(Q50500527)

14 March 2018

title

Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice. (English)

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14 March 2018

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Dixon MJ

1

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14 March 2018

Gazzard J

2

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14 March 2018

Chaudhry SS

3

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14 March 2018

Sampson N

4

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14 March 2018

Schulte BA

5

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14 March 2018

Steel KP

6

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14 March 2018

publication date

1 August 1999

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14 March 2018

published in

Human Molecular Genetics

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14 March 2018

volume

8

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14 March 2018

issue

8

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14 March 2018

page(s)

1579-1584

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14 March 2018

Inherited hearing defects in mice

cites work

1 reference

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The original shaker-with-syndactylism mutation (sy) is a contiguous gene deletion syndrome

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Immunohistochemical localization of the Na-K-Cl co-transporter (NKCC1) in the gerbil inner ear.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1579

Expression and localization of the Na-K-2Cl cotransporter in the rat cochlea.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1579

Ultrastructural localization of the Na-K-Cl cotransporter in the lateral wall of the rabbit cochlear duct.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1579

Na-K-Cl cotransporter expression in the developing and senescent gerbil cochlea.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1579

Gap junctions in the rat cochlea: immunohistochemical and ultrastructural analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1579

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1579

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1579

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

21 January 2018

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Connexin 26 gene linked to a dominant deafness.

21 January 2018

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Comparison of ion transport mechanisms between vestibular dark cells and strial marginal cells

21 January 2018

1 reference

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A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1579

KCNE1 mutations cause jervell and Lange-Nielsen syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1579

Deafness and imbalance associated with inactivation of the secretory Na-K-2Cl co-transporter

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F8.8.1579

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

21 January 2018

1 reference

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21 January 2018

Identifiers

DOI

10.1093/HMG/8.8.1579

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14 March 2018

PubMed ID

10401008

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14 March 2018