Results 181 to 190 of about 115,363 (220)

Enhancement of lentiviral vectors gene delivery against VEGFR2 expressing cells by co-display of the binding and fusogenic moieties: a two molecules targeting approach. [PDF]

Virol J
Ahani R, Etemadzadeh MH, Mohajel N, Behdani M, Cohan RA, Kalani MR, Madani N, Roohvand F, Azadmanesh K.   +8 more
europepmc   +1 more source

Engineering baculo- and lentiviral vectors for enhanced and targeted gene delivery (Geeninsiirron tehostaminen ja kohdentaminen pintamuokatuilla bakulo- ja lentiviruksilla) [PDF]

Kaikkonen, Minna
core  

Lentiviral Vectors: From Wild-Type Viruses to Efficient Multi-Functional Delivery Vectors. [PDF]

Int J Mol Sci
Arrasate A, Lopez-Robles C, Zuazo M, Banos-Mateos S, Martin C, Lamsfus-Calle A, Fertin MJ.   +6 more
europepmc   +1 more source

Hematopoietic stem cell therapy with gene modification to treat sickle cell disease. [PDF]

Stem Cells Transl Med
Ball J, Bradley A, Le A, Tisdale JF, Uchida N.   +4 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

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).
Anna, Bellizzi, Nicholas, Ahye, Hassen S, Wollebo   +2 more
openaire   +2 more sources

Lentiviral Gene Transduction of Kidney

Human Gene Therapy, 2002
Gene transfer into kidney holds great potential as a novel therapeutic approach. We have studied the transduction of kidney in vivo after delivery of lentiviral vectors by various routes of administration. A lentiviral vector expressing the bacterial lacZ gene from the cytomegalovirus early promoter was used.
G Luca, Gusella, Elena, Fedorova, Basil, Hanss, Daniele, Marras, Mary E, Klotman, Paul E, Klotman   +5 more
openaire   +2 more sources

Lentiviral transduction of murine oligodendrocytes in vivo

Journal of Neuroscience Research, 2005
Lentiviral vectors are used widely to direct efficient gene transfer in vivo. We examined cell-specific expression in adult murine white matter after stereotaxic microinjection of four lentiviral constructs. We synthesized vesicular stomatitis virus glycoprotein (VSV-G) pseudotyped lentiviruses with combinations of two promoters, cytomegalovirus (CMV ...
Sally R, McIver, Chul-Sang, Lee, Jin-Moo, Lee, Steven H, Green, Mark S, Sands, B Joy, Snider, Mark P, Goldberg   +6 more
openaire   +2 more sources

Lentiviral Transduction of Cultured Microglia

2013
Microglial cells are the resident immune-related glial cells of the central nervous system (CNS) that are crucial for maintaining homeostasis and sensing pathological alterations in the nervous system. To improve our understanding of the biological function of microglia, gene-transfer techniques have been improved and become widely used over the past ...
Takahiro, Masuda, Makoto, Tsuda, Hidetoshi, Tozaki-Saitoh, Kazuhide, Inoue   +3 more
openaire   +2 more sources