Works by Rivella, Stefano
Results: 52
Development of K562 cell clones expressing β-globin mRNA carrying the β039 thalassaemia mutation for the screening of correctors of stop-codon mutations.
- Published in:
- Biotechnology & Applied Biochemistry, 2009, v. 54, n. 1, p. 41, doi. 10.1042/BA20080266
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- Publication type:
- Article
Downregulation of hepcidin and haemojuvelin expression in the hepatocyte cell-line HepG2 induced by thalassaemic sera.
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- British Journal of Haematology, 2006, v. 135, n. 1, p. 129, doi. 10.1111/j.1365-2141.2006.06258.x
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- Publication type:
- Article
Decreased hepcidin mRNA expression in thalassemic mice.
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- 2004
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- Publication type:
- Letter
A combined approach for β-thalassemia based on gene therapy-mediated adult hemoglobin (HbA) production and fetal hemoglobin (HbF) induction.
- Published in:
- Annals of Hematology, 2012, v. 91, n. 8, p. 1201, doi. 10.1007/s00277-012-1430-5
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- Publication type:
- Article
HMGB1 Mediates Anemia of Inflammation in Murine Sepsis Survivors.
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- Molecular Medicine, 2015, v. 21, n. 1, p. 951, doi. 10.2119/molmed.2015.00243
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- Publication type:
- Article
Development and characterization of cellular biosensors for HTS of erythroid differentiation inducers targeting the transcriptional activity of γ-globin and β-globin gene promoters.
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- Analytical & Bioanalytical Chemistry, 2019, v. 411, n. 29, p. 7669, doi. 10.1007/s00216-019-01959-z
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- Publication type:
- Article
Generation and Characterization of a Transgenic Mouse Carrying a Functional Human β -Globin Gene with the IVSI-6 Thalassemia Mutation.
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- BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/687635
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- Publication type:
- Article
Recent trends in the gene therapy of β-thalassemia.
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- Journal of Blood Medicine, 2015, v. 6, p. 69, doi. 10.2147/JBM.S46256
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- Publication type:
- Article
Hepcidin inhibits Smad3 phosphorylation in hepatic stellate cells by impeding ferroportin-mediated regulation of Akt.
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- Nature Communications, 2016, v. 7, n. 12, p. 13817, doi. 10.1038/ncomms13817
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- Publication type:
- Article
β-Thalassemia: HiJAKing Ineffective Erythropoiesis and Iron Overload.
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- Advances in Hematology, 2010, v. 2010, p. 1, doi. 10.1155/2010/938640
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- Publication type:
- Article
Crosstalk between Erythropoiesis and Iron Metabolism.
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- Advances in Hematology, 2010, v. 2010, p. 1, doi. 10.1155/2010/317095
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- Publication type:
- Article
Mitochondria Biogenesis Modulates Iron–Sulfur Cluster Synthesis to Increase Cellular Iron Uptake.
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- DNA & Cell Biology, 2020, v. 39, n. 5, p. 756, doi. 10.1089/dna.2019.5123
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- Publication type:
- Article
Inhibition of fibroblast growth factor 23 (FGF23) signaling rescues renal anemia.
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- FASEB Journal, 2018, v. 32, n. 7, p. 3752, doi. 10.1096/fj.201700667R
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- Publication type:
- Article
Cytoskeletal organization during terminal differentiation and enucleation of mammalian erythroblasts (538.3).
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- FASEB Journal, 2014, v. 28, p. N.PAG, doi. 10.1096/fasebj.28.1_supplement.538.3
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- Publication type:
- Article
Revisiting the non‐transfusion‐dependent (NTDT) vs. transfusion‐dependent (TDT) thalassemia classification 10 years later.
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- American Journal of Hematology, 2021, v. 96, n. 2, p. E54, doi. 10.1002/ajh.26056
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- Publication type:
- Article
FOXO3-mTOR metabolic cooperation in the regulation of erythroid cell maturation and homeostasis.
