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Search results 1 to 100 out of 267 for Slc26a4

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0.044s
Type Details Score
Gene
Type: gene
Organism: human
Gene
Type: gene
Organism: cattle
Gene
Type: gene
Organism: chicken
Gene
Type: gene
Organism: zebrafish
Gene
Type: gene
Organism: macaque, rhesus
Gene
Type: gene
Organism: rat
Gene
Type: gene
Organism: dog, domestic
Gene
Type: gene
Organism: chimpanzee
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Gene
Type: gene
Organism: human
Publication
First Author: Choi BY
Year: 2011
Journal: J Clin Invest
Title: Mouse model of enlarged vestibular aqueducts defines temporal requirement of Slc26a4 expression for hearing acquisition.
Volume: 121
Issue: 11
Pages: 4516-25
Publication  
First Author: Nishio A
Year: 2016
Journal: Neuroscience
Title: Slc26a4 expression prevents fluctuation of hearing in a mouse model of large vestibular aqueduct syndrome.
Volume: 329
Pages: 74-82
Publication
First Author: Li X
Year: 2013
Journal: PLoS Genet
Title: SLC26A4 targeted to the endolymphatic sac rescues hearing and balance in Slc26a4 mutant mice.
Volume: 9
Issue: 7
Pages: e1003641
Publication
First Author: Takeda H
Year: 2019
Journal: Sci Rep
Title: Prenatal electroporation-mediated gene transfer restores Slc26a4 knock-out mouse hearing and vestibular function.
Volume: 9
Issue: 1
Pages: 17979
Publication
First Author: Dror AA
Year: 2010
Journal: J Biol Chem
Title: Calcium oxalate stone formation in the inner ear as a result of an Slc26a4 mutation.
Volume: 285
Issue: 28
Pages: 21724-35
Publication
First Author: Wen Z
Year: 2019
Journal: Biochem Biophys Res Commun
Title: A knock-in mouse model of Pendred syndrome with Slc26a4 L236P mutation.
Volume: 515
Issue: 2
Pages: 359-365
Publication
First Author: Lu YC
Year: 2011
Journal: PLoS One
Title: Establishment of a knock-in mouse model with the SLC26A4 c.919-2A>G mutation and characterization of its pathology.
Volume: 6
Issue: 7
Pages: e22150
Publication  
First Author: Xu J
Year: 2022
Journal: Front Mol Biosci
Title: Identification of IQGAP1 as a SLC26A4 (Pendrin)-Binding Protein in the Kidney.
Volume: 9
Pages: 874186
Publication
First Author: Yamaguchi N
Year: 2022
Journal: Sci Rep
Title: The iodide transporter Slc26a7 impacts thyroid function more strongly than Slc26a4 in mice.
Volume: 12
Issue: 1
Pages: 11259
Publication
First Author: Yang T
Year: 2007
Journal: Am J Hum Genet
Title: Transcriptional control of SLC26A4 is involved in Pendred syndrome and nonsyndromic enlargement of vestibular aqueduct (DFNB4).
Volume: 80
Issue: 6
Pages: 1055-63
Publication
First Author: Hu CJ
Year: 2021
Journal: Sci Rep
Title: Insights into phenotypic differences between humans and mice with p.T721M and other C-terminal variants of the SLC26A4 gene.
Volume: 11
Issue: 1
Pages: 20983
Publication
First Author: Lu YC
Year: 2014
Journal: PLoS One
Title: Differences in the pathogenicity of the p.H723R mutation of the common deafness-associated SLC26A4 gene in humans and mice.
Volume: 8
Issue: 6
Pages: e64906
Publication
First Author: Kim YH
Year: 2005
Journal: Am J Physiol Renal Physiol
Title: Intercalated cell H+/OH- transporter expression is reduced in Slc26a4 null mice.
