(Q48913468)

16 February 2018

title

Expression of connexin 30 in the developing mouse cochlea. (English)

1 reference

16 February 2018

author name string

Xia A

1

1 reference

16 February 2018

Katori Y

2

1 reference

16 February 2018

Oshima T

3

1 reference

16 February 2018

Watanabe K

4

1 reference

16 February 2018

Kikuchi T

5

1 reference

16 February 2018

Ikeda K

6

1 reference

16 February 2018

language of work or name

English

0 references

publication date

1 April 2001

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16 February 2018

number of pages

4

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based on heuristic

inferred from page(s)

published in

Brain Research

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16 February 2018

volume

898

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16 February 2018

page(s)

364-367

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16 February 2018

issue

2

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16 February 2018

Connexin mutations in X-linked Charcot-Marie-Tooth disease

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2801%2902216-8

Molecular cloning and functional expression of mouse connexin-30,a gap junction gene highly expressed in adult brain and skin.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2801%2902216-8

Connexin-26 mutations in sporadic and inherited sensorineural deafness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2801%2902216-8

Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2801%2902216-8

The Na-K-Cl cotransporters in the rat cochlea: RT-PCR and partial sequence analysis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2801%2902216-8

Human connexin 30 (GJB6), a candidate gene for nonsyndromic hearing loss: molecular cloning, tissue-specific expression, and assignment to chromosome 13q12

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2801%2902216-8

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2801%2902216-8

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2801%2902216-8

Expression of the gap-junction connexins 26 and 30 in the rat cochlea

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2801%2902216-8

Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2801%2902216-8

Development of endocochlear potential and its negative component in mouse cochlea.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2801%2902216-8

Expression of alpha and beta subunit isoforms of Na,K-ATPase in the mouse inner ear and changes with mutations at the Wv or Sld loci

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2801%2902216-8

The fine structure of spiral ligament cells relates to ion return to the stria and varies with place-frequency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2801%2902216-8

Perspectives: biomedicine. The benefits of recycling.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2801%2902216-8

Expression of connexin 26 and Na,K-ATPase in the developing mouse cochlear lateral wall: functional implications

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2801%2902216-8

Expression of connexin 31 in the developing mouse cochlea.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2801%2902216-8

Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2801%2902216-8

10.1016/S0006-8993(01)02216-8

7 January 2021

Identifiers

DOI

1 reference

16 February 2018

PubMed ID

11306024

1 reference

16 February 2018