C Portulano, M Paroder-Belenitsky… - Endocrine …, 2014 - academic.oup.com
Abstract The Na+/I− symporter (NIS) is the plasma membrane glycoprotein that mediates active I− transport in the thyroid and other tissues, such as salivary glands, stomach …
Human milk is considered the optimal nutrition for infants as it provides additional attributes other than nutritional support for the infant and contributes to the mother's health as well …
HM Targovnik, CE Citterio, CM Rivolta - Best Practice & Research Clinical …, 2017 - Elsevier
Iodide Handling Disorders lead to defects of the biosynthesis of thyroid hormones (thyroid dyshormonogenesis, TD) and thereafter congenital hypothyroidism (CH), the most common …
E Darrouzet, S Lindenthal, D Marcellin… - … et Biophysica Acta (BBA …, 2014 - Elsevier
The sodium/iodide symporter (NIS or SLC5A5) is an intrinsic membrane protein implicated in iodide uptake into thyroid follicular cells. It plays a crucial role in iodine metabolism and …
ZC Hannoush, RE Weiss - Endocrinology and Metabolism …, 2017 - endo.theclinics.com
In the beginning (before the genomic revolution) thyroid disorders were primarily diagnosed by the presence of a goiter and thought to be due to either deficiency or excess of iodine …
HR Zhekova, T Sakuma, R Johnson… - Journal of chemical …, 2020 - ACS Publications
The human sodium iodide symporter (hNIS) is a theranostic reporter gene which concentrates several clinically approved SPECT and PET radiotracers and plays an …
N Mostofizade, P Nikpour, SH Javanmard… - … Journal of Preventive …, 2013 - ncbi.nlm.nih.gov
Background: Considering the high prevalence of congenital hypothyroidism (CH) in Isfahan and its different etiologies in comparison with other countries, the high rate of parental …
ЕЛ Джикия, ОН Авилов, ЯЮ Киселева… - Вестник Российского …, 2018 - cyberleninka.ru
Натрий-йод симпортёр (NIS) трансмембранный белок, участвующий в поглощении йодида в фолликулярных клетках щитовидной железы. Он играет критическую роль в …
S Fukata, A Hishinuma, N Nakatake, J Tajiri - Thyroid, 2010 - liebertpub.com
Background: Iodide transport defect (ITD) is an infrequent condition associated with congenital dyshormonogenetic goiter due to mutations in the Na+/I− symporter (NIS) gene …