Fornari, Thais A <br/><br/>
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 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1535-3699 
<br/><br/><label>Standard No.: </label>10.1177/1535370216668052  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Antigens, CD34--metabolism<br/>Base Sequence<br/>Carrier Proteins--genetics<br/>Down-Regulation--genetics<br/>Female<br/>Fetal Hemoglobin--genetics<br/>Humans<br/>Male<br/>MicroRNAs--biosynthesis<br/>Nuclear Proteins--genetics<br/>Real-Time Polymerase Chain Reaction<br/>Repressor Proteins<br/>SOXD Transcription Factors--genetics<br/>Sequence Analysis, DNA<br/>Sequence Deletion--genetics<br/>beta-Globins--genetics<br/>beta-Thalassemia--genetics<br/>delta-Thalassemia--genetics<br/>gamma-Globins--genetics