2022
DOI: 10.3390/medicina58101470
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miRNA Expression Associated with HbF in Saudi Sickle Cell Anemia

Abstract: Background and Objectives: Sickle cell anemia (SCA) is a hereditary monogenic disease due to a single β-globin gene mutation that codes for the production of sickle hemoglobin. Its phenotype is modulated by fetal hemoglobin (HbF), a product of γ-globin genes. Exploring the molecules that regulate γ-globin genes at both transcriptional and translational levels, including microRNA (miRNA), might help identify alternative therapeutic targets. Materials and Methods: Using next-generation sequencing we identified p… Show more

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“…Patients with high fetal hemoglobin (HbF) status, which is a product of γ-globin genes and modulates SCD, experience fewer painful crises and enhanced survival rates [ 75 ]. Examining the factors that control γ-globin genes at both transcriptional and translational levels, including miRNAs, can assist in the identification of possible therapeutic avenues for SCD [ 76 , 77 ].…”
Section: The Advent Of New Technologiesmentioning
confidence: 99%
“…Patients with high fetal hemoglobin (HbF) status, which is a product of γ-globin genes and modulates SCD, experience fewer painful crises and enhanced survival rates [ 75 ]. Examining the factors that control γ-globin genes at both transcriptional and translational levels, including miRNAs, can assist in the identification of possible therapeutic avenues for SCD [ 76 , 77 ].…”
Section: The Advent Of New Technologiesmentioning
confidence: 99%