A forkhead-domain gene is mutated in a severe speech and language disorder
about
Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolutionComparative genomics search for losses of long-established genes on the human lineageIncomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X.Gene losses during human originsAuditory hallucinations in schizophrenia: the role of cognitive, brain structural and genetic disturbances in the left temporal lobe.Accelerated FoxP2 evolution in echolocating batsFoxp2 regulates gene networks implicated in neurite outgrowth in the developing brainUltrasonic songs of male mice.Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.Genome-wide matching of genes to cellular roles using guilt-by-association models derived from single sample analysisEvolution at two levels: on genes and formNeanderthal genomics and the evolution of modern humansMolecular evolution of FOXP2, a gene involved in speech and languageGenetics of austim: complex aetiology for a heterogeneous disorderLinguistic tone is related to the population frequency of the adaptive haplogroups of two brain size genes, ASPM and MicrocephalinCommon neural substrates for inhibition of spoken and manual responsesIntervention for childhood apraxia of speechFOXC1 transcriptional regulation is mediated by N- and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domainTranscriptional regulation by FOXP1, FOXP2, and FOXP4 dimerizationDe novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairmentFoxp2 inhibits Nkx2.1-mediated transcription of SP-C via interactions with the Nkx2.1 homeodomainA functional genetic link between distinct developmental language disordersFoxP1 stimulates angiogenesis by repressing the inhibitory guidance protein semaphorin 5B in endothelial cellsMutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disordersSevere defects in proliferation and differentiation of lens cells in Foxe3 null miceThe human language-associated gene SRPX2 regulates synapse formation and vocalization in miceAltered ultrasonic vocalization in mice with a disruption in the Foxp2 geneIdentification of FOXP2 truncation as a novel cause of developmental speech and language deficitsFOXP2 is not a major susceptibility gene for autism or specific language impairmentFOXP2Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficitsA high-coverage genome sequence from an archaic Denisovan individualHuman brain evolution: from gene discovery to phenotype discoveryHuman chromosome 7: DNA sequence and biologyA locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3.Evo-devo, deep homology and FoxP2: implications for the evolution of speech and language.Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactionsChildhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.Genetic advances in the study of speech and language disordersA genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27
P2860
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P2860
A forkhead-domain gene is mutated in a severe speech and language disorder
description
2001 nî lūn-bûn
@nan
2001 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
A forkhead-domain gene is mutated in a severe speech and language disorder
@ast
A forkhead-domain gene is mutated in a severe speech and language disorder
@en
A forkhead-domain gene is mutated in a severe speech and language disorder
@nl
type
label
A forkhead-domain gene is mutated in a severe speech and language disorder
@ast
A forkhead-domain gene is mutated in a severe speech and language disorder
@en
A forkhead-domain gene is mutated in a severe speech and language disorder
@nl
prefLabel
A forkhead-domain gene is mutated in a severe speech and language disorder
@ast
A forkhead-domain gene is mutated in a severe speech and language disorder
@en
A forkhead-domain gene is mutated in a severe speech and language disorder
@nl
P2093
P3181
P356
P1433
P1476
A forkhead-domain gene is mutated in a severe speech and language disorder
@en
P2093
P2888
P304
P3181
P356
10.1038/35097076
P407
P577
2001-10-04T00:00:00Z
P5875
P6179
1027123435