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Paper Details

Control of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translation.
Nat Genet
60
2020
-thalassemia1, BCL11A, BCL11A mRNA, BCL11A protein, HbF, LIN28B, fetal hemoglobin, genes, human, human hemoglobin, let-7 microRNAs, mRNA, messenger RNA, sickle cell disease
Author NameAffiliation
Jacob C UlirschBoston Children's Hospital, Harvard Medical School
Jacob C UlirschHarvard Medical School
Jacob C UlirschBroad Institute of Massachusetts Institute of Technology and Harvard
Jacob C UlirschDana-Farber Cancer Institute, Harvard Medical School
Charles M RiceThe Rockefeller University
Steven A CarrBroad Institute of Massachusetts Institute of Technology and Harvard
Steven A CarrBroad Institute of Massachusetts Institute of Technology and Harvard
Stuart H OrkinBoston Children's Hospital, Harvard Medical School
Stuart H OrkinDana-Farber Cancer Institute, Harvard Medical School
Stuart H OrkinBroad Institute of Massachusetts Institute of Technology and Harvard
Eric S LanderBroad Institute of Massachusetts Institute of Technology and Harvard
Eric S LanderMassachusetts Institute of Technology
Eric S LanderHarvard Medical School
Eric S LanderBroad Institute of Massachusetts Institute of Technology and Harvard
Eric S LanderMassachusetts Institute of Technology
Eric S LanderHarvard Medical School
Vijay G SankaranBoston Children's Hospital, Harvard Medical School
Vijay G SankaranDana-Farber Cancer Institute, Harvard Medical School
Vijay G SankaranBroad Institute of Massachusetts Institute of Technology and Harvard
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Release 1.2