Inherited defects of thyroid hormone-cell-membrane transport-Reference-Cited by-同舟云学术

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Inherited defects of thyroid hormone-cell-membrane transport

Published:2013-10 Issue:5 Volume:20 Page:434-440
ISSN:1752-296X
Container-title:Current Opinion in Endocrinology, Diabetes & Obesity
language:en
Short-container-title:

Author:

Fu Jiao,Refetoff Samuel,Dumitrescu Alexandra M.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Nutrition and Dietetics,Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference44 articles.

1. Identification of monocarboxylate transporter 8 as a specific thyroid hormone transporter.;Friesema;J Biol Chem,2003

2. A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene.;Dumitrescu;Am J Hum Genet,2004

3. Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation.;Friesema;Lancet,2004

4. Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene.;Schwartz;Am J Hum Genet,2005

5. Genotype-phenotype relationship in patients with mutations in thyroid hormone transporter MCT8.;Jansen;Endocrinology,2008

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2. Tsh Induces Agrp1 Neuron Proliferation in Oatp1c1-Deficient Zebrafish;The Journal of Neuroscience;2022-09-23

3. Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley Syndrome;Molecular Genetics and Metabolism;2022-01

4. Monocarboxylate Transporter 8 Deficiency: From Pathophysiological Understanding to Therapy Development;Frontiers in Endocrinology;2021-09-01

5. Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by MCT8 Gene Mutation;Thyroid;2021-05-01

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