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Last Updated: 10/31/2025
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Found 55 publications
Structural insights into brain thyroid hormone transport via MCT8 and OATP1C1.
Journal: Cell
Published: October 26, 2024
Inherited Disorders of Thyroid Hormone Metabolism Defect Caused by the Dysregulation of Selenoprotein Expression.
Journal: Frontiers in endocrinology
Published: October 27, 2021
PKM1 Exerts Critical Roles in Cardiac Remodeling Under Pressure Overload in the Heart.
Journal: Circulation
Published: June 09, 2021
A Novel SLC5A5 Variant Reveals the Crucial Role of Kinesin Light Chain 2 in Thyroid Hormonogenesis.
Journal: The Journal of clinical endocrinology and metabolism
Published: January 07, 2021
Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by MCT8 Gene Mutation.
Journal: Thyroid : official journal of the American Thyroid Association
Published: August 05, 2020
The Protein Translocation Defect of MCT8L291R Is Rescued by Sodium Phenylbutyrate.
Journal: European thyroid journal
Published: December 20, 2019
Novel Sodium/Iodide Symporter Compound Heterozygous Pathogenic Variants Causing Dyshormonogenic Congenital Hypothyroidism.
Journal: Thyroid : official journal of the American Thyroid Association
Published: May 23, 2019
Implications of Na+/I- Symporter Transport to the Plasma Membrane for Thyroid Hormonogenesis and Radioiodide Therapy.
Journal: Journal of the Endocrine Society
Published: April 12, 2018
Structural Investigation of a Dimeric Variant of Pyruvate Kinase Muscle Isoform 2.
Journal: Biochemistry
Published: November 29, 2017
Interdependence of thyroglobulin processing and thyroid hormone export in the mouse thyroid gland.
Journal: European journal of cell biology
Published: December 22, 2016
Hypomyelinating leukodystrophies - a molecular insight into the white matter pathology.
Journal: Clinical genetics
Published: February 29, 2016
Last Updated: 10/31/2025