Transporters MCT8 and OATP1C1 maintain murine brain thyroid hormone homeostasis
Author:
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Reference55 articles.
1. Identification of Monocarboxylate Transporter 8 as a Specific Thyroid Hormone Transporter
2. A Novel Syndrome Combining Thyroid and Neurological Abnormalities Is Associated with Mutations in a Monocarboxylate Transporter Gene
3. Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation
4. Allan-Herndon-Dudley Syndrome and the Monocarboxylate Transporter 8 (MCT8) Gene
5. Mechanisms of Disease: psychomotor retardation and high T3 levels caused by mutations in monocarboxylate transporter 8
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