(Q42509720)

1 November 2017

title

Cochlear pathology of the circling mouse: a new mouse model of DFNB6. (English)

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1 November 2017

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Won-Ho Chung

1

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1 November 2017

Ki Ryung Kim

2

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1 November 2017

Yang-Sun Cho

3

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1 November 2017

Do-Yeon Cho

4

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1 November 2017

Ji Hwan Woo

5

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1 November 2017

Zae Young Ryoo

6

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1 November 2017

Kyoung In Cho

7

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1 November 2017

Sung Hwa Hong

8

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1 November 2017

language of work or name

English

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publication date

1 March 2007

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1 November 2017

published in

Acta Oto-Laryngologica

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1 November 2017

volume

127

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1 November 2017

issue

3

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1 November 2017

page(s)

244-251

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Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound

1 November 2017

cites work

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https://api.crossref.org/works/10.1080%2F00016480600827071

Human Nonsyndromic Sensorineural Deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016480600827071

Mouse models for human deafness: current tools for new fashions

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016480600827071

Circling mouse, a spontaneous mutant in the inner ear.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016480600827071

An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016480600827071

Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016480600827071

Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016480600827071

Cochlear pathology induced by aminoglycoside ototoxicity during postnatal maturation in cats

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016480600827071

Cochlear pathology of long term neomycin induced deafness in cats

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016480600827071

Inherited hearing defects in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016480600827071

Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016480600827071

Genomic structure of the human unconventional myosin VI gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016480600827071

Unconventional myosins and the genetics of hearing loss

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016480600827071

Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016480600827071

Stereocilia defects in the sensory hair cells of the inner ear in mice deficient in integrin alpha8beta1

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016480600827071

The deaf jerker mouse has a mutation in the gene encoding the espin actin-bundling proteins of hair cell stereocilia and lacks espins.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F00016480600827071

10.1080/00016480600827071

21 January 2018

Identifiers

DOI

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1 November 2017

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