(Q23914819)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15811708%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

title

Characterization of a new allele of Ames waltzer generated by ENU mutagenesis (English)

2 references

12 July 2017

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15811708%20AND%20SRC:MED&resulttype=core&format=json

NIOSH Division of Applied Research and Technology

10 January 2020

sponsor

object named as

DART

1 reference

25 September 2023

1 reference

GOA release 2020-03-11

author

Rickie R. Davis

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15811708%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

author name string

Darrell Pitts

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15811708%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Kumar Alagramam

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15811708%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Jesse L Washington

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15811708%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Charles G Wright

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15811708%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

L C Erway

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15811708%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

language of work or name

English

1 reference

inferred from title

process of elimination

publication date

1 April 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15811708%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15811708%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

volume

202

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15811708%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

issue

1-2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15811708%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

page(s)

161-169

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15811708%20AND%20SRC:MED&resulttype=core&format=json

on focus list of Wikimedia project

10 January 2020

Wikimedia–NIOSH collaboration

0 references

2 references

2 February 2024

inferred from email address

cites work

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

1 reference

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7 January 2021

Genetics of age-related hearing loss in mice. III. Susceptibility of inbred and F1 hybrid strains to noise-induced hearing loss

1 reference

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7 January 2021

Drosophila Rho-associated kinase (Drok) links Frizzled-mediated planar cell polarity signaling to the actin cytoskeleton.

1 reference

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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%2FJ.HEARES.2004.09.014

7 January 2021

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

1 reference

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7 January 2021

Planar polarization of Drosophila and vertebrate epithelia

1 reference

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7 January 2021

Planar polarity: out of joint?

1 reference

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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%2FJ.HEARES.2004.09.014

7 January 2021

An allelic series of mutations in Smad2 and Smad4 identified in a genotype-based screen of N-ethyl-N- nitrosourea-mutagenized mouse embryonic stem cells

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.HEARES.2004.09.014

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FJ.HEARES.2004.09.014

7 January 2021