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Development of lentiviral vectors expressing multiple small interfering RNAs as a gene therapy approach against HIV-1 infectionud

机译：表达多种小干扰RNA的慢病毒载体的开发作为抗HIV-1感染的基因治疗方法 ud

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Spanevello Francesca;
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年度 2014
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1. Optimized lentiviral vectors for HIV gene therapy: Multiplexed expression of small RNAs and inclusion of MGMT P140K drug resistance gene [J] . ChungJ., SchererL.J., GuA., Molecular therapy: the journal of the American Society of Gene Therapy . 2014,第5期

机译：用于HIV基因治疗的优化慢病毒载体：小RNA的多重表达和MGMT P140K耐药基因的纳入
2. Gene therapy of HIV-1 infection using lentiviral vectors expressing anti-HIV-1 genes. [J] . Mautino MarioR, Morgan RichardA AIDS patient care and STDs . 2002,第1期

机译：使用表达抗HIV-1基因的慢病毒载体对HIV-1感染进行基因治疗。
3. A general method for gene knockdown in mice by using lentiviral vectors expressing small interfering RNA. [J] . Tiscornia G, Singer O, Ikawa M, Proceedings of the National Academy of Sciences of the United States of America . 2003,第4期

机译：通过使用表达小干扰RNA的慢病毒载体在小鼠中进行基因敲低的一般方法。
4. Lentiviral Vector-Mediated in Vitro Down-Regulation of Porcine Somatostatin Expression Using shRNA [C] . Jing-hua Ding, Qian-yun Xi, Hong-yi Li International Conference on Materials for Environmental Protection and Energy Application . 2012

机译：慢病毒载体介导的在体外下调猪生长抑制素的表达使用shRNA
5. Engineering lentiviral vectors for gene therapy and development of live cell arrays for dynamic gene expression profiling. [D] . Tian, Jun. 2010

机译：用于基因治疗的工程慢病毒载体，以及用于动态基因表达谱分析的活细胞阵列的开发。
6. Development of Lentiviral Vectors Simultaneously Expressing Multiple siRNAs Against CCR5 vif and tat/rev Genes for an HIV-1 Gene Therapy Approach [O] . Francesca Spanevello, Arianna Calistri, Claudia Del Vecchio, 2016

机译：同时表达针对CCR5vif和tat / rev基因的多种siRNA的慢病毒载体的开发用于HIV-1基因治疗方法
7. Development of Lentiviral Vectors Simultaneously Expressing Multiple siRNAs Against CCR5, vif and tat/rev Genes for an HIV-1 Gene Therapy Approach [O] . SPANEVELLO, F, CALISTRI, A, DEL VECCHIO, C, 2016

机译：同时表达针对CCR5，vif和tat / rev基因的多种siRNA的慢病毒载体的开发，用于HIV-1基因治疗方法

Development of lentiviral vectors expressing multiple small interfering RNAs as a gene therapy approach against HIV-1 infectionud

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