A unified model of human hemoglobin switching through single-cell genome editing

Key mechanisms of fetal hemoglobin (HbF) regulation and switching have been elucidated through studies of human genetic variation, including mutations in the HBG1/2 promoters, deletions in the β-globin locus, and variation impacting BCL11A. While this has led to substantial insights, there has not b...

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Detalles Bibliográficos
Autores principales: Shen, Yong, Verboon, Jeffrey M., Zhang, Yuannyu, Liu, Nan, Kim, Yoon Jung, Marglous, Samantha, Nandakumar, Satish K., Voit, Richard A., Fiorini, Claudia, Ejaz, Ayesha, Basak, Anindita, Orkin, Stuart H., Xu, Jian, Sankaran, Vijay G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8371164/
https://www.ncbi.nlm.nih.gov/pubmed/34404810
http://dx.doi.org/10.1038/s41467-021-25298-9

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