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首页> 外文期刊>Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation >Early Results of a Phase I/II Study of Gene Therapy for beta-Thalassemia Major Via Transplantation of Autologous Hematopoietic Stem Cells Transduced Ex-Vivo with a Lentiviral beta(AT87Q)-Globin Vector

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Early Results of a Phase I/II Study of Gene Therapy for beta-Thalassemia Major Via Transplantation of Autologous Hematopoietic Stem Cells Transduced Ex-Vivo with a Lentiviral beta(AT87Q)-Globin Vector

机译：通过慢病毒β（AT87Q）-Globin载体体外转导的自体造血干细胞移植，对β-地中海贫血基因治疗的I / II期研究的早期结果

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来源
《Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation 》 |2015年第1期| 共2页
作者
Soni Sandeep; Thompson Alexis A.; Walters Mark; Leboulch Philippe; Cavazzana Marina;
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正文语种 eng
中图分类治疗学 ;
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1. 小剂量5-FU提高携带VEGF siRNA的腺病毒载体对肿瘤细胞的转导效率和基因治疗效果的研究 [J] . 王丰, 李惠明, 陈霞芳癌症（英文版） . 2010 ,第007期
2. Early Results of a Phase I/II Study of Gene Therapy for beta-Thalassemia Major Via Transplantation of Autologous Hematopoietic Stem Cells Transduced Ex-Vivo with a Lentiviral beta(AT87Q)-Globin Vector [J] . Soni Sandeep, Thompson Alexis A., Walters Mark, Biology of blood and marrow transplantation: journal of the American Society for Blood and Marrow Transplantation . 2015 ,第2Suppla1期

机译：通过慢病毒β（AT87Q）-Globin载体体外转导的自体造血干细胞移植，对β-地中海贫血基因治疗的I / II期研究的早期结果
3. Amelioration of murine beta-thalassemia through drug selection of hematopoietic stem cells transduced with a lentiviral vector encoding both gamma-globin and the MGMT drug-resistance gene. [J] . Zhao H, Pestina TI, Nasimuzzaman M, Blood: The Journal of the American Society of Hematology . 2009 ,第23期

机译：通过用编码γ-珠蛋白和MGMT耐药基因的慢病毒载体转导的造血干细胞的药物选择来改善鼠β地中海贫血。
4. Efficacy and safety of multiple doses of NEPA without dexamethasone in preventing nausea and vomiting induced by multiple-day and high-dose chemotherapy in patients with non-Hodgkin's lymphoma undergoing autologous hematopoietic stem cell transplantation: a phase IIa, multicenter study [J] . Di Renzo Nicola, Musso Maurizio, Scime Rosanna, Bone marrow transplantation . 2020 ,第11期

机译：多剂量Nepa的疗效和安全性没有地塞米松预防多日和高剂量化疗诱导的非Hodgkin淋巴瘤患者患者进行自体造血干细胞移植患者的恶心和呕吐：A相IIA，多中心研究
5. HIGH DOSE THERAPY WITH AUTOLOGOUS HEMATOPOIETIC STEM CELL TRANSPLANTATION (HSCT) FOR PATIENTS WITH PRIMARY SYSTEMIC AMYLOIDOSIS (AL): AN ABMTR STUDY [C] . DH Vesole, W Perez, D Reece, International Symposium on Amyloidosis . 2005

机译：具有自体造血干细胞移植（HSCT）的高剂量治疗用于初级全身淀粉样蛋白症（AL）的患者：ABMTR研究
6. Transduction of hematopoietic stem cells using lentiviral vectors in models of drug resistance gene therapy: Determinants of transduction and selection. [D] . Zielske, Steven Paul. 2003

机译：在耐药基因治疗模型中使用慢病毒载体对造血干细胞的转导：转导和选择的决定因素。
7. Gene Therapy: Sustained high-level polyclonal hematopoietic marking and transgene expression 4 years after autologous transplantation of rhesus macaques with SIV lentiviral vector–transduced CD34+ cells [O] . Yoo-Jin Kim, Yoon-Sang Kim, Andre Larochelle, -1

机译：基因治疗：自体移植恒河猴猕猴与SIV慢病毒载体转导的CD34 +细胞后4年持续的高水平多克隆造血标记和转基因表达
8. Early Results of a Phase I/ II Study of Gene Therapy for β-Thalassemia Major Via Transplantation of Autologous Hematopoietic Stem Cells Transduced Ex-Vivo with a Lentiviral βAT87Q -Globin Vector [O] . Soni Sandeep, Thompson Alexis A., Walters Mark, 2015

机译：通过慢病毒βAT87Q-球蛋白载体体外转导的自体造血干细胞的移植，对β-地中海贫血基因治疗的I / II期研究的早期结果

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