Humanized Foxp2 specifically affects cortico-basal ganglia circuits (Q42480395)

1 November 2017

Humanized Foxp2 specifically affects cortico-basal ganglia circuits (English)

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1 November 2017

3

S Pääbo

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1 November 2017

S Reimers-Kipping

1

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1 November 2017

W Hevers

series ordinal

2

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1 November 2017

W Enard

series ordinal

4

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1 November 2017

language of work or name

English

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publication date

25 November 2010

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1 November 2017

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75-84

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FOXP2 as a molecular window into speech and language

1 November 2017

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Language fMRI abnormalities associated with FOXP2 gene mutation

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

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A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice

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

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

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Dopamine receptor activation is required for corticostriatal spike-timing-dependent plasticity.

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The forkhead transcription factors, Foxp1 and Foxp2, identify different subpopulations of projection neurons in the mouse cerebral cortex

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FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder.

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Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells

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Behavioural analysis of an inherited speech and language disorder: comparison with acquired aphasia.

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

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

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Start/stop signals emerge in nigrostriatal circuits during sequence learning

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Conservation and diversity of Foxp2 expression in muroid rodents: functional implications

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Dendritic size of pyramidal neurons differs among mouse cortical regions.

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Foxp2 and Foxp1 cooperatively regulate lung and esophagus development

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Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain.

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

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Branching out: mechanisms of dendritic arborization

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Identifiers

DOI

10.1016/J.NEUROSCIENCE.2010.11.042

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1 November 2017

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