Amelioration of Sardinian 0 thalassemia by genetic modifiers
Author:
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Reference11 articles.
1. Genotype-phenotype correlations in β-thalassemias
2. Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults
3. A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15
4. Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of -thalassemia
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3. The Long Scientific Journey of Sirolimus (Rapamycin): From the Soil of Easter Island (Rapa Nui) to Applied Research and Clinical Trials on β-Thalassemia and Other Hemoglobinopathies;Biology;2023-09-02
4. 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
5. Frequency of secondary modifiers in Beta Thalassemia intermedia in patients from Northern Punjab;Pakistan Journal of Medical Sciences;2023-07-10
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