(Q73635186)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751668%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

review article

1 reference

title

Functional analysis of human Cx26 mutations associated with deafness (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751668%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751668%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

publication date

1 April 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751668%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

volume

32

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751668%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751668%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

page(s)

181-183

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751668%20AND%20SRC:MED&resulttype=core&format=json

Connections with connexins: the molecular basis of direct intercellular signaling

5 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

Connexin 26 gene linked to a dominant deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

Altered trafficking of mutant connexin32

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

Connexin-26 mutations in sporadic and inherited sensorineural deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

Connexin-26 mutations in sporadic non-syndromal sensorineural deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

Connexin mutations and hearing loss.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

Extracellular Potassium in the Mammalian Central Nervous System

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

Equilibrium properties of a voltage-dependent junctional conductance.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

Formation of gap junctions by expression of connexins in Xenopus oocyte pairs

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

The connexin family of intercellular channel forming proteins

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

Connexin mutations in deafness.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900079-X

7 January 2021

10.1016/S0165-0173(99)00079-X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751668%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

1 reference