Quantification of HBG mRNA in primary erythroid cultures: prediction of the response to hydroxyurea in sickle cell and beta-thalassemia.
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Variation in Gamma-Globin Expression before and after Induction with Hydroxyurea Associated with BCL11A, KLF1 and TAL1.Recent trends for novel options in experimental biological therapy of β-thalassemia.Recent trends in the gene therapy of β-thalassemia.Study on Hydroxyurea Response in Hemoglobinopathies Patients Using Genetic Markers and Liquid Erythroid Cultures.Efficacy of Rapamycin as Inducer of Hb F in Primary Erythroid Cultures from Sickle Cell Disease and β-Thalassemia Patients.In Vitro Hb Production in B-thalassemia Patients Is Not a Predictor of Clinical Responsiveness to HydroxyureaHistone deacetylase inhibitors suppress ABO transcription in vitro, leading to reduced expression of the antigens.Orphan Drugs and Potential Novel Approaches for Therapies of β-Thalassemia: Current Status and Future Expectations
P2860
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P2860
Quantification of HBG mRNA in primary erythroid cultures: prediction of the response to hydroxyurea in sickle cell and beta-thalassemia.
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name
Quantification of HBG mRNA in ...... kle cell and beta-thalassemia.
@en
Quantification of HBG mRNA in ...... kle cell and beta-thalassemia.
@nl
type
label
Quantification of HBG mRNA in ...... kle cell and beta-thalassemia.
@en
Quantification of HBG mRNA in ...... kle cell and beta-thalassemia.
@nl
prefLabel
Quantification of HBG mRNA in ...... kle cell and beta-thalassemia.
@en
Quantification of HBG mRNA in ...... kle cell and beta-thalassemia.
@nl
P2093
P2860
P50
P356
P1476
Quantification of HBG mRNA in ...... kle cell and beta-thalassemia.
@en
P2093
Antonio Troia
Concetta Scazzone
Paolo Rigano
Roberta Calzolari
Rosalba Di Marzo
P2860
P356
10.1111/EJH.12204
P577
2013-10-22T00:00:00Z