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PUBMED FOR HANDHELDS

Journal Abstract Search


177 related items for PubMed ID: 23782080

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  • 4. Therapeutic levels of fetal hemoglobin in erythroid progeny of β-thalassemic CD34+ cells after lentiviral vector-mediated gene transfer.
    Wilber A, Hargrove PW, Kim YS, Riberdy JM, Sankaran VG, Papanikolaou E, Georgomanoli M, Anagnou NP, Orkin SH, Nienhuis AW, Persons DA.
    Blood; 2011 Mar 10; 117(10):2817-26. PubMed ID: 21156846
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  • 5. Recent trends for novel options in experimental biological therapy of β-thalassemia.
    Finotti A, Gambari R.
    Expert Opin Biol Ther; 2014 Oct 10; 14(10):1443-54. PubMed ID: 24934764
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  • 6. Co-Treatment of Erythroid Cells from β-Thalassemia Patients with CRISPR-Cas9-Based β039-Globin Gene Editing and Induction of Fetal Hemoglobin.
    Cosenza LC, Zuccato C, Zurlo M, Gambari R, Finotti A.
    Genes (Basel); 2022 Sep 26; 13(10):. PubMed ID: 36292612
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  • 7. Clinical experience with fetal hemoglobin induction therapy in patients with β-thalassemia.
    Musallam KM, Taher AT, Cappellini MD, Sankaran VG.
    Blood; 2013 Mar 21; 121(12):2199-212; quiz 2372. PubMed ID: 23315167
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  • 8. Reactivation of Fetal Hemoglobin for Treating β-Thalassemia and Sickle Cell Disease.
    Cui S, Engel JD.
    Adv Exp Med Biol; 2017 Mar 21; 1013():177-202. PubMed ID: 29127681
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  • 9. Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypes.
    Sheehan VA, Luo Z, Flanagan JM, Howard TA, Thompson BW, Wang WC, Kutlar A, Ware RE, BABY HUG Investigators.
    Am J Hematol; 2013 Jul 21; 88(7):571-6. PubMed ID: 23606168
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  • 12. Lentiviral and genome-editing strategies for the treatment of β-hemoglobinopathies.
    Magrin E, Miccio A, Cavazzana M.
    Blood; 2019 Oct 10; 134(15):1203-1213. PubMed ID: 31467062
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  • 14. Alternative options for DNA-based experimental therapy of β-thalassemia.
    Gambari R.
    Expert Opin Biol Ther; 2012 Apr 10; 12(4):443-62. PubMed ID: 22413823
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  • 15. [γ-Globin Inductive Therapy of β-thalassemia and Its Relationship with MicroRNA].
    Li YY, Gu J, Yu DN.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2016 Apr 10; 24(2):627-31. PubMed ID: 27151042
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  • 16. [Reaserch Advances on Induction of Fetal Hemoglobin (HbF) by Drugs in the Treatment of β-Thalassemia--Review].
    Li L, Sun ZQ.
    Zhongguo Shi Yan Xue Ye Xue Za Zhi; 2020 Aug 10; 28(4):1424-1428. PubMed ID: 32798438
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  • 17. Efficacy of Rapamycin as Inducer of Hb F in Primary Erythroid Cultures from Sickle Cell Disease and β-Thalassemia Patients.
    Pecoraro A, Troia A, Calzolari R, Scazzone C, Rigano P, Martorana A, Sacco M, Maggio A, Di Marzo R.
    Hemoglobin; 2015 Aug 10; 39(4):225-9. PubMed ID: 26016899
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  • 18. Common fetal hemoglobin variants in Lebanese patients bearing the codon 29 beta gene mutation associated with different thalassemia phenotypes.
    Brancaleoni V, Moukhadder HM, Consonni D, Koussa S, Di Pierro E, Cappellini MD, Taher A.
    Ann Hematol; 2019 Apr 10; 98(4):833-840. PubMed ID: 30506348
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  • 20. Induction of hemoglobin F synthesis in patients with beta thalassemia.
    Ley TJ, Nienhuis AW.
    Annu Rev Med; 1985 Apr 10; 36():485-98. PubMed ID: 2581500
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