Genetics and phenomics of thyroid hormone transport by MCT8.
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Inherited defects in thyroid hormone cell-membrane transport and metabolismGenetic disorders of thyroid metabolism and brain developmentThe syndromes of reduced sensitivity to thyroid hormoneFurther Insights into the Allan-Herndon-Dudley Syndrome: Clinical and Functional Characterization of a Novel MCT8 MutationThe Concise Guide to PHARMACOLOGY 2013/14: transporters.A diagnostic approach for cerebral palsy in the genomic era.In vitro and mouse studies supporting therapeutic utility of triiodothyroacetic acid in MCT8 deficiencyMaternal thyroid hormones are essential for neural development in zebrafish.Mutations in MCT8 in patients with Allan-Herndon-Dudley-syndrome affecting its cellular distributionMinireview: thyroid hormone transporters: the knowns and the unknowns.Inherited defects of thyroid hormone-cell-membrane transport: review of recent findings.The role and potential sites of action of thyroid hormone in timing the onset of puberty in male primates.Monocarboxylate transporter 8 modulates the viability and invasive capacity of human placental cells and fetoplacental growth in mice.Thyroid hormone action in cerebellum and cerebral cortex development.Insights into molecular properties of the human monocarboxylate transporter 8 by combining functional with structural information.Gender-specific regulation of response to thyroid hormone in agingSLC16A2 mutations in two Japanese patients with Allan-Herndon-Dudley syndrome.Recent insights into the cell biology of thyroid angiofollicular units.Opening the black box: revealing the molecular basis of thyroid hormone transport.Regulation of the pituitary-thyroid axis in adulthood is not related to birth weight: evidence from extremely birth weight-discordant monozygotic Danish twin pairs.Novel SLC16A2 mutations in patients with Allan-Herndon-Dudley syndrome.A Novel Deletion Mutation of SLC16A2 Encoding Monocarboxylate Transporter (MCT) 8 in a 26-year-old Japanese Patient with Allan-Herndon-Dudley SyndromeThyroid hormone role on cerebellar development and maintenance: a perspective based on transgenic mouse modelsThree novel mutations of the MCT8 (SLC16A2) gene: individual and temporal variations of endocrinological and radiological features.Understanding the hypothalamus-pituitary-thyroid axis in mct8 deficiency.Essential molecular determinants for thyroid hormone transport and first structural implications for monocarboxylate transporter 8.Novel mutation in MCT8 gene in a Brazilian boy with thyroid hormone resistance and severe neurologic abnormalities.Transcriptomics reveal an integrative role for maternal thyroid hormones during zebrafish embryogenesis.Clinical and Molecular Characteristics of SLC16A2 (MCT8) Mutations in Three Families with the Allan-Herndon-Dudley Syndrome.Redefining the Pediatric Phenotype of X-Linked Monocarboxylate Transporter 8 (MCT8) Deficiency: Implications for Diagnosis and Therapies.Membrane-traversing mechanism of thyroid hormone transport by monocarboxylate transporter 8.New insights into thyroid hormone action.Hypothalamus-Pituitary-Thyroid Axis.
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Genetics and phenomics of thyroid hormone transport by MCT8.
description
article científic
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article scientifique
@fr
articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 18 January 2010
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Genetics and phenomics of thyroid hormone transport by MCT8.
@en
Genetics and phenomics of thyroid hormone transport by MCT8.
@nl
type
label
Genetics and phenomics of thyroid hormone transport by MCT8.
@en
Genetics and phenomics of thyroid hormone transport by MCT8.
@nl
prefLabel
Genetics and phenomics of thyroid hormone transport by MCT8.
@en
Genetics and phenomics of thyroid hormone transport by MCT8.
@nl
P2093
P1476
Genetics and phenomics of thyroid hormone transport by MCT8.
@en
P2093
Edith C H Friesema
Theo J Visser
W Edward Visser
P304
P356
10.1016/J.MCE.2010.01.016
P577
2010-01-18T00:00:00Z