Development and characterization of K562 cell clones expressing BCL11A-XL: Decreased hemoglobin production with fetal hemoglobin inducers and its rescue with mithramycin

Induction of fetal hemoglobin (HbF) is considered a promising strategy in the treatment of β-thalassemia, in which production of adult hemoglobin (HbA) is impaired by mutations affecting the β-globin gene. Recent results indicate that B-cell lymphoma/leukemia 11A (BCL11A) is a major repressor of γ-g...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Exp Hematol
Hauptverfasser: Finotti, Alessia, Gasparello, Jessica, Breveglieri, Giulia, Cosenza, Lucia Carmela, Montagner, Giulia, Bresciani, Alberto, Altamura, Sergio, Bianchi, Nicoletta, Martini, Elisa, Gallerani, Eleonora, Borgatti, Monica, Gambari, Roberto
Format: Artigo
Sprache:Inglês
Veröffentlicht: Elsevier Science Inc 2015
Schlagworte:
Normal Hematopoiesis
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4670904/
https://ncbi.nlm.nih.gov/pubmed/26342260
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.exphem.2015.08.011
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!

Ähnliche Einträge