Deafness induced by Connexin 26 (GJB2) deficiency is not determined by endocochlear potential (EP) reduction but is associated with cochlear developmental disorders (Q41968817)

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scientific article published on 13 April 2014

Language	Label	Description	Also known as
English	Deafness induced by Connexin 26 (GJB2) deficiency is not determined by endocochlear potential (EP) reduction but is associated with cochlear developmental disorders	scientific article published on 13 April 2014

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

Deafness induced by Connexin 26 (GJB2) deficiency is not determined by endocochlear potential (EP) reduction but is associated with cochlear developmental disorders (English)

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

1 reference

based on heuristic

inferred from title

author name string

Jin Chen

1

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

Jing Chen

2

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

Yan Zhu

3

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

Chun Liang

4

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

Hong-Bo Zhao

5

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

13 April 2014

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

Biochemical and Biophysical Research Communications

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

448

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

1

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

28-32

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

The role of an inwardly rectifying K(+) channel (Kir4.1) in the inner ear and hearing loss

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

5 June 2018

Active cochlear amplification is dependent on supporting cell gap junctions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

5 June 2018

Cell degeneration is not a primary causer for Connexin26 (GJB2) deficiency associated hearing loss

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

5 June 2018

The DFNB1 subtype of autosomal recessive non-syndromic hearing impairment

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

5 June 2018

Connexin30 null and conditional connexin26 null mice display distinct pattern and time course of cellular degeneration in the cochlea

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

5 June 2018

Targeted connexin26 ablation arrests postnatal development of the organ of Corti

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

5 June 2018

Connexin-caused genetic diseases and corresponding mouse models.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

5 June 2018

Cochlear amplification, outer hair cells and prestin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

5 June 2018

Making an effort to listen: mechanical amplification in the ear

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

5 June 2018

Cellular characterization of Connexin26 and Connnexin30 expression in the cochlear lateral wall

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

5 June 2018

Distinct and gradient distributions of connexin26 and connexin30 in the cochlear sensory epithelium of guinea pigs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

5 June 2018

Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

5 June 2018

Gap junctions and cochlear homeostasis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

5 June 2018

Non-syndromic, autosomal-recessive deafness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

5 June 2018

Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

5 June 2018

https://pubmed.ncbi.nlm.nih.gov/24732355

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

5 June 2018

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

5 June 2018

Down regulated connexin26 at different postnatal stage displayed different types of cellular degeneration and formation of organ of Corti.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

18 August 2018

Cochlear outer hair cells in a dominant-negative connexin26 mutant mouse preserve non-linear capacitance in spite of impaired distortion product otoacoustic emission

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

18 August 2018

Postnatal development of the organ of Corti in dominant-negative Gjb2 transgenic mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

18 August 2018

Inducible Cre recombinase activity in mouse cerebellar granule cell precursors and inner ear hair cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

18 August 2018

Universal Infant Hearing Screening by Automated Auditory Brainstem Response Measurement

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4105360

18 August 2018

Identifiers

10.1016/J.BBRC.2014.04.016

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 October 2017

ResearchGate publication ID

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