Pendrin is an iodide-specific apical porter responsible for iodide efflux from thyroid cells
about
Genetic factors that might lead to different responses in individuals exposed to perchlorate.Genetic disorders coupled to ROS deficiencyExcess iodide decreases transcription of NIS and VEGF genes in rat FRTL-5 thyroid cellsIodine excess as an environmental risk factor for autoimmune thyroid disease.Altered ion transport by thyroid epithelia from CFTR(-/-) pigs suggests mechanisms for hypothyroidism in cystic fibrosis.Protective effect of KI in mtDNA in porcine thyroid: comparison with KIO₃ and nDNA.TSH regulates pendrin membrane abundance and enhances iodide efflux in thyroid cells.The pendrin anion exchanger gene is transcriptionally regulated by uroguanylin: a novel enterorenal linkPropylthiouracil increases sodium/iodide symporter gene expression and iodide uptake in rat thyroid cells in the absence of TSH.Expression of pendrin in benign and malignant human thyroid tissues.Current and potential rodent screens and tests for thyroid toxicants.Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVAFunctional characterization of pendrin mutations found in the Israeli and Palestinian populations.Identification of allelic variants of pendrin (SLC26A4) with loss and gain of function.TRPM7 is regulated by halides through its kinase domainMinireview: The sodium-iodide symporter NIS and pendrin in iodide homeostasis of the thyroidIodide excess regulates its own efflux: a possible involvement of pendrin.Developmental delays consistent with cochlear hypothyroidism contribute to failure to develop hearing in mice lacking Slc26a4/pendrin expression.Iodine mediated mechanisms and thyroid carcinoma.Intrinsic regulation of thyroid function by thyroglobulin.Thiocyanate: a review and evaluation of the kinetics and the modes of action for thyroid hormone perturbations.Molecular mechanisms of epithelial cell-specific expression and regulation of the human anion exchanger (pendrin) gene.Targeted Next-Generation Sequencing Analysis of a Pendred Syndrome-Associated Thyroid Carcinoma.Pendred syndrome in a large consanguineous Brazilian family caused by a homozygous mutation in the SLC26A4 gene.The Effect on Sodium/Iodide Symporter and Pendrin in Thyroid Colloid Retention Developed by Excess Iodide Intake.Atrophic thyroid follicles and inner ear defects reminiscent of cochlear hypothyroidism in Slc26a4-related deafness.Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects.
P2860
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P2860
Pendrin is an iodide-specific apical porter responsible for iodide efflux from thyroid cells
description
2002 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2002
@ast
im Juli 2002 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2002/07/01)
@sk
vědecký článek publikovaný v roce 2002
@cs
wetenschappelijk artikel (gepubliceerd op 2002/07/01)
@nl
наукова стаття, опублікована в липні 2002
@uk
مقالة علمية (نشرت في يوليو 2002)
@ar
name
Pendrin is an iodide-specific ...... dide efflux from thyroid cells
@ast
Pendrin is an iodide-specific ...... dide efflux from thyroid cells
@en
Pendrin is an iodide-specific ...... dide efflux from thyroid cells
@nl
type
label
Pendrin is an iodide-specific ...... dide efflux from thyroid cells
@ast
Pendrin is an iodide-specific ...... dide efflux from thyroid cells
@en
Pendrin is an iodide-specific ...... dide efflux from thyroid cells
@nl
prefLabel
Pendrin is an iodide-specific ...... dide efflux from thyroid cells
@ast
Pendrin is an iodide-specific ...... dide efflux from thyroid cells
@en
Pendrin is an iodide-specific ...... dide efflux from thyroid cells
@nl
P2093
P356
P1476
Pendrin is an iodide-specific ...... dide efflux from thyroid cells
@en
P2093
Akio Yoshida
Ichiro Hisatome
Ines E. Royaux
Koichi Suzuki
Leonard D. Kohn
Shinichi Taniguchi
P304
P356
10.1210/JCEM.87.7.8679
P407
P577
2002-07-01T00:00:00Z