Articles dans des revues avec comité de lecture (129)
  1. 83. Siffroi-Fernandez, S., Costagliola, S., Paumel, S., Giraud, A., Banga, J. P., & Franc, J. L. (2001). Role of complex asparagine-linked oligosaccharides in the expression of a functional thyrotropin receptor. Biochemical journal, 354(Pt 2), 331-336.
  2. 84. Vilain, C., Rydlewski, C., Duprez, L., Heinrichs, C., Abramowicz, M., Malvaux, P., Renneboog, B., Parma, J., Costagliola, S., & Vassart, G. (2001). Autosomal dominant transmission of congenital thyroid hypoplasia due to loss-of-function mutation of PAX8. The Journal of clinical endocrinology and metabolism, 86(1), 234-238. doi:10.1210/jc.86.1.234
  3. 85. Chin, H. S., Chin, D. K., Morgenthaler, N. G., Vassart, G., & Costagliola, S. (2000). Rarity of anti- Na+/I- symporter (NIS) antibody with iodide uptake inhibiting activity in autoimmune thyroid diseases (AITD). The Journal of clinical endocrinology and metabolism, 85(10), 3937-3940.
  4. 86. Pohlenz, J., Duprez, L., Weiss, R. E., Vassart, G., Refetoff, S., & Costagliola, S. (2000). Failure of membrane targeting causes the functional defect of two mutant sodium iodide symporters. The Journal of clinical endocrinology and metabolism, 85(7), 2366-2369. doi:10.1210/jc.85.7.2366
  5. 87. Costagliola, S., Many, M.-C., Denef, J. F., Pohlenz, J., Refetoff, S., & Vassart, G. (2000). Genetic immunization of outbred mice with thyrotropin receptor cDNA provides a model of Graves' disease. The Journal of clinical investigation, 105(6), 803-811. doi:10.1172/JCI7665
  6. 88. De Deken, X., Wang, D., Many, M.-C., Costagliola, S., Libert, F., Vassart, G., Dumont, J., & Miot, F. (2000). Cloning of two human thyroid cDNAs encoding new members of the NADPH oxidase family. The Journal of biological chemistry, 275(30), 23227-23233. doi:10.1074/jbc.M000916200
  7. 89. Costagliola, S., Sunthorntepvarakul, T., Migeotte, I., Van Sande, J., Kajava, A. M., Refetoff, S., & Vassart, G. (1999). Structure-function relationships of two loss-of-function mutations of the thyrotropin receptor gene. Thyroid, 9(10), 995-1000.
  8. 90. Many, M.-C., Costagliola, S., Detrait, M., Deneft, F., Vassart, G., & Ludgate, M. (1999). Development of an animal model of autoimmune thyroid eye disease. The Journal of immunology, 162(8), 4966-4974.
  9. 91. Costagliola, S., Morgenthaler, N. G., Hoermann, R., Badenhoop, K., Struck, J., Freitag, D., Poertl, S., Weglöhner, W., Hollidt, J. M., Quadbeck, B., Dumont, J., Schumm-Draeger, P. M., Bergmann, A., Mann, K., Vassart, G., & Usadel, K. H. (1999). Second generation assay for thyrotropin receptor antibodies has superior diagnostic sensitivity for Graves' disease. The Journal of clinical endocrinology and metabolism, 84(1), 90-97. doi:10.1210/jc.84.1.90
  10. 92. Uyttersprot, N., Costagliola, S., Dumont, J., & Miot, F. (1999). Requirement for cAMP-response element (CRE) binding protein/CRE modulator transcription factors in thyrotropin-induced proliferation of dog thyroid cells in primary culture. European journal of biochemistry / FEBS, 259(1-2), 370-378. doi:10.1046/j.1432-1327.1999.00049.x
  11. 93. Rodien, P., Cetani, F., Costagliola, S., Tonacchera, M., Duprez, L., Minegishi, T., Govaerts, C., & Vassart, G. (1998). Evidences for an allelic variant of the human LC/CG receptor rather than a gene duplication: functional comparison of wild-type and variant receptors. The Journal of clinical endocrinology and metabolism, 83(12), 4431-4434.
  12. 94. Rodien, P., Brémont, C., Sanson, M. L., Parma, J., Van Sande, J., Costagliola, S., Luton, J. P., Vassart, G., & Duprez, L. (1998). Familial gestational hyperthyroidism caused by a mutant thyrotropin receptor hypersensitive to human chorionic gonadotropin. The New England journal of medicine, 339(25), 1823-1826. doi:10.1056/NEJM199812173392505
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