28 results on '"Rivella, Stefano"'
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2. New strategies to target iron metabolism for the treatment of beta thalassemia
3. Altered erythropoiesis and iron metabolism in carriers of thalassemia
4. Cancer cells with irons in the fire
5. FOXO3-mTOR metabolic cooperation in the regulation of erythroid cell maturation and homeostasis
6. CANCER, CELLS WITH IRONS IN THE FIRE: P15
7. Isocitrate ameliorates anemia by suppressing the erythroid iron restriction response
8. Combining gene therapy and fetal hemoglobin induction for treatment of β-thalassemia
9. Gene therapy for hemoglobinopathies: progress and challenges
10. Reducing TMPRSS6 ameliorates hemochromatosis and β-thalassemia in mice
11. A combined approach for β-thalassemia based on gene therapy-mediated adult hemoglobin (HbA) production and fetal hemoglobin (HbF) induction
12. Prospects for a hepcidin mimic to treat β-thalassemia and hemochromatosis
13. Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice
14. Analysis of alpha hemoglobin stabilizing protein overexpression in murine β-thalassemia
15. A preclinical approach for gene therapy of β-thalassemia
16. Hepcidin and Hfe in iron overload in β-thalassemia
17. Iron metabolism and ineffective erythropoiesis in β-thalassemia mouse models
18. Future alternative therapies for β-thalassemia
19. Development of K562 cell clones expressing β-globin mRNA carrying the β039 thalassaemia mutation for the screening of correctors of stop-codon mutations
20. Protective role of calreticulin in HFE hemochromatosis
21. Downregulation of hepcidin and haemojuvelin expression in the hepatocyte cell-line HepG2 induced by thalassaemic sera
22. mRNA Expression of Iron Regulatory Genes in β-Thalassemia Intermedia and β-Thalassemia Major Mouse Models
23. Exploring the Role of Hepcidin, an Antimicrobial and Iron Regulatory Peptide, in Increased Iron Absorption in β-Thalassemia
24. Progress Toward the Genetic Treatment of the β-Thalassemias
25. Role of Iron in Inducing Oxidative Stress in Thalassemia: Can It Be Prevented by Inhibition of Absorption and by Antioxidants?
26. Decreased hepcidin mRNA expression in thalassemic mice
27. Globin gene transfer: a paradigm for transgene regulation and vector safety
28. Therapeutic haemoglobin synthesis in β-thalassaemic mice expressing lentivirus-encoded human β-globin
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