Control of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translation

Increased production of fetal hemoglobin (HbF) can ameliorate the severity of sickle cell disease and β-thalassemia(1). BCL11A represses the genes encoding HbF and regulates human hemoglobin switching through variation in its expression during development(2–7). However, the mechanisms underlying the...

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Detalles Bibliográficos
Autores principales: Basak, Anindita, Munschauer, Mathias, Lareau, Caleb A., Montbleau, Kara E., Ulirsch, Jacob C., Hartigan, Christina R., Schenone, Monica, Lian, John, Wang, Yaomei, Huang, Yumin, Wu, Xianfang, Gehrke, Lee, Rice, Charles M., An, Xiuli, Christou, Helen A., Mohandas, Narla, Carr, Steven A., Chen, Jane-Jane, Orkin, Stuart H., Lander, Eric S., Sankaran, Vijay G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031047/
https://www.ncbi.nlm.nih.gov/pubmed/31959994
http://dx.doi.org/10.1038/s41588-019-0568-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7031047/
https://www.ncbi.nlm.nih.gov/pubmed/31959994
http://dx.doi.org/10.1038/s41588-019-0568-7

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