Volume: 289
Issue: 6
Pages: F1262-72
Publication
First Author: Shcheynikov N
Year: 2008
Journal: J Physiol
Title: The Slc26a4 transporter functions as an electroneutral Cl-/I-/HCO3- exchanger: role of Slc26a4 and Slc26a6 in I- and HCO3- secretion and in regulation of CFTR in the parotid duct.
Volume: 586
Issue: 16
Pages: 3813-24
Publication
First Author: Kim MA
Year: 2019
Journal: Theranostics
Title: Gene therapy for hereditary hearing loss by SLC26A4 mutations in mice reveals distinct functional roles of pendrin in normal hearing.
Volume: 9
Issue: 24
Pages: 7184-7199
Publication
First Author: Amlal H
Year: 2010
Journal: Am J Physiol Cell Physiol
Title: Deletion of the anion exchanger Slc26a4 (pendrin) decreases apical Cl(-)/HCO3(-) exchanger activity and impairs bicarbonate secretion in kidney collecting duct.
Volume: 299
Issue: 1
Pages: C33-41
Publication      
First Author: Gagnon LH
Year: 2007
Journal: MGI Direct Data Submission
Title: Pendred syndrome model, pdsm, a spontaneous mouse mutation in the Slc26a4 gene with associated inner ear abnormalities
Publication
First Author: Yang T
Year: 2009
Journal: Am J Hum Genet
Title: Mutations of KCNJ10 together with mutations of SLC26A4 cause digenic nonsyndromic hearing loss associated with enlarged vestibular aqueduct syndrome.
Volume: 84
Issue: 5
Pages: 651-7
Publication  
First Author: Hu CJ
Year: 2021
Journal: Int J Mol Sci
Title: Toward the Pathogenicity of the SLC26A4 p.C565Y Variant Using a Genetically Driven Mouse Model.
Volume: 22
Issue: 6
Publication  
First Author: Ito T
Year: 2015
Journal: Neuroscience
Title: Progressive irreversible hearing loss is caused by stria vascularis degeneration in an Slc26a4-insufficient mouse model of large vestibular aqueduct syndrome.
Volume: 310
Pages: 188-97
Publication  
First Author: Ito T
Year: 2014
Journal: Neurobiol Dis
Title: Slc26a4-insufficiency causes fluctuating hearing loss and stria vascularis dysfunction.
Volume: 66
Pages: 53-65
Publication
First Author: Trepiccione F
Year: 2017
Journal: Nephrol Dial Transplant
Title: Acute genetic ablation of pendrin lowers blood pressure in mice.
Volume: 32
Issue: 7
Pages: 1137-1145
Publication
First Author: Dror AA
Year: 2014
Journal: Mamm Genome
Title: Atrophic thyroid follicles and inner ear defects reminiscent of cochlear hypothyroidism in Slc26a4-related deafness.
Volume: 25
Issue: 7-8
Pages: 304-16
Publication
First Author: Dror AA
Year: 2020
Journal: Genes Brain Behav
Title: A mouse model for benign paroxysmal positional vertigo with genetic predisposition for displaced otoconia.
Volume: 19
Issue: 5
Pages: e12635
Publication
First Author: Wangemann P
Year: 2009
Journal: Am J Physiol Renal Physiol
Title: Developmental delays consistent with cochlear hypothyroidism contribute to failure to develop hearing in mice lacking Slc26a4/pendrin expression.
Volume: 297
Issue: 5
Pages: F1435-47
Publication
First Author: Verlander JW
Year: 2006
Journal: Am J Physiol Renal Physiol
Title: Dietary Cl(-) restriction upregulates pendrin expression within the apical plasma membrane of type B intercalated cells.
Volume: 291
Issue: 4
Pages: F833-9
Publication  
First Author: Bronckers AL
Year: 2011
Journal: Eur J Oral Sci
Title: Developmental expression of solute carrier family 26A member 4 (SLC26A4/pendrin) during amelogenesis in developing rodent teeth.