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- American Journal of Hematology, 2014, v. 89, n. 10, p. 954, doi. 10.1002/ajh.23786
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- Publication type:
- Article
Analysis of alpha hemoglobin stabilizing protein overexpression in murine β-thalassemia.
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- American Journal of Hematology, 2010, v. 85, n. 10, p. 820, doi. 10.1002/ajh.21829
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- Publication type:
- Article
Production of β-globin and adult hemoglobin following G418 treatment of erythroid precursor cells from homozygous β<sup>0</sup>39 thalassemia patients.
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- American Journal of Hematology, 2009, v. 84, n. 11, p. 720, doi. 10.1002/ajh.21539
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- Publication type:
- Article
mRNA expression of iron regulatory genes in β‐thalassemia intermedia and β‐thalassemia major mouse models.
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- American Journal of Hematology, 2006, v. 81, n. 7, p. 479, doi. 10.1002/ajh.20549
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- Publication type:
- Article
Normal and dysregulated crosstalk between iron metabolism and erythropoiesis.
- Published in:
- eLife, 2023, p. 1, doi. 10.7554/eLife.90189
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- Publication type:
- Article
DNA binding to TLR9 expressed by red blood cells promotes innate immune activation and anemia.
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- Science Translational Medicine, 2021, v. 13, n. 616, p. 1, doi. 10.1126/scitranslmed.abj1008
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- Publication type:
- Article
Altered erythropoiesis and iron metabolism in carriers of thalassemia.
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- European Journal of Haematology, 2015, v. 94, n. 6, p. 511, doi. 10.1111/ejh.12464
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- Publication type:
- Article
CYP450 Mediates Reactive Oxygen Species Production in a Mouse Model of β-Thalassemia through an Increase in 20-HETE Activity.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 3, p. 1106, doi. 10.3390/ijms22031106
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- Publication type:
- Article
Exploring the Role of Hepcidin, an Antimicrobial and Iron Regulatory Peptide, in Increased Iron Absorption in β-Thalassemia.
- Published in:
- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 417, doi. 10.1196/annals.1345.069
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- Publication type:
- Article
Role of Iron in Inducing Oxidative Stress in Thalassemia: Can It Be Prevented by Inhibition of Absorption and by Antioxidants?
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 118, doi. 10.1196/annals.1345.014
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- Publication type:
- Article
Progress Toward the Genetic Treatment of the β- Thalassemias.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 78, doi. 10.1196/annals.1345.010
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- Publication type:
- Article
341. Lentivirus Transduction of Murine Embryonic Stem Cells with Truncated Human Low-Affinity Nerve Growth Factor Permits Efficient Purification of Genetically Modified Cells without Loss of Stem Cell Characteristics.
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- Molecular Therapy, 2006, v. 13, p. S130, doi. 10.1016/j.ymthe.2006.08.399
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- Publication type:
- Article
4. Optimization of Globin Lentiviral Vector Design for the Treatment of β-Thalassemia
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- 2005
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- Publication type:
- Abstract
Macrophages support pathological erythropoiesis in polycythemia vera and β-thalassemia.
- Published in:
- Nature Medicine, 2013, v. 19, n. 4, p. 437, doi. 10.1038/nm.3126
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- Publication type:
- Article
Identification of erythroferrone as an erythroid regulator of iron metabolism.
- Published in:
- Nature Genetics, 2014, v. 46, n. 7, p. 678, doi. 10.1038/ng.2996
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- Publication type:
- Article
New strategies to target iron metabolism for the treatment of beta thalassemia.
- Published in:
- Annals of the New York Academy of Sciences, 2016, v. 1368, n. 1, p. 162, doi. 10.1111/nyas.13018
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- Publication type:
- Article
A preclinical approach for gene therapy of β-thalassemia.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 134, doi. 10.1111/j.1749-6632.2010.05594.x
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- Publication type:
- Article
Hepcidin and Hfe in iron overload in β-thalassemia.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 221, doi. 10.1111/j.1749-6632.2010.05595.x
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- Publication type:
- Article
Iron metabolism and ineffective erythropoiesis in β-thalassemia mouse models.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 24, doi. 10.1111/j.1749-6632.2010.05596.x
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- Publication type:
- Article
The hepcidin regulator erythroferrone is a new member of the erythropoiesis-iron-bone circuitry.
