LEVI, SONIA MARIA ROSA
LEVI, SONIA MARIA ROSA
Facoltà di Medicina e Chirurgia
A human mitochondrial ferritin encoded by an intronless gene
2001-01-01 Levi, SONIA MARIA ROSA; Corsi, B; Bosisio, M; Invernizzi, R; Volz, A; Sanford, D; Arosio, P; Drysdale, J.
A mutational analysis of the epitopes of recombinant human H-ferritin.
1990-01-01 Arosio, P; Cozzi, A; Ingrassia, R; Levi, SONIA MARIA ROSA; Luzzago, A; Ruggeri, G; Iacobello, C; Santambrogio, P; Albertini, A.
A new G51C mutation in the IRE of L-ferritin in hyperferritinemia cataract syndrome decreases the binding affinity of the mutant IRE to IRP.
1999-01-01 Camaschella, Clara; Zecchina, G; Lockitch, G; Roetto, A; Campanella, A; Arosio, P; Levi, SONIA MARIA ROSA
A new mutation (G51C) in the iron-responsive element (IRE) of L-ferritin associated with hyperferritinaemia-cataract syndrome decreases the binding affinity of the mutated IRE for iron-regulatory proteins
2000-01-01 Camaschella, Clara; Zecchina, G; Lockitch, G; Roetto, A; Campanella, A; Arosio, P; Levi, SONIA MARIA ROSA
A new mutation in the IRE of L-ferritin (G51C) associated with hyperferritinemia-cataract syndrome decreases the binding affinity of IRE to IRPS
2000-01-01 Camaschella, Clara; ., ZECCHINA G; Lockitch, G; Campanella, A.; Arosio, P.; Levi, SONIA MARIA ROSA
A novel deletion of the L-ferritin iron-responsive element responsible for severe hereditary hyperferritinaemia-cataract syndrome
2002-01-01 Cazzola, M; Foglieni, B; Bergamaschi, G; Levi, SONIA MARIA ROSA; Lazzarino, M; Arosio, P.
A novel neuroferritinopathy mouse model (FTL 498InsTC) shows progressive brain iron dysregulation, morphological signs of early neurodegeneration and motor coordination deficits
2015-01-01 Maccarinelli, F; Pagani, A; Cozzi, A; Codazzi, Franca; DI GIACOMO, Giuseppina; Capoccia, S; Rapino, S; Finazzi, D; Politi, Ls; Cirulli, F; Giorgio, M; Cremona, Ottavio; Grohovaz, Fabio; Levi, SONIA MARIA ROSA
Actions of H-subunit ferritin and lactoferrin as suppressor molecules of myelopoiesis in vitro and in vivo.
1991-01-01 Broxmeyer, H. E.; Mantel, C; Gentile, P; Srivastava, C; Miyazawa, K; Zucali, J. R.; Rado, T. A.; Levi, SONIA MARIA ROSA; Arosio, P.
An approach for screening of Hereditary Hyperferritinemia Cataract Syndrome (HHCS) by a new DG-DGGE method for rapid mutational scanning in ferritin L-chain IRE.
1999-01-01 Cremonesi, L; Fumagalli, A; Soriani, N; Ferrari, Maurizio; Tinazzi, E; Camparini, M; Aldigeri, R; Girelli, D; Arosio, P; Levi, SONIA MARIA ROSA
Analysis of ferritin genes in Parkinson disease.
2007-01-01 Foglieni, B; Ferrari, F; Goldwurm, S; Santambrogio, P; Castiglioni, E; Sessa, M; Volontè, Ma; Lalli, S; Galli, C; Wang, Xs; Connor, J; Sironi, F; Canesi, M; Biasiotto, G; Pezzoli, G; Levi, SONIA MARIA ROSA; Ferrari, Maurizio; Arosio, P; Cremonesi, L.
Analysis of ferritins in lymphoblastoid cell lines and in the lens of subjects with hereditary hyperferritinemia-cataract syndrome
1998-01-01 Levi, SONIA MARIA ROSA; Girelli, D; Perrone, F; Pasti, M; Beaumont, C; Corrocher, R; Albertini, A; Arosio, P.
Analysis of the biologic functions of H- and L-ferritins in HeLa cells by transfection with siRNAs and cDNAs: evidence for a proliferative role of L-ferritin
2004-01-01 Cozzi, A; Corsi, B; Levi, SONIA MARIA ROSA; Santambrogio, P; Biasiotto, G; Arosio, P.
Analysis of the iron status of professional cyclists during a 3-week road race.
1988-01-01 Campanini, S; Arosio, P; Levi, SONIA MARIA ROSA; Ceriotti, F; Murone, M; Marconi, C.