Volume: 119 Suppl 1
Pages: 185-92
Publication  
First Author: Choi HJ
Year: 2020
Journal: Mol Ther Methods Clin Dev
Title: DNAJC14 Ameliorates Inner Ear Degeneration in the DFNB4 Mouse Model.
Volume: 17
Pages: 188-197
Publication  
First Author: Wangemann P
Year: 2004
Journal: BMC Med
Title: Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model.
Volume: 2
Pages: 30
Publication  
First Author: Do DC
Year: 2021
Journal: JCI Insight
Title: Type II alveolar epithelial cell-specific loss of RhoA exacerbates allergic airway inflammation through SLC26A4.
Volume: 6
Issue: 14
Publication
First Author: Kim HM
Year: 2010
Journal: PLoS One
Title: Failure of fluid absorption in the endolymphatic sac initiates cochlear enlargement that leads to deafness in mice lacking pendrin expression.
Volume: 5
Issue: 11
Pages: e14041
Publication
First Author: Pelzl L
Year: 2013
Journal: Cell Physiol Biochem
Title: Sgk1 sensitive pendrin expression in murine platelets.
Volume: 32
Issue: 7
Pages: 210-20
Publication    
First Author: Honda K
Year: 2017
Journal: Elife
Title: Molecular architecture underlying fluid absorption by the developing inner ear.
Volume: 6
Publication
First Author: Eskalli Z
Year: 2016
Journal: Thyroid
Title: Overexpression of Interleukin-4 in the Thyroid of Transgenic Mice Upregulates the Expression of Duox1 and the Anion Transporter Pendrin.
Volume: 26
Issue: 10
Pages: 1499-1512
Publication
First Author: Li X
Year: 2013
Journal: PLoS One
Title: Endolymphatic Na⁺ and K⁺ concentrations during cochlear growth and enlargement in mice lacking Slc26a4/pendrin.
Volume: 8
Issue: 5
Pages: e65977
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus caroli
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus pahari
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus spretus
Publication
First Author: Royaux IE
Year: 2001
Journal: Proc Natl Acad Sci U S A
Title: Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion.
Volume: 98
Issue: 7
Pages: 4221-6
Publication
First Author: López-Cayuqueo KI
Year: 2018
Journal: Kidney Int
Title: A mouse model of pseudohypoaldosteronism type II reveals a novel mechanism of renal tubular acidosis.
Volume: 94
Issue: 3
Pages: 514-523
Publication
First Author: Barone S
Year: 2012
Journal: Nephrol Dial Transplant
Title: Deletion of the Cl-/HCO3- exchanger pendrin downregulates calcium-absorbing proteins in the kidney and causes calcium wasting.
Volume: 27
Issue: 4
Pages: 1368-79
Publication
First Author: Wangemann P
Year: 2007
Journal: Am J Physiol Renal Physiol
Title: Loss of cochlear HCO3- secretion causes deafness via endolymphatic acidification and inhibition of Ca2+ reabsorption in a Pendred syndrome mouse model.
Volume: 292
Issue: 5
Pages: F1345-53
Publication
First Author: Everett LA
Year: 2001
Journal: Hum Mol Genet
Title: Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome.
Volume: 10
Issue: 2
Pages: 153-61
Publication
First Author: Nakagami Y
Year: 2008
Journal: J Immunol
Title: The epithelial anion transporter pendrin is induced by allergy and rhinovirus infection, regulates airway surface liquid, and increases airway reactivity and inflammation in an asthma model.
Volume: 181
Issue: 3
Pages: 2203-10
Publication
First Author: Nanami M
Year: 2015
Journal: Am J Physiol Renal Physiol
Title: ENaC inhibition stimulates HCl secretion in the mouse cortical collecting duct. II. Bafilomycin-sensitive H+ secretion.
Volume: 309
Issue: 3
Pages: F259-68
Publication
First Author: Kim BG
Year: 2014
Journal: PLoS One
Title: 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.
