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Search results 1 to 100 out of 146 for Slc26a4

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Category: Publication
Type Details Score
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: 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: 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: 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: 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: 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: 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: 2014
Journal: Neurobiol Dis
Title: Slc26a4-insufficiency causes fluctuating hearing loss and stria vascularis dysfunction.
Volume: 66
Pages: 53-65
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: 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: 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: 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: 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: 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: 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: 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: 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: 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
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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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
Publication
First Author: Knauf F
Year: 2001
Journal: Proc Natl Acad Sci U S A
Title: Identification of a chloride-formate exchanger expressed on the brush border membrane of renal proximal tubule cells.
Volume: 98
Issue: 16
Pages: 9425-30
Publication
First Author: Blomqvist SR
Year: 2004
Journal: J Clin Invest
Title: Distal renal tubular acidosis in mice that lack the forkhead transcription factor Foxi1.
Volume: 113
Issue: 11
Pages: 1560-70
Publication
First Author: Soleimani M
Year: 2016
Journal: PLoS One
Title: Prostaglandin-E2 Mediated Increase in Calcium and Phosphate Excretion in a Mouse Model of Distal Nephron Salt Wasting.
Volume: 11
Issue: 7
Pages: e0159804
Publication
First Author: Patel-Chamberlin M
Year: 2016
Journal: PLoS One
Title: The Role of Epithelial Sodium Channel ENaC and the Apical Cl-/HCO3- Exchanger Pendrin in Compensatory Salt Reabsorption in the Setting of Na-Cl Cotransporter (NCC) Inactivation.
Volume: 11
Issue: 3
Pages: e0150918
Publication
First Author: Soleimani M
Year: 2012
Journal: Proc Natl Acad Sci U S A
Title: Double knockout of pendrin and Na-Cl cotransporter (NCC) causes severe salt wasting, volume depletion, and renal failure.
Volume: 109
Issue: 33
Pages: 13368-73
Publication
First Author: Alshahrani S
Year: 2017
Journal: Kidney Blood Press Res
Title: Ablation of the Cl-/HCO3- Exchanger Pendrin Enhances Hydrochlorothiazide-Induced Diuresis.
Volume: 42
Issue: 3
Pages: 444-455
Publication
First Author: Kim YH
Year: 2007
Journal: Am J Physiol Renal Physiol
Title: Reduced ENaC protein abundance contributes to the lower blood pressure observed in pendrin-null mice.
Volume: 293
Issue: 4
Pages: F1314-24
Publication
First Author: Pech V
Year: 2010
Journal: J Am Soc Nephrol
Title: Pendrin modulates ENaC function by changing luminal HCO3-.
Volume: 21
Issue: 11
Pages: 1928-41
Publication
First Author: Wall SM
Year: 2003
Journal: Am J Physiol Renal Physiol
Title: Localization of pendrin in mouse kidney.
Volume: 284
Issue: 1
Pages: F229-41
Publication
First Author: Rozenfeld J
Year: 2012
Journal: Am J Physiol Renal Physiol
Title: The pendrin anion exchanger gene is transcriptionally regulated by uroguanylin: a novel enterorenal link.
Volume: 302
Issue: 5
Pages: F614-24
Publication
First Author: Thumova M
Year: 2012
Journal: Am J Physiol Renal Physiol
Title: Pendrin protein abundance in the kidney is regulated by nitric oxide and cAMP.
Volume: 303
Issue: 6
Pages: F812-20
Publication
First Author: Nanami M
Year: 2018
Journal: J Am Soc Nephrol
Title: The Role of Intercalated Cell Nedd4-2 in BP Regulation, Ion Transport, and Transporter Expression.
Volume: 29
Issue: 6
Pages: 1706-1719
Publication  
First Author: Berg P
Year: 2022
Journal: Proc Natl Acad Sci U S A
Title: Alkalosis-induced hypoventilation in cystic fibrosis: The importance of efficient renal adaptation.
Volume: 119
Issue: 8
Publication
First Author: Singh R
Year: 2008
Journal: Am J Physiol Renal Physiol
Title: Free radical stress-mediated loss of Kcnj10 protein expression in stria vascularis contributes to deafness in Pendred syndrome mouse model.
