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Lentiviral gene

Xem 1-13 trên 13 kết quả Lentiviral gene
  • Lentiviral gene delivery is now considered as a major candidate in the future of cancer therapy. To avoid common side-effects associated with methods of cancer therapy, the survivin promoter shows great promise due to its high expression level in multiple cancers.

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  • High-Level Recombinant Protein Production in CHO Cells Using Lentiviral Vectors and the Cumate Gene-Switch developed  an efficient system to generate in less than 2 months, starting from the cDNA, pools of CHO cells stably expressing high-level of recombinant  proteins. It is based on lentiviral vectors (LVs) for stable transduction coupled with the cumate gene-switch for inducible and efficient gene expression.

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  • In the first section of this book, ‘Retroviral Vector’, chapter one discusses the efficiency of retroviral DNA integration, the preferences of integration for certain regions, and advances on integration site selection and gene therapy. Chapter two reviews and discusses the current cell lines and bioreaction platforms used for production of retroviral and lentiviral vectors, focusing on the current bottlenecks and future directions with a particular emphasis in the metabolic constrains.

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  • In the section on ‘Lentiviral Vector’, the generation of high-titre lentiviral vectors capable of efficiently expressing transgenes over long periods of time is governed by a number of vector design rules. Chapter thirteen highlights the guiding design principles and the technical of the successful lentiviral gene vector design. Chapter fourteen reviews current status of lentiviral vector development, especially the progress in the lentiviral vector systems allowing the controlling of gene expression.

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  • According to the most recent updates, retroviral and lentiviral vectors represent 23% of all the vector types and 33% of the viral vectors used in Gene Therapy clinical trials. Moreover, retroviral vectors are currently the blockbuster vectors for the treatment of monogenic and infectious diseases and gene marking clinical trials (Edelstein 2010). Retroviruses are double stranded RNA enveloped viruses mainly characterized by the ability to “reverse-transcribe” their genome from RNA to DNA.

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  • Tuyển tập các báo cáo nghiên cứu về sinh học được đăng trên tạp chí sinh học Journal of Biology đề tài: Lentiviral-mediated gene correction of mucopolysaccharidosis type IIIA

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  • They found that AAV5 and 7-syn-GFP resulted in the highest percentage of nigral dopaminergic neurons transduction, where AAV7 showed the highest efficiency in transducing the nigrostriatal projection pathway. Accordingly, they conclude that AAV7-syn-GFP is the most suitable SN gene delivery vehicle in mice. In the eleventh chapter, Okada et al. developed a new method of producing AAV vectors. They applied these AAV vectors in muscle transduction for the treatment of Duchenne muscular dystrophy (DMD). In chapter twelve, Sunico et al.

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  • Tuyển tập các báo cáo nghiên cứu về sinh học được đăng trên tạp chí sinh học Journal of Biology đề tài: Comparative analysis of HIV-1-based lentiviral vectors bearing lyssavirus glycoproteins for neuronal gene transfer

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  • Tuyển tập báo cáo các nghiên cứu khoa học quốc tế ngành hóa học dành cho các bạn yêu hóa học tham khảo đề tài: Multicistronic lentiviral vectors containing the FMDV 2A cleavage factor demonstrate robust expression of encoded genes at limiting MOI

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  • Tuyển tập các báo cáo nghiên cứu về hóa học được đăng trên tạp chí sinh học đề tài :Multicistronic lentiviral vectors containing the FMDV 2A cleavage factor demonstrate robust expression of encoded genes at limiting MOI

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  • Mucopolysaccharidosis type I (MPS I) results from a deficiency in the enzyme a-L-iduronidase (IDUA), and is characterized by skeletal abnormalities, hepatosplenomegaly and neurological dysfunction. In this study, we used a late generation lentiviral vector to evaluate the utility of this vector system for the transfer and expression of the human IDUA cDNA in MPS I fibroblasts. We observed that the level of enzyme expression in transduced cells was 1.5-fold the level found in normal cells; the expression persisted for at least two months....

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  • Tuyển tập các báo cáo nghiên cứu về sinh học được đăng trên tạp chí sinh học Journal of Biology đề tài: The significance of controlled conditions in lentiviral vector titration and in the use of multiplicity of infection (MOI) for predicting gene transfer events

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  • Gamma-retroviral vectors, commonly designated retroviral vectors, were the first viral vector employed in Gene Therapy clinical trials in 1990 and are still one of the most used. More recently, the interest in lentiviral vectors, derived from complex retroviruses such as the human immunodeficiency virus (HIV), has been growing due to their ability to transduce non-dividing cells (Lewis et al. 1992; Naldini et al. 1996), an attribute that distinguishes them from other viral vectors, including their simple counterparts, gammaretroviral vectors.

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