Generation of mice with a conditional Foxp2 null allele (Q28586785)

31 January 2017

title

Generation of mice with a conditional Foxp2 null allele (English)

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31 January 2017

1 reference

GOA release 2020-03-11

Catherine A. French

1

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Matthias Groszer

object named as

Matthias Groszer

2

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Klaus Rajewsky

object named as

Klaus Rajewsky

5

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author name string

Christopher Preece

3

1 reference

31 January 2017

Anne-Marie Coupe

4

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31 January 2017

Simon E. Fisher

6

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31 January 2017

publication date

1 July 2007

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31 January 2017

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31 January 2017

volume

45

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31 January 2017

issue

7

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31 January 2017

page(s)

440–446

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

31 January 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

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

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

FOXP2 and the neuroanatomy of speech and language

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

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

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

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

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

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

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

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

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

High-efficiency deleter mice show that FLPe is an alternative to Cre-loxP

17 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

FoxP2 expression in avian vocal learners and non-learners

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

Forkhead transcription factors: key players in development and metabolism

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

The eloquent ape: genes, brains and the evolution of language

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

Language fMRI abnormalities associated with FOXP2 gene mutation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

Multiple Domains Define the Expression and Regulatory Properties of Foxp1 Forkhead Transcriptional Repressors

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

Conditional control of gene expression in the mouse

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

Maternal inheritance of Cre activity in a Sox2Cre deleter strain

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

FOXP2 in focus: what can genes tell us about speech and language?

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

Targeted disruption of the MHC class II Aa gene in C57BL/6 mice

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

Isolation and characterization of a novel cDNA clone encoding a homeodomain that is developmentally regulated in the ventral forebrain

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2.

3 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FDVG.20305

Molecular cloning and developmental expression of foxP2 in zebrafish

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

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

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

Domain-restricted expression of two glutamic acid decarboxylase genes in midgestation mouse embryos.

27 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2682329

Highly efficient transgene-independent recombination directed by a maternally derived SOX2CRE transgene

27 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/17619227

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Conditional gene mutagenesis in B-lineage cells

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FDVG.20305

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/DVG.20305

1 reference

1 reference

1 reference

1 reference