Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss
about
Functional analysis of nonsynonymous single nucleotide polymorphisms in human SLC26A9SLC26A9 is a Cl(-) channel regulated by the WNK kinasesReview series: The cell biology of hearingAutosomal recessive nonsyndromic deafness genes: a reviewThe ultrastructural distribution of prestin in outer hair cells: a post-embedding immunogold investigation of low-frequency and high-frequency regions of the rat cochlea.A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosisPrestin and the cochlear amplifierCoupling modes and stoichiometry of Cl-/HCO3- exchange by slc26a3 and slc26a6High frequency of the IVS2-2A>G DNA sequence variation in SLC26A5, encoding the cochlear motor protein prestin, precludes its involvement in hereditary hearing loss.Genetics of Nonsyndromic Congenital Hearing LossSTAS domain structure and functionSolution Structure of the Guanine Nucleotide-binding STAS Domain of SLC26-related SulP Protein Rv1739c from Mycobacterium tuberculosisThe motor protein prestin is a bullet-shaped molecule with inner cavitiesConserved dimeric subunit stoichiometry of SLC26 multifunctional anion exchangersAnion transport by the cochlear motor protein prestinMolecular screening of patients with nonsyndromic hearing loss from Nanjing city of ChinaIn vivo Drosophilia genetic model for calcium oxalate nephrolithiasisFinding new genes for non-syndromic hearing loss through an in silico prioritization studyEvolutionary insights into the unique electromotility motor of mammalian outer hair cells.The hearing gene Prestin reunites echolocating bats.Prestin is an anion transporter dispensable for mechanical feedback amplification in Drosophila hearingThe sound of silence: mouse models for hearing lossMolecular biology of hearing.The derived allele of ASPM is associated with lexical tone perception.Function and expression pattern of nonsyndromic deafness genesInteraction between CFTR and prestin (SLC26A5)Gene expression associated with the onset of hearing detected by differential display in rat organ of CortiAnalysis and functional evaluation of the hair-cell transcriptome.Molecular architecture and the structural basis for anion interaction in prestin and SLC26 transporters.The solute carrier 26 family of proteins in epithelial ion transport.DNA sequence analysis of SLC26A5, encoding prestin, in a patient-control cohort: identification of fourteen novel DNA sequence variationsGenotyping with a 198 mutation arrayed primer extension array for hereditary hearing loss: assessment of its diagnostic value for medical practice.Regulated transport of sulfate and oxalate by SLC26A2/DTDST.Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing studyNovel autosomal recessive nonsyndromic hearing impairment locus DFNB90 maps to 7p22.1-p15.3.Slc26a6 regulates CFTR activity in vivo to determine pancreatic duct HCO3- secretion: relevance to cystic fibrosisSolute carrier family 26 member a2 (Slc26a2) protein functions as an electroneutral SOFormula/OH-/Cl- exchanger regulated by extracellular Cl-.Deafness in Claudin 11-null mice reveals the critical contribution of basal cell tight junctions to stria vascularis function.Applying Genomic Analysis to Newborn ScreeningThe SLC26 gene family of anion transporters and channels.
P2860
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P2860
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss
description
2003 nî lūn-bûn
@nan
2003 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss
@ast
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss
@en
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss
@nl
type
label
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss
@ast
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss
@en
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss
@nl
prefLabel
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss
@ast
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss
@en
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss
@nl
P2093
P50
P356
P1476
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss
@en
P2093
Arti Pandya
David Corey
Denise Yan
Jing Zheng
Katherine O Welch
Kathleen S Arnos
Peter Dallos
Walter E Nance
P304
P356
10.1093/HMG/DDG127
P407
P577
2003-05-01T00:00:00Z