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https://currentprotocols.onlinelibrary.wiley.com/doi/abs/10.1002/0471142735.im1017cs31
Rapid Production of Retroviruses for Efficient Gene Delivery to Mammalian Cells Using 293T Cell–Based Systems Susan Swift Rigel, Inc, South San Francisco, CaliforniaAuthor: Susan Swift, James Lorens, Philip Achacoso, Garry P. Nolan
https://www.ncbi.nlm.nih.gov/pubmed/18432682
Rapid production of retroviruses for efficient gene delivery to mammalian cells using 293T cell-based systems. Swift S(1), Lorens J, Achacoso P, Nolan GP. Author information: (1)Rigel, Inc., South San Francisco, California, USA.Author: Susan Swift, James Lorens, Philip Achacoso, Garry P. Nolan
https://www.researchgate.net/publication/5419599_Rapid_Production_of_Retroviruses_for_Efficient_Gene_Delivery_to_Mammalian_Cells_Using_293T_Cell-Based_Systems
Rapid Production of Retroviruses for Efficient Gene Delivery to Mammalian Cells Using 293T Cell-Based Systems Article in Current protocols in immunology / edited by John E. Coligan ...
https://www.microbiologyresearch.org/content/journal/jgv/10.1099/vir.0.020255-0
Genetically modified cells of haematopoietic and lymphocytic lineages could provide potentially curative treatments for a wide range of inherited and acquired diseases. However, this application is limited in mouse models by the low efficiency of lentiviral vectors. To facilitate the rapid production of high-titre helper-free retroviral vectors for enhanced gene delivery, multiple ...Author: Chengxiang Wu, Yuanan Lu
https://www.atcc.org/products/all/CRL-3214.aspx
Swift S et al. Rapid Production of Retroviruses for Efficient Gene Delivery to Mammalian Cells Using 293T Cell-Based Systems. Current Protocols in Immunology,Unit 10.17C, 2001 Pear WS, et al. Production of High-Titer Helper-Free Retroviruses by Transient Transfection.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5449975/
Apr 28, 2017 · With the rapid development of nanotechnology in the recent decade, novel DNA and RNA delivery systems for gene therapy have become available that can be used instead of viral vectors. These non-viral vectors can be made of a variety of materials, including ...Author: Michael K. Riley, Wilfred Vermerris
https://www.researchgate.net/publication/8571604_Portal_branch_ligation_induces_efficient_retrovirus-mediated_gene_delivery_in_rat_liver
Portal branch ligation induces efficient retrovirus-mediated gene delivery in rat liver Article in The Journal of Gene Medicine 6(5):507-13 · May 2004 with 8 Reads How we measure 'reads'
https://www.intechopen.com/books/recent-advances-in-novel-drug-carrier-systems/gene-delivery-systems-recent-progress-in-viral-and-non-viral-therapy
Current gene delivery systems are divided into three categories: viral-based, non-viral based, and combined hybrid systems. Viral gene delivery systems consist of viruses that are modified to be replication-deficient which can deliver genes to the target cells to provide expression.Author: Erdal Cevher, Ali Demir Sezer, Emre Şefik Çağlar
https://link.springer.com/protocol/10.1007/978-1-4939-2809-5_8
Swift S, Lorens J, Achacoso P et al (2001) Rapid production of retroviruses for efficient gene delivery to mammalian cells using 293T cell-based systems. Curr Protoc …Author: Amie Simmons, José Alberola-Ila
https://www.sciencedirect.com/science/article/pii/S1549963417301685
However, there are serious obstacles to the broad clinical use of GE, the main challenge being an old problem of gene therapy—safe and efficient delivery. Gene transfer methods can be divided into viral and non-viral. 11 Viral platforms are probably the most efficient method of getting foreign genetic material into large numbers of cells, but ...Author: Alexander S. Timin, Albert R. Muslimov, Kirill V. Lepik, Olga S. Epifanovskaya, Alena I. Shakirova, ...
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