Induction of gamma-globin gene transcription by hydroxycarbamide in primary erythroid cell cultures from Lepore patients
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2008.07041.x/fullpdf
Reference43 articles.
1. Flow Cytometric Analysis of Hydroxyurea Effects on Fetal Hemoglobin Production in Cultures of β‐Thalassemia Erythroid Precursors
2. Localization of the site of recombination in formation of the Lepore Boston globin gene.
3. Fetal hemoglobin in acute and chronic states of erythroid expansion
4. Hydroxyurea can eliminate transfusion requirements in children with severe β-thalassemia
5. The Corfu δβ thalassemia deletion disrupts γ-globin gene silencing and reveals post-transcriptional regulation of HbF expression
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1. Emerging therapies in β-thalassemia: toward a new era in management;Expert Opinion on Emerging Drugs;2020-04-02
2. Efficacy of Rapamycin as Inducer of Hb F in Primary Erythroid Cultures from Sickle Cell Disease andβ-Thalassemia Patients;Hemoglobin;2015-05-27
3. Non-Transfusion Dependent Thalassemia: Translating Evidence to Guidelines;Thalassemia Reports;2014-12-04
4. Quantification ofHBGmRNA in primary erythroid cultures: prediction of the response to hydroxyurea in sickle cell and beta-thalassemia;European Journal of Haematology;2013-10-22
5. Clinical experience with fetal hemoglobin induction therapy in patients with β-thalassemia;Blood;2013-03-21
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