(Q73635190)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751669%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

review article

1 reference

title

Connexin 26: required for normal auditory function (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751669%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

author name string

P M Kelley

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751669%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

E Cohn

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751669%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

W J Kimberling

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751669%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:10751669%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:10751669%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:10751669%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

page(s)

184-188

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751669%20AND%20SRC:MED&resulttype=core&format=json

Central visual, acoustic, and motor pathway involvement in a Charcot-Marie-Tooth family with an Asn205Ser mutation in the connexin 32 gene

5 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

7 January 2021

Connexin 26 R143W mutation associated with recessive nonsyndromic sensorineural deafness in Africa

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

7 January 2021

Connections with connexins: the molecular basis of direct intercellular signaling

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

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%2900080-6

7 January 2021

Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1)

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

7 January 2021

Connexin 26 gene linked to a dominant deafness.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

7 January 2021

Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

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%2900080-6

7 January 2021

Connexin-26 mutations in sporadic and inherited sensorineural deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

7 January 2021

Transplacental uptake of glucose is decreased in embryonic lethal connexin26-deficient mice

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

7 January 2021

Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

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%2900080-6

7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

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%2900080-6

7 January 2021

Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

7 January 2021

Transcriptional downregulation of gap-junction proteins blocks junctional communication in human mammary tumor cell lines

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

7 January 2021

A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2).

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

7 January 2021

Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

7 January 2021

Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

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%2900080-6

7 January 2021

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

7 January 2021

Connexin mutations and hearing loss.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

7 January 2021

Connexin mutations in deafness.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

7 January 2021

Genetic diseases and gene knockouts reveal diverse connexin functions.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6

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%2900080-6

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%2900080-6

7 January 2021

10.1016/S0165-0173(99)00080-6

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751669%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

1 reference