(Q30352521)

16 August 2017

Progression of inner ear pathology in Ames waltzer mice and the role of protocadherin 15 in hair cell development. (English)

1 reference

16 August 2017

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Karen S Pawlowski

1

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16 August 2017

Yayoi S Kikkawa

series ordinal

2

1 reference

16 August 2017

Charles G Wright

series ordinal

3

1 reference

16 August 2017

Kumar N Alagramam

series ordinal

4

1 reference

16 August 2017

12 January 2006

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16 August 2017

1 reference

16 August 2017

7

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16 August 2017

2

1 reference

16 August 2017

83-94

1 reference

https://scigraph.springernature.com/pub.10.1007/s10162-005-0024-5

16 August 2017

0 references

cites work

Characterization of vestibular dysfunction in the mouse model for Usher syndrome 1F

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504581

TRPA1 is a candidate for the mechanosensitive transduction channel of vertebrate hair cells

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504581

PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504581

The functional age of hearing loss in a mouse model of presbycusis. II. Neuroanatomical correlates.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504581

Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504581

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504581

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504581

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504581

Recent progress in protocadherin research

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504581

Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504581

A new mouse insertional mutation that causes sensorineural deafness and vestibular defects

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504581

Expression of Pcdh15 in the inner ear, nervous system and various epithelia of the developing embryo.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2504581

26 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16408167

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S10162-005-0024-5

1 reference

Dimensions Publication ID

16 August 2017

0 references

1 reference

16 August 2017

1 reference