Novel players in β-thalassemia dyserythropoiesis and new therapeutic strategies
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Hematology
Reference27 articles.
1. Phenotype—genotype relationships in monogenic disease: lessons from the thalassaemias
2. Protein Quality Control During Erythropoiesis and Hemoglobin Synthesis
3. β-thalassemia: a model for elucidating the dynamic regulation of ineffective erythropoiesis and iron metabolism
4. Erythroferrone contributes to hepcidin suppression and iron overload in a mouse model of β-thalassemia
5. Suppression of Fas-FasL coexpression by erythropoietin mediates erythroblast expansion during the erythropoietic stress response in vivo
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1. Therapeutic Relevance of Inducing Autophagy in β-Thalassemia;Cells;2024-05-25
2. Increased Expression of α-Hemoglobin Stabilizing Protein (AHSP) mRNA in Erythroid Precursor Cells Isolated from β-Thalassemia Patients Treated with Sirolimus (Rapamycin);Journal of Clinical Medicine;2024-04-24
3. The interactions between ineffective erythropoiesis and ferroptosis in β-thalassemia;Frontiers in Physiology;2024-02-26
4. Effects of Beta-Thalassemia on COVID-19 Outcomes;Thalassemia Syndromes - New Insights and Transfusion Modalities;2023-11-22
5. Luspatercept stimulates erythropoiesis, increases iron utilization, and redistributes body iron in transfusion‐dependent thalassemia;American Journal of Hematology;2023-10-02
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