Volume: 9
Issue: 4
Pages: e95730
Publication
First Author: Lazo-Fernandez Y
Year: 2015
Journal: Am J Physiol Endocrinol Metab
Title: Pendrin localizes to the adrenal medulla and modulates catecholamine release.
Volume: 309
Issue: 6
Pages: E534-45
Publication
First Author: Karniski LP
Year: 2002
Journal: Am J Physiol Renal Physiol
Title: Formate-stimulated NaCl absorption in the proximal tubule is independent of the pendrin protein.
Volume: 283
Issue: 5
Pages: F952-6
Publication
First Author: Royaux IE
Year: 2003
Journal: J Assoc Res Otolaryngol
Title: Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in pendred syndrome.
Volume: 4
Issue: 3
Pages: 394-404
Publication
First Author: Hirohama D
Year: 2018
Journal: J Am Soc Nephrol
Title: Aldosterone Is Essential for Angiotensin II-Induced Upregulation of Pendrin.
Volume: 29
Issue: 1
Pages: 57-68
Publication
First Author: Sutliff RL
Year: 2014
Journal: PLoS One
Title: Contractile force is enhanced in Aortas from pendrin null mice due to stimulation of angiotensin II-dependent signaling.
Volume: 9
Issue: 8
Pages: e105101
Publication
First Author: Verlander JW
Year: 2003
Journal: Hypertension
Title: Deoxycorticosterone upregulates PDS (Slc26a4) in mouse kidney: role of pendrin in mineralocorticoid-induced hypertension.
Volume: 42
Issue: 3
Pages: 356-62
Publication      
First Author: SoRelle J
Year: 2016
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for cul-de-sac
Publication      
First Author: SoRelle J
Year: 2016
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for discobolus
Publication
First Author: Vallet M
Year: 2006
Journal: J Am Soc Nephrol
Title: Pendrin regulation in mouse kidney primarily is chloride-dependent.
Volume: 17
Issue: 8
Pages: 2153-63
Publication
First Author: Kim YH
Year: 2002
Journal: Am J Physiol Renal Physiol
Title: Immunocytochemical localization of pendrin in intercalated cell subtypes in rat and mouse kidney.
Volume: 283
Issue: 4
Pages: F744-54
Publication
First Author: Azroyan A
Year: 2011
Journal: Biochem J
Title: Regulation of pendrin by pH: dependence on glycosylation.
Volume: 434
Issue: 1
Pages: 61-72
Publication
First Author: Azroyan A
Year: 2012
Journal: Am J Physiol Renal Physiol
Title: Regulation of pendrin by cAMP: possible involvement in β-adrenergic-dependent NaCl retention.
Volume: 302
Issue: 9
Pages: F1180-7
GXD Expression        
Probe: MGI:4361833
Assay Type: RT-PCR
Annotation Date: 2009-10-21
Strength: Not Specified
Sex: Not Specified
Emaps: EMAPS:1737321
Stage: TS21
Assay Id: MGI:4361900
Age: embryonic day 13.5
Specimen Label: E13.5
Specimen Num: 1
GXD Expression      
Probe: MGI:4361833
Assay Type: RT-PCR
Annotation Date: 2009-10-21
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1737323
Stage: TS23
Assay Id: MGI:4361900
Age: embryonic day 15.5
Specimen Label: E15.5
Detected: true
Specimen Num: 2
GXD Expression      
Probe: MGI:4361833
Assay Type: RT-PCR
Annotation Date: 2009-10-21
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1737325
Stage: TS25
Assay Id: MGI:4361900
Age: embryonic day 17.5
Specimen Label: E17.5
Detected: true
Specimen Num: 3
GXD Expression      
Probe: MGI:4361833
Assay Type: RT-PCR
Annotation Date: 2009-10-21
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1737327
Stage: TS27
