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Connexin 26: required for normal auditory function
scientific article published on 01 April 2000
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10751669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751669%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
review article
1 reference
stated in
Europe PubMed Central
title
Connexin 26: required for normal auditory function
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10751669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751669%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
author name string
P M Kelley
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10751669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751669%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
E Cohn
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10751669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751669%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
W J Kimberling
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10751669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751669%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
publication date
1 April 2000
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10751669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751669%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
volume
32
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10751669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751669%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10751669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751669%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
page(s)
184-188
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10751669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751669%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
cites work
Central visual, acoustic, and motor pathway involvement in a Charcot-Marie-Tooth family with an Asn205Ser mutation in the connexin 32 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connexin 26 R143W mutation associated with recessive nonsyndromic sensorineural deafness in Africa
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connections with connexins: the molecular basis of direct intercellular signaling
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connexin 26 gene linked to a dominant deafness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connexin-26 mutations in sporadic and inherited sensorineural deafness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transplacental uptake of glucose is decreased in embryonic lethal connexin26-deficient mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of the gap-junction connexins 26 and 30 in the rat cochlea
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transcriptional downregulation of gap-junction proteins blocks junctional communication in human mammary tumor cell lines
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional defects of Cx26 resulting from a heterozygous missense mutation in a family with dominant deaf-mutism and palmoplantar keratoderma.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connexin mutations and hearing loss.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connexin mutations in deafness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic diseases and gene knockouts reveal diverse connexin functions.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-0173%2899%2900080-6
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0165-0173(99)00080-6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10751669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751669%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
PubMed publication ID
10751669
1 reference
stated in
Europe PubMed Central
PubMed publication ID
10751669
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10751669%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 November 2019
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