The transcription factor CREB3L1 is expressed in a wide variety of tissues including
cartilage, pancreas, and bone. It is located in the endoplasmic reticulum and upon …

Context Iodide transport defect (ITD)(Online Mendelian Inheritance in Man No. 274400) is
an uncommon cause of dyshormonogenic congenital hypothyroidism due to loss-of-function …

The sodium/iodide symporter (NIS) expresses at the basolateral plasma membrane of the
thyroid follicular cell and mediates iodide accumulation required for normal thyroid …

Background: The sodium/iodide symporter (NIS) mediates active iodide accumulation in the
thyroid follicular cell. Autosomal recessive iodide transport defect (ITD)-causing loss-of …

Congenital iodide transport defect is an uncommon autosomal recessive disorder caused by
loss-of-function variants in the sodium iodide symporter (NIS)-coding SLC5A5 gene and …

Introduction Iodide is an essential micronutrient for the synthesis of thyroid hormones and its
imbalance is involved in the origin of different thyroid pathological processes. Selenium (Se) …

Instructive signals that delineate the formation of thyroid follicles by thyrotropin (TSH) in stem
cells are complex. Here, we have examined the role of protein kinase C (PKC) by using a …

Introduction: Thyrotropin receptor-stimulating antibody (TSAb) is a pathogenic antibody in
the serum of patients with Graves' disease. The binding of TSAb to thyroid-stimulating …

Purpose: To investigate the signi cance of TSHR and NF-κB P65 expression difference in
thyroid papillary carcinoma, and to explore how TSHR affects the biological behavior of PTC …

Las hormonas tiroideas juegan un papel crucial en la diferenciación y el desarrollo del
sistema nervioso central. Su deficiencia funcional al nacimiento se conoce como …