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Thyroid : Official Journal of the American Thyroid Association|December 21, 2019
Sorting Variants of Unknown Significance Identified by Whole Exome Sequencing: Genetic and Laboratory Investigations of Two Novel MCT8 VariantsJiao Fu, Manassawee Korwutthikulrangsri, Leigh Ramos-Platt, et al.
Endocrinology|September 26, 2022
Foxe1 Deletion in the Adult Mouse Is Associated With Increased Thyroidal Mast Cells and HypothyroidismGrace Lim, Alexander Widiapradja, Scott P Levick, et al.
Endocrinology|May 23, 2013
Changes in thyroid status during perinatal development of MCT8-deficient male miceAlfonso Massimiliano Ferrara, Xiao-Hui Liao, Pilar Gil-Ibáñez, et al.
Endocrinology|May 5, 2017
Thyroid Hormone Signaling Pathways: Time for a More Precise NomenclatureFrédéric Flamant, Sheue-Yann Cheng, Anthony N Hollenberg, et al.
The Journal of Clinical Endocrinology and Metabolism|March 9, 2013
Evidence of primary aldosteronism in a predominantly female cohort of normotensive individuals: a very high odds ratio for progression into arterial hypertensionAthina Markou, Theodora Pappa, Gregory Kaltsas, et al.
Hormone Research in Paediatrics|January 9, 2020
Central Congenital Hypothyroidism Caused by a Novel Mutation, C47W, in the Cysteine Knot Region of TSHβReham S Ebrhim, Ryan J Bruellman, Yui Watanabe, et al.
The Journal of Clinical Investigation|February 21, 2002
Partial deficiency of thyroid transcription factor 1 produces predominantly neurological defects in humans and miceJoachim Pohlenz, Alexandra Dumitrescu, Dorothee Zundel, et al.
The Journal of Clinical Investigation|October 31, 2017
GLIS3 is indispensable for TSH/TSHR-dependent thyroid hormone biosynthesis and follicular cell proliferationHong Soon Kang, Dhirendra Kumar, Grace Liao, et al.
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