Showing results (221-230 of 238) with videos related to

Sort By:
Pageof 24
Thyroid : Official Journal of the American Thyroid Association|August 5, 2020
Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by MCT8 Gene MutationSamuel Refetoff, Theodora Pappa, Meredith K Williams, et al.
Molecular Endocrinology (Baltimore, Md.)|October 13, 2007
A lack of thyroid hormones rather than excess thyrotropin causes abnormal skeletal development in hypothyroidismJ H Duncan Bassett, Allan J Williams, Elaine Murphy, et al.
Thyroid : Official Journal of the American Thyroid Association|March 30, 2022
AAV9-MCT8 Delivery at Juvenile Stage Ameliorates Neurological and Behavioral Deficits in a Mouse Model of MCT8-DeficiencyXiao-Hui Liao, Pablo Avalos, Oksana Shelest, et al.
The Journal of Clinical Investigation|November 23, 2011
Small-molecule MAPK inhibitors restore radioiodine incorporation in mouse thyroid cancers with conditional BRAF activationDebyani Chakravarty, Elmer Santos, Mabel Ryder, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 12, 2011
Thyrotrophin receptor signaling dependence of Braf-induced thyroid tumor initiation in miceAime T Franco, Roberta Malaguarnera, Samuel Refetoff, et al.
The Journal of Clinical Investigation|March 2, 2021
DUOX2 variants associate with preclinical disturbances in microbiota-immune homeostasis and increased inflammatory bowel disease riskHelmut Grasberger, Andrew T Magis, Elisa Sheng, et al.
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.
Pageof 24