首页> 外文OA文献 >548. Recombinant AAV3 Serotype Vectors Generated by Using AAV3 ITRs and AAV3 Rep Proteins Efficiently Transduce Human Liver Cancer Cell Lines In Vitro and Human Liver Tumors in a Murine Xenograft Model In Vivo

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548. Recombinant AAV3 Serotype Vectors Generated by Using AAV3 ITRs and AAV3 Rep Proteins Efficiently Transduce Human Liver Cancer Cell Lines In Vitro and Human Liver Tumors in a Murine Xenograft Model In Vivo

机译：548.通过使用AAV3 ITR和AAV3 Rep蛋白产生的重组AAV3血清型载体在小鼠异种移植模型体内有效地体外转导人肝癌细胞系和人肝肿瘤。

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2017-08-30T02:06:24Z

机译：2017-08-30T02：06：24Z

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Pediatrics, University of Florida College of Medicine, Gainesville, FL ( host institution ); Ling, Chen ( UF author ); Yin, Zifei ( author ); Li, Jun ( UF author ); Zhang, Daniel ( UF author ); Aslanidi, George ( UF author ); Srivastava, Arun ( UF author );
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年度 2016
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专利

1. Selective In Vivo Targeting of Human Liver Tumors by Optimized AAV3 Vectors in a Murine Xenograft Model [J] . Ling Chen, Wang Yuan, Zhang Yuanhui, Human gene therapy . 2014,第12期

机译：通过优化的AAV3载体在小鼠异种移植模型中对人肝肿瘤的选择性体内靶向。
2. Development of optimized AAV3 serotype vectors: Mechanism of high-efficiency transduction of human liver cancer cells [J] . ChengB., LingC., DaiY., Gene therapy . 2012,第4期

机译：优化的AAV3血清型载体的开发：人肝癌细胞高效转导的机制
3. Strategies to generate high-titer, high-potency recombinant AAV3 serotype vectors [J] . Chen Ling, Zifei Yin, Jun Li, Molecular Therapy - Methods & Clinical Development . 2016,第9期

机译：产生高滴度，高效率的重组AAV3血清型载体的策略
4. Intracellular Delivery of Recombinant Human Proteins into Mammalian cells as a Potential Therapeutic Approach [C] . Papadopoulou LC, Foltopoulou PF Tsiftsoglou AS European Biological Inorganic Chemistry Conference . 2010

机译：将重组人蛋白的细胞内递送到哺乳动物细胞中作为潜在的治疗方法
5. Clinical predictive value of pre-clinical cancer models: A study of the predictive value of the in vitro cell line, human xenograft and murine allograft pre-clinical cancer models for phase II clinical trials of cytotoxic cancer drugs [D] . Voskoglou-Nomikos, Theodora 2001

机译：临床前癌症模型的临床预测价值：体外细胞系，人异种移植和小鼠同种异体移植临床前癌症模型对细胞毒性癌症药物II期临床试验的预测价值研究
6. Selective In Vivo Targeting of Human Liver Tumors by Optimized AAV3 Vectors in a Murine Xenograft Model [O] . Chen Ling, Yuan Wang, Yuanhui Zhang, -1

机译：通过优化的AAV3载体在小鼠异种移植模型中对人肝肿瘤的选择性体内靶向。
7. 77. Targeted Delivery and Suppression of Human Liver Tumorigenesis By Optimized Recombinant AAV3 Vectors in a Murine Xenograft Model [O] . 2014

机译：77.通过优化的重组AAV3载体在鼠异叶移植模型中的靶向递送和抑制人肝肿瘤

548. Recombinant AAV3 Serotype Vectors Generated by Using AAV3 ITRs and AAV3 Rep Proteins Efficiently Transduce Human Liver Cancer Cell Lines In Vitro and Human Liver Tumors in a Murine Xenograft Model In Vivo

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