Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits - Wikidata - wikimedia - TriplyDB

Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits

Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits

http://www.wikidata.org/entity/Q24594611

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Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain Human and great ape red blood cells differ in plasmalogen levels and composition Gestures, vocalizations, and memory in language origins.The human language-associated gene SRPX2 regulates synapse formation and vocalization in mice FOXP2 Human brain evolution: from gene discovery to phenotype discovery A 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.Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.Genes and social behavior The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia Shaping action sequences in basal ganglia circuits Neurogenomics of speech and language disorders: the road ahead Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3.Drosophila FoxP mutants are deficient in operant self-learning Knockout of Foxp2 disrupts vocal development in mice.Mass Spectrometry-Based Approaches to Understand the Molecular Basis of Memory Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder Challenging the use of adult neuropsychological models for explaining neurodevelopmental disorders: developed versus developing brains Convergent evidence for the molecular basis of musical traits.Functional characterization of rare FOXP2 variants in neurodevelopmental disorder.Communication impairments in mice lacking Shank1: reduced levels of ultrasonic vocalizations and scent marking behavior.A Foxp2 Mutation Implicated in Human Speech Deficits Alters Sequencing of Ultrasonic Vocalizations in Adult Male Mice.The language-related transcription factor FOXP2 is post-translationally modified with small ubiquitin-like modifiers Animal Models of Speech and Vocal Communication Deficits Associated With Psychiatric Disorders Recent Advances in the Genetics of Vocal Learning Social cognition and the evolution of language: constructing cognitive phylogenies Behavior-linked FoxP2 regulation enables zebra finch vocal learning Globularity and language-readiness: generating new predictions by expanding the set of genes of interest Humanized Foxp2 accelerates learning by enhancing transitions from declarative to procedural performance Single nucleotide polymorphism in the neuroplastin locus associates with cortical thickness and intellectual ability in adolescents Diminished FoxP2 levels affect dopaminergic modulation of corticostriatal signaling important to song variability.ASD-relevant Animal Models of the Foxp Family of Transcription Factors Rapid diversification of FoxP2 in teleosts through gene duplication in the teleost-specific whole genome duplication event Imaging-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 finches An aetiological Foxp2 mutation causes aberrant striatal activity and alters plasticity during skill learning Mice do not require auditory input for the normal development of their ultrasonic vocalizations.Foxp2 mutations impair auditory-motor association learning.

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P2860

Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits

http://www.wikidata.org/entity/Q24594611

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2008 nî lūn-bûn

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Günter Ehret

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J Nicholas P Rawlins

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Joseph P de Bono

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Julie A Coventry

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Jérôme Nicod

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Martin Fray

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Muriel G Baum

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Shweta Prasad-Mulcare

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Simone Gaub

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P2860

Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X.

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

Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene

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

FoxP2 regulation during undirected singing in adult songbirds.

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

Short-term synaptic plasticity

FOXP2 and the neuroanatomy of speech and language

Foxp2 and Foxp1 cooperatively regulate lung and esophagus development

Generation of mice with a conditional Foxp2 null allele

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Catherine A. French

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