High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders - Wikidata - wikimedia - TriplyDB

High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders

High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders

http://www.wikidata.org/entity/Q24648773

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Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain Transcriptional regulation by FOXP1, FOXP2, and FOXP4 dimerization A functional genetic link between distinct developmental language disorders The human language-associated gene SRPX2 regulates synapse formation and vocalization in mice FOXP2 Human brain evolution: from gene discovery to phenotype discovery Evo-devo, deep homology and FoxP2: implications for the evolution of speech and language.PCSK6 is associated with handedness in individuals with dyslexia Genetic advances in the study of speech and language disorders The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia Human-specific transcriptional regulation of CNS development genes by FOXP2 Neurogenomics of speech and language disorders: the road ahead Mice with Dab1 or Vldlr insufficiency exhibit abnormal neonatal vocalization patterns Knockout of Foxp2 disrupts vocal development in mice.Detecting signatures of positive selection associated with musical aptitude in the human genome 22q13.2q13.32 genomic regions associated with severity of speech delay, developmental delay, and physical features in Phelan-McDermid syndrome Implications of Oxytocin in Human Linguistic Cognition: From Genome to Phenome Network analysis of microRNA and mRNA seasonal dynamics in a highly plastic sensorimotor neural circuit Possible functional links among brain- and skull-related genes selected in modern humans Globularity and language-readiness: generating new predictions by expanding the set of genes of interest FOXP2, retinoic acid, and language: a promising direction Core and region-enriched networks of behaviorally regulated genes and the singing genome Diminished FoxP2 levels affect dopaminergic modulation of corticostriatal signaling important to song variability.ASD-relevant Animal Models of the Foxp Family of Transcription Factors Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.miR-9 and miR-140-5p target FoxP2 and are regulated as a function of the social context of singing behavior in zebra finches From the ultrasonic to the infrared: molecular evolution and the sensory biology of bats.An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning What is comparable in comparative cognition?Foxp2 mutations impair auditory-motor association learning.Molecular microcircuitry underlies functional specification in a basal ganglia circuit dedicated to vocal learning Recent advances in the genetics of language impairment Song practice promotes acute vocal variability at a key stage of sensorimotor learning Striatal FoxP2 is actively regulated during songbird sensorimotor learning.The structure of innate vocalizations in Foxp2-deficient mouse pups.Genes and vocal learning Motor learning: the FoxP2 puzzle piece.Domain-specific regulation of foxP2 CNS expression by lef1

P2860

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P2860

High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders

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2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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High-throughput analysis of pr ...... speech and language disorders

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High-throughput analysis of pr ...... speech and language disorders

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Elizabeth Spiteri

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Jennifer M Taylor

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Jérôme Nicod

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Kay E Davies

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P2860

A global transcriptional regulatory role for c-Myc in Burkitt's lymphoma cells

Molecular evolution of FOXP2, a gene involved in speech and language

Gene ontology: tool for the unification of biology

Scurfin (FOXP3) acts as a repressor of transcription and regulates T cell activation

MRI analysis of an inherited speech and language disorder: structural brain abnormalities

Wnt genes define distinct boundaries in the developing human brain: implications for human forebrain patterning

FOXP3 controls regulatory T cell function through cooperation with NFAT

Structure of the forkhead domain of FOXP2 bound to DNA

Characterization of a family of related cellular transcription factors which can modulate human immunodeficiency virus type 1 transcription in vitro

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits

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