(Q24530590)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

title

Altered ultrasonic vocalization in mice with a disruption in the Foxp2 gene (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

1 reference

GOA release 2020-03-11

0 references

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

Julie Y Cho

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

8

Rita De Gasperi

1 reference

13 January 2020

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

7

James Schmeidler

1 reference

13 January 2020

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

Weiguo Shu

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

Yuhui Jiang

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

Minhua Zhang

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

Donald Weisz

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

Gregory A Elder

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

Miguel A Gama Sosa

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

Donald Rabidou

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

Anthony C Santucci

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

Daniel Perl

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

Edward Morrisey

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

language of work or name

English

0 references

publication date

27 June 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

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

13 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

volume

102

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

page(s)

9643-9648

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

issue

27

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

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

13 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

Chromosome 7q: where autism meets language disorder?

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

FOXP2 and the neuroanatomy of speech and language

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

Mutation screening of FOXP2 in individuals diagnosed with autistic disorder

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

An extended family with a dominantly inherited speech disorder

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

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

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

FoxP2 expression in avian vocal learners and non-learners

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

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=1160518

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

Acoustic variability and distinguishability among mouse ultrasound vocalizations.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

A genome scan for developmental dyslexia confirms linkage to chromosome 2p11 and suggests a new locus on 7q32

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

Association of specific language impairment (SLI) to the region of 7q31.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

FOXP2: novel exons, splice variants, and CAG repeat length stability

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

Evaluation of FOXP2 as an autism susceptibility gene

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

Regional meta-analysis of published data supports linkage of autism with markers on chromosome 7.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

Ultrasonic vocalisation emitted by infant rodents: a tool for assessment of neurobehavioural development.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

Central nervous system neuronal migration

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

A cell cycle alteration precedes apoptosis of granule cell precursors in the weaver mouse cerebellum

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

Effects of scopolamine on spatial working memory in rats pretreated with the serotonergic depleter p-chloroamphetamine.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

Maternal responses to infant vocalizations and olfactory cues in rats and mice.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

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

30 May 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0503739102

Entorhinal cortex lesioning promotes neurogenesis in the hippocampus of adult mice

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0503739102

Association between the FOXP2 gene and autistic disorder in Chinese population.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1160518

Support for the MnlI polymorphism of SNAP25; a Korean ADHD case-control study

29 November 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0503739102

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1073/PNAS.0503739102

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

OpenCitations bibliographic resource ID

13 January 2020

ADS bibcode

2005PNAS..102.9643S

0 references

1602719

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1602719

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15983371%20AND%20SRC:MED&resulttype=core&format=json

13 January 2020

1 reference