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Results: 1-17 |
Results: 17
A novel germline mutation in the TSH receptor gene causes non-autoimmune autosomal dominant hyperthyroidism
Authors: Alberti, L Proverbio, MC Costagliola, S Weber, G Beck-Peccoz, P Chiumello, G Persani, L
Citation: L. Alberti et al., A novel germline mutation in the TSH receptor gene causes non-autoimmune autosomal dominant hyperthyroidism, EUR J ENDOC, 145(3), 2001, pp. 249-254
Role of complex asparagine-linked oligosaccharides in the expression of a functional thyrotropin receptor
Authors: Siffroi-Fernandez, S Costagliola, S Paumel, S Giraud, A Banga, JP Franc, JL
Citation: S. Siffroi-fernandez et al., Role of complex asparagine-linked oligosaccharides in the expression of a functional thyrotropin receptor, BIOCHEM J, 354, 2001, pp. 331-336
Autosomal dominant transmission of congenital thyroid hypoplasia due to loss-of-function mutation of PAX8
Authors: Vilain, C Rydlewski, C Duprez, L Heinrichs, C Abramowicz, M Malvaux, P Renneboog, B Parma, J Costagliola, S Vassart, G
Citation: C. Vilain et al., Autosomal dominant transmission of congenital thyroid hypoplasia due to loss-of-function mutation of PAX8, J CLIN END, 86(1), 2001, pp. 234-238
A conserved Asn in transmembrane helix 7 is an on/off switch in the activation of the thyrotropin receptor
Authors: Govaerts, C Lefort, A Costagliola, S Wodak, SJ Ballesteros, JA Van Sande, J Pardo, L Vassart, G
Citation: C. Govaerts et al., A conserved Asn in transmembrane helix 7 is an on/off switch in the activation of the thyrotropin receptor, J BIOL CHEM, 276(25), 2001, pp. 22991-22999
Effects of mutations involving the highly conserved S281HCC motif in the extracellular domain of the thyrotropin (TSH) receptor on TSH binding and constitutive activity
Authors: Ho, SC van Sande, J Lefort, A Vassart, G Costagliola, S
Citation: Sc. Ho et al., Effects of mutations involving the highly conserved S281HCC motif in the extracellular domain of the thyrotropin (TSH) receptor on TSH binding and constitutive activity, ENDOCRINOL, 142(7), 2001, pp. 2760-2767
Purification and characterization of a soluble bioactive amino-terminal extracellular domain of the human thyrotropin receptor
Authors: Cornelis, S Uttenweiler-Joseph, S Panneels, V Vassart, G Costagliola, S
Citation: S. Cornelis et al., Purification and characterization of a soluble bioactive amino-terminal extracellular domain of the human thyrotropin receptor, BIOCHEM, 40(33), 2001, pp. 9860-9869
Comparison of human and porcine TSH receptors
Authors: Costagliola, S Vassart, G
Citation: S. Costagliola et G. Vassart, Comparison of human and porcine TSH receptors, THYROID, 10(5), 2000, pp. 446-446
Genetic immunization of outbred mice with thyrotropin receptor cDNA provides a model of Graves' disease
Authors: Costagliola, S Many, MC Denef, JF Pohlenz, J Refetoff, S Vassart, G
Citation: S. Costagliola et al., Genetic immunization of outbred mice with thyrotropin receptor cDNA provides a model of Graves' disease, J CLIN INV, 105(6), 2000, pp. 803-811
Failure of membrane targeting causes the functional defect of two mutant sodium iodide symporters
Authors: Pohlenz, J Duprez, L Weiss, RE Vassart, G Refetoff, S Costagliola, S
Citation: J. Pohlenz et al., Failure of membrane targeting causes the functional defect of two mutant sodium iodide symporters, J CLIN END, 85(7), 2000, pp. 2366-2369
Rarity of anti- Na+/I- symporter (NIS) antibody with iodide uptake inhibiting activity in autoimmune thyroid diseases (AITD).
Authors: Chin, HS Chin, DKH Morgenthaler, NG Vassart, G Costagliola, S
Citation: Hs. Chin et al., Rarity of anti- Na+/I- symporter (NIS) antibody with iodide uptake inhibiting activity in autoimmune thyroid diseases (AITD)., J CLIN END, 85(10), 2000, pp. 3937-3940
Cloning of two human thyroid cDNAs encoding new members of the NADPH oxidase family
Authors: De Deken, X Wang, DT Many, MC Costagliola, S Libert, F Vassart, G Dumont, JE Miot, F
Citation: X. De Deken et al., Cloning of two human thyroid cDNAs encoding new members of the NADPH oxidase family, J BIOL CHEM, 275(30), 2000, pp. 23227-23233
Structure-function relationships of two loss-of-function mutations of the thyrotropin receptor gene
Authors: Costagliola, S Sunthorntepvarakul, T Migeotte, I Van Sande, J Kajava, AM Refetoff, S Vassart, G
Citation: S. Costagliola et al., Structure-function relationships of two loss-of-function mutations of the thyrotropin receptor gene, THYROID, 9(10), 1999, pp. 995-1000
Development of an animal model of autoimmune thyroid eye disease
Authors: Many, MC Costagliola, S Detrait, M Denef, JF Vassart, G Ludgate, M
Citation: Mc. Many et al., Development of an animal model of autoimmune thyroid eye disease, J IMMUNOL, 162(8), 1999, pp. 4966-4974
Second generation assay for thyrotropin receptor antibodies has superior diagnostic sensitivity for Graves' disease
Authors: Costagliola, S Morgenthaler, NG Hoermann, R Badenhoop, K Struck, J Freitag, D Poertl, S Weglohner, W Hollidt, JM Quadbeck, B Dumont, JE Schumm-Draeger, PM Bergmann, A Mann, K Vassart, G Usadel, KH
Citation: S. Costagliola et al., Second generation assay for thyrotropin receptor antibodies has superior diagnostic sensitivity for Graves' disease, J CLIN END, 84(1), 1999, pp. 90-97
Requirement for cAMP-response element (CRE) binding protein CRE modulator transcription factors in thyrotropin-induced proliferation of dog thyroid cells in primary culture
Authors: Uyttersprot, N Costagliola, S Dumont, JE Miot, F
Citation: N. Uyttersprot et al., Requirement for cAMP-response element (CRE) binding protein CRE modulator transcription factors in thyrotropin-induced proliferation of dog thyroid cells in primary culture, EUR J BIOCH, 259(1-2), 1999, pp. 370-378
Familial gestational hyperthyroidism caused by a mutant thyrotropin receptor hypersensitive to human chorionic gonadotropin
Authors: Rodien, P Bremont, C Parma, J Van Sande, J Costagliola, S Luton, JP Vassart, G Duprez, L
Citation: P. Rodien et al., Familial gestational hyperthyroidism caused by a mutant thyrotropin receptor hypersensitive to human chorionic gonadotropin, N ENG J MED, 339(25), 1998, pp. 1823-1826
Evidences for an allelic variant of the human LC/CG receptor rather than agene duplication: Functional comparison of wild-type and variant receptors
Authors: Rodien, P Cetani, F Costagliola, S Tonacchera, M Duprez, L Minegishi, T Govaerts, C Vassart, G
Citation: P. Rodien et al., Evidences for an allelic variant of the human LC/CG receptor rather than agene duplication: Functional comparison of wild-type and variant receptors, J CLIN END, 83(12), 1998, pp. 4431-4434
Risultati: 1-17 |