CCND3 Suppression Ameliorates β-Thalassaemia in a Murine Disease Model: A Potential Therapeutic Strategy. [PDF]
Caria CA +9 more
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Orai1 acts as a novel Ca<sup>2+</sup> signal switch, balancing erythropoiesis through KLF1 regulation. [PDF]
Lee YY +5 more
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Revisiting hemoglobin constant spring: molecular insights, pathophysiological mechanisms, and clinical perspectives. [PDF]
Wongkhammul N +3 more
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A functional overlap between actively transcribed genes and chromatin insulator elements. [PDF]
Cornell LJ +16 more
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Transcriptomic data of piglet blood compartments with 3' mRNA sequencing. [PDF]
Payros G +5 more
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Systematic Review of Non-Coding Genomic Variants in Globin and Non-Globin Clusters and Their Impact on Phenotypic Severity in Thalassemia and Sickle Cell Disease. [PDF]
Al-Subaie AM, Borgio JF.
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Lentiviral vectors for hematopoietic stem cell gene therapy restore α-globin expression in α-thalassemia red blood cells. [PDF]
Segura EER +18 more
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Multiomics analysis of red blood cells reveals thalassemia severity beyond globin gene mutations. [PDF]
Mitra N +6 more
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Functional correction and genome integrity with duplex base editing of β-thalassemic hematopoietic stem cells. [PDF]
Papaioannou NY +11 more
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Clinical value of miR-329-3p in thalassemia and its regulation of TNRC6B expression. [PDF]
Zhao Y, Gao J, Li Y, Li S, Li W, Cen M.
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