ANALYSIS OF THE MITOCHONDRIAL FERRITIN PHYSIOPATHOLOGICAL ROLE IN SIDEROBLASTIC ERYTHROPOIESIS
2009-01-01 Invernizzi, R.; Della Porta, M. G.; Rosti, V.; Galli, A.; Travaglino, E.; Santambrogio, P.; Marseglia, C.; Matti, V.; Malcovati, L.; Bergamaschi, G.; Cazzola, M.; Levi, SONIA MARIA ROSA
ANIMAL MODELS OF NEUROFERRITINOPATHY
2013-01-01 Maccarinelli, F; Asperti, M; Capoccia, S; Pagani, A; Buffoli, B; Codazzi, F; Finazzi, D; Pelizzoni, I; Cozzi, A; Strippoli, M; Politi, L; Cremona, ; Grohovaz, Fabio; Levi, SONIA MARIA ROSA; Arosio, P.
ANTIBODIES FOR DENATURED HUMAN H-FERRITIN STAIN ONLY RETICULOENDOTHELIAL CELLS WITHIN THE BONE-MARROW
1992-01-01 Ruggeri, G; Santambrogio, P; Bonfiglio, F; Levi, SONIA MARIA ROSA; Bugari, G; Verardi, R; Cazzola, M; Invernizzi, R; Zambelli, Lm; Albertini, A; Arosio, P.
BINDING AND SUPPRESSIVE ACTIVITY OF HUMAN RECOMBINANT FERRITINS ON ERYTHROID-CELLS
1992-01-01 Fargion, S; Cappellini, Md; Fracanzani, Al; Defeo, Tm; Levi, SONIA MARIA ROSA; Arosio, P; Fiorelli, G.
Blotting Analysis of Native IRP1: A Novel Approach to Distinguish the Different Forms of IRP1 in Cells and Tissues
2004-01-01 Campanella, Alessandro; Levi, Sonia Maria; Gaetano, Cairo; Giorgio, Biasiotto; Paolo, Arosio
C29G in the iron-responsive element of L-ferritin: a new mutation associated with hyperferritinemia-cataract
2004-01-01 Bosio, S; Campanella, A; Gramaglia, E; Porporato, P; Longo, F; Cremonesi, L; Levi, SONIA MARIA ROSA; Camaschella, Clara
Case report: a subject with a mutation in the ATG start codon of L-ferritin has no hematological or neurological symptoms
2004-01-01 Cremonesi, L; Cozzi, A; Girelli, D; Ferrari, F; Fermo, I; Foglieni, B; Levi, S; Bozzini, C; Camparini, M; Ferrari, M; Arosio, P
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A human mitochondrial ferritin encoded by an intronless gene | 1-gen-2001 | Levi, SONIA MARIA ROSA; Corsi, B; Bosisio, M; Invernizzi, R; Volz, A; Sanford, D; Arosio, P; Drysdale, J. | |
| A mutational analysis of the epitopes of recombinant human H-ferritin. | 1-gen-1990 | Arosio, P; Cozzi, A; Ingrassia, R; Levi, SONIA MARIA ROSA; Luzzago, A; Ruggeri, G; Iacobello, C; Santambrogio, P; Albertini, A. | |
| A new G51C mutation in the IRE of L-ferritin in hyperferritinemia cataract syndrome decreases the binding affinity of the mutant IRE to IRP. | 1-gen-1999 | Camaschella, Clara; Zecchina, G; Lockitch, G; Roetto, A; Campanella, A; Arosio, P; Levi, SONIA MARIA ROSA | |
| A new mutation (G51C) in the iron-responsive element (IRE) of L-ferritin associated with hyperferritinaemia-cataract syndrome decreases the binding affinity of the mutated IRE for iron-regulatory proteins | 1-gen-2000 | Camaschella, Clara; Zecchina, G; Lockitch, G; Roetto, A; Campanella, A; Arosio, P; Levi, SONIA MARIA ROSA | |
| A new mutation in the IRE of L-ferritin (G51C) associated with hyperferritinemia-cataract syndrome decreases the binding affinity of IRE to IRPS | 1-gen-2000 | Camaschella, Clara; ., ZECCHINA G; Lockitch, G; Campanella, A.; Arosio, P.; Levi, SONIA MARIA ROSA | |
| A novel deletion of the L-ferritin iron-responsive element responsible for severe hereditary hyperferritinaemia-cataract syndrome | 1-gen-2002 | Cazzola, M; Foglieni, B; Bergamaschi, G; Levi, SONIA MARIA ROSA; Lazzarino, M; Arosio, P. | |
| A novel neuroferritinopathy mouse model (FTL 498InsTC) shows progressive brain iron dysregulation, morphological signs of early neurodegeneration and motor coordination deficits | 1-gen-2015 | Maccarinelli, F; Pagani, A; Cozzi, A; Codazzi, Franca; DI GIACOMO, Giuseppina; Capoccia, S; Rapino, S; Finazzi, D; Politi, Ls; Cirulli, F; Giorgio, M; Cremona, Ottavio; Grohovaz, Fabio; Levi, SONIA MARIA ROSA | |
