Featured Article: Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting microRNAs.

Fornari, Thais A

Featured Article: Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting microRNAs. [electronic resource] - Experimental biology and medicine (Maywood, N.J.) 02 2017 - 267-274 p. digital

Publication Type: Journal Article

1535-3699

10.1177/1535370216668052 doi


Antigens, CD34--metabolism
Base Sequence
Carrier Proteins--genetics
Down-Regulation--genetics
Female
Fetal Hemoglobin--genetics
Humans
Male
MicroRNAs--biosynthesis
Nuclear Proteins--genetics
Real-Time Polymerase Chain Reaction
Repressor Proteins
SOXD Transcription Factors--genetics
Sequence Analysis, DNA
Sequence Deletion--genetics
beta-Globins--genetics
beta-Thalassemia--genetics
delta-Thalassemia--genetics
gamma-Globins--genetics