Volume: 294
Issue: 1
Pages: F139-48
Publication
First Author: Pech V
Year: 2013
Journal: Am J Physiol Renal Physiol
Title: Nitric oxide reduces Cl⁻ absorption in the mouse cortical collecting duct through an ENaC-dependent mechanism.
Volume: 304
Issue: 11
Pages: F1390-7
Publication
First Author: Nakaya K
Year: 2007
Journal: Am J Physiol Renal Physiol
Title: Lack of pendrin HCO3- transport elevates vestibular endolymphatic [Ca2+] by inhibition of acid-sensitive TRPV5 and TRPV6 channels.
Volume: 292
Issue: 5
Pages: F1314-21
Publication
First Author: Everett LA
Year: 1999
Journal: Proc Natl Acad Sci U S A
Title: Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear.
Volume: 96
Issue: 17
Pages: 9727-32
Publication
First Author: Chambrey R
Year: 2013
Journal: Proc Natl Acad Sci U S A
Title: Renal intercalated cells are rather energized by a proton than a sodium pump.
Volume: 110
Issue: 19
Pages: 7928-33
Publication
First Author: Scanlon KM
Year: 2014
Journal: Infect Immun
Title: Epithelial anion transporter pendrin contributes to inflammatory lung pathology in mouse models of Bordetella pertussis infection.
Volume: 82
Issue: 10
Pages: 4212-21
Publication
First Author: Verlander JW
Year: 2011
Journal: Am J Physiol Renal Physiol
Title: Angiotensin II acts through the angiotensin 1a receptor to upregulate pendrin.
Volume: 301
Issue: 6
Pages: F1314-25
Publication
First Author: Frank H
Year: 2008
Journal: J Biol Chem
Title: Lactaturia and loss of sodium-dependent lactate uptake in the colon of SLC5A8-deficient mice.
Volume: 283
Issue: 36
Pages: 24729-37
Publication
First Author: Alshahrani S
Year: 2017
Journal: PLoS One
Title: The non-diuretic hypotensive effects of thiazides are enhanced during volume depletion states.
Volume: 12
Issue: 7
Pages: e0181376
Publication
First Author: Pech V
Year: 2015
Journal: Am J Physiol Renal Physiol
Title: Pendrin gene ablation alters ENaC subcellular distribution and open probability.
Volume: 309
Issue: 2
Pages: F154-63
Publication
First Author: Dou H
Year: 2004
Journal: J Histochem Cytochem
Title: Co-expression of pendrin, vacuolar H+-ATPase alpha4-subunit and carbonic anhydrase II in epithelial cells of the murine endolymphatic sac.
Volume: 52
Issue: 10
Pages: 1377-84
Publication
First Author: Verlander JW
Year: 2003
Journal: Am J Physiol Renal Physiol
Title: Localization of the ammonium transporter proteins RhBG and RhCG in mouse kidney.
Volume: 284
Issue: 2
Pages: F323-37
Publication
First Author: Stehberger PA
Year: 2007
Journal: J Am Soc Nephrol
Title: Distal renal tubular acidosis in mice lacking the AE1 (band3) Cl-/HCO3- exchanger (slc4a1).
Volume: 18
Issue: 5
Pages: 1408-18
Publication
First Author: Lazo-Fernandez Y
Year: 2018
Journal: Am J Physiol Renal Physiol
Title: α-Ketoglutarate stimulates pendrin-dependent Cl- absorption in the mouse CCD through protein kinase C.
Volume: 315
Issue: 1
Pages: F7-F15
Publication
First Author: Merves M
Year: 2003
Journal: J Assoc Res Otolaryngol
Title: Expression of aquaporin 1 and 5 in the developing mouse inner ear and audiovestibular assessment of an Aqp5 null mutant.
Volume: 4
Issue: 2
Pages: 264-75
Publication
First Author: Trepiccione F
Year: 2016
Journal: Am J Physiol Renal Physiol
Title: A fate-mapping approach reveals the composite origin of the connecting tubule and alerts on "single-cell"-specific KO model of the distal nephron.
