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Stem Cell Res ; 73: 103228, 2023 12.
Artículo en Inglés | MEDLINE | ID: mdl-37890329

RESUMEN

Hemoglobin E (HbE), a common variant in Southeast Asian populations, results from a G to A substitution at codon 26 of the HBB gene, causing abnormal Hb and mild ß-thalassemia-like symptoms. Here, we derived an induced pluripotent stem cell (iPSC) line, named MUi033-A, from a male homozygous for HbE. The iPSC line demonstrates a normal karyotype and embryonic stem cell-like properties including pluripotency gene expression, and tri-lineage differentiation potential. This iPSC resource holds the potential for investigating gene therapy targeting HbE mutation.


Asunto(s)
Hemoglobina E , Células Madre Pluripotentes Inducidas , Talasemia beta , Humanos , Masculino , Hemoglobina E/genética , Hemoglobina E/metabolismo , Células Madre Pluripotentes Inducidas/metabolismo , Mutación , Talasemia beta/genética , Talasemia beta/metabolismo , Talasemia beta/terapia , Homocigoto
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