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English
One connexin, two diseases
scientific article published on 01 December 1998
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
9843196
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843196%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
title
One connexin, two diseases
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
9843196
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843196%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
author name string
Steel KP
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1
1 reference
stated in
Europe PubMed Central
PubMed ID
9843196
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843196%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
publication date
1 December 1998
1 reference
stated in
Europe PubMed Central
PubMed ID
9843196
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843196%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
9843196
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843196%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
volume
20
1 reference
stated in
Europe PubMed Central
PubMed ID
9843196
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843196%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
page(s)
319-320
1 reference
stated in
Europe PubMed Central
PubMed ID
9843196
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843196%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed ID
9843196
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843196%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
exact match
https://scigraph.springernature.com/pub.10.1038/3781
0 references
cites work
Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3781
retrieved
7 January 2021
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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/10.1038%2F3781
retrieved
7 January 2021
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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/10.1038%2F3781
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connexins, connexons, and intercellular communication
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3781
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Switch in gap junction protein expression is associated with selective changes in junctional permeability during keratinocyte differentiation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3781
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Connexin mutations in X-linked Charcot-Marie-Tooth disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3781
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/10.1038%2F3781
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/10.1038%2F3781
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/10.1038%2F3781
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular markers for cell types of the inner ear and candidate genes for hearing disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3781
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/10.1038%2F3781
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1p
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3781
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Opposite voltage gating polarities of two closely related connexins.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3781
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a proline residue as a transduction element involved in voltage gating of gap junctions.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3781
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Altered trafficking of mutant connexin32
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3781
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Null mutations of connexin32 in patients with X-linked Charcot-Marie-Tooth disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F3781
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/3781
1 reference
stated in
Europe PubMed Central
PubMed ID
9843196
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843196%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
PubMed ID
9843196
1 reference
stated in
Europe PubMed Central
PubMed ID
9843196
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9843196%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 December 2019
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