Combining gene therapy and fetal hemoglobin induction for treatment of β-thalassemia
Author:
Publisher
Informa UK Limited
Subject
Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1586/ehm.13.24
Reference117 articles.
1. Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies
2. Screening and genetic diagnosis of haemoglobin disorders
3. Beta-thalassemia
4. Global burden, distribution and prevention of β-thalassemias and hemoglobin E disorders
5. Molecular therapies in ?-thalassaemia
Cited by 13 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Combined approaches for increasing fetal hemoglobin (HbF) and de novo production of adult hemoglobin (HbA) in erythroid cells from β-thalassemia patients: treatment with HbF inducers and CRISPR-Cas9 based genome editing;Frontiers in Genome Editing;2023-07-17
2. Co-Treatment of Erythroid Cells from β-Thalassemia Patients with CRISPR-Cas9-Based β039-Globin Gene Editing and Induction of Fetal Hemoglobin;Genes;2022-09-26
3. Gene Therapy of the Hemoglobinopathies;HemaSphere;2020-09-11
4. Gene Therapy for Beta-Hemoglobinopathies: Milestones, New Therapies and Challenges;Molecular Diagnosis & Therapy;2019-01-30
5. Novel and innovative approaches for treatment of β-thalassemia;Pediatric Hematology Oncology Journal;2017-12
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