Language fMRI abnormalities associated with FOXP2 gene mutation.
about
Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X.Auditory hallucinations in schizophrenia: the role of cognitive, brain structural and genetic disturbances in the left temporal lobe.Accelerated FoxP2 evolution in echolocating batsGestures, vocalizations, and memory in language origins.Common neural substrates for inhibition of spoken and manual responsesIntervention for childhood apraxia of speechIdentification of FOXP2 truncation as a novel cause of developmental speech and language deficitsFOXP2Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficitsHuman brain evolution: from gene discovery to phenotype discoveryThe distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disordersHigh-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disordersThe role of the basal ganglia and cerebellum in language processingFoxP2 regulation during undirected singing in adult songbirds.Singing mice, songbirds, and more: models for FOXP2 function and dysfunction in human speech and languageNeural Correlates of Developmental Speech and Language Disorders: Evidence from NeuroimagingNeurogenomics of speech and language disorders: the road aheadGeneration of mice with a conditional Foxp2 null alleleA Gradualist Scenario for Language Evolution: Precise Linguistic Reconstruction of Early Human (and Neandertal) GrammarsA Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice.Neural FoxP2 and FoxP1 expression in the budgerigar, an avian species with adult vocal learningHumanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performanceLeft brain, right brain: facts and fantasiesImaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.Young and intense: FoxP2 immunoreactivity in Area X varies with age, song stereotypy, and singing in male zebra finchesAn aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learningCNTNAP2 and language processing in healthy individuals as measured with ERPsFoxp2 mutations impair auditory-motor association learning.Recent advances in the genetics of language impairmentStriatal FoxP2 is actively regulated during songbird sensorimotor learning.Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cellsDomain-specific regulation of foxP2 CNS expression by lef1Birdsong decreases protein levels of FoxP2, a molecule required for human speech.Functional and evolutionary insights into human brain development through global transcriptome analysisTo transduce a zebra finch: interrogating behavioral mechanisms in a model system for speechBrain mechanisms of acoustic communication in humans and nonhuman primates: an evolutionary perspective.Knockdown of FoxP2 alters spine density in Area X of the zebra finch.Abnormal functional lateralization and activity of language brain areas in typical specific language impairment (developmental dysphasia).Neurophysiology of speech differences in childhood apraxia of speech.Structural brain differences in school-age children with residual speech sound errors.
P2860
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P2860
Language fMRI abnormalities associated with FOXP2 gene mutation.
description
2003 nî lūn-bûn
@nan
2003 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Language fMRI abnormalities associated with FOXP2 gene mutation.
@ast
Language fMRI abnormalities associated with FOXP2 gene mutation.
@en
Language fMRI abnormalities associated with FOXP2 gene mutation.
@nl
type
label
Language fMRI abnormalities associated with FOXP2 gene mutation.
@ast
Language fMRI abnormalities associated with FOXP2 gene mutation.
@en
Language fMRI abnormalities associated with FOXP2 gene mutation.
@nl
prefLabel
Language fMRI abnormalities associated with FOXP2 gene mutation.
@ast
Language fMRI abnormalities associated with FOXP2 gene mutation.
@en
Language fMRI abnormalities associated with FOXP2 gene mutation.
@nl
P2093
P356
P1433
P1476
Language fMRI abnormalities associated with FOXP2 gene mutation.
@en
P2093
Alan Connelly
David G Gadian
Frédérique Liégeois
Torsten Baldeweg
P2888
P304
P356
10.1038/NN1138
P407
P577
2003-10-12T00:00:00Z