(Q28588493)

GOA release 2020-03-11

Hiroshi Kiyama

6

0 references

author name string

Hideshi Yagi

1

1 reference

31 January 2017

Hisashi Tokano

2

1 reference

31 January 2017

Mitsuyo Maeda

3

1 reference

31 January 2017

Tetsuji Takabayashi

4

1 reference

31 January 2017

Takashi Nagano

5

1 reference

31 January 2017

Shigeharu Fujieda

7

1 reference

31 January 2017

Ken Kitamura

8

1 reference

31 January 2017

Makoto Sato

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

9

1 reference

31 January 2017

language of work or name

1 reference

1 February 2007

1 reference

31 January 2017

1 reference

31 January 2017

12

1 reference

31 January 2017

2

1 reference

31 January 2017

235–250

1 reference

31 January 2017

1 reference

https://api.crossref.org/works/10.1111/J.1365-2443.2007.01046.X

Math1: an essential gene for the generation of inner ear hair cells

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1365-2443.2007.01046.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1365-2443.2007.01046.X

The Mass1frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC.

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1365-2443.2007.01046.X

The very large G-protein-coupled receptor VLGR1: a component of the ankle link complex required for the normal development of auditory hair bundles.

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1365-2443.2007.01046.X

Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1365-2443.2007.01046.X

Calx, a Na-Ca exchanger gene of Drosophila melanogaster

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1365-2443.2007.01046.X

A novel gene causing a mendelian audiogenic mouse epilepsy

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1365-2443.2007.01046.X

Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1365-2443.2007.01046.X

The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1365-2443.2007.01046.X

Prestin is the motor protein of cochlear outer hair cells

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1365-2443.2007.01046.X

Cleavage of Ig-Hepta at a "SEA" module and at a conserved G protein-coupled receptor proteolytic site

21 April 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2007.01046.X

Physiological, behavioral and anatomical correlates of the development of hearing in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2007.01046.X

Hereditary deafness and phenotyping in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2007.01046.X

Calcium imaging of single stereocilia in hair cells: localization of transduction channels at both ends of tip links

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2007.01046.X

Genetic insights into the morphogenesis of inner ear hair cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2007.01046.X

Development and properties of stereociliary link types in hair cells of the mouse cochlea

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2007.01046.X

Genetics of hearing impairment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2007.01046.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2007.01046.X

Postnatal development of the hamster cochlea. II. Growth and differentiation of stereocilia bundles

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2007.01046.X

Very large G protein-coupled receptor-1, the largest known cell surface protein, is highly expressed in the developing central nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2007.01046.X

Loss of the transmembrane and cytoplasmic domains of the very large G-protein-coupled receptor-1 (VLGR1 or Mass1) causes audiogenic seizures in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2007.01046.X

21 January 2018

The genetics of deafness

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2007.01046.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2007.01046.X

Effect of absence of cochlear outer hair cells on behavioural auditory threshold

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2007.01046.X

Neurons in Golgi-stain-like images revealed by GFP-adenovirus infection in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2007.01046.X

Histopathologic features of the temporal bone in usher syndrome type I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2007.01046.X

Vlgr1 knockout mice show audiogenic seizure susceptibility.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2007.01046.X

Development of the auditory receptors of the rat: a SEM study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2443.2007.01046.X