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The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene
scientific journal article
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scholarly article
1 reference
stated in
PubMed
PubMed ID
11138007
retrieved
31 January 2017
title
The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene
(English)
1 reference
stated in
PubMed
PubMed ID
11138007
retrieved
31 January 2017
main subject
Protocadherin 15
1 reference
stated in
GOA release 2020-03-11
hearing loss
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based on heuristic
inferred from title
author
Richard P Woychik
1 reference
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ORCID Public Data File 2021
author name string
K. N. Alagramam
series ordinal
1
1 reference
stated in
PubMed
PubMed ID
11138007
retrieved
31 January 2017
C. L. Murcia
series ordinal
2
1 reference
stated in
PubMed
PubMed ID
11138007
retrieved
31 January 2017
H. Y. Kwon
series ordinal
3
1 reference
stated in
PubMed
PubMed ID
11138007
retrieved
31 January 2017
K. S. Pawlowski
series ordinal
4
1 reference
stated in
PubMed
PubMed ID
11138007
retrieved
31 January 2017
C. G. Wright
series ordinal
5
1 reference
stated in
PubMed
PubMed ID
11138007
retrieved
31 January 2017
R. P. Woychik
series ordinal
6
1 reference
stated in
PubMed
PubMed ID
11138007
retrieved
31 January 2017
language of work or name
English
0 references
publication date
1 January 2001
1 reference
stated in
PubMed
PubMed ID
11138007
retrieved
31 January 2017
published in
Nature Genetics
1 reference
stated in
PubMed
PubMed ID
11138007
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31 January 2017
volume
27
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stated in
PubMed
PubMed ID
11138007
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31 January 2017
issue
1
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stated in
PubMed
PubMed ID
11138007
retrieved
31 January 2017
page(s)
99–102
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stated in
PubMed
PubMed ID
11138007
retrieved
31 January 2017
cites work
The fundamental and medical impacts of recent progress in research on hereditary hearing loss.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83837
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifying the genes of hearing, deafness, and dysequilibrium
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83837
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic causes of hearing loss
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83837
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Electron Microscopic Studies of Capillary Permeability in Normal and Ames Waltzer Deaf Mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83837
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83837
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83837
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83837
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Structural and functional diversity of cadherin superfamily: are new members of cadherin superfamily involved in signal transduction pathway?
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83837
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A unique variant of a homeobox gene related to Drosophila cut is expressed in mouse testis.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83837
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83837
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83837
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83837
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
WWW-query: an on-line retrieval system for biological sequence banks
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83837
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular characterization of the mouse agouti locus.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F83837
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/83837
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1357405
OpenCitations bibliographic resource ID
1357405
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1357405
PubMed ID
11138007
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1357405
ResearchGate publication ID
12191217
0 references
Springer Nature article ID
10.1038/83837
0 references
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