- Published in:
- eLife, 2021, p. 1, doi. 10.7554/eLife.68217
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- Publication type:
- Article
Gene therapy of hemoglobinopathies: progress and future challenges.
- Published in:
- Human Molecular Genetics, 2019, v. 28, p. R24, doi. 10.1093/hmg/ddz172
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- Publication type:
- Article
Tmprss6-ASO as a tool for the treatment of Polycythemia Vera mice.
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- PLoS ONE, 2021, v. 16, n. 12, p. 1, doi. 10.1371/journal.pone.0251995
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- Publication type:
- Article
Gene Therapy for Beta-Hemoglobinopathies: Milestones, New Therapies and Challenges.
- Published in:
- Molecular Diagnosis & Therapy, 2019, v. 23, n. 2, p. 173, doi. 10.1007/s40291-019-00383-4
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- Publication type:
- Article
Isocitrate ameliorates anemia by suppressing the erythroid iron restriction response.
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- Journal of Clinical Investigation, 2013, v. 123, n. 8, p. 3614, doi. 10.1172/JCI68487
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- Publication type:
- Article
Reducing TMPRSS6 ameliorates hemochromatosis and β-thalassemia in mice.
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- Journal of Clinical Investigation, 2013, v. 123, n. 4, p. 1531, doi. 10.1172/JCI66969
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- Publication type:
- Article
Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice.
- Published in:
- 2010
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- Publication type:
- journal article
Therapeutic haemoglobin synthesis in beta-thalassaemic mice expressing lentivirus-encoded human beta-globin.
- Published in:
- Nature, 2000, v. 406, n. 6791, p. 82, doi. 10.1038/35017565
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- Publication type:
- Article
Pleckstrin-2 is essential for erythropoiesis in β-thalassemic mice, reducing apoptosis and enhancing enucleation.
- Published in:
- Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02046-9
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- Publication type:
- Article
TMPRSS6 as a Therapeutic Target for Disorders of Erythropoiesis and Iron Homeostasis.
- Published in:
- Advances in Therapy, 2023, v. 40, n. 4, p. 1317, doi. 10.1007/s12325-022-02421-w
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- Publication type:
- Article
Changes in bone microarchitecture and biomechanical properties in the th3 thalassemia mouse are associated with decreased bone turnover and occur during the period of bone accrual.
- Published in:
- 2010
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- Publication type:
- journal article
Combination of a TGF‐β ligand trap (RAP‐GRL) and TMPRSS6‐ASO is superior for correcting β‐thalassemia.
- Published in:
- American Journal of Hematology, 2024, v. 99, n. 7, p. 1300, doi. 10.1002/ajh.27332
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- Publication type:
- Article
Iron restriction in sickle cell disease: When less is more.
- Published in:
- American Journal of Hematology, 2024, v. 99, n. 7, p. 1349, doi. 10.1002/ajh.27267
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- Publication type:
- Article
Transferrin receptor 2 (Tfr2) genetic deletion makes transfusion‐independent a murine model of transfusion‐dependent β‐thalassemia.
- Published in:
- American Journal of Hematology, 2022, v. 97, n. 10, p. 1324, doi. 10.1002/ajh.26673
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- Publication type:
- Article
Management of non‐transfusion‐dependent β‐thalassemia (NTDT): The next 5 years.
- Published in:
- American Journal of Hematology, 2021, v. 96, n. 3, p. E57, doi. 10.1002/ajh.26055
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- Publication type:
- Article
Therapeutic Hemoglobin Levels after Gene Transfer in β-Thalassemia Mice and in Hematopoietic Cells of β-Thalassemia and Sickle Cells Disease Patients.
- Published in:
- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0032345
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- Publication type:
- Article