(Q30494661)

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Loss of cochlear HCO3- secretion causes deafness via endolymphatic acidification and inhibition of Ca2+ reabsorption in a Pendred syndrome mouse model

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Loss of cochlear HCO3- secretion causes deafness via endolymphatic acidification and inhibition of Ca2+ reabsorption in a Pendred syndrome mouse model (English)

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Pendred syndrome

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Philine Wangemann

1

object named as

Philine Wangemann

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

author name string

Kazuhiro Nakaya

2

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Tao Wu

3

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Rajanikanth J Maganti

4

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Erin M Itza

5

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Joel D Sanneman

6

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Donald G Harbidge

7

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Sara Billings

8

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Daniel C Marcus

9

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

publication date

13 February 2007

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

American Journal of Physiology - Renal Physiology

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

292

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

5

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

F1345-53

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

Lack of pendrin HCO3- transport elevates vestibular endolymphatic [Ca2+] by inhibition of acid-sensitive TRPV5 and TRPV6 channels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Macrophage invasion contributes to degeneration of stria vascularis in Pendred syndrome mouse model

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Low endolymph calcium concentrations in deafwaddler2J mice suggest that PMCA2 contributes to endolymph calcium maintenance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Expression of an inwardly rectifying K+ channel, Kir5.1, in specific types of fibrocytes in the cochlear lateral wall suggests its functional importance in the establishment of endocochlear potential

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Blindness and auditory impairment caused by loss of the sodium bicarbonate cotransporter NBC3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Modulation of the epithelial Ca2+ channel ECaC by extracellular pH.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Pendrin: an apical Cl-/OH-/HCO3- exchanger in the kidney cortex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

A rat kidney-specific calcium transporter in the distal nephron

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

The Pendred syndrome gene encodes a chloride-iodide transport protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Effects of barium and ion substitutions in artificial blood on endocochlear potential

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Adaptation of mechanoelectrical transduction in hair cells of the bullfrog's sacculus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Ionic changes in cochlear endolymph of the guinea pig induced by acoustic injury

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Calcium transport mechanism in the endolymph of the chinchilla

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Early effects of acetazolamide on anionic activities of the guinea pig endolymph: evidence for active function of carbonic anhydrase in the cochlea

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Mechano-electrical transduction currents in isolated vestibular hair cells of the chick

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Carbonic anhydrase activity in the inner ear.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

The actions of calcium on the mechano-electrical transducer current of turtle hair cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Respiratory quotient of stria vascularis of guinea pig in vitro

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Very low calcium content of cochlear endolymph, an extracellular fluid

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

20 June 2018

Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndrome.

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00487.2006

21 January 2018

Expression of plasma membrane Ca-ATPase in the adult and developing gerbil cochlea.

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00487.2006

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00487.2006

21 January 2018

DEAF-MUTISM AND GOITRE

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00487.2006

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00487.2006

21 January 2018

Localization of pH regulating proteins H+ATPase and Cl-/HCO3- exchanger in the guinea pig inner ear.

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00487.2006

21 January 2018

Potentials of outer hair cells and their membrane properties in cationic environments.

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00487.2006

21 January 2018

Vitamin D upregulates expression of ECaC1 mRNA in semicircular canal

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00487.2006

21 January 2018

Molecular analysis of the Pendred's syndrome gene and magnetic resonance imaging studies of the inner ear are essential for the diagnosis of true Pendred's syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2020516

26 November 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17299139

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Electrochemical heterogeneity of the cochlear endolymph: effect of acetazolamide

1 reference

https://pubmed.ncbi.nlm.nih.gov/17299139

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid, active hair bundle movements in hair cells from the bullfrog's sacculus

1 reference

https://pubmed.ncbi.nlm.nih.gov/17299139

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17299139

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alternatively spliced isoforms of the Na+/Ca2+ exchanger in the guinea pig cochlea

1 reference

https://pubmed.ncbi.nlm.nih.gov/17299139

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plasma membrane Ca2+-ATPase extrudes Ca2+ from hair cell stereocilia

1 reference

https://pubmed.ncbi.nlm.nih.gov/17299139

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17299139

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1152/AJPRENAL.00487.2006

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

11 August 2017

ResearchGate publication ID

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