(Q28512445)

25 January 2017

title

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

1 reference

Cadherin 23 (otocadherin)

25 January 2017

main subject

1 reference

GOA release 2020-03-11

Myosin VIIA

1 reference

GOA release 2020-03-11

2

Karen P. Steel

1 reference

25 January 2017

Ralph H. Holme

1

1 reference

25 January 2017

language of work or name

1 reference

1 July 2002

1 reference

25 January 2017

1 reference

25 January 2017

volume

169

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25 January 2017

issue

1-2

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25 January 2017

page(s)

13–23

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

25 January 2017

cites work

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

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/S0378-5955(02)00334-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

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/S0378-5955(02)00334-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

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/S0378-5955(02)00334-9

7 January 2021

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/S0378-5955(02)00334-9

7 January 2021

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/S0378-5955(02)00334-9

7 January 2021

Planar polarity: out of joint?

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

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/S0378-5955(02)00334-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

Unconventional myosins in inner-ear sensory epithelia

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expression

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

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/S0378-5955(02)00334-9

7 January 2021

Tailchaser (Tlc): a new mouse mutation affecting hair bundle differentiation and hair cell survival.

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

Ultrastructural findings in the inner ear of Jackson shaker mice

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

A role for cadherins in cellular signaling and differentiation

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

Mutation analysis of the mouse myosin VIIA deafness gene

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

mdfw:A Deafness Susceptibility Locus That Interacts with Deaf Waddler (dfw)

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

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/S0378-5955(02)00334-9

7 January 2021

Severe vestibular and auditory impairment in three alleles of Ames waltzer (av) mice

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

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/S0378-5955(02)00334-9

7 January 2021

Mutations in a plasma membrane Ca2 -ATPase gene cause deafness in deafwaddler mice

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

Unconventional myosins: new frontiers in actin-based motors

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

Flamingo, a seven-pass transmembrane cadherin, regulates planar cell polarity under the control of Frizzled

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

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/S0378-5955(02)00334-9

7 January 2021

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/S0378-5955(02)00334-9

7 January 2021

Defective myosin VIIA gene responsible for Usher syndrome type 1B

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

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/S0378-5955(02)00334-9

7 January 2021

Mutations in Cdh23 cause nonsyndromic hearing loss in waltzer mice

1 reference

https://api.crossref.org/works/10.1016/S0378-5955(02)00334-9

7 January 2021

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/S0378-5955(02)00334-9

7 January 2021

10.1016/S0378-5955(02)00334-9

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017