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Article

Expression ofPDS/Pds, the Pendred Syndrome Gene, in Endometrium

1 Feb 2002

Abstract excerpt

Expression of the Pendred syndrome gene (PDS/Pds) is thought to be responsible for the iodide transport in the thyroid as well as the formation and function of the inner ear. Its mRNA is also expressed in the kidney and placenta. We report here that PDS and its encoded protein (pendrin) are also expressed in the endometrium. The RNA levels of rat PDS in the endometrium and kidney were much higher than those of...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 11836344
DOI: 10.1210/jcem.87.2.8390

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Related research

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Research trail→

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Expression ofPDS/Pds, the Pendred Syndrome Gene, in EndometriumPMID 11836344Read ↗

Expression pattern of the mouse ortholog of the Pendred’s syndrome gene ( Pds ) suggests a key role for pendrin in the inner earSemantic proximity Read ↗

[Pendrin: physiology, molecular biology and clinical importance].Semantic proximity Read ↗

The role of pendrin in iodide regulation.Semantic proximity Read ↗

Mutations of the PDS Gene, Encoding Pendrin, Are Associated with Protein Mislocalization and Loss of Iodide Efflux: Implications for Thyroid Dysfunction in Pendred SyndromeSemantic proximity Read ↗

Mutations of the PDS gene, encoding pendrin, are associated with protein mislocalization and loss of iodide efflux: implications for thyroid dysfunction in Pendred syndrome.Semantic proximity Read ↗

Expression of Na+/I- Symporter and Pendred Syndrome Genes in Trophoblast CellsSemantic proximity Read ↗

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS).Semantic proximity Read ↗

Expression of Na<sup>+</sup>/I<sup>−</sup>Symporter and Pendred Syndrome Genes in Trophoblast Cells<sup>1</sup>Semantic proximity Read ↗

Pendred's Syndrome: Identification of the Genetic Defect a Century After Its RecognitionSemantic proximity Read ↗

Pendred syndrome.Semantic proximity Read ↗

Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndromeSemantic proximity Read ↗

Pendrin, the Protein Encoded by the Pendred Syndrome Gene (PDS), Is an Apical Porter of Iodide in the Thyroid and Is Regulated by Thyroglobulin in FRTL-5 CellsSemantic proximity Read ↗

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