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Molecular Endocrinology (Baltimore, Md.)|February 5, 2011
Thyroid hormone receptor α and regulation of type 3 deiodinaseOlga Barca-Mayo, Xiao-Hui Liao, Manuela Alonso, et al.The Journal of Clinical Endocrinology and Metabolism|May 7, 2023
Effect of the Fetal THRB Genotype on the PlacentaFederico Salas-Lucia, Marius N Stan, Haleigh James, et al.The American Journal of Gastroenterology|September 25, 2013
Identification of a functional TPH1 polymorphism associated with irritable bowel syndrome bowel habit subtypesHelmut Grasberger, Lin Chang, Wendy Shih, et al.Gastroenterology|July 5, 2016
Genetic Complexity of Crohn's Disease in Two Large Ashkenazi Jewish FamiliesAdam P Levine, Nikolas Pontikos, Elena R Schiff, et al.General and Comparative Endocrinology|August 6, 2002
Type 1 iodothyronine deiodinase in the house musk shrew (Suncus murinus, Insectivora: Soricidae): cloning and characterization of complementary DNA, unique tissue distribution and regulation by T(3)Margarita Rogatcheva, Yoshitaka Hayashi, Sen Oda, et al.The Journal of Clinical Endocrinology and Metabolism|July 16, 2009
Clinical and molecular characterization of a novel selenocysteine insertion sequence-binding protein 2 (SBP2) gene mutation (R128X)Caterina Di Cosmo, Neil McLellan, Xiao-Hui Liao, et al.Plos One|October 8, 2013
Increased oxidative metabolism and neurotransmitter cycling in the brain of mice lacking the thyroid hormone transporter SLC16A2 (MCT8)Tiago B Rodrigues, Ainhoa Ceballos, Carmen Grijota-Martínez, et al.General and Comparative Endocrinology|January 24, 2006
Unique regulation of thyroid hormone metabolism during fasting in the house musk shrew (Suncus murinus, Insectivora: Soricidae)Yoko Takeuchi, Daisuke Suzuki, Sen-Ichi Oda, et al.Thyroid : Official Journal of the American Thyroid Association|December 24, 2019
Insertion of an Alu Element in Thyroglobulin Gene as a Novel Cause of Congenital HypothyroidismRyan Bruellman, Yui Watanabe, Reham Shareef, et al.Journal of Molecular Medicine (Berlin, Germany)|September 2, 2006
TBG deficiency: description of two novel mutations associated with complete TBG deficiency and review of the literatureDeborah Mannavola, Guia Vannucchi, Laura Fugazzola, et al.Pageof 24