Works by Breda, Laura
Results: 22
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.
- Published in:
- 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:
- 2012
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- Publication type:
- journal article
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
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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- Article
Quand l'ubiquitination se mêle du mélanome cutané: Un mécanisme à explorer.
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- Médecine Sciences, 2024, v. 40, n. 3, p. 308, doi. 10.1051/medsci/2024021
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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.
- Published in:
- 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
Complexation to Cationic Microspheres of Double-Stranded Peptide Nucleic Acid-DNA Chimeras Exhibiting Decoy Activity.
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- Journal of Biomedical Science, 2004, v. 11, n. 5, p. 697, doi. 10.1007/BF02256136
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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
Formulations for natural and peptide nucleic acids based on cationic polymeric submicron particles.
- Published in:
- AAPS Journal, 2004, v. 6, n. 1, p. 10, doi. 10.1208/ps060102
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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.
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- 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
The challenging diagnosis of cranial congenital anomalies in a newborn from an Italian 20th century documented skeletal collection.
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- International Journal of Osteoarchaeology, 2021, v. 31, n. 2, p. 309, doi. 10.1002/oa.2952
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- Article
Macrophages support pathological erythropoiesis in polycythemia vera and β-thalassemia.
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- Nature Medicine, 2013, v. 19, n. 4, p. 437, doi. 10.1038/nm.3126
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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
Gene Therapy for Beta-Hemoglobinopathies: Milestones, New Therapies and Challenges.
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- Molecular Diagnosis & Therapy, 2019, v. 23, n. 2, p. 173, doi. 10.1007/s40291-019-00383-4
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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 Hemoglobin Levels after Gene Transfer in β-Thalassemia Mice and in Hematopoietic Cells of β-Thalassemia and Sickle Cells Disease Patients.
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- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0032345
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- Publication type:
- Article
A validated cellular biobank for β-thalassemia.
- Published in:
- 2016
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- Publication type:
- journal article