| Actions of H-subunit ferritin and lactoferrin as suppressor molecules of myelopoiesis in vitro and in vivo. | 1-gen-1991 | Broxmeyer, H. E.; Mantel, C; Gentile, P; Srivastava, C; Miyazawa, K; Zucali, J. R.; Rado, T. A.; Levi, SONIA MARIA ROSA; Arosio, P. | |
| An approach for screening of Hereditary Hyperferritinemia Cataract Syndrome (HHCS) by a new DG-DGGE method for rapid mutational scanning in ferritin L-chain IRE. | 1-gen-1999 | Cremonesi, L; Fumagalli, A; Soriani, N; Ferrari, Maurizio; Tinazzi, E; Camparini, M; Aldigeri, R; Girelli, D; Arosio, P; Levi, SONIA MARIA ROSA | |
| Analysis of ferritin genes in Parkinson disease. | 1-gen-2007 | Foglieni, B; Ferrari, F; Goldwurm, S; Santambrogio, P; Castiglioni, E; Sessa, M; Volontè, Ma; Lalli, S; Galli, C; Wang, Xs; Connor, J; Sironi, F; Canesi, M; Biasiotto, G; Pezzoli, G; Levi, SONIA MARIA ROSA; Ferrari, Maurizio; Arosio, P; Cremonesi, L. | |
| Analysis of ferritins in lymphoblastoid cell lines and in the lens of subjects with hereditary hyperferritinemia-cataract syndrome | 1-gen-1998 | Levi, SONIA MARIA ROSA; Girelli, D; Perrone, F; Pasti, M; Beaumont, C; Corrocher, R; Albertini, A; Arosio, P. | |
| Analysis of the biologic functions of H- and L-ferritins in HeLa cells by transfection with siRNAs and cDNAs: evidence for a proliferative role of L-ferritin | 1-gen-2004 | Cozzi, A; Corsi, B; Levi, SONIA MARIA ROSA; Santambrogio, P; Biasiotto, G; Arosio, P. | |
| Analysis of the iron status of professional cyclists during a 3-week road race. | 1-gen-1988 | Campanini, S; Arosio, P; Levi, SONIA MARIA ROSA; Ceriotti, F; Murone, M; Marconi, C. | |
| ANALYSIS OF THE MITOCHONDRIAL FERRITIN PHYSIOPATHOLOGICAL ROLE IN SIDEROBLASTIC ERYTHROPOIESIS | 1-gen-2009 | Invernizzi, R.; Della Porta, M. G.; Rosti, V.; Galli, A.; Travaglino, E.; Santambrogio, P.; Marseglia, C.; Matti, V.; Malcovati, L.; Bergamaschi, G.; Cazzola, M.; Levi, SONIA MARIA ROSA | |
| ANIMAL MODELS OF NEUROFERRITINOPATHY | 1-gen-2013 | Maccarinelli, F; Asperti, M; Capoccia, S; Pagani, A; Buffoli, B; Codazzi, F; Finazzi, D; Pelizzoni, I; Cozzi, A; Strippoli, M; Politi, L; Cremona, ; Grohovaz, Fabio; Levi, SONIA MARIA ROSA; Arosio, P. | |
| ANTIBODIES FOR DENATURED HUMAN H-FERRITIN STAIN ONLY RETICULOENDOTHELIAL CELLS WITHIN THE BONE-MARROW | 1-gen-1992 | Ruggeri, G; Santambrogio, P; Bonfiglio, F; Levi, SONIA MARIA ROSA; Bugari, G; Verardi, R; Cazzola, M; Invernizzi, R; Zambelli, Lm; Albertini, A; Arosio, P. | |
| BINDING AND SUPPRESSIVE ACTIVITY OF HUMAN RECOMBINANT FERRITINS ON ERYTHROID-CELLS | 1-gen-1992 | Fargion, S; Cappellini, Md; Fracanzani, Al; Defeo, Tm; Levi, SONIA MARIA ROSA; Arosio, P; Fiorelli, G. | |
| Blotting Analysis of Native IRP1: A Novel Approach to Distinguish the Different Forms of IRP1 in Cells and Tissues | 1-gen-2004 | Campanella, Alessandro; Levi, Sonia Maria; Gaetano, Cairo; Giorgio, Biasiotto; Paolo, Arosio | |
| C29G in the iron-responsive element of L-ferritin: a new mutation associated with hyperferritinemia-cataract | 1-gen-2004 | Bosio, S; Campanella, A; Gramaglia, E; Porporato, P; Longo, F; Cremonesi, L; Levi, SONIA MARIA ROSA; Camaschella, Clara | |
| Case report: a subject with a mutation in the ATG start codon of L-ferritin has no hematological or neurological symptoms | 1-gen-2004 | Cremonesi, L; Cozzi, A; Girelli, D; Ferrari, F; Fermo, I; Foglieni, B; Levi, S; Bozzini, C; Camparini, M; Ferrari, M; Arosio, P |