The Pendred syndrome gene encodes a chloride-iodide transport protein
about
Tat1, a novel sulfate transporter specifically expressed in human male germ cells and potentially linked to rhogtpase signalingFunctional characterization of three novel tissue-specific anion exchangers SLC26A7, -A8, and -A9Isoforms of SLC26A6 mediate anion transport and have functional PDZ interaction domainsPendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretionThe epithelial anion transporter pendrin is induced by allergy and rhinovirus infection, regulates airway surface liquid, and increases airway reactivity and inflammation in an asthma modelExpression profiling of the solute carrier gene family in the mouse brainAcute regulation of the SLC26A3 congenital chloride diarrhoea anion exchanger (DRA) expressed in Xenopus oocytesLoss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model.Thyroid iodide efflux: a team effort?Collecting duct intercalated cell function and regulationSLC26A4 genotypes and phenotypes associated with enlargement of the vestibular aqueductControversies concerning the role of pendrin as an apical iodide transporter in thyroid follicular cellsSLC26A4 targeted to the endolymphatic sac rescues hearing and balance in Slc26a4 mutant mice.Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype-phenotype correlationsPhysiological roles and regulation of mammalian sulfate transportersPendrin: an apical Cl-/OH-/HCO3- exchanger in the kidney cortexSLC26A2 (diastrophic dysplasia sulfate transporter) is expressed in developing and mature cartilage but also in other tissues and cell typesIdentification of seven novel mutations including the first two genomic rearrangements in SLC26A3 mutated in congenital chloride diarrheaHuman pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchangeIdentification of a chloride-formate exchanger expressed on the brush border membrane of renal proximal tubule cellsIntercalated cell H+/OH- transporter expression is reduced in Slc26a4 null miceExpression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner earRegulation of anion exchanger Slc26a6 by protein kinase CSugar transport by mammalian members of the SLC26 superfamily of anion-bicarbonate exchangersMolecular characterization of the murine Slc26a6 anion exchanger: functional comparison with Slc26a1Evolutionary insights into the unique electromotility motor of mammalian outer hair cells.Free radical stress-mediated loss of Kcnj10 protein expression in stria vascularis contributes to deafness in Pendred syndrome mouse model.Developmental changes of ENaC expression and function in the inner ear of pendrin knock-out mice as a perspective on the development of endolymphatic hydrops.Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in pendred syndrome.Loss of cochlear HCO3- secretion causes deafness via endolymphatic acidification and inhibition of Ca2+ reabsorption in a Pendred syndrome mouse model.Age-related functional and histopathological changes of the ear in the MPS I mouse.Macrophage invasion contributes to degeneration of stria vascularis in Pendred syndrome mouse modelImmunocytochemical localization of pendrin in intercalated cell subtypes in rat and mouse kidney.The solute carrier 26 family of proteins in epithelial ion transport.Deafness and cochlear fibrocyte alterations in mice deficient for the inner ear protein otospiralin.Diagnostic yield of high-resolution computed tomography for pediatric sensorineural hearing loss.Autosomal recessive nonsyndromic hearing loss.Calcium oxalate stone formation in the inner ear as a result of an Slc26a4 mutation.The clinical chemistry of inorganic sulfate.Molecular mechanisms of renal sulfate regulation.
P2860
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P2860
The Pendred syndrome gene encodes a chloride-iodide transport protein
description
1999 nî lūn-bûn
@nan
1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
The Pendred syndrome gene encodes a chloride-iodide transport protein
@ast
The Pendred syndrome gene encodes a chloride-iodide transport protein
@en
The Pendred syndrome gene encodes a chloride-iodide transport protein
@en-gb
The Pendred syndrome gene encodes a chloride-iodide transport protein
@nl
type
label
The Pendred syndrome gene encodes a chloride-iodide transport protein
@ast
The Pendred syndrome gene encodes a chloride-iodide transport protein
@en
The Pendred syndrome gene encodes a chloride-iodide transport protein
@en-gb
The Pendred syndrome gene encodes a chloride-iodide transport protein
@nl
prefLabel
The Pendred syndrome gene encodes a chloride-iodide transport protein
@ast
The Pendred syndrome gene encodes a chloride-iodide transport protein
@en
The Pendred syndrome gene encodes a chloride-iodide transport protein
@en-gb
The Pendred syndrome gene encodes a chloride-iodide transport protein
@nl
P2093
P356
P1433
P1476
The Pendred syndrome gene encodes a chloride-iodide transport protein
@en
P2093
L P Karniski
T M Kreman
V C Sheffield
P2888
P356
10.1038/7783
P407
P577
1999-04-01T00:00:00Z
P6179
1045700175