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Displaying 7 results.
    • Journal article
    Genetic immunization of outbred mice with thyrotropin receptor cDNA provides a model of Graves' disease.
    Costagliola, S Denef, Jean-François[UCL] Many, Marie-Christine[UCL] Pohlenz, J Refetoff, S. Vassart, G. (2000) The Journal of clinical investigation — Vol. 105, no. 6, p. 803-11 (2000)
    • Journal article
    Tyrosine sulfation is required for agonist recognition by glycoprotein hormone receptors.
    Costagliola, S Panneels, V Bonomi, M Koch, J Many, Marie-Christine[UCL] Smits, G Vassart, G (2002) The EMBO journal — Vol. 21, no.4, p. 504-13 (2002)
    • Journal article
    Evidence for thyrotropin receptor immunoreactivity in pretibial connective tissue from patients with thyroid-associated dermopathy.
    Daumerie, Chantal[UCL] Ludgate, M Costagliola, S Many, Marie-Christine[UCL] (2002) European journal of endocrinology / European Federation of Endocrine Societies — Vol. 146, no. 1, p. 35-8 (2002)
    • Journal article
    Quantification of cells expressing the thyrotropin receptor in extraocular muscles in thyroid associated orbitopathy.
    Boschi, Antonella[UCL] Daumerie, Chantal[UCL] Spiritus, Micheline[UCL] Beguin, Claire[UCL] Senou, Maximin[UCL] Yüksel, Demet[UCL] Duplicy, M[UCL] Costagliola, S Ludgate, M Many, Marie-Christine[UCL] (2005) The British journal of ophthalmology — Vol. 89, no. 6, p. 724-9 (2005)
    • Journal article
    Sphingolipid-cholesterol domains (lipid rafts) in normal human and dog thyroid follicular cells are not involved in thyrotropin receptor signaling
    Costa, MJ Song, Y. Macours, P Massart, C Many, Marie-Christine[UCL] Costagliola, S Dumont, JE Van Sande, J. Vanvooren, V (2004) Endocrinology — Vol. 145, no. 3, p. 1464-1472 (2004)
    • Speech
    The thyrotropin receptor in thyroid eye disease
    Ludgate, M Crisp, M Lane, C Costagliola, S Vassart, G. Weetman, A Daumerie, Chantal[UCL] Many, Marie-Christine[UCL] (1998) International Satellite Symposium of the 25th Annual Meeting of the European-Thyroid-Association on Advances in Thyroid Eye Disease — PIERIA (Greece)
    • Journal article
    Autosomal dominant transmission of congenital thyroid hypoplasia due to loss-of-function mutation of PAX8
    Vilain, C. Rydlewski, C. Duprez, L Heinrichs, C. Abramowicz, Marc J. Malvaux, Paul[UCL] Renneboog, B Parma, J Costagliola, S Vassart, G. (2001) Journal of Clinical Endocrinology and Metabolism — Vol. 86, no. 1, p. 234-238 (2001)