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Article

The MCT8 thyroid hormone transporter and Allan–Herndon–Dudley syndrome

1 Jun 2007

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 17574010
DOI: 10.1016/j.beem.2007.03.009

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The MCT8 thyroid hormone transporter and Allan–Herndon–Dudley syndromePMID 17574010Read ↗

[MCT8-specific thyroid hormone cell transporter deficiency: a case report and review of the literature].Semantic proximity Read ↗

Clinical and endocrine features of two Allan-Herndon-Dudley syndrome patients with monocarboxylate transporter 8 mutations.Semantic proximity Read ↗

Allan-Herndon-Dudley Syndrome.Semantic proximity Read ↗

Psychomotor retardation caused by a defective thyroid hormone transporter: report of two families with different MCT8 mutations.Semantic proximity Read ↗

Decreased cellular uptake and metabolism in Allan-Herndon-Dudley syndrome (AHDS) due to a novel mutation in the MCT8 thyroid hormone transporterSemantic proximity Read ↗

MCT8 mutation analysis and identification of the first female with Allan–Herndon–Dudley syndrome due to loss of MCT8 expressionSemantic proximity Read ↗

Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene.Semantic proximity Read ↗

Clinical phenotype and endocrinological investigations in a patient with a mutation in the MCT8 thyroid hormone transporter.Semantic proximity Read ↗

Disorder of thyroid hormone transport into the tissues.Semantic proximity Read ↗

Genetics and phenomics of thyroid hormone transport by MCT8.Semantic proximity Read ↗

Further Insights into the Allan-Herndon-Dudley Syndrome: Clinical and Functional Characterization of a Novel MCT8 Mutation.Semantic proximity Read ↗

Molecular aspects of thyroid hormone transporters, including MCT8, MCT10, and OATPs, and the effects of genetic variation in these transporters.Semantic proximity Read ↗

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