Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues
about
Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretionTranscriptional control of SLC26A4 is involved in Pendred syndrome and nonsyndromic enlargement of vestibular aqueduct (DFNB4)Requirements for sulfate transport and the diastrophic dysplasia sulfate transporter in fibronectin matrix assemblyLoss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model.Novel Roles for Chloride Channels, Exchangers, and Regulators in Chronic Inflammatory Airway DiseasesLocalization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in pendred syndrome.Macrophage invasion contributes to degeneration of stria vascularis in Pendred syndrome mouse modelIodine and thyroid function.Establishment of a knock-in mouse model with the SLC26A4 c.919-2A>G mutation and characterization of its pathologyExpression of pendrin in benign and malignant human thyroid tissues.The SLC26 gene family of anion transporters and channels.Minireview: The sodium-iodide symporter NIS and pendrin in iodide homeostasis of the thyroidDevelopmental delays consistent with cochlear hypothyroidism contribute to failure to develop hearing in mice lacking Slc26a4/pendrin expression.The Thyroid Na+/I- Symporter: Molecular Characterization and Genomic Regulation.Pendrin is a novel in vivo downstream target gene of the TTF-1/Nkx-2.1 homeodomain transcription factor in differentiated thyroid cells.Screening of SLC26A4 gene in autoimmune thyroid diseases.Overexpression of Interleukin-4 in the Thyroid of Transgenic Mice Upregulates the Expression of Duox1 and the Anion Transporter Pendrin.Functional characterization of pendrin in a polarized cell system. Evidence for pendrin-mediated apical iodide efflux.Differential diagnosis between Pendred and pseudo-Pendred syndromes: clinical, radiologic, and molecular studies.Association of intronic repetition of SLC26A4 gene with Hashimoto thyroiditis disease.
P2860
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P2860
Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues
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2000 nî lūn-bûn
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2000 թուականի Մայիսին հրատարակուած գիտական յօդուած
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2000 թվականի մայիսին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年论文
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name
Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues
@ast
Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues
@en
Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues
@nl
type
label
Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues
@ast
Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues
@en
Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues
@nl
prefLabel
Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues
@ast
Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues
@en
Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues
@nl
P2093
P356
P1476
Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues
@en
P2093
J M Bidart
M Schlumberger
P304
P356
10.1210/JC.85.5.2028
P407
P577
2000-05-01T00:00:00Z