ROETTO, Antonella
ROETTO, Antonella
SCIENZE CLINICHE E BIOLOGICHE
A child with hyperferritinemia: case report
2011-01-01 M. Serra; F. Longo; A. Roetto; A. Sandri; A. Piga
A comparative study of myocardial molecular phenotypes of two tfr2β null mice: Role in ischemia/reperfusion
2015-01-01 Boero, Martina; Pagliaro, Pasquale; Tullio, Francesca; Pellegrino, Rosa M.; Palmieri, Antonietta; Ferbo, Ludovica; Saglio, Giuseppe; De Gobbi, Marco; Penna, Claudia; Roetto, Antonella
A frequent polymorphism in the 5' region of the BCMA gene
1997-01-01 Roetto, A; Cicilano, M.; Gottardi, E.; Totaro, A.; Carella, M.; Gasparini, P.; Camaschella, C.
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 C;Zecchina G;Lockitch G;Roetto A;Campanella A;Arosio P;Levi S
A novel mutation in the CUB sequence of matriptase-2 (TMPRSS6) is implicated in iron-resistant iron deficiency anaemia - response to Jasperset al
2013-01-01 Antonella Roetto;Graça Porto
A pilot C282Y hemochromatosis screening in Italian newborns by TaqMan technology.
2000-01-01 Restagno G; Gomez AM; Sbaiz L; De Gobbi M; Roetto A; Bertino E; Fabris C; Fiorucci GC; Fortina P; Camaschella C.
A Portuguese patient homozygous for the -25G>A mutation of the HAMP promoter shows evidence of steady-state transcription but fails to up-regulate hepcidin levels by iron.
2005-01-01 Porto G;Roetto A;Daraio F;Pinto JP;Almeida S;Bacelar C;Nemeth E;Ganz T;Camaschella C
A recombination event close to HFE gene in hereditary hemochromatosis
1997-01-01 Roetto, A; Sbaiz, L; Bosio, S; Piperno, A; Fargion, S; Carella, M; Totaro, A; Grifa, A; Gasparini, P; Camaschella, C
A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4
2002-01-01 A. ROETTO; A.T. MERRYWEATHER-CLARKE; F. DARAIO; K. LIVESEY; J.J. POINTON; G. BARBABIETOLA; A. PIGA; P.H. MACKIE; K.J. ROBSON; C. CAMASCHELLA
Activation of the Hepcidin-Ferroportin1 pathway in the brain and astrocytic–neuronal crosstalk to counteract iron dyshomeostasis during aging
2022-01-01 Mariarosa Mezzanotte, Giorgia Ammirata, Marina Boido, Serena Stanga, Antonella Roetto
Ailanthone increases oxidative stress in CDDP-resistant ovarian and bladder cancer cells by inhibiting of Nrf2 and YAP expression through a post-translational mechanism
2020-01-01 Cucci M.A.; Grattarola M.; Dianzani C.; Damia G.; Ricci F.; Roetto A.; Trotta F.; Barrera G.; Pizzimenti S.
Allelic association of microsatellites of 6p in Italian hemochromatosis patients
1996-01-01 Camaschella, C; Roetto, A; Gasparini, P; Piperno, A; Fortina, P; Surrey, S; Rappaport, E
Altered Erythropoiesis in Mouse Models of Type 3 Hemochromatosis
2017-01-01 Pellegrino, R M; Riondato, F; Ferbo, L; Boero, M; Palmieri, A; Osella, L; Pollicino, P; Miniscalco, B; Saglio, G; Roetto, A
Altered erythropoiesis in mouse models of type 3 Hemochromatosis (Hh3)
2014-01-01 F. Riondato; L. Ferbo; R.M. Pellegrino; M. Boero; B. Miniscalco; G. Saglio; M. De Gobbi; A. Roetto.
ALTERED MRNAS EXPRESSION OF GENES INVOLVED IN CELLULAR IRON HOMEOSTASIS IN LUNG NON SMALL CELLS CARCINOMA
2012-01-01 Lo Iacono M; Roetto A; Monica V; Boero M; Vavala T; Saviozzi S; Bracco E; Novello S; Papotti M; Scagliotti GV
ANALYSIS OF IRON METABOLISM IN TFR2 TARGETED ANIMALS BRAIN
2013-01-01 Rosa Maria Pellegrino;Enrica Boda;Martina Boero;Francesca Montarolo;Alessandro Volpengo;Giuseppe Saglio;Annalisa Buffo; Antonella Roetto
Analysis of microsatellite instability in chronic lymphoproliferative disorders
1996-01-01 Volpe, G; Gamberi, B; Pastore, C; Roetto, A; Pautasso, M; Parvis, G; Camaschella, C; Mazza, U; Saglio, G; Gaidano, G
Analysis of NCOA4/Tfr2 as PB markers of iron increase during ageing
2019-01-01 M. Mezzanotte, D. Galeno, G. Ammirata, A. Roetto
Anemia and iron overload due to compound heterozygosity for novel ceruloplasmin mutations.