Assay Id: MGI:4361900
Age: postnatal newborn
Specimen Label: Newborn
Detected: true
Specimen Num: 4
GXD Expression      
Probe: MGI:4361833
Assay Type: RT-PCR
Annotation Date: 2009-10-21
Strength: Present
Sex: Male
Emaps: EMAPS:1737328
Stage: TS28
Assay Id: MGI:4361900
Age: postnatal week 12
Specimen Label: Adult
Detected: true
Specimen Num: 5
GXD Expression      
Probe: MGI:4361731
Assay Type: Western blot
Annotation Date: 2009-10-21
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:1737321
Stage: TS21
Assay Id: MGI:4361914
Age: embryonic day 13.5
Specimen Label: E13.5
Detected: false
Specimen Num: 1
GXD Expression      
Probe: MGI:4361731
Assay Type: Western blot
Annotation Date: 2009-10-21
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:1737322
Stage: TS22
Assay Id: MGI:4361914
Age: embryonic day 14.5
Specimen Label: E14.5
Detected: false
Specimen Num: 2
GXD Expression      
Probe: MGI:4361731
Assay Type: Western blot
Annotation Date: 2009-10-21
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:1737323
Stage: TS23
Assay Id: MGI:4361914
Age: embryonic day 15.5
Specimen Label: E15.5
Detected: false
Specimen Num: 3
GXD Expression      
Probe: MGI:4361731
Assay Type: Western blot
Annotation Date: 2009-10-21
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1737324
Stage: TS24
Assay Id: MGI:4361914
Age: embryonic day 16.5
Specimen Label: E16.5
Detected: true
Specimen Num: 4
GXD Expression      
Probe: MGI:4361731
Assay Type: Western blot
Annotation Date: 2009-10-21
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1737325
Stage: TS25
Assay Id: MGI:4361914
Age: embryonic day 17.5
Specimen Label: E17.5
Detected: true
Specimen Num: 5
GXD Expression      
Probe: MGI:4361731
Assay Type: Western blot
Annotation Date: 2009-10-21
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1737326
Stage: TS26
Assay Id: MGI:4361914
Age: embryonic day 18.5
Specimen Label: E18.5
Detected: true
Specimen Num: 6
GXD Expression      
Probe: MGI:4361731
Assay Type: Western blot
Annotation Date: 2009-10-21
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1737327
Stage: TS27
Assay Id: MGI:4361914
Age: postnatal newborn
Specimen Label: Newborn
Detected: true
Specimen Num: 7
GXD Expression      
Probe: MGI:4361731
Assay Type: Western blot
Annotation Date: 2009-10-21
Strength: Present
Sex: Male
Emaps: EMAPS:1737328
Stage: TS28
Assay Id: MGI:4361914
Age: postnatal week 12
Specimen Label: Adult
Detected: true
Specimen Num: 8
GXD Expression      
Probe: MGI:4361731
Assay Type: Western blot
Annotation Date: 2009-10-21
Strength: Present
Sex: Male
Emaps: EMAPS:1795228
Stage: TS28
Assay Id: MGI:4361935
Age: postnatal week 12
Specimen Label: cortex
Detected: true
Specimen Num: 1
GXD Expression      
Probe: MGI:4361731
Assay Type: Western blot
Annotation Date: 2009-10-21
Strength: Present
Sex: Male
Emaps: EMAPS:1927928
Stage: TS28
Assay Id: MGI:4361935
Age: postnatal week 12
Specimen Label: medulla
Detected: true
Specimen Num: 2
GXD Expression  
Probe: MGI:4424900
Assay Type: RNA in situ
Annotation Date: 2010-09-14
Strength: Weak
Sex: Not Specified
Emaps: EMAPS:1689423
Pattern: Regionally restricted
Stage: TS23
Assay Id: MGI:4828166
Age: embryonic day 14.5
Image: euxassay_014488_09
Specimen Label: euxassay_014488_09
Detected: true
Specimen Num: 1