Sfoglia per Autore
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
Overexpression of the hereditary hemochromatosis protein, HFE, in HeLa cells induces and iron-deficient phenotype
1999-01-01 Corsi, B; Levi, SONIA MARIA ROSA; Cozzi, A; Corti, Angelo; Altimare, D; Albertini, A; Arosio, P.
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
Functional and immunological analysis of recombinant mouse H- and L-ferritins from Escherichia coli
2000-01-01 Santambrogio, P; Cozzi, A; Levi, SONIA MARIA ROSA; Rovida, E; Magni, F; Albertini, A; Arosio, P.
Relationship between TNF-alpha and iron metabolism in differentiating human monocytic THP-1 cells
2000-01-01 Scaccabarozzi, A; Arosio, P; Weiss, G; Valenti, L; Dongiovanni, P; Fracanzani, Al; Mattioli, M; Levi, SONIA MARIA ROSA; Fiorelli, G; Fargion, S.
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
Early embryonic lethality of H ferritin gene deletion in mice
2000-01-01 Ferreira, C; Bucchini, D; Martin, Me; Levi, SONIA MARIA ROSA; Arosio, P; Grandchamp, B; Beaumont, C.
Immunohistochemistry of HFE in the duodenum of C282Y homozygotes with antisera for recombinant HFE protein
2000-01-01 Zuccon, L; Corsi, B; Levi, SONIA MARIA ROSA; Mattioli, M; Fracanzani, Al; Corti, Angelo; Albertini, A; Sampietro, M; Fargion, S; Arosio, P.
Overexpression of wild type and mutated human ferritin H-chain in HeLa cells
2000-01-01 Cozzi, A.; Corsi, B.; Levi, SONIA MARIA ROSA; Santambrogio, P.; Albertini, A.; Arosio, P.
Mitochondrial ferritin expression in the erythroblasts of normal subjects and patients with sideroblastic anemia.
2001-01-01 Cazzola, M; Invernizzi, R; Levi, SONIA MARIA ROSA; Corsi, B; Drysdale, J; Arosio, P.
Double-Gradient Denaturing Gradient Gel Electrophoresis Assay for Identification of L-Ferritin Iron-responsive Element Mutations Responsible for Hereditary Hyperferritinemia-Cataract Syndrome: Identification of the New Mutation C14G
2001-01-01 Cremonesi, L; Fumagalli, A; Soriani, N; Ferrari, Maurizio; Levi, SONIA MARIA ROSA; Belloli, S; Ruggeri, G; Arosio, P.
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.
Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndrome
2001-01-01 Girelli, D; Bozzini, C; Zecchina, G; Tinazzi, E; Bosio, S; Piperno, A; Ramenghi, U; Peters, J; Levi, SONIA MARIA ROSA; Camaschella, Clara; Corrocher, R.
Ferritins
2002-01-01 Arosio, P; Levi, SONIA MARIA ROSA
Ferritin, iron homeostasis, and oxidative damage
2002-01-01 Arosio, P; Levi, SONIA MARIA ROSA
Human mitochondrial ferritin expressed in HeLa cells incorporates iron and affects cellular iron metabolism
2002-01-01 Corsi, B; Cozzi, A; Arosio, P; Drysdale, J; Santambrogio, P; Campanella, A; Biasiotto, G; Albertini, A; 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.
Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3)
2002-01-01 Cazzola, M; Cremonesi, L; Papaioannou, M; Soriani, N; Kioumi, A; Charalambidou, A; Paroni, R; Romtsou, K; Levi, SONIA MARIA ROSA; Ferrari, Maurizio; Arosio, P; Christakis, J.
Mitochondrial ferritin: a new player in iron metabolism
2002-01-01 Drysdale, J; Arosio, P; Invernizzi, R; Cazzola, M; Volz, A; Corsi, B; Biasiotto, G; Levi, SONIA MARIA ROSA
Identification of two novel mutations in the 5 ' untranslated region of H-ferritin using denaturing high performance liquid chromatography scanning
2003-01-01 Cremonesi, L; Foglieni, B; Fermo, I; Cozzi, A; Paroni, R; Ruggeri, G; Belloli, S; Levi, SONIA MARIA ROSA; Fargion, S; Ferrari, Maurizio; Arosio, P.
