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104. Therapeutic haemoglobin synthesis in β-thalassaemic mice expressing lentivirus-encoded human β-globin

110. 2'-O-Methoxyethyl Splice-Switching Oligos to Reverse Splicing from IVS2-745 β-Thalassemia Patient Cells: A Foundation for Potential Therapies

112. PP-14, a Novel Structurally-Enhanced Antisickling Allosteric Hemoglobin Effector, Increases Oxygen Affinity and Disrupts Hemoglobin S Polymer Formation

113. Erythroferrone Regulates Bone Remodeling in β-Thalassemia

128. Development and characterization of cellular biosensors for HTS of erythroid differentiation inducers targeting the transcriptional activity of γ-globin and β-globin gene promoters

130. Interleukin-6 Contributes to the Development of Anemia in Juvenile CKD

132. Correcting Non-Transfusion Dependent β-Thalassemia by Utilizing a Combined Therapy that Modulates EPO Activity by Limiting Erythroid Cellular Iron Intake

133. Lack of GDF11 Does Not Ameliorate Erythropoiesis in β-Thalassemia and Does Not Prevent the Activity of the Trap-Ligand RAP-536

134. Improved Lentiviral Vectors for the Cure of Hemoglobinopathies

137. The European Hematology Association Roadmap for European Hematology Research: a consensus document

138. Hepcidin is an HDAC3 regulated gene and its expression is determined by promoter-associated histone acetylation

141. Emerging Therapies

145. The multicenter THALAMOSS cellular Biobank for β-Thalassemia

146. MOESM2 of A validated cellular biobank for β-thalassemia

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