Thyroid Hormone Plasma Membrane Transport Defect Latest Advances

Find the Latest Research About Thyroid Hormone Plasma Membrane Transport Defect

Last Updated: 09/26/2026

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Found 56 publications

Loss of Thyroid Hormone Transporters MCT8 and OATP1C1 in Mouse Oligodendroglia Cells Results in a Delayed Oligodendrocyte Maturation and Myelination.

Loss of Thyroid Hormone Transporters MCT8 and OATP1C1 in Mouse Oligodendroglia Cells Results in a Delayed Oligodendrocyte Maturation and Myelination.

Journal: Thyroid : official journal of the American Thyroid Association
Published: July 15, 2026

Structural insights into brain thyroid hormone transport via MCT8 and OATP1C1.

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.

Inherited Disorders of Thyroid Hormone Metabolism Defect Caused by the Dysregulation of Selenoprotein Expression.

Journal: Frontiers in endocrinology
Published: October 27, 2021

Case of Resistance to Thyroid Hormones With a Relatively Rare Mutation in Thyroid Hormones Receptor.

Case of Resistance to Thyroid Hormones With a Relatively Rare Mutation in Thyroid Hormones Receptor.

Journal: Cureus
Published: June 11, 2021

PKM1 Exerts Critical Roles in Cardiac Remodeling Under Pressure Overload in the Heart.

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.

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.

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.

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.

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.

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.

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.

Interdependence of thyroglobulin processing and thyroid hormone export in the mouse thyroid gland.

Journal: European journal of cell biology
Published: December 22, 2016
Showing 1-12 of 56

Last Updated: 09/26/2026