Ultrasonic vocalization impairment of Foxp2 (R552H) knockin mice related to speech-language disorder and abnormality of Purkinje cells (Q28755340)

22 June 2017

title

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

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22 June 2017

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Eriko Fujita

1

1 reference

22 June 2017

Yuko Tanabe

2

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22 June 2017

Akira Shiota

3

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22 June 2017

Masatsugu Ueda

4

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22 June 2017

Kiyotaka Suwa

5

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22 June 2017

Mariko Y Momoi

6

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22 June 2017

Takashi Momoi

7

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22 June 2017

language of work or name

English

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publication date

19 February 2008

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Proceedings of the National Academy of Sciences of the United States of America

22 June 2017

number of pages

6

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based on heuristic

inferred from page(s)

published in

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22 June 2017

volume

105

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22 June 2017

issue

8

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22 June 2017

page(s)

3117-3122

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A neuroligin-3 mutation implicated in autism increases inhibitory synaptic transmission in mice

22 June 2017

cites work

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

16 March 2017

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

16 March 2017

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FOXP2 and the neuroanatomy of speech and language

16 March 2017

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Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions

16 March 2017

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Expression of Foxp2, a gene involved in speech and language, in the developing and adult striatum

16 March 2017

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The G protein-coupled receptor repertoires of human and mouse

16 March 2017

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

16 March 2017

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

16 March 2017

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Characterization of a new subfamily of winged-helix/forkhead (Fox) genes that are expressed in the lung and act as transcriptional repressors

16 March 2017

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Localisation of a gene implicated in a severe speech and language disorder

16 March 2017

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Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice

16 March 2017

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FoxP2 expression in avian vocal learners and non-learners

7 April 2017

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Intracellular distribution of a speech/language disorder associated FOXP2 mutant

7 April 2017

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Functional genetic analysis of mutations implicated in a human speech and language disorder

3 June 2018

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The G0/G1 switch gene 2 is a novel PPAR target gene.

3 June 2018

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Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients

3 June 2018

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3 June 2018

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Microarray analysis uncovers retinoid targets in human bronchial epithelial cells

3 June 2018

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

3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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3 June 2018

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ER stress (PERK/eIF2alpha phosphorylation) mediates the polyglutamine-induced LC3 conversion, an essential step for autophagy formation.

3 June 2018

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Localization of metabotropic GABA receptor subunits GABAB1 and GABAB2 relative to synaptic sites in the rat developing cerebellum.

27 November 2018

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Immunohistochemical characterization of the orphan nuclear receptor ROR alpha in the mouse nervous system.

27 November 2018

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Polyglutamine aggregates stimulate ER stress signals and caspase-12 activation

27 November 2018

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Expression of the helix-loop-helix genes Id-1 and NSCL-1 during cerebellar development.

27 November 2018

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27 November 2018

Identifiers

DOI

10.1073/PNAS.0712298105

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OpenCitations bibliographic resource ID

22 June 2017

0 references

1602718

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1602718

1 reference