Activation of γ-globin gene expression by GATA1 and NF-Y in hereditary persistence of fetal hemoglobin

Hereditary persistence of fetal hemoglobin (HPFH) ameliorates β-hemoglobinopathies by inhibiting the developmental switch from γ-globin (HBG1/HBG2) to β-globin (HBB) gene expression. Some forms of HPFH are associated with γ-globin promoter variants that either disrupt binding motifs for transcriptio...

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Detalles Bibliográficos
Autores principales: Doerfler, Phillip A., Feng, Ruopeng, Li, Yichao, Palmer, Lance E., Porter, Shaina N., Bell, Henry W., Crossley, Merlin, Pruett-Miller, Shondra M., Cheng, Yong, Weiss, Mitchell J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8610173/
https://www.ncbi.nlm.nih.gov/pubmed/34341563
http://dx.doi.org/10.1038/s41588-021-00904-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8610173/
https://www.ncbi.nlm.nih.gov/pubmed/34341563
http://dx.doi.org/10.1038/s41588-021-00904-0

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