Optimized production and concentration of lentiviral vectors containing large inserts
暂无分享,去创建一个
J. Foerster | John Foerster | M. Romanowska | Nadya al Yacoub | Malgorzata Romanowska | Natalie Haritonova | N. Haritonova | Nadya al Yacoub
[1] A. Consiglio,et al. A new-generation stable inducible packaging cell line for lentiviral vectors. , 2001, Human gene therapy.
[2] J. Reiser. Production and concentration of pseudotyped HIV-1-based gene transfer vectors , 2000, Gene Therapy.
[3] M. Fussenegger,et al. Detailed design and comparative analysis of protocols for optimized production of high-performance HIV-1-derived lentiviral particles. , 2005, Metabolic engineering.
[4] T. Crombleholme,et al. Optimized large-scale production of high titer lentivirus vector pseudotypes. , 2004, Journal of virological methods.
[5] Y. Ron,et al. An inducible packaging cell system for safe, efficient lentiviral vector production in the absence of HIV-1 accessory proteins. , 2001, Virology.
[6] H. Bujard,et al. Doxycycline-regulated lentiviral vector system with a novel reverse transactivator rtTA2S-M2 shows a tight control of gene expression in vitro and in vivo , 2003, Gene Therapy.
[7] L. Kedes,et al. A high-titer lentiviral production system mediates efficient transduction of differentiated cells including beating cardiac myocytes. , 1999, Journal of molecular and cellular cardiology.
[8] B. Karolewski,et al. Comparison of transfection conditions for a lentivirus vector produced in large volumes. , 2003, Human gene therapy.
[9] D. Israeli,et al. Transactivator and structurally optimized inducible lentiviral vectors. , 2004, Molecular Therapy.
[10] C. Lois,et al. Retroviruses as tools to study the immune system. , 2001, Current opinion in immunology.
[11] T. Kafri,et al. A trans-lentiviral packaging cell line for high-titer conditional self-inactivating HIV-1 vectors. , 2006, Molecular therapy : the journal of the American Society of Gene Therapy.
[12] L. Crofford,et al. Highly efficient genetic transduction of primary human synoviocytes with concentrated retroviral supernatant , 2002, Arthritis Research & Therapy.
[13] I. Verma,et al. Generation of a stable cell line producing high-titer self-inactivating lentiviral vectors. , 2001, Molecular therapy : the journal of the American Society of Gene Therapy.
[14] Michael T. McManus,et al. A lentivirus-based system to functionally silence genes in primary mammalian cells, stem cells and transgenic mice by RNA interference , 2003, Nature Genetics.
[15] D. Trono,et al. A Third-Generation Lentivirus Vector with a Conditional Packaging System , 1998, Journal of Virology.
[16] D. Trono,et al. Lentiviral vectors and antiretroviral intrinsic immunity. , 2005, Human gene therapy.
[17] Brian Davis,et al. Generation of a packaging cell line for prolonged large‐scale production of high‐titer HIV‐1‐based lentiviral vector , 2005, The journal of gene medicine.
[18] M. Kumar,et al. Systematic determination of the packaging limit of lentiviral vectors. , 2001, Human gene therapy.
[19] R. Fässler. Lentiviral transgene vectors , 2004, EMBO reports.
[20] G. Cleghorn,et al. A highly efficient and consistent method for harvesting large volumes of high-titre lentiviral vectors , 2001, Gene Therapy.
[21] A. Logan,et al. Factors influencing the titer and infectivity of lentiviral vectors. , 2004, Human gene therapy.
[22] D. Nesbeth,et al. Metabolic biotinylation of lentiviral pseudotypes for scalable paramagnetic microparticle-dependent manipulation. , 2006, Molecular therapy : the journal of the American Society of Gene Therapy.
[23] D. Trono,et al. A stable system for the high-titer production of multiply attenuated lentiviral vectors. , 2000, Molecular therapy : the journal of the American Society of Gene Therapy.
[24] M. Wiznerowicz,et al. A versatile tool for conditional gene expression and knockdown , 2006, Nature Methods.
[25] A. Blesch. Lentiviral and MLV based retroviral vectors for ex vivo and in vivo gene transfer. , 2004, Methods.
[26] L. Naldini,et al. Gene therapy of storage disorders by retroviral and lentiviral vectors. , 2005, Human Gene Therapy.