Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness (Q30478884)

12 November 2017

Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness (English)

1 reference

12 November 2017

1 reference

Shoeb Ahmad

1

1 reference

12 November 2017

Wenxue Tang

2

1 reference

12 November 2017

Qing Chang

3

1 reference

12 November 2017

Yan Qu

4

1 reference

12 November 2017

Jill Hibshman

5

1 reference

12 November 2017

Yuhua Li

6

1 reference

12 November 2017

Goran Söhl

7

1 reference

12 November 2017

Klaus Willecke

8

1 reference

12 November 2017

Ping Chen

9

1 reference

12 November 2017

Xi Lin

10

1 reference

12 November 2017

language of work or name

English

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publication date

16 January 2007

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

12 November 2017

5

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based on heuristic

inferred from page(s)

published in

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12 November 2017

104

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12 November 2017

4

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12 November 2017

1337-1341

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Cochlear gap junctions coassembled from Cx26 and 30 show faster intercellular Ca2+ signaling than homomeric counterparts.

12 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783143

Acid-sensing ion channel 2 contributes a major component to acid-evoked excitatory responses in spiral ganglion neurons and plays a role in noise susceptibility of mice

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783143

Gap junctions in the inner ear: comparison of distribution patterns in different vertebrates and assessement of connexin composition in mammals

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783143

Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783143

The role of connexins in human disease.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783143

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

20 June 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783143

20 June 2018

https://pubmed.ncbi.nlm.nih.gov/17227867

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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=1783143

A deletion involving the connexin 30 gene in nonsyndromic hearing impairment

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783143

Unique and redundant connexin contributions to lens development

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783143

Gap junction systems in the mammalian cochlea

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783143

Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783143

Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783143

Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783143

Expression of the gap-junction connexins 26 and 30 in the rat cochlea

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783143

Connexin-26 mutations in sporadic and inherited sensorineural deafness

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783143

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783143

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783143

Defective propagation of signals generated by sympathetic nerve stimulation in the liver of connexin32-deficient mice

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783143

A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1783143

The prevalence of connexin 26 ( GJB2) mutations in the Chinese population.

20 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0606855104

Homologous recombination based modification in Escherichia coli and germline transmission in transgenic mice of a bacterial artificial chromosome.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0606855104

Expression patterns of aquaporins in the inner ear: evidence for concerted actions of multiple types of aquaporins to facilitate water transport in the cochlea.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.0606855104

Connexins 26 and 30 are co-assembled to form gap junctions in the cochlea of mice

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17227867

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.0606855104

1 reference

12 November 2017

0 references

1 reference

12 November 2017

1 reference