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Results: 1-12 |
Results: 12
Flt-3 and its ligand are expressed in neural crest-derived tumors and promote survival and proliferation of their cell lines
Authors: Timeus, F Ricotti, E Crescenzio, N Garelli, E Doria, A Spinelli, M Ramenghi, U Basso, G
Citation: F. Timeus et al., Flt-3 and its ligand are expressed in neural crest-derived tumors and promote survival and proliferation of their cell lines, LAB INV, 81(7), 2001, pp. 1025-1037
Defective function of Fas in patients with type 1 diabetes associated withother autoimmune diseases
Authors: DeFranco, S Bonissoni, S Cerutti, F Bona, G Bottarel, F Cadario, F Brusco, A Loffredo, G Rabbone, I Corrias, A Pignata, C Ramenghi, U Dianzani, A
Citation: S. Defranco et al., Defective function of Fas in patients with type 1 diabetes associated withother autoimmune diseases, DIABETES, 50(3), 2001, pp. 483-488
Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndrome
Authors: Girelli, D Bozzini, C Zecchina, G Tinazzi, E Bosio, S Piperno, A Ramenghi, U Peters, J Levi, S Camaschella, C Corrocher, R
Citation: D. Girelli et al., Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndrome, BR J HAEM, 115(2), 2001, pp. 334-340
Diamond-Blackfan anemia: Report of seven further mutations in the RPS19 gene and evidence of mutation heterogeneity in the Italian population
Authors: Ramenghi, U Campagnoli, MF Garelli, E Carando, A Brusco, A Bagnara, GP Strippoli, P Izzi, GC Brandalise, S Riccardi, R Dianzani, I
Citation: U. Ramenghi et al., Diamond-Blackfan anemia: Report of seven further mutations in the RPS19 gene and evidence of mutation heterogeneity in the Italian population, BL CELL M D, 26(5), 2000, pp. 417-422
Cell cycle analysis in the diagnosis of Fanconi's anemia
Authors: Timeus, F Crescenzio, N Saracco, P Leone, L Ponzio, G Ramenghi, U
Citation: F. Timeus et al., Cell cycle analysis in the diagnosis of Fanconi's anemia, HAEMATOLOG, 85(4), 2000, pp. 431-432
Clustering of distinct autoimmune diseases associated with functional abnormalities of T cell survival in children
Authors: Pignata, C Alessio, M Ramenghi, U Bonissoni, S Difranco, D Brusco, A Matrecano, E Franzese, A Dianzani, I Dianzani, U
Citation: C. Pignata et al., Clustering of distinct autoimmune diseases associated with functional abnormalities of T cell survival in children, CLIN EXP IM, 121(1), 2000, pp. 53-58
Stem cell transplantation in patients with severe congenital neutropenia without evidence of leukemic transformation
Authors: Zeidler, C Welte, K Barak, Y Barriga, F Bolyard, AA Boxer, L Cornu, G Cowan, MJ Dale, DC Flood, T Freedman, M Gadner, H Mandel, H O'Reilly, RJ Ramenghi, U Reiter, A Skinner, R Vermylen, C Levine, JE
Citation: C. Zeidler et al., Stem cell transplantation in patients with severe congenital neutropenia without evidence of leukemic transformation, BLOOD, 95(4), 2000, pp. 1195-1198
Deficiency of the Fas apoptosis pathway without Fas gene mutations is a familial trait predisposing to development of autoimmune diseases and cancer
Authors: Ramenghi, U Bonissoni, S Migliaretti, G DeFranco, S Bottarel, F Gambaruto, C DiFranco, D Priori, R Conti, F Dianzani, I Valesini, G Merletti, F Dianzani, U
Citation: U. Ramenghi et al., Deficiency of the Fas apoptosis pathway without Fas gene mutations is a familial trait predisposing to development of autoimmune diseases and cancer, BLOOD, 95(10), 2000, pp. 3176-3182
The cell death-inducing ability of glycoprotein 120 from different HIV strains correlates with their ability to induce CD4 lateral association with CD95 on CD4(+) T cells
Authors: Bottarel, F Feito, MO Bragardo, M Bonissoni, S Buonfiglio, D DeFranco, S Malavasi, F Bensi, T Ramenghi, U Dianzani, U
Citation: F. Bottarel et al., The cell death-inducing ability of glycoprotein 120 from different HIV strains correlates with their ability to induce CD4 lateral association with CD95 on CD4(+) T cells, AIDS RES H, 15(14), 1999, pp. 1255-1263
Long-term bone marrow cultures in Diamond-Blackfan anemia reveal a defect of both granulomacrophage and erythroid progenitors
Authors: Santucci, MA Bagnara, GP Strippoli, P Bonsi, L Vitale, L Tonelli, R Locatelli, F Gabutti, V Ramenghi, U D'Avanzo, M Paolucci, G Rosito, P Pession, A Freedman, MH
Citation: Ma. Santucci et al., Long-term bone marrow cultures in Diamond-Blackfan anemia reveal a defect of both granulomacrophage and erythroid progenitors, EXP HEMATOL, 27(1), 1999, pp. 9-18
Diamond-Blackfan anaemia in the Italian population
Authors: Ramenghi, U Garelli, E Valtolina, S Campagnoli, MF Timeus, F Crescenzio, N Mair, M Varotto, S D'Avanzo, M Nobili, B Massolo, F Mori, PG Locatelli, F Gustavsson, P Dahl, N Dianzani, I
Citation: U. Ramenghi et al., Diamond-Blackfan anaemia in the Italian population, BR J HAEM, 104(4), 1999, pp. 841-848
Mutations in ribosomal protein S19 gene and Diamond Blackfan anemia: Wide variations in phenotypic expression
Authors: Willig, TN Draptchinskaia, N Dianzani, I Ball, S Niemeyer, C Ramenghi, U Orfali, K Gustavsson, P Garelli, E Brusco, A Tiemann, C Perignon, JL Bouchier, C Cicchiello, L Dahl, N Mohandas, N Tchernia, G
Citation: Tn. Willig et al., Mutations in ribosomal protein S19 gene and Diamond Blackfan anemia: Wide variations in phenotypic expression, BLOOD, 94(12), 1999, pp. 4294-4306
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