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Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice
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scholarly article
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PubMed
PubMed ID
12121736
retrieved
25 January 2017
title
Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice
(English)
1 reference
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PubMed
PubMed ID
12121736
retrieved
25 January 2017
main subject
Cadherin 23 (otocadherin)
1 reference
stated in
GOA release 2020-03-11
Myosin VIIA
1 reference
stated in
GOA release 2020-03-11
author
Karen Steel
series ordinal
2
object named as
Karen P. Steel
1 reference
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PubMed
PubMed ID
12121736
retrieved
25 January 2017
author name string
Ralph H. Holme
series ordinal
1
1 reference
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PubMed
PubMed ID
12121736
retrieved
25 January 2017
language of work or name
English
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publication date
1 July 2002
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PubMed
PubMed ID
12121736
retrieved
25 January 2017
published in
Hearing Research
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stated in
PubMed
PubMed ID
12121736
retrieved
25 January 2017
volume
169
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stated in
PubMed
PubMed ID
12121736
retrieved
25 January 2017
issue
1-2
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stated in
PubMed
PubMed ID
12121736
retrieved
25 January 2017
page(s)
13–23
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stated in
PubMed
PubMed ID
12121736
retrieved
25 January 2017
cites work
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
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inferred from DOI database lookup
The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
retrieved
7 January 2021
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inferred from DOI database lookup
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
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inferred from DOI database lookup
Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer
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reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
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inferred from DOI database lookup
Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.
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reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
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A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
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inferred from DOI database lookup
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
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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
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
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inferred from DOI database lookup
Planar polarity: out of joint?
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
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inferred from DOI database lookup
High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and Waltzer (Cdh23v).
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
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inferred from DOI database lookup
The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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/10.1016%2FS0378-5955%2802%2900334-9
retrieved
7 January 2021
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inferred from DOI database lookup
A type VII myosin encoded by the mouse deafness gene shaker-1
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
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inferred from DOI database lookup
Unconventional myosins in inner-ear sensory epithelia
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expression
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
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inferred from DOI database lookup
A major gene affecting age-related hearing loss in C57BL/6J mice
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
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A major gene affecting age-related hearing loss is common to at least ten inbred strains of mice.
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reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Tailchaser (Tlc): a new mouse mutation affecting hair bundle differentiation and hair cell survival.
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
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inferred from DOI database lookup
Ultrastructural findings in the inner ear of Jackson shaker mice
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
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inferred from DOI database lookup
Morphological changes of cochlea in a strain of new-mutant mice
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
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inferred from DOI database lookup
A role for cadherins in cellular signaling and differentiation
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
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Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complex
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the myosin VIIA gene cause non-syndromic recessive deafness
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation analysis of the mouse myosin VIIA deafness gene
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw)
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
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Phylogenetic analysis of the cadherin superfamily allows identification of six major subfamilies besides several solitary members
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Severe vestibular and auditory impairment in three alleles of Ames waltzer (av) mice
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A strategy for fine-structure functional analysis of a 6- to 11-centimorgan region of mouse chromosome 7 by high-efficiency mutagenesis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in a plasma membrane Ca2+-ATPase gene cause deafness in deafwaddler mice
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Unconventional myosins: new frontiers in actin-based motors.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
based on heuristic
inferred from DOI database lookup
Flamingo, a seven-pass transmembrane cadherin, regulates planar cell polarity under the control of Frizzled
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
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7 January 2021
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Usher's syndrome--deafness and progressive blindness. Clinical cases, prevention, theory and literature survey
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A point mutation in a cadherin gene, Cdh23, causes deafness in a novel mutant, Waltzer mouse niigata
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defective myosin VIIA gene responsible for Usher syndrome type 1B
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in Cdh23 cause nonsyndromic hearing loss in waltzer mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The deaf jerker mouse has a mutation in the gene encoding the espin actin-bundling proteins of hair cell stereocilia and lacks espins.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0378-5955(02)00334-9
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
438038
OpenCitations bibliographic resource ID
438038
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
438038
PubMed ID
12121736
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
438038
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