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Results: 1-25 | 26-47
Results: 1-25/47
Chimeraplasty validation
Authors: Albuquerque-Silva, J Vassart, G Lavinha, J Abramowicz, MJ
Citation: J. Albuquerque-silva et al., Chimeraplasty validation, NAT BIOTECH, 19(11), 2001, pp. 1011-1011
A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene
Authors: Bretones, P Duprez, L Parma, J David, M Vassart, G Rodien, P
Citation: P. Bretones et al., A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene, THYROID, 11(10), 2001, pp. 977-980
Genomic organization of the human thyroglobulin gene: the complete intron-exon structure
Authors: Mendive, FM Rivolta, CM Moya, CM Vassart, G Targovnik, HM
Citation: Fm. Mendive et al., Genomic organization of the human thyroglobulin gene: the complete intron-exon structure, EUR J ENDOC, 145(4), 2001, pp. 485-496
Somatic and germline mutations of the TSH receptor and thyroid diseases
Authors: Corvilain, B Van Sande, J Dumont, JE Vassart, G
Citation: B. Corvilain et al., Somatic and germline mutations of the TSH receptor and thyroid diseases, CLIN ENDOCR, 55(2), 2001, pp. 143-158
Urokinase plasminogen activator and plasmin efficiently convert hemofiltrate CC chemokine 1 into its active [9-74] processed variant
Authors: Vakili, J Standker, L Detheux, M Vassart, G Forssmann, WG Parmentier, M
Citation: J. Vakili et al., Urokinase plasminogen activator and plasmin efficiently convert hemofiltrate CC chemokine 1 into its active [9-74] processed variant, J IMMUNOL, 167(6), 2001, pp. 3406-3413
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
The metastasis suppressor gene KiSS-1 encodes kisspeptins, the natural ligands of the orphan G protein-coupled receptor GPR54
Authors: Kotani, M Detheux, M Vandenbbogaerde, A Communi, D Vanderwinden, JM Le Poul, E Brezillon, S Tyldesley, R Suarez-Huerta, N Vandeput, F Blanpain, C Schiffmann, SN Vassart, G Parmentier, M
Citation: M. Kotani et al., The metastasis suppressor gene KiSS-1 encodes kisspeptins, the natural ligands of the orphan G protein-coupled receptor GPR54, J BIOL CHEM, 276(37), 2001, pp. 34631-34636
Palmitoylation of CCR5 is critical for receptor trafficking and efficient activation of intracellular signaling pathways
Authors: Blanpain, C Wittamer, V Vanderwinden, JM Boom, A Renneboog, B Lee, B Le Poul, E El Asmar, L Govaerts, C Vassart, G Doms, RW Parmentier, M
Citation: C. Blanpain et al., Palmitoylation of CCR5 is critical for receptor trafficking and efficient activation of intracellular signaling pathways, J BIOL CHEM, 276(26), 2001, pp. 23795-23804
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
The TXP motif in the second transmembrane helix of CCR5 - A structural determinant of chemokine-induced activation
Authors: Govaerts, C Blanpain, C Deupi, X Ballet, S Ballesteros, JA Wodak, SJ Vassart, G Pardo, L Parmentier, M
Citation: C. Govaerts et al., The TXP motif in the second transmembrane helix of CCR5 - A structural determinant of chemokine-induced activation, J BIOL CHEM, 276(16), 2001, pp. 13217-13225
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
Fusion of a novel gene, RCC17, to the TFE3 gene in t(X;17)(p11.2;q25,3)-bearing papillary renal cell carcinomas
Authors: Heimann, P El Housni, H Ogur, G Weterman, MAJ Petty, EM Vassart, G
Citation: P. Heimann et al., Fusion of a novel gene, RCC17, to the TFE3 gene in t(X;17)(p11.2;q25,3)-bearing papillary renal cell carcinomas, CANCER RES, 61(10), 2001, pp. 4130-4135
Functional characterization of a human receptor for neuropeptide FF and related peptides
Authors: Kotani, M Mollereau, C Detheux, M Le Poul, E Brezillon, S Vakili, J Mazarguil, H Vassart, G Zajac, JM Parmentier, M
Citation: M. Kotani et al., Functional characterization of a human receptor for neuropeptide FF and related peptides, BR J PHARM, 133(1), 2001, pp. 138-144
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
Congenital central isolated hypothyroidism caused by a homozygous mutationin the TSH-beta subunit gene
Authors: Heinrichs, C Parma, J Scherberg, NH Delange, F Van Vliet, G Duprez, L Bourdoux, P Bergmann, P Vassart, G Refetoff, S
Citation: C. Heinrichs et al., Congenital central isolated hypothyroidism caused by a homozygous mutationin the TSH-beta subunit gene, THYROID, 10(5), 2000, pp. 387-391
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
Genomic organization of the 5 ' region of the human thyroglobulin gene
Authors: Moya, CM Mendive, FM Rivolta, CM Vassart, G Targovnik, HM
Citation: Cm. Moya et al., Genomic organization of the 5 ' region of the human thyroglobulin gene, EUR J ENDOC, 143(6), 2000, pp. 789-798
Re-analysis by fluorescence in situ hybridisation of spare embryos cultured until Day 5 after preimplantation genetic diagnosis for a 47, XYY infertile patient demonstrates a high incidence of diploid mosaic embryos: a case report
Authors: Emiliani, S Merino, EG Van den Bergh, M Abramowicz, M Vassart, G Englert, Y Delneste, D
Citation: S. Emiliani et al., Re-analysis by fluorescence in situ hybridisation of spare embryos cultured until Day 5 after preimplantation genetic diagnosis for a 47, XYY infertile patient demonstrates a high incidence of diploid mosaic embryos: a case report, PRENAT DIAG, 20(13), 2000, pp. 1063-1066
Hyperfunctioning malignant thyroid nodule in an 11-year-old girl: Pathologic and molecular studies
Authors: Mircescu, H Parma, J Huot, C Deal, C Oligny, LL Vassart, G Van Vliet, G
Citation: H. Mircescu et al., Hyperfunctioning malignant thyroid nodule in an 11-year-old girl: Pathologic and molecular studies, J PEDIAT, 137(4), 2000, pp. 585-587
Natural proteolytic processing of hemofiltrate CC chemokine 1 generates a potent CC chemokine receptor (CCR)1 and CCR5 agonist with anti-HIV properties
Authors: Detheux, M Standker, L Vakili, J Munch, J Forssmann, U Adermann, K Pohlmann, S Vassart, G Kirchhoff, F Parmentier, M Forssmann, WG
Citation: M. Detheux et al., Natural proteolytic processing of hemofiltrate CC chemokine 1 generates a potent CC chemokine receptor (CCR)1 and CCR5 agonist with anti-HIV properties, J EXP MED, 192(10), 2000, pp. 1501-1508
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
Multiple nonfunctional alleles of CCR5 are frequent in various human populations
Authors: Blanpain, C Lee, B Tackoen, M Puffer, B Boom, A Libert, F Sharron, M Wittamer, V Vassart, G Doms, RW Parmentier, M
Citation: C. Blanpain et al., Multiple nonfunctional alleles of CCR5 are frequent in various human populations, BLOOD, 96(5), 2000, pp. 1638-1645
Risultati: 1-25 | 26-47