2002-01-01 S. Bosio;M. De Gobbi;A. Roetto;G. Zecchina;E. Leonardo;M. Rizzetto;C. Lucetti;L. Petrozzi;U. Bonuccelli;C. Camaschella
Anemia and iron overload due to genetic defects of iron recycling, aceruloplasminemia and hemochromatosis type 4
2002-01-01 M. De Gobbi; A. Roetto; S. Bosio; F. Daraio; F. Alberti; M.R. Barilaro; F. Longo; U. Bonuccelli; C. Camaschella
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A child with hyperferritinemia: case report | 2011 | M. Serra; F. Longo; A. Roetto; A. Sandri; A. Piga | |
| A comparative study of myocardial molecular phenotypes of two tfr2β null mice: Role in ischemia/reperfusion | 2015 | Boero, Martina; Pagliaro, Pasquale; Tullio, Francesca; Pellegrino, Rosa M.; Palmieri, Antonietta; Ferbo, Ludovica; Saglio, Giuseppe; De Gobbi, Marco; Penna, Claudia; Roetto, Antonella | |
| A frequent polymorphism in the 5' region of the BCMA gene | 1997 | Roetto, A; Cicilano, M.; Gottardi, E.; Totaro, A.; Carella, M.; Gasparini, P.; Camaschella, C. | |
| 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 | Camaschella C;Zecchina G;Lockitch G;Roetto A;Campanella A;Arosio P;Levi S | |
| A novel mutation in the CUB sequence of matriptase-2 (TMPRSS6) is implicated in iron-resistant iron deficiency anaemia - response to Jasperset al | 2013 | Antonella Roetto;Graça Porto | |
| A pilot C282Y hemochromatosis screening in Italian newborns by TaqMan technology. | 2000 | Restagno G; Gomez AM; Sbaiz L; De Gobbi M; Roetto A; Bertino E; Fabris C; Fiorucci GC; Fortina P; Camaschella C. | |
| A Portuguese patient homozygous for the -25G>A mutation of the HAMP promoter shows evidence of steady-state transcription but fails to up-regulate hepcidin levels by iron. | 2005 | Porto G;Roetto A;Daraio F;Pinto JP;Almeida S;Bacelar C;Nemeth E;Ganz T;Camaschella C | |
| A recombination event close to HFE gene in hereditary hemochromatosis | 1997 | Roetto, A; Sbaiz, L; Bosio, S; Piperno, A; Fargion, S; Carella, M; Totaro, A; Grifa, A; Gasparini, P; Camaschella, C | |
| A valine deletion of ferroportin 1: a common mutation in hemochromastosis type 4 | 2002 | A. ROETTO; A.T. MERRYWEATHER-CLARKE; F. DARAIO; K. LIVESEY; J.J. POINTON; G. BARBABIETOLA; A. PIGA; P.H. MACKIE; K.J. ROBSON; C. CAMASCHELLA | |
| Activation of the Hepcidin-Ferroportin1 pathway in the brain and astrocytic–neuronal crosstalk to counteract iron dyshomeostasis during aging | 2022 | Mariarosa Mezzanotte, Giorgia Ammirata, Marina Boido, Serena Stanga, Antonella Roetto | |
| Ailanthone increases oxidative stress in CDDP-resistant ovarian and bladder cancer cells by inhibiting of Nrf2 and YAP expression through a post-translational mechanism | 2020 | Cucci M.A.; Grattarola M.; Dianzani C.; Damia G.; Ricci F.; Roetto A.; Trotta F.; Barrera G.; Pizzimenti S. | |
| Allelic association of microsatellites of 6p in Italian hemochromatosis patients | 1996 | Camaschella, C; Roetto, A; Gasparini, P; Piperno, A; Fortina, P; Surrey, S; Rappaport, E | |
| Altered Erythropoiesis in Mouse Models of Type 3 Hemochromatosis | 2017 | Pellegrino, R M; Riondato, F; Ferbo, L; Boero, M; Palmieri, A; Osella, L; Pollicino, P; Miniscalco, B; Saglio, G; Roetto, A | |
| Altered erythropoiesis in mouse models of type 3 Hemochromatosis (Hh3) | 2014 | F. Riondato; L. Ferbo; R.M. Pellegrino; M. Boero; B. Miniscalco; G. Saglio; M. De Gobbi; A. Roetto. | |
| ALTERED MRNAS EXPRESSION OF GENES INVOLVED IN CELLULAR IRON HOMEOSTASIS IN LUNG NON SMALL CELLS CARCINOMA | 2012 | Lo Iacono M; Roetto A; Monica V; Boero M; Vavala T; Saviozzi S; Bracco E; Novello S; Papotti M; Scagliotti GV | |
| ANALYSIS OF IRON METABOLISM IN TFR2 TARGETED ANIMALS BRAIN | 2013 | Rosa Maria Pellegrino;Enrica Boda;Martina Boero;Francesca Montarolo;Alessandro Volpengo;Giuseppe Saglio;Annalisa Buffo; Antonella Roetto | |
| Analysis of microsatellite instability in chronic lymphoproliferative disorders | 1996 | Volpe, G; Gamberi, B; Pastore, C; Roetto, A; Pautasso, M; Parvis, G; Camaschella, C; Mazza, U; Saglio, G; Gaidano, G | |
| Analysis of NCOA4/Tfr2 as PB markers of iron increase during ageing | 2019 | M. Mezzanotte, D. Galeno, G. Ammirata, A. Roetto | |
| Anemia and iron overload due to compound heterozygosity for novel ceruloplasmin mutations. | 2002 | S. Bosio;M. De Gobbi;A. Roetto;G. Zecchina;E. Leonardo;M. Rizzetto;C. Lucetti;L. Petrozzi;U. Bonuccelli;C. Camaschella | |
| Anemia and iron overload due to genetic defects of iron recycling, aceruloplasminemia and hemochromatosis type 4 | 2002 | M. De Gobbi; A. Roetto; S. Bosio; F. Daraio; F. Alberti; M.R. Barilaro; F. Longo; U. Bonuccelli; C. Camaschella |