The Role of Pendrin in the Development of the Murine Inner Ear (Q37960787)

26 August 2017

title

The Role of Pendrin in the Development of the Murine Inner Ear (English)

1 reference

18 December 2024

1

Philine Wangemann

1 reference

26 August 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=22116367

18 December 2024

publication date

18 November 2011

1 reference

full work available at URL

26 August 2017

https://www.karger.com/Article/Pdf/335113

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:22116367

https://europepmc.org/articles/PMC7077107

18 December 2024

file format

HyperText Markup Language

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:22116367

https://doi.org/10.1159/000335113

18 December 2024

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:22116367

http://www.karger.com/Article/Pdf/335113

18 December 2024

1 reference

Cellular Physiology and Biochemistry

18 December 2024

published in

1 reference

26 August 2017

volume

28

1 reference

26 August 2017

issue

3

1 reference

26 August 2017

page(s)

527-534

1 reference

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

26 August 2017

cites work

1 reference

Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?

21 January 2018

1 reference

SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities

21 January 2018

1 reference

Characteristics of vestibular evoked myogenic potentials in children with enlarged vestibular aqueduct

21 January 2018

1 reference

Long-term follow-up in patients with Pendred syndrome: vestibular, auditory and other phenotypes

21 January 2018

1 reference

Amniotic fluid volume and composition in mouse pregnancy

21 January 2018

1 reference

Failure of Fluid Absorption in the Endolymphatic Sac Initiates Cochlear Enlargement that Leads to Deafness in Mice Lacking Pendrin Expression

21 January 2018

1 reference

Supporting sensory transduction: cochlear fluid homeostasis and the endocochlear potential

21 January 2018

1 reference

Patterning of the mammalian cochlea

21 January 2018

1 reference

Developmental acquisition of sensory transduction in hair cells of the mouse inner ear

21 January 2018

1 reference

Tonotopic gradient in the developmental acquisition of sensory transduction in outer hair cells of the mouse cochlea

21 January 2018

1 reference

Afferent innervation patterns in crista ampullaris of the mouse during ontogenesis

21 January 2018

1 reference

Development of monovalent ions in the endolymph in mouse cochlea.

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in pendred syndrome

21 January 2018

1 reference

Regulation of sodium transport in the inner ear.

21 January 2018

1 reference

Epithelial Cell Stretching and Luminal Acidification Lead to a Retarded Development of Stria Vascularis and Deafness in Mice Lacking Pendrin

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Free radical stress-mediated loss of Kcnj10 protein expression in stria vascularis contributes to deafness in Pendred syndrome mouse model

21 January 2018

1 reference

Developmental delays consistent with cochlear hypothyroidism contribute to failure to develop hearing in mice lacking Slc26a4/pendrin expression

21 January 2018

1 reference

Calcium oxalate stone formation in the inner ear as a result of an Slc26a4 mutation

21 January 2018

1 reference

Establishment of a knock-in mouse model with the SLC26A4 c.919-2A>G mutation and characterization of its pathology

21 January 2018

1 reference

Type 2 iodothyronine deiodinase expression in the cochlea before the onset of hearing

21 January 2018

1 reference

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

21 January 2018

1 reference

K cycling and the endocochlear potential

21 January 2018

1 reference

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

21 January 2018

1 reference

KCNE1 reverses the response of the human K channel KCNQ1 to cytosolic pH changes and alters its pharmacology and sensitivity to temperature

21 January 2018

1 reference

Clinical characteristics and genotype-phenotype correlation of hearing loss patients with SLC26A4 mutations

21 January 2018

1 reference

Identification of a novel mutation in the SLC26A4 gene in an Italian with fluctuating sensorineural hearing loss

21 January 2018

1 reference

Mutations of the Pendred syndrome gene (PDS) in patients with large vestibular aqueduct

21 January 2018

1 reference

Expression of epithelial calcium transport system in rat cochlea and vestibular labyrinth.

21 January 2018

1 reference

Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice

21 January 2018

1 reference

The winged helix transcription factor Fkh10 is required for normal development of the inner ear.

21 January 2018

1 reference

Toward a systems biology of mouse inner ear organogenesis: gene expression pathways, patterns and network analysis

21 January 2018

1 reference

Postnatal Development of the Vestibular Sensory Epithelium in the Mouse

21 January 2018

1 reference

K( )-induced stimulation of K secretion involves activation of the IsK channel in vestibular dark cells

21 January 2018

1 reference

12 December 2020

The large vestibular aqueduct syndrome and sensorineural hearing loss in the pediatric population

1 reference

12 December 2020

SLC26A4 genotypes and phenotypes associated with enlargement of the vestibular aqueduct

1 reference

12 December 2020

The Large Vestibular Aqueduct Syndrome

1 reference

12 December 2020

Phenotypic Analyses and Mutation Screening of the SLC26A4 and FOXI1 Genes in 101 Taiwanese Families with Bilateral Nonsyndromic Enlarged Vestibular Aqueduct (DFNB4) or Pendred Syndrome

1 reference

12 December 2020

Co-expression of pendrin, vacuolar H -ATPase alpha4-subunit and carbonic anhydrase II in epithelial cells of the murine endolymphatic sac

1 reference

12 December 2020

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

1 reference

12 December 2020

Elemental composition of the developing inner ear.

1 reference

12 December 2020

Another role for melanocytes: their importance for normal stria vascularis development in the mammalian inner ear.

1 reference

12 December 2020

Deletion of the Cl-/HCO3- exchanger pendrin downregulates calcium-absorbing proteins in the kidney and causes calcium wasting

1 reference

12 December 2020

Hearing loss associated with enlargement of the vestibular aqueduct: Mechanistic insights from clinical phenotypes, genotypes, and mouse models

1 reference

12 December 2020

Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisition

1 reference

12 December 2020

The Journal of otolaryngology

2

20

247

Arcand P

1991

1 reference

Journal of Clinical Investigation

18 December 2024

series ordinal

48

author name string

Choi BY

publication date

2011

1 reference

18 December 2024

Identifiers

DOI

10.1159/000335113

1 reference

release_ikg2fr3xjbaedl4bycbbmec35a

26 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ikg2fr3xjbaedl4bycbbmec35a

24 November 2022

mapped directly with Wikidata item

PMC publication ID

7077107

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=22116367

18 December 2024

1 reference