In vivo gene delivery and stable transduction of nondividing cells
by a lentiviral vector.
These images show the development of cancer (dark purple) in the mouse lung, initiated
by lentiviral vector.
The study, titled «Restoration of spermatogenesis
by lentiviral gene transfer: Offspring from infertile mice,» was funded by the National Institutes of Health, the March of Dimes Birth Defects Foundation, the Wayne and Gladys Valley Foundation, and the H. N. and Frances C. Berger Foundation.
This is a derivative of the TZM - bl cell line, engineered
by lentiviral transduction to stably express human FcγRIIIa on the surface.
This is a derivative of the TZM - bl cell line, engineered
by lentiviral transduction to stably express human FcγRI on the surface.
This is a derivative of the TZM - bl cell line, engineered
by lentiviral transduction to stably express human FcγRIIb on the surface.
Germline Transmission and Tissue - Specific Expression of Transgenes Delivered
by Lentiviral Vectors
Not exact matches
Single - cell mouse embryos were infected in vitro with recombinant
lentiviral vectors to generate transgenic mice carrying the green fluorescent protein (GFP) gene driven
by a ubiquitously expressing promoter.
The treatment involves collected blood stem cells carrying the genetic anomaly of patients and corrected them in the laboratory
by introducing a healthy WAS gene using a
lentiviral vector developed and produced
by Genethon.
The plasmids expressing hsa - mir -7-1 and hsa - mir -7-2 precursors in
lentiviral pCDH - CMV - MCS - EF1 - copGFP vector (System Bioscience) were supplied
by Yin - Yuan Mo (University of Mississippi Medical Center).
(The test was the perfect complement for one conducted earlier
by the Zhang lab for GeCKO, a
lentiviral CRISPR library enabling genome - scale, knockout screening).
OMC also aims at potentiating the existing Conditional Mutagenesis Facility
by implementing novel approaches to attain tissue -, stage - and site - specific transgene expression in mouse mutant strains, mainly through
lentiviral vector - mediated transduction of blastocysts.
Provasi E, Genovese P, Lombardo A, Magnani Z, Liu PQ, Reik A, Chu V, Paschon DE, Zhang L, Kuball J, Camisa B, Bondanza A, Casorati G, Ponzoni M, Ciceri F, Bordignon C, Greenberg PD, Holmes MC, Gregory PD, Naldini L, Bonini C. Editing T cell specificity towards leukemia
by zinc finger nucleases and
lentiviral gene transfer.
Role of the endocytic pathway in the counteraction of BST - 2
by human
lentiviral pathogens.
Functional KL2 genes were delivered to the mice using
lentiviral vectors, based on a crippled version of HIV that was first developed
by Verma and Salk Institute colleagues in 1996.
Review of «Safety and efficacy of a tCD25 pre-selective combination anti-HIV
lentiviral vector in human hematopoietic stem and progenitor cells» from Stem Cells
by Stuart P. Atkinson
Preintegration HIV - 1 inhibition
by a combination
lentiviral vector containing a chimeric TRIM5 alpha protein, a CCR5 shRNA, and a TAR decoy.
Suppression of clonal dominance in cultured human lymphoid cells
by addition of the cHS4 insulator to a
lentiviral vector.
The degree of phenotypic correction of murine ß — thalassemia intermedia following
lentiviral - mediated transfer of a human γ — globin gene is influenced
by chromosomal position effects and vector copy number.
HEK293T cells were transfected with the following retroviral or
lentiviral constructs, with their packaging vectors indicated in the parentheses, using FuGENE 6 reagent (Promega): pMX - puro - STAT5A * (provided
by T. Kitamura, University of Tokyo; pCMV - Gag - Pol and pCMV - VSV - G); pLenti - EF - FH - TAZ - S89A (psPAX2 and pVSV - G); PLKO - NS and shTAZ
lentiviral construct (provided
by C. Linardic, Duke University; pCMV - Rev, pCVM - VSVG; pMDL).
Prior to transplantation, we analyzed the in vitro production of specific growth factors
by unmodified hNPCctx and
by hNPCctx transduced with a
lentiviral gene construct designed to constitutively express GDNF (hNPCctx - GDNF)[11], [44].
Adenoviral vectors can be produced
by human embryonic kidney (HEK293) and human embryonic retinal (PER.C6) cell lines (31), both of which also can be used for
lentiviral vector production.
Lentivirus was produced
by cotransfecting replication incompetent
lentiviral vector with psPAX2 (Addgene, 12260) and pLP / VSV - G (Invitrogen).
We also demonstrated that this observation was not caused incidentally
by a particular vectoring system: using intraductal injection of a
lentiviral vector (Bu et al., 2009) to introduce caErbb2 to ductal epithelia, we also observed accelerated tumorigenesis in the parous group relative to the virgin group (Figure 1 — figure supplement 2).