Results 251 to 260 of about 368,855 (303)

BaEV-pseudotyped lentiviral vectors enable stable CAR expression and cytotoxic function in NK cells. [PDF]

PLoS One
Park M, Lim Y, Jo Y, Jo DH, Kim SK, Kim HY, Lee SH, Lee M, Cho D.   +8 more
europepmc   +1 more source

Lentiviral-mediated gene complementation to rescue pathogenic ABCA3 variants. [PDF]

Am J Respir Cell Mol Biol
Cooney AL, Lamer S, Yang P, Wegner DJ, White FV, Cole FS, Wohlford-Lenane C, Hennessey E, Bawa P, Kotton DN, Sinn PL, Wambach JA, McCray PB.   +12 more
europepmc   +1 more source

Efficient NK cell transduction with VSV-G-pseudotyped lentiviral vectors. [PDF]

Mol Ther Adv
Järvelä E, Koski J, Jahan F, Tuhkala A, Saari M, Elmadani M, Salokas K, Veltman L, Andersson L, Kerkelä E, Can H, Nyman M, Ylä-Herttuala S, Varjosalo M, Schenkwein D, Paavilainen H, Vettenranta K, Korhonen M, Göös H.   +18 more
europepmc   +1 more source

Safe and Localized Lentiviral Gene Delivery via Injectable Mesoporous Scaffolds for Potent Antitumor Immunity. [PDF]

Adv Mater
Nguyen TL, Kim YJ, Im J, Min DK, Shin H, Trinh TA, Phan NM, Son MJ, Shim JY, Lee YL, Ha Y, Lim KI, Kim J.   +12 more
europepmc   +1 more source

[Transduction of hematopoietic stem cells by lentiviral vectors].

Uirusu, 2003
openaire   +1 more source

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Lentiviral Transduction of Neuronal Cells.

Methods in molecular biology, 2021
Lentiviruses are a very reliable class of viral vectors wildly used in gene therapy. In this chapter, we described a general method for the construction of lentiviral delivery system by using a derived HIV-1 based lentivirus expression vector pKLV-Puro containing a monomeric blue fluorescent protein mammalian codon-optimized (TagBFP).
A. Bellizzi, Nicholas Ahye, Hassen S Wollebo   +2 more
semanticscholar   +3 more sources

Lentiviral Transduction of Mammary Epithelial Cells.

Methods in molecular biology, 2022
Lentiviral vectors are the workhorses of modern cell biology. They can infect a wide variety of cells including non-dividing cells and stem cells. They integrate into the genome of infected cells leading to stable expression. It is easy to transduce 100% of the cells in a culture and possible to infect cells simultaneously with multiple vectors ...
R. Iggo
semanticscholar   +3 more sources

Generation of CAR-T Cells by Lentiviral Transduction.

Methods in molecular biology, 2021
CAR-T cell therapy is one of the most successful cell-based therapies. T cells are the most common cells to be genetically modified for cancer therapy, not only because T cells have cytotoxicity but also because they are easily cultured ex vivo and genetically modified with viral vectors.
Atsushi Okuma
semanticscholar   +3 more sources

Stable Expression by Lentiviral Transduction of Cells.

Methods in molecular biology, 2018
Lentiviral gene transfer represents a versatile and powerful method for genetic transduction of many cell lines and primary cells including "hard-to-transfect" cells. As a consequence of the integration of the recombinant lentiviral vector into the cellular genome, the transgene is stably maintained, and long-term producing cells are established. Here,
Natascha Gödecke, H. Hauser, D. Wirth
semanticscholar   +4 more sources