23 results on '"Rivella, Stefano"'
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2. Iron restriction in sickle cell disease: When less is more.
3. Transferrin receptor 2 (Tfr2) genetic deletion makes transfusion‐independent a murine model of transfusion‐dependent β‐thalassemia.
4. Management of non‐transfusion‐dependent β‐thalassemia (NTDT): The next 5 years.
5. Revisiting the non‐transfusion‐dependent (NTDT) vs. transfusion‐dependent (TDT) thalassemia classification 10 years later.
6. Inhibition of fibroblast growth factor 23 (FGF23) signaling rescues renal anemia.
7. New strategies to target iron metabolism for the treatment of beta thalassemia.
8. Altered erythropoiesis and iron metabolism in carriers of thalassemia.
9. FOXO3-mTOR metabolic cooperation in the regulation of erythroid cell maturation and homeostasis.
10. Hepcidin and Hfe in iron overload in β-thalassemia.
11. A preclinical approach for gene therapy of β-thalassemia.
12. Iron metabolism and ineffective erythropoiesis in β-thalassemia mouse models.
13. Production of β-globin and adult hemoglobin following G418 treatment of erythroid precursor cells from homozygous β039 thalassemia patients.
14. Downregulation of hepcidin and haemojuvelin expression in the hepatocyte cell-line HepG2 induced by thalassaemic sera.
15. Exploring the Role of Hepcidin, an Antimicrobial and Iron Regulatory Peptide, in Increased Iron Absorption in β-Thalassemia.
16. Role of Iron in Inducing Oxidative Stress in Thalassemia: Can It Be Prevented by Inhibition of Absorption and by Antioxidants?
17. Progress Toward the Genetic Treatment of the β- Thalassemias.
18. Analysis of alpha hemoglobin stabilizing protein overexpression in murine β-thalassemia.
19. Decreased hepcidin mRNA expression in thalassemic mice.
20. Cytoskeletal organization during terminal differentiation and enucleation of mammalian erythroblasts (538.3).
21. Production of beta-globin and adult hemoglobin following G418 treatment of erythroid precursor cells from homozygous beta(0)39 thalassemia patients.
22. Development of K562 cell clones expressing beta-globin mRNA carrying the beta039 thalassaemia mutation for the screening of correctors of stop-codon mutations.
23. mRNA expression of iron regulatory genes in beta-thalassemia intermedia and beta-thalassemia major mouse models.
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