Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits - Wikidata - awgldk - TriplyDB

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

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

http://www.wikidata.org/entity/Q24530823

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Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X.Accelerated FoxP2 evolution in echolocating bats Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.Transcriptional regulation by FOXP1, FOXP2, and FOXP4 dimerization De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment A functional genetic link between distinct developmental language disorders Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene FOXP2 Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits Evo-devo, deep homology and FoxP2: implications for the evolution of speech and language.Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder Genetic advances in the study of speech and language disorders Severe expressive-language delay related to duplication of the Williams-Beuren locus.The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders At the height of fashion: what genetics can teach us about neurodevelopmental disabilities Genes, cognition, and communication: insights from neurodevelopmental disorders Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia The human lexinome: genes of language and reading Human-specific transcriptional regulation of CNS development genes by FOXP2 FoxP2 regulation during undirected singing in adult songbirds.Singing mice, songbirds, and more: models for FOXP2 function and dysfunction in human speech and language Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia The language faculty that wasn't: a usage-based account of natural language recursion Increased glutamate and homocysteine and decreased glutamine levels in autism: a review and strategies for future studies of amino acids in autism Neurogenomics of speech and language disorders: the road ahead Knockout of Foxp2 disrupts vocal development in mice.Generation of mice with a conditional Foxp2 null allele Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.Animal Models of Speech and Vocal Communication Deficits Associated With Psychiatric Disorders Recent Advances in the Genetics of Vocal Learning Differential FoxP2 and FoxP1 expression in a vocal learning nucleus of the developing budgerigar.Association study of stuttering candidate genes GNPTAB, GNPTG and NAGPA with dyslexia in Chinese population.Globularity and language-readiness: generating new predictions by expanding the set of genes of interest Stuttering candidate genes DRD2 but not SLC6A3 is associated with developmental dyslexia in Chinese population 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.

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P2860

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

http://www.wikidata.org/entity/Q24530823

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2005 nî lūn-bûn

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2005 թուականի Յունիսին հրատարակուած գիտական յօդուած

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2005年の論文

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Identification of FOXP2 trunca ...... l speech and language deficits

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Identification of FOXP2 trunca ...... l speech and language deficits

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Anne-Marie Coupe

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Cecilia S L Lai

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Fiona McKenzie

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Kay D MacDermot

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Nuala Sykes

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Robert L Smith

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P2860

Predicting deleterious amino acid substitutions

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

Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1

FOXP2 is not a major susceptibility gene for autism or specific language impairment

Neural basis of an inherited speech and language disorder.

FoxP4, a novel forkhead transcription factor

Mutation screening of FOXP2 in individuals diagnosed with autistic disorder

A forkhead-domain gene is mutated in a severe speech and language disorder

Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia

FOXP2 and the neuroanatomy of speech and language

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1074-80

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Faraneh Vargha-Khadem

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