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JAMA|August 12, 2004
Fetal loss associated with excess thyroid hormone exposureJoão Anselmo, Dingcai Cao, Theodore Karrison, et al.
The Journal of Laboratory and Clinical Medicine|August 16, 2005
Tissue responses to thyroid hormone in a kindred with resistance to thyroid hormone harboring a commonly occurring mutation in the thyroid hormone receptor beta gene (P453T)Sharon Y Wu, Peter M Sadow, Samuel Refetoff, et al.
Thyroid : Official Journal of the American Thyroid Association|November 17, 2020
Early Diagnosis and Treatment of an Infant with a Novel Thyroid Hormone Receptor α Gene (pC380SfsX9) MutationAry E Furman, Alexandra M Dumitrescu, Samuel Refetoff, et al.
Redox Biology|March 25, 2018
Peroxidasin-mediated crosslinking of collagen IV is independent of NADPH oxidasesGábor Sirokmány, Hajnal A Kovács, Enikő Lázár, et al.
European Journal of Endocrinology|December 14, 2004
Multiple endocrine neoplasia 2A syndrome presenting as peripartum cardiomyopathy due to catecholamine excessJaime Kim, Sirimon Reutrakul, Dawn Belt Davis, et al.
The Journal of Clinical Endocrinology and Metabolism|November 3, 2005
Identification of a functional polymorphism of the human type 5 17beta-hydroxysteroid dehydrogenase gene associated with polycystic ovary syndromeKenan Qin, David A Ehrmann, Nancy Cox, et al.
European Thyroid Journal|August 9, 2017
A Novel Mutation in the TBG Gene Producing Partial Thyroxine-Binding Globulin Deficiency (Glencoe) Identified in 2 FamiliesTheodora Pappa, Lars C Moeller, Deborah V Edidin, et al.
Nuclear Receptor Signaling|July 25, 2006
Thyroid hormone mediated changes in gene expression can be initiated by cytosolic action of the thyroid hormone receptor beta through the phosphatidylinositol 3-kinase pathwayLars C Moeller, Xia Cao, Alexandra M Dumitrescu, et al.
The Journal of Clinical Endocrinology and Metabolism|May 7, 2010
Autoimmunity in patients with resistance to thyroid hormoneMarla S Barkoff, Masha Kocherginsky, João Anselmo, et al.
JCI Insight|February 20, 2024
Impaired T3 uptake and action in MCT8-deficient cerebral organoids underlie Allan-Herndon-Dudley syndromeFederico Salas-Lucia, Sergio Escamilla, Antonio C Bianco, et al.
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