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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.
Thyroid : Official Journal of the American Thyroid Association|January 8, 2020
Nonautoimmune Hyperthyroidism Caused by a Somatic Mosaic GNAS Mutation Involving Part of the Thyroid GlandMonica M França, Robert L Levine, Theodora Pappa, et al.
The Journal of Biological Chemistry|May 26, 2022
Maintaining the thyroid gland in mutant thyroglobulin-induced hypothyroidism requires thyroid cell proliferation that must continue in adulthoodXiaohan Zhang, Bhoomanyu Malik, Crystal Young, et al.
Thyroid : Official Journal of the American Thyroid Association|October 15, 2021
XB130 Plays an Essential Role in Folliculogenesis Through Mediating Interactions Between Microfilament and Microtubule Systems in ThyrocytesYingchun Wang, Yun-Yan Xiang, Junichi Sugihara, et al.
Cells|March 25, 2022
Thyroidal Transcriptomic Profiles of Pathoadaptive Responses to Congenital Hypothyroidism in XB130 Knockout MiceJunichi Sugihara, Aaron Wong, Hiroki Shimizu, et al.
Clinical Endocrinology|March 27, 2007
Clinical and genetic characteristics of congenital hypothyroidism due to mutations in the thyroid peroxidase (TPO) gene in IsraelisYardena Tenenbaum-Rakover, Sunee Mamanasiri, Carrie Ris-Stalpers, et al.
Molecular Endocrinology (Baltimore, Md.)|December 13, 2005
Repulsive separation of the cytoplasmic ends of transmembrane helices 3 and 6 is linked to receptor activation in a novel thyrotropin receptor mutant (M626I)Usanee Ringkananont, Joost Van Durme, Lucia Montanelli, et al.
Endocrinology|July 23, 2014
Placenta passage of the thyroid hormone analog DITPA to male wild-type and Mct8-deficient miceAlfonso Massimiliano Ferrara, Xiao-Hui Liao, Pilar Gil-Ibáñez, et al.
Thyroid : Official Journal of the American Thyroid Association|October 31, 2018
Congenital Hypothyroidism due to Oligogenic Mutations in Two Sudanese FamiliesYui Watanabe, Ryan J Bruellman, Reham S Ebrhim, et al.
Thyroid : Official Journal of the American Thyroid Association|July 29, 2020
Human Type 1 Iodothyronine Deiodinase (DIO1) Mutations Cause Abnormal Thyroid Hormone MetabolismMonica M França, Alina German, Gustavo W Fernandes, et al.
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