Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice (Q28512445)

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scientific journal article

Language	Label	Description	Also known as
English	Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice	scientific journal article

Statements

scholarly article

1 reference

PubMed publication ID

25 January 2017

Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice (English)

1 reference

PubMed publication ID

25 January 2017

Cadherin 23 (otocadherin)

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GOA release 2020-03-11

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GOA release 2020-03-11

2

object named as

Karen P. Steel

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PubMed publication ID

25 January 2017

author name string

Ralph H. Holme

1

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PubMed publication ID

25 January 2017

language of work or name

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based on heuristic

inferred from title

publication date

1 July 2002

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PubMed publication ID

25 January 2017

Hearing Research

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PubMed publication ID

25 January 2017

169

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PubMed publication ID

25 January 2017

1-2

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PubMed publication ID

25 January 2017

13–23

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PubMed publication ID

25 January 2017

Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

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

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

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

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

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

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Planar polarity: out of joint?

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and Waltzer (Cdh23v).

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

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

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

A type VII myosin encoded by the mouse deafness gene shaker-1

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Unconventional myosins in inner-ear sensory epithelia

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

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

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

A major gene affecting age-related hearing loss in C57BL/6J mice

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

A major gene affecting age-related hearing loss is common to at least ten inbred strains of mice

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

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.

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Ultrastructural findings in the inner ear of Jackson shaker mice

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Morphological changes of cochlea in a strain of new-mutant mice

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

A role for cadherins in cellular signaling and differentiation

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complex

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

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

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutation analysis of the mouse myosin VIIA deafness gene

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw)

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Phylogenetic analysis of the cadherin superfamily allows identification of six major subfamilies besides several solitary members

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

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

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

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A strategy for fine-structure functional analysis of a 6- to 11-centimorgan region of mouse chromosome 7 by high-efficiency mutagenesis

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

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

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Unconventional myosins: new frontiers in actin-based motors

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

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

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Usher's syndrome--deafness and progressive blindness. Clinical cases, prevention, theory and literature survey

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

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

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

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

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Defective myosin VIIA gene responsible for Usher syndrome type 1B

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

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

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in Cdh23 cause nonsyndromic hearing loss in waltzer mice

1 reference

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

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

https://api.crossref.org/works/10.1016%2FS0378-5955%2802%2900334-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0378-5955(02)00334-9

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

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