Volume: 311
Issue: 5
Pages: F901-F906
Publication
First Author: Ranieri M
Year: 2018
Journal: FASEB J
Title: CaSR signaling down-regulates AQP2 expression via a novel microRNA pathway in pendrin and NaCl cotransporter knockout mice.
Volume: 32
Issue: 4
Pages: 2148-2159
Publication
First Author: Kim HM
Year: 2011
Journal: PLoS One
Title: Epithelial cell stretching and luminal acidification lead to a retarded development of stria vascularis and deafness in mice lacking pendrin.
Volume: 6
Issue: 3
Pages: e17949
Publication
First Author: Norgett EE
Year: 2012
Journal: Proc Natl Acad Sci U S A
Title: Atp6v0a4 knockout mouse is a model of distal renal tubular acidosis with hearing loss, with additional extrarenal phenotype.
Volume: 109
Issue: 34
Pages: 13775-80
Publication
First Author: Song HK
Year: 2007
Journal: J Am Soc Nephrol
Title: Origin and fate of pendrin-positive intercalated cells in developing mouse kidney.
Volume: 18
Issue: 10
Pages: 2672-82
Publication
First Author: Huebner AK
Year: 2019
Journal: J Assoc Res Otolaryngol
Title: Early Hearing Loss upon Disruption of Slc4a10 in C57BL/6 Mice.
Volume: 20
Issue: 3
Pages: 233-245
Publication
First Author: Guo Q
Year: 2015
Journal: J Am Soc Nephrol
Title: Adam10 mediates the choice between principal cells and intercalated cells in the kidney.
Volume: 26
Issue: 1
Pages: 149-59
Publication    
First Author: Werth M
Year: 2017
Journal: Elife
Title: Transcription factor TFCP2L1 patterns cells in the mouse kidney collecting ducts.
Volume: 6
Publication
First Author: Hulander M
Year: 2003
Journal: Development
Title: Lack of pendrin expression leads to deafness and expansion of the endolymphatic compartment in inner ears of Foxi1 null mutant mice.
Volume: 130
Issue: 9
Pages: 2013-25
Publication
First Author: Rossier BC
Year: 2013
Journal: FEBS Lett
Title: Genetic dissection of sodium and potassium transport along the aldosterone-sensitive distal nephron: importance in the control of blood pressure and hypertension.
Volume: 587
Issue: 13
Pages: 1929-41
Publication
First Author: Choo D
Year: 2006
Journal: Dev Biol
Title: Molecular mechanisms underlying inner ear patterning defects in kreisler mutants.
Volume: 289
Issue: 2
Pages: 308-17
Publication
First Author: Jeong HW
Year: 2009
Journal: J Clin Invest
Title: Inactivation of Notch signaling in the renal collecting duct causes nephrogenic diabetes insipidus in mice.
Volume: 119
Issue: 11
Pages: 3290-300
Publication
First Author: Hinze C
Year: 2018
Journal: J Am Soc Nephrol
Title: GRHL2 Is Required for Collecting Duct Epithelial Barrier Function and Renal Osmoregulation.
Volume: 29
Issue: 3
Pages: 857-868
Publication
First Author: Burton Q
Year: 2004
Journal: Dev Biol
Title: The role of Pax2 in mouse inner ear development.
Volume: 272
Issue: 1
Pages: 161-75
Publication
First Author: Jouret F
Year: 2005
Journal: J Am Soc Nephrol
Title: Ubiquitous and kidney-specific subunits of vacuolar H+-ATPase are differentially expressed during nephrogenesis.
Volume: 16
Issue: 11
Pages: 3235-46
Publication
First Author: Wu L
Year: 2013
Journal: Dev Dyn
Title: A systematic survey of carbonic anhydrase mRNA expression during mammalian inner ear development.
Volume: 242
Issue: 3
Pages: 269-80
Publication
First Author: Yamaguchi Y
Year: 2006
Journal: Development
Title: Grainyhead-related transcription factor is required for duct maturation in the salivary gland and the kidney of the mouse.
Volume: 133
Issue: 23
Pages: 4737-48