(Q30428046)

English

Compound heterozygosity of the functionally null Cdh23(v-ngt) and hypomorphic Cdh23(ahl) alleles leads to early-onset progressive hearing loss in mice

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scholarly article

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Europe PubMed Central

PMC publication ID

9 November 2017

Compound heterozygosity of the functionally null Cdh23(v-ngt) and hypomorphic Cdh23(ahl) alleles leads to early-onset progressive hearing loss in mice (English)

1 reference

Europe PubMed Central

PMC publication ID

9 November 2017

1 reference

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inferred from title

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inferred from title

Yoshiaki Kikkawa

11

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Europe PubMed Central

PMC publication ID

9 November 2017

author name string

Yuki Miyasaka

1

1 reference

Europe PubMed Central

PMC publication ID

9 November 2017

Sari Suzuki

2

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Europe PubMed Central

PMC publication ID

9 November 2017

Yasuhiro Ohshiba

3

1 reference

Europe PubMed Central

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9 November 2017

Kei Watanabe

4

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Europe PubMed Central

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9 November 2017

Yoshihiko Sagara

5

1 reference

Europe PubMed Central

PMC publication ID

9 November 2017

Shumpei P Yasuda

6

1 reference

Europe PubMed Central

PMC publication ID

9 November 2017

Kunie Matsuoka

7

1 reference

Europe PubMed Central

PMC publication ID

9 November 2017

Hiroshi Shitara

8

1 reference

Europe PubMed Central

PMC publication ID

9 November 2017

Hiromichi Yonekawa

9

1 reference

Europe PubMed Central

PMC publication ID

9 November 2017

Ryo Kominami

10

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Europe PubMed Central

PMC publication ID

9 November 2017

publication date

1 January 2013

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Europe PubMed Central

PMC publication ID

9 November 2017

number of pages

14

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Experimental Animals

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Europe PubMed Central

PMC publication ID

9 November 2017

62

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Europe PubMed Central

PMC publication ID

9 November 2017

4

1 reference

Europe PubMed Central

PMC publication ID

9 November 2017

333-346

1 reference

Europe PubMed Central

PMC publication ID

9 November 2017

describes a project that uses

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Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4160959/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

Structure of a force-conveying cadherin bond essential for inner-ear mechanotransduction

1 reference

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20 June 2018

Advantages of a mouse model for human hearing impairment

1 reference

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20 June 2018

Digenic inheritance of deafness caused by 8J allele of myosin-VIIA and mutations in other Usher I genes

1 reference

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20 June 2018

A mutation in the cdh23 gene causes age-related hearing loss in Cdh23(nmf308/nmf308) mice

1 reference

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20 June 2018

Structures of usher syndrome 1 proteins and their complexes

1 reference

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20 June 2018

An ENU-induced mutation of Cdh23 causes congenital hearing loss, but no vestibular dysfunction, in mice

1 reference

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20 June 2018

Mechanotransduction by hair cells: models, molecules, and mechanisms

1 reference

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20 June 2018

Rethinking how hearing happens

1 reference

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20 June 2018

A mouse model for nonsyndromic deafness (DFNB12) links hearing loss to defects in tip links of mechanosensory hair cells

1 reference

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20 June 2018

Inheritance patterns of progressive hearing loss in laboratory strains of mice

1 reference

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20 June 2018

Cadherins and mechanotransduction by hair cells

1 reference

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20 June 2018

A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth

1 reference

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20 June 2018

Development of the hair bundle and mechanotransduction

1 reference

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Shaping the mammalian auditory sensory organ by the planar cell polarity pathway

1 reference

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20 June 2018

Cadherin 23 and protocadherin 15 interact to form tip-link filaments in sensory hair cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4160959

20 June 2018

Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4160959

20 June 2018

Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4160959

20 June 2018

Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4160959

20 June 2018

Cadherin 23 is a component of the tip link in hair-cell stereocilia

1 reference

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20 June 2018

Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4160959

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4160959

20 June 2018

CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4160959

20 June 2018

Mutations in Cdh23 cause nonsyndromic hearing loss in waltzer mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4160959

20 June 2018

A point mutation in a cadherin gene, Cdh23, causes deafness in a novel mutant, Waltzer mouse niigata

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4160959

20 June 2018

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4160959

20 June 2018

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4160959

20 June 2018

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4160959

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Genealogies of mouse inbred strains

1 reference

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20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4160959

20 June 2018

Hereditary inner-ear abnormalities in animals. Relationships with human abnormalities.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4160959

20 June 2018

Effects of aging, hearing loss, and anatomical location on thresholds of inferior colliculus neurons in C57BL/6 and CBA mice.

1 reference

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Development and degeneration of hearing in the C57/b16 mouse: relation of electrophysiologic responses from the round window and cochlear nucleus to cochlear anatomy and behavioral responses

1 reference

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20 June 2018

Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4160959

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Fates of Cdh23/CDH23 with mutations affecting the cytoplasmic region.

1 reference

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A physiological place-frequency map of the cochlea in the CBA/J mouse.

1 reference

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Mutations in cadherin 23 affect tip links in zebrafish sensory hair cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4160959

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A compendium of mouse knockouts with inner ear defects.

1 reference

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26 November 2018

Genomic structure, alternative splice forms and normal and mutant alleles of cadherin 23 (Cdh23).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4160959

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Genetics of age-related hearing loss in mice: I. Inbred and F1 hybrid strains.

1 reference

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1 reference

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12 December 2020

based on heuristic

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Identifiers

10.1538/EXPANIM.62.333

1 reference

Europe PubMed Central

PMC publication ID

9 November 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

9 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

9 November 2017

ResearchGate publication ID

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