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Thyroid : Official Journal of the American Thyroid Association|September 5, 2013
American Thyroid Association Guide to investigating thyroid hormone economy and action in rodent and cell modelsAntonio C Bianco, Grant Anderson, Douglas Forrest, et al.Development (Cambridge, England)|April 13, 2016
Thyroid follicle development requires Smad1/5- and endothelial cell-dependent basement membrane assemblyMylah Villacorte, Anne-Sophie Delmarcelle, Manon Lernoux, et al.The Journal of Clinical Endocrinology and Metabolism|October 18, 2007
Pendred syndrome in two Galician families: insights into clinical phenotypes through cellular, genetic, and molecular studiesFernando Palos, María E R García-Rendueles, David Araujo-Vilar, et al.Nature Communications|November 17, 2022
Transplantable human thyroid organoids generated from embryonic stem cells to rescue hypothyroidismMírian Romitti, Adrien Tourneur, Barbara de Faria da Fonseca, et al.Thyroid : Official Journal of the American Thyroid Association|March 7, 2023
Iodotyrosines Are Biomarkers for Preclinical Stages of Iodine-Deficient Hypothyroidism in Dehal1-Knockout MiceCristian González-Guerrero, Marco Borsò, Pouya Alikhani, et al.Cancer Discovery|December 15, 2020
SWI/SNF Complex Mutations Promote Thyroid Tumor Progression and Insensitivity to Redifferentiation TherapiesMahesh Saqcena, Luis Javier Leandro-Garcia, Jesper L V Maag, et al.Cell Stem Cell|May 21, 2017
Modeling Psychomotor Retardation using iPSCs from MCT8-Deficient Patients Indicates a Prominent Role for the Blood-Brain BarrierGad D Vatine, Abraham Al-Ahmad, Bianca K Barriga, et al.Thyroid : Official Journal of the American Thyroid Association|May 11, 2018
NFE2-Related Transcription Factor 2 Coordinates Antioxidant Defense with Thyroglobulin Production and Iodination in the Thyroid GlandPanos G Ziros, Ioannis G Habeos, Dionysios V Chartoumpekis, et al.Nature Genetics|May 7, 2024
STR mutations on chromosome 15q cause thyrotropin resistance by activating a primate-specific enhancer of MIR7-2/MIR1179Helmut Grasberger, Alexandra M Dumitrescu, Xiao-Hui Liao, et al.JCI Insight|October 19, 2018
Homozygous loss-of-function mutations in SLC26A7 cause goitrous congenital hypothyroidismHakan Cangul, Xiao-Hui Liao, Erik Schoenmakers, et al.Pageof 21