(Q44697326)

English

The inner ear contains heteromeric channels composed of cx26 and cx30 and deafness-related mutations in cx26 have a dominant negative effect on cx30.

scientific article published in July 2003

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14681039%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

The inner ear contains heteromeric channels composed of cx26 and cx30 and deafness-related mutations in cx26 have a dominant negative effect on cx30 (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14681039%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

1 reference

based on heuristic

inferred from title

Daniel J Jagger

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14681039%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

Stefano O Casalotti

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14681039%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

author name string

Andrew Forge

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14681039%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

Nerissa K Marziano

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14681039%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

David L Becker

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14681039%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

publication date

1 July 2003

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14681039%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

Cell Communication & Adhesion

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14681039%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

10

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14681039%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

4-6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14681039%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

341-346

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14681039%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

Hereditary deafness and phenotyping in humans

1 reference

https://api.crossref.org/works/10.1080%2FCAC.10.4-6.341.346

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1080%2FCAC.10.4-6.341.346

21 January 2018

A technique for slicing the rat cochlea around the onset of hearing.

1 reference

https://api.crossref.org/works/10.1080%2FCAC.10.4-6.341.346

21 January 2018

De novo mutation of the connexin 26 gene associated with dominant non-syndromic sensorineural hearing loss.

1 reference

https://api.crossref.org/works/10.1080%2FCAC.10.4-6.341.346

21 January 2018

Transgenic expression of a dominant-negative connexin26 causes degeneration of the organ of Corti and non-syndromic deafness

1 reference

https://api.crossref.org/works/10.1080%2FCAC.10.4-6.341.346

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1080%2FCAC.10.4-6.341.346

21 January 2018

Intracellular domains of mouse connexin26 and -30 affect diffusional and electrical properties of gap junction channels

1 reference

https://api.crossref.org/works/10.1080%2FCAC.10.4-6.341.346

21 January 2018

Mutations in the gene for connexin 26 (GJB2) that cause hearing loss have a dominant negative effect on connexin 30.

1 reference

https://api.crossref.org/works/10.1080%2FCAC.10.4-6.341.346

21 January 2018

Isolation and purification of gap junction channels

1 reference

https://api.crossref.org/works/10.1080%2FCAC.10.4-6.341.346

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1080%2FCAC.10.4-6.341.346

21 January 2018

Identifiers

10.1080/CAC.10.4-6.341.346

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14681039%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14681039%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

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