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Communications Biology|June 4, 2021
The chaperonin CCT8 controls proteostasis essential for T cell maturation, selection, and functionBergithe E Oftedal, Stefano Maio, Adam E Handel, et al.The Journal of Clinical Endocrinology and Metabolism|June 7, 2014
ARMC5 mutations are common in familial bilateral macronodular adrenal hyperplasiaLucia Gagliardi, Andreas W Schreiber, Christopher N Hahn, et al.The Journal of Clinical Endocrinology and Metabolism|November 23, 2006
Autoimmune polyendocrine syndrome type 1 in Norway: phenotypic variation, autoantibodies, and novel mutations in the autoimmune regulator geneAnette S B Wolff, Martina M Erichsen, Anthony Meager, et al.The Journal of Clinical Endocrinology and Metabolism|January 7, 2023
Systemic Activation of the Kynurenine Pathway in Graves Disease With and Without OphthalmopathyHans Olav Ueland, Arve Ulvik, Kristian Løvås, et al.Frontiers in Immunology|April 2, 2024
Rare copy number variation in autoimmune Addison's diseaseHaydee Artaza, Daniel Eriksson, Ksenia Lavrichenko, et al.Journal of Immunology (Baltimore, Md. : 1950)|September 19, 2014
Clinical and serologic parallels to APS-I in patients with thymomas and autoantigen transcripts in their tumorsAnette S B Wolff, Jaanika Kärner, Jone F Owe, et al.The Journal of Clinical Endocrinology and Metabolism|June 3, 2016
A Longitudinal Follow-up of Autoimmune Polyendocrine Syndrome Type 1Øyvind Bruserud, Bergithe E Oftedal, Nils Landegren, et al.The Journal of Experimental Medicine|September 3, 2021
Mechanistic dissection of dominant AIRE mutations in mouse models reveals AIRE autoregulationYael Goldfarb, Tal Givony, Noam Kadouri, et al.Acta Ophthalmologica|July 7, 2025
Exploring tear fluid biomarkers and the ocular surface in thyroid eye diseaseMikael Thomassen Neset, Roy Miodini Nilsen, Kristian Løvås, et al.Cell|July 19, 2016
AIRE-Deficient Patients Harbor Unique High-Affinity Disease-Ameliorating AutoantibodiesSteffen Meyer, Martin Woodward, Christina Hertel, et al.Pageof 6