor-6 Is Required for CNS Myelination (Q27342581) (← links)
• (Q28174666) (redirect page) (← links)
• Genetic malformations of cortical development (Q28242257) (← links)
• Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy (Q28260777) (← links)
• The LIM-homeobox gene Islet-1 is required for the development of restricted forebrain cholinergic neurons (Q28504624) (← links)
• The RHOX5 homeodomain protein mediates transcriptional repression of the netrin-1 receptor gene Unc5c (Q28505825) (← links)
• Arx is required for normal enteroendocrine cell development in mice and humans (Q28506459) (← links)
• High-throughput analysis of promoter occupancy reveals new targets for Arx, a gene mutated in mental retardation and interneuronopathies (Q28506691) (← links)
• Lis1 is necessary for normal non-radial migration of inhibitory interneurons (Q28507800) (← links)
• A regulatory path associated with X-linked intellectual disability and epilepsy links KDM5C to the polyalanine expansions in ARX (Q28508740) (← links)
• Cell-autonomous roles of ARX in cell proliferation and neuronal migration during corticogenesis (Q28571585) (← links)
• 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) (← links)
• Pdgfr-alpha mediates testis cord organization and fetal Leydig cell development in the XY gonad (Q28594102) (← links)
• Possible functional links among brain- and skull-related genes selected in modern humans (Q28648399) (← links)
• Caenorhabditis elegans aristaless/Arx gene alr-1 restricts variable gene expression (Q28742056) (← links)
• A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3 (Q29147508) (← links)
• De Novo Mutations in EBF3 Cause a Neurodevelopmental Syndrome (Q29147516) (← links)
• Model of autism: increased ratio of excitation/inhibition in key neural systems (Q29547530) (← links)
• The origin and specification of cortical interneurons (Q29622901) (← links)
• Identification of a Protein Network Driving Neuritogenesis of MGE-Derived GABAergic Interneurons. (Q30354530) (← links)
• Xenopus mutant reveals necessity of rax for specifying the eye field which otherwise forms tissue with telencephalic and diencephalic character. (Q30366238) (← links)
• Disturbances in the positioning, proliferation and apoptosis of neural progenitors contribute to subcortical band heterotopia formation (Q30427891) (← links)
• Expression of the Ladybird-like homeobox 2 transcription factor in the developing mouse testis and epididymis (Q30443270) (← links)
• 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) (← links)
• Targeted loss of Arx results in a developmental epilepsy mouse model and recapitulates the human phenotype in heterozygous females (Q30487790) (← links)
• KCC2 expression promotes the termination of cortical interneuron migration in a voltage-sensitive calcium-dependent manner. (Q30512206) (← links)
• The LIM homeodomain protein Lhx6 regulates maturation of interneurons and network excitability in the mammalian cortex (Q30541076) (← links)
• The c.429_452 duplication of the ARX gene: a unique developmental-model of limb kinetic apraxia (Q30577795) (← links)
• Neonatal estradiol stimulation prevents epilepsy in Arx model of X-linked infantile spasms syndrome. (Q30578899) (← links)
• The role of Rhox homeobox factors in tumorigenesis (Q30583656) (← links)
• The genetics of lissencephaly (Q30826834) (← links)
• Neuronal migration disorders, genetics, and epileptogenesis (Q30990797) (← links)
• Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity. (Q31106338) (← links)