(Q28511832)

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Hearing and vestibular deficits in the Coch null mouse model: Comparison to the Coch mouse and to DFNA9 hearing and balance disorder

scientific article published on November 10, 2010

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Europe PubMed Central

PubMed publication ID

21 June 2017

Hearing and vestibular deficits in the Coch(-/-) null mouse model: comparison to the Coch(G88E/G88E) mouse and to DFNA9 hearing and balance disorder (English)

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

Hearing and vestibular deficits in the Coch null mouse model: Comparison to the Coch mouse and to DFNA9 hearing and balance disorder (English)

1 reference

10.1016/J.HEARES.2010.11.002

https://api.crossref.org/works/10.1016/J.HEARES.2010.11.002

25 August 2024

1 reference

GOA release 2020-03-11

postural balance

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21073934

25 August 2024

M Charles Liberman

5

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M Charles Liberman

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

author name string

Shelly Given

3

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

Sherri M. Jones

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21073934

25 August 2024

Nahid G. Robertson

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21073934

25 August 2024

Anne B. S. Giersch

4

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21073934

25 August 2024

Cynthia C. Morton

6

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21073934

25 August 2024

language of work or name

1 reference

National Center for Biotechnology Information

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=21073934

25 August 2024

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10 November 2010

1 reference

Europe PubMed Central

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21 June 2017

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21073934

25 August 2024

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21073934/?tool=EBI

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21073934

25 August 2024

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21073934/pdf/?tool=EBI

Portable Document Format

online access status

content deliverer

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21073934

25 August 2024

https://europepmc.org/articles/PMC3039082

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21073934

25 August 2024

https://europepmc.org/articles/PMC3039082?pdf=render

Portable Document Format

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content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21073934

25 August 2024

https://doi.org/10.1016/j.heares.2010.11.002

online access status

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A21073934

25 August 2024

https://api.elsevier.com/content/article/PII:S0378595510004247?httpAccept=text/xml

1 reference

10.1016/J.HEARES.2010.11.002

https://api.crossref.org/works/10.1016/J.HEARES.2010.11.002

25 August 2024

https://api.elsevier.com/content/article/PII:S0378595510004247?httpAccept=text/plain

1 reference

10.1016/J.HEARES.2010.11.002

https://api.crossref.org/works/10.1016/J.HEARES.2010.11.002

25 August 2024

Hearing Research

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

272

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

1-2

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

42-48

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

Functional role of GABAergic innervation of the cochlea: phenotypic analysis of mice lacking GABA(A) receptor subunits alpha 1, alpha 2, alpha 5, alpha 6, beta 2, beta 3, or delta.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

19 March 2017

Mice with altered KCNQ4 K+ channels implicate sensory outer hair cells in human progressive deafness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

19 March 2017

Type IX collagen knock-out mouse shows progressive hearing loss

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

19 March 2017

Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

19 March 2017

Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

19 March 2017

COCH5B2 is a target antigen of anti-inner ear antibodies in autoimmune inner ear diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

19 March 2017

Identification of a novel COCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

19 March 2017

Vestibular responses to linear acceleration are absent in otoconia-deficient C57BL/6JEi-het mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

19 March 2017

High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

19 March 2017

A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

19 March 2017

Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

19 March 2017

Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

7 April 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

7 April 2017

Muscarinic signaling in the cochlea: presynaptic and postsynaptic effects on efferent feedback and afferent excitability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

29 September 2017

Role of protein misfolding in DFNA9 hearing loss.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

29 September 2017

Inheritance patterns of progressive hearing loss in laboratory strains of mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

29 September 2017

A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

29 September 2017

Vestibular deterioration precedes hearing deterioration in the P51S COCH mutation (DFNA9): an analysis in 74 mutation carriers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

29 September 2017

A novel COCH mutation, V104del, impairs folding of the LCCL domain of cochlin and causes progressive hearing loss

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

29 September 2017

The Trp117Arg mutation of the COCH gene causes deafness in Koreans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

27 November 2018

Novel mutations in the vWFA2 domain of COCH in two Chinese DFNA9 families

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

27 November 2018

Antibody reactivity to heat shock protein 70 and inner ear-specific proteins in patients with idiopathic sensorineural hearing loss

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

27 November 2018

Increased frequencies of cochlin-specific T cells in patients with autoimmune sensorineural hearing loss

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

27 November 2018

Audiometric, vestibular, and genetic aspects of a DFNA9 family with a G88E COCH mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

27 November 2018

Targeted disruption of mouse Coch provides functional evidence that DFNA9 hearing loss is not a COCH haploinsufficiency disorder.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

27 November 2018

A physiological place-frequency map of the cochlea in the CBA/J mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

27 November 2018

Gravity receptor function in mice with graded otoconial deficiencies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3039082

27 November 2018

Stimulus and recording variables and their effects on mammalian vestibular evoked potentials

1 reference

https://pubmed.ncbi.nlm.nih.gov/21073934

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Short latency compound action potentials from mammalian gravity receptor organs

1 reference

https://pubmed.ncbi.nlm.nih.gov/21073934

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel DFNA9 mutation in the vWFA2 domain of COCH alters a conserved cysteine residue and intrachain disulfide bond formation resulting in progressive hearing loss and site-specific vestibular and central oculomotor dysfunction

1 reference

https://pubmed.ncbi.nlm.nih.gov/21073934

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a novel COCH mutation, G87W, causing autosomal dominant hearing impairment (DFNA9)

1 reference

https://pubmed.ncbi.nlm.nih.gov/21073934

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotype description of a novel DFNA9/COCH mutation, I109T.

22

1 reference

10.1016/J.HEARES.2010.11.002

https://api.crossref.org/works/10.1016/J.HEARES.2010.11.002

25 August 2024

Identifiers

10.1016/J.HEARES.2010.11.002

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

PMC publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 June 2017

ResearchGate publication ID

0 references

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