Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model (Q24805411)

23 June 2017

title

Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model (English)

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23 June 2017

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11

Eric D Green

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23 June 2017

1

Philine Wangemann

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23 June 2017

Rajanikanth J Maganti

6

object named as

Rajanikanth J Maganti

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23 June 2017

10

Ines E Royaux

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23 June 2017

8

Lorraine A Everett

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23 June 2017

Erin M Itza

2

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23 June 2017

Beatrice Albrecht

3

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23 June 2017

Tao Wu

4

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23 June 2017

Sairam V Jabba

5

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23 June 2017

Jun Ho Lee

7

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23 June 2017

Susan M Wall

9

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23 June 2017

Daniel C Marcus

12

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23 June 2017

language of work or name

English

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publication date

20 August 2004

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23 June 2017

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23 June 2017

volume

2

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23 June 2017

issue

1

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page(s)

30

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Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion

23 June 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

The Pendred syndrome gene encodes a chloride-iodide transport protein

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

K+ cycling and the endocochlear potential

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Enlarged vestibular aqueduct: a radiological marker of pendred syndrome, and mutation of the PDS gene

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange

7 April 2017

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Metabolic regulation of potassium channels.

7 April 2017

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Targeted disruption of the Kcnq1 gene produces a mouse model of Jervell and Lange-Nielsen Syndrome.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Dye-coupling of melanocytes with endothelial cells and pericytes in the cochlea of gerbils

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Inner ear defects induced by null mutation of the isk gene

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Fine structure of the intracochlear potential field. I. The silent current

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

The ultrastructural cytochemistry of peroxisomes in the guinea pig cochlea: A metabolic hypothesis for the stria vascularis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

KCNJ10 (Kir4.1) potassium channel knockout abolishes endocochlear potential

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Various glutathione S-transferase isoforms in the rat cochlea

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Expression of Na+/I- symporter and Pendred syndrome genes in trophoblast cells

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Differential cellular distribution of glutathione--an endogenous antioxidant--in the guinea pig inner ear.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Ion transport mechanisms responsible for K+ secretion and the transepithelial voltage across marginal cells of stria vascularis in vitro

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

The junctions of the spindle-shaped cells of the stria vascularis: a link that completes the barrier between perilymph and endolymph

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Embryogenesis of the inner ear. IV. Post-natal maturation of the secretory epithelia of the inner ear in correlation with the elemental composition in the endolymphatic space

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Histochemical localization of carbonic anhydrase in the inner ear.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Deterioration of hearing function in mice with neural crest defect

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Endocochlear potential generation is associated with intercellular communication in the stria vascularis: structural analysis in the viable dominant spotting mouse mutant

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Hyperpigmentation of chinchilla stria vascularis following acoustic trauma

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

30 May 2018

DEAF-MUTISM AND GOITRE

1 reference

https://api.crossref.org/works/10.1186%2F1741-7015-2-30

Prolactin regulation of the pendrin-iodide transporter in the mammary gland

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1741-7015-2-30

Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1741-7015-2-30

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1741-7015-2-30

P2X2 receptor mediates stimulation of parasensory cation absorption by cochlear outer sulcus cells and vestibular transitional cells.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=516044

Expression of PDS/Pds, the Pendred syndrome gene, in endometrium

28 November 2018

1 reference

12 December 2020

1 reference

12 December 2020

Enzyme-histochemical localization of carbonic anhydrase in the inner ear of the guinea pig and several improvements of the technique

1 reference

12 December 2020

Quantification of insulin-like growth factor-1 (IGF-1) mRNA: development and validation of an internally standardised competitive reverse transcription-polymerase chain reaction

1 reference

12 December 2020

Voltage-dependent outward K(+) current in intermediate cell of stria vascularis of gerbil cochlea

1 reference

12 December 2020

L-lactate inhibits L-cystine/L-glutamate exchange transport and decreases glutathione content in rat cultured astrocytes

1 reference

12 December 2020

Na(+)/I(-) symporter and Pendred syndrome gene and protein expressions in human extra-thyroidal tissues

1 reference

12 December 2020

Identifiers

DOI

10.1186/1741-7015-2-30

1 reference

Dimensions Publication ID

23 June 2017

1051578359

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OpenCitations bibliographic resource ID

213779

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

213779

1 reference