(Q27302149)

21 June 2017

title

Hearing loss in a mouse model of 22q11.2 Deletion Syndrome (English)

1 reference

21 June 2017

1 reference

Jennifer F Linden

8

Jennifer F

Linden

1 reference

19 October 2023

Abigail S Tucker

7

Abigail S

Tucker

1 reference

19 October 2023

Peter J Scambler

5

Peter J

Scambler

1 reference

19 October 2023

Jennifer C Fuchs

1

Jennifer C

Fuchs

1 reference

21 June 2017

Fhatarah A Zinnamon

2

Fhatarah A

Zinnamon

1 reference

21 June 2017

Ruth R Taylor

3

Ruth R

Taylor

1 reference

21 June 2017

Sarah Ivins

4

Sarah

Ivins

1 reference

21 June 2017

Andrew Forge

6

Andrew

Forge

1 reference

21 June 2017

language of work or name

English

0 references

publication date

14 November 2013

1 reference

21 June 2017

1 reference

21 June 2017

volume

8

1 reference

21 June 2017

issue

11

1 reference

21 June 2017

page(s)

e80104

1 reference

Creative Commons Attribution 3.0 Unported

21 June 2017

copyright license

start time

14 November 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Grommets (ventilation tubes) for hearing loss associated with otitis media with effusion in children

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Hearing loss and otitis media in velo-cardio-facial syndrome

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Eya4-deficient mice are a model for heritable otitis media

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

TBX1 is required for inner ear morphogenesis

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses

21 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

22q11 deletion syndrome: a role for TBX1 in pharyngeal and cardiovascular development

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Can you hear me now? A genetic model of otitis media with effusion

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Mouse models of 22q11 deletion syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Lower prepulse inhibition in children with the 22q11 deletion syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Otolaryngologic manifestations of the 22q11.2 deletion syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Schizophrenia and velo-cardio-facial syndrome.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Developing models of DiGeorge syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Genetic factors are major determinants of phenotypic variability in a mouse model of the DiGeorge/del22q11 syndromes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

The 22q11 deletion syndromes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Otolaryngological manifestations of velocardiofacial syndrome: a retrospective review of 35 patients

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Otitis media in 2253 Pittsburgh-area infants: prevalence and risk factors during the first two years of life

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

A meta-analytic review of the risk factors for acute otitis media

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Congenital heart defects and 22q11 deletions: which genes count?

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Distortion product otoacoustic emissions in the C57BL/6J mouse model of age-related hearing loss

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

The cellular mechanism of ossicular erosion in chronic suppurative otitis media.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Defects in middle ear cavitation cause conductive hearing loss in the Tcof1 mutant mouse

31 May 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0080104

Grommets (ventilation tubes) for hearing loss associated withotitis media with effusion in children

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0080104

A region of mouse chromosome 16 is syntenic to the DiGeorge, velocardiofacial syndrome minimal critical region

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0080104

Cloning and comparative mapping of the DiGeorge syndrome critical region in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0080104

Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0080104

Audiological findings in patients with microdeletion 22q11 (di George/velocardiofacial syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0080104

Dual origin of the epithelium of the mammalian middle ear.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0080104

Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3828191

Congenital heart disease in mice deficient for the DiGeorge syndrome region

28 November 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0080104

The heritability of otitis media: a twin and triplet study

21 January 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/24244619

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic dissection of the DiGeorge syndrome phenotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/24244619

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0080104

1 reference

21 June 2017

0 references

0 references

1 reference