Titolo | Data di pubblicazione | Autore(i) | File |
---|---|---|---|
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 | |
Overexpression of the hereditary hemochromatosis protein, HFE, in HeLa cells induces and iron-deficient phenotype | 1-gen-1999 | Corsi, B; Levi, SONIA MARIA ROSA; Cozzi, A; Corti, Angelo; Altimare, D; Albertini, A; Arosio, P. | |
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 | |
Functional and immunological analysis of recombinant mouse H- and L-ferritins from Escherichia coli | 1-gen-2000 | Santambrogio, P; Cozzi, A; Levi, SONIA MARIA ROSA; Rovida, E; Magni, F; Albertini, A; Arosio, P. | |
Relationship between TNF-alpha and iron metabolism in differentiating human monocytic THP-1 cells | 1-gen-2000 | Scaccabarozzi, A; Arosio, P; Weiss, G; Valenti, L; Dongiovanni, P; Fracanzani, Al; Mattioli, M; Levi, SONIA MARIA ROSA; Fiorelli, G; Fargion, S. | |
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 | |
Early embryonic lethality of H ferritin gene deletion in mice | 1-gen-2000 | Ferreira, C; Bucchini, D; Martin, Me; Levi, SONIA MARIA ROSA; Arosio, P; Grandchamp, B; Beaumont, C. | |
Immunohistochemistry of HFE in the duodenum of C282Y homozygotes with antisera for recombinant HFE protein | 1-gen-2000 | Zuccon, L; Corsi, B; Levi, SONIA MARIA ROSA; Mattioli, M; Fracanzani, Al; Corti, Angelo; Albertini, A; Sampietro, M; Fargion, S; Arosio, P. | |
Overexpression of wild type and mutated human ferritin H-chain in HeLa cells | 1-gen-2000 | Cozzi, A.; Corsi, B.; Levi, SONIA MARIA ROSA; Santambrogio, P.; Albertini, A.; Arosio, P. | |
Mitochondrial ferritin expression in the erythroblasts of normal subjects and patients with sideroblastic anemia. | 1-gen-2001 | Cazzola, M; Invernizzi, R; Levi, SONIA MARIA ROSA; Corsi, B; Drysdale, J; Arosio, P. | |
Double-Gradient Denaturing Gradient Gel Electrophoresis Assay for Identification of L-Ferritin Iron-responsive Element Mutations Responsible for Hereditary Hyperferritinemia-Cataract Syndrome: Identification of the New Mutation C14G | 1-gen-2001 | Cremonesi, L; Fumagalli, A; Soriani, N; Ferrari, Maurizio; Levi, SONIA MARIA ROSA; Belloli, S; Ruggeri, G; Arosio, P. | |
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. | |
Clinical, biochemical and molecular findings in a series of families with hereditary hyperferritinaemia-cataract syndrome | 1-gen-2001 | Girelli, D; Bozzini, C; Zecchina, G; Tinazzi, E; Bosio, S; Piperno, A; Ramenghi, U; Peters, J; Levi, SONIA MARIA ROSA; Camaschella, Clara; Corrocher, R. | |
Ferritins | 1-gen-2002 | Arosio, P; Levi, SONIA MARIA ROSA | |
Ferritin, iron homeostasis, and oxidative damage | 1-gen-2002 | Arosio, P; Levi, SONIA MARIA ROSA | |
Human mitochondrial ferritin expressed in HeLa cells incorporates iron and affects cellular iron metabolism | 1-gen-2002 | Corsi, B; Cozzi, A; Arosio, P; Drysdale, J; Santambrogio, P; Campanella, A; Biasiotto, G; Albertini, A; 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. | |
Genetic hyperferritinaemia and reticuloendothelial iron overload associated with a three base pair deletion in the coding region of the ferroportin gene (SLC11A3) | 1-gen-2002 | Cazzola, M; Cremonesi, L; Papaioannou, M; Soriani, N; Kioumi, A; Charalambidou, A; Paroni, R; Romtsou, K; Levi, SONIA MARIA ROSA; Ferrari, Maurizio; Arosio, P; Christakis, J. | |
Mitochondrial ferritin: a new player in iron metabolism | 1-gen-2002 | Drysdale, J; Arosio, P; Invernizzi, R; Cazzola, M; Volz, A; Corsi, B; Biasiotto, G; Levi, SONIA MARIA ROSA | |
Identification of two novel mutations in the 5 ' untranslated region of H-ferritin using denaturing high performance liquid chromatography scanning | 1-gen-2003 | Cremonesi, L; Foglieni, B; Fermo, I; Cozzi, A; Paroni, R; Ruggeri, G; Belloli, S; Levi, SONIA MARIA ROSA; Fargion, S; Ferrari, Maurizio; Arosio, P. |
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