000 01765 a2200469 4500
005 20250517113638.0
264 0 _c20170626
008 201706s 0 0 eng d
022 _a1535-3699
024 7 _a10.1177/1535370216668052
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aFornari, Thais A
245 0 0 _aFeatured 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.
_h[electronic resource]
260 _bExperimental biology and medicine (Maywood, N.J.)
_c02 2017
300 _a267-274 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAntigens, CD34
_xmetabolism
650 0 4 _aBase Sequence
650 0 4 _aCarrier Proteins
_xgenetics
650 0 4 _aDown-Regulation
_xgenetics
650 0 4 _aFemale
650 0 4 _aFetal Hemoglobin
_xgenetics
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMicroRNAs
_xbiosynthesis
650 0 4 _aNuclear Proteins
_xgenetics
650 0 4 _aReal-Time Polymerase Chain Reaction
650 0 4 _aRepressor Proteins
650 0 4 _aSOXD Transcription Factors
_xgenetics
650 0 4 _aSequence Analysis, DNA
650 0 4 _aSequence Deletion
_xgenetics
650 0 4 _abeta-Globins
_xgenetics
650 0 4 _abeta-Thalassemia
_xgenetics
650 0 4 _adelta-Thalassemia
_xgenetics
650 0 4 _agamma-Globins
_xgenetics
700 1 _aLanaro, Carolina
700 1 _aAlbuquerque, Dulcinéia M
700 1 _aFerreira, Regiane
700 1 _aCosta, Fernando F
773 0 _tExperimental biology and medicine (Maywood, N.J.)
_gvol. 242
_gno. 3
_gp. 267-274
856 4 0 _uhttps://doi.org/10.1177/1535370216668052
_zAvailable from publisher's website
999 _c26387050
_d26387050