196 related articles for article (PubMed ID: 16982327)
21. Lentivirus-based gene delivery in mouse embryonic stem cells.
Kosaka Y; Kobayashi N; Fukazawa T; Totsugawa T; Maruyama M; Yong C; Arata T; Ikeda H; Kobayashi K; Ueda T; Kurabayashi Y; Tanaka N
Artif Organs; 2004 Mar; 28(3):271-7. PubMed ID: 15046626
[TBL] [Abstract][Full Text] [Related]
22. Aberrant expression of alpha-Gal on primary human endothelium does not confer susceptibility to NK cell cytotoxicity or increased NK cell adhesion.
He Z; Ehrnfelt C; Kumagai-Braesch M; Islam KB; Holgersson J
Eur J Immunol; 2004 Apr; 34(4):1185-95. PubMed ID: 15048730
[TBL] [Abstract][Full Text] [Related]
23. Transcriptional targeting of virus-mediated gene transfer by the human hexokinase II promoter.
Määttä AM; Korja S; Venhoranta H; Hakkarainen T; Pirinen E; Heikkinen S; Pellinen R; Mäkinen K; Wahlfors J
Int J Mol Med; 2006 Nov; 18(5):901-8. PubMed ID: 17016620
[TBL] [Abstract][Full Text] [Related]
24. Expression of human factor IX gene in murine plasma through lentiviral vector-infected haematopoietic stem cells.
Chen H; Yao H; Huang L; Shen Q; Jia W; Xue J
Clin Exp Pharmacol Physiol; 2006 Dec; 33(12):1196-201. PubMed ID: 17184501
[TBL] [Abstract][Full Text] [Related]
25. Efficient transduction of monocyte- and CD34+-derived Langerhans cells with lentiviral vectors in the absence of phenotypic and functional maturation.
Veron P; Boutin S; Bernard J; Danos O; Davoust J; Masurier C
J Gene Med; 2006 Aug; 8(8):951-61. PubMed ID: 16741998
[TBL] [Abstract][Full Text] [Related]
26. Simian immunodeficiency virus vector pseudotypes differ in transduction efficiency and target cell specificity in brain.
Liehl B; Hlavaty J; Moldzio R; Tonar Z; Unger H; Salmons B; Günzburg WH; Renner M
Gene Ther; 2007 Sep; 14(18):1330-43. PubMed ID: 17611586
[TBL] [Abstract][Full Text] [Related]
27. The combined use of viral transcriptional and post-transcriptional regulatory elements to improve baculovirus-mediated transient gene expression in human embryonic stem cells.
Du J; Zeng J; Zhao Y; Boulaire J; Wang S
J Biosci Bioeng; 2010 Jan; 109(1):1-8. PubMed ID: 20129073
[TBL] [Abstract][Full Text] [Related]
28. Efficient infection of human natural killer cells with an EBV/retroviral hybrid vector.
Becknell B; Trotta R; Yu J; Ding W; Mao HC; Hughes T; Marburger T; Caligiuri MA
J Immunol Methods; 2005 Jan; 296(1-2):115-23. PubMed ID: 15680156
[TBL] [Abstract][Full Text] [Related]
29. Inducible and reversible transgene expression in human stem cells after efficient and stable gene transfer.
Zhou BY; Ye Z; Chen G; Gao ZP; Zhang YA; Cheng L
Stem Cells; 2007 Mar; 25(3):779-89. PubMed ID: 17158240
[TBL] [Abstract][Full Text] [Related]
30. Gene transfer system derived from the caprine arthritis-encephalitis lentivirus.
Mselli-Lakhal L; Guiguen F; Greenland T; Mornex JF; Chebloune Y
J Virol Methods; 2006 Sep; 136(1-2):177-84. PubMed ID: 16797087
[TBL] [Abstract][Full Text] [Related]
31. Regeneration of a well-differentiated human airway surface epithelium by spheroid and lentivirus vector-transduced airway cells.
Castillon N; Avril-Delplanque A; Coraux C; Delenda C; Péault B; Danos O; Puchelle E
J Gene Med; 2004 Aug; 6(8):846-56. PubMed ID: 15293343
[TBL] [Abstract][Full Text] [Related]
32. Gene transfer of human TCR in primary murine T cells is improved by pseudo-typing with amphotropic and ecotropic envelopes.
Pouw NM; Westerlaken EJ; Willemsen RA; Debets R
J Gene Med; 2007 Jul; 9(7):561-70. PubMed ID: 17471588
[TBL] [Abstract][Full Text] [Related]
33. Efficient in vitro transduction of naive murine B cells with lentiviral vectors.
Warncke M; Vogt B; Ulrich J; von Laer MD; Beyer W; Klump H; Micheel B; Sheriff A
Biochem Biophys Res Commun; 2004 Jun; 318(3):673-9. PubMed ID: 15144890
[TBL] [Abstract][Full Text] [Related]
34. [Transduction of recombinant marrow stem cells using lentiviral vector and adenoviral vector: a comparative study].
Ma XS; Jiang JY; Lü FZ; Ma X; Li XK; Huang HY
Zhonghua Yi Xue Za Zhi; 2006 Dec; 86(47):3340-4. PubMed ID: 17313830
[TBL] [Abstract][Full Text] [Related]
35. Lentiviral vector-mediated gene delivery into human embryonic stem cells.
Gropp M; Reubinoff B
Methods Enzymol; 2006; 420():64-81. PubMed ID: 17161694
[TBL] [Abstract][Full Text] [Related]
36. Comparison of HIV-1 and EIAV-based lentiviral vectors in corneal transduction.
Beutelspacher SC; Ardjomand N; Tan PH; Patton GS; Larkin DF; George AJ; McClure MO
Exp Eye Res; 2005 Jun; 80(6):787-94. PubMed ID: 15939034
[TBL] [Abstract][Full Text] [Related]
37. Lentiviral vectors mediate stable and efficient gene delivery into primary murine natural killer cells.
Tran J; Kung SK
Mol Ther; 2007 Jul; 15(7):1331-9. PubMed ID: 17505478
[TBL] [Abstract][Full Text] [Related]
38. Lentiviral vector gene transfer into human T cells.
Verhoeyen E; Costa C; Cosset FL
Methods Mol Biol; 2009; 506():97-114. PubMed ID: 19110622
[TBL] [Abstract][Full Text] [Related]
39. Induction of human histo-blood group A antigen expression in mouse cells by gene therapy using lentiviral vectors harbouring human ABH-related glycosyltransferase genes.
Fan X; Ang A; Tao K; West LJ
Transplant Proc; 2005; 37(1):265-7. PubMed ID: 15808615
[TBL] [Abstract][Full Text] [Related]
40. Functional characterization of interleukin-15 gene transduction into the human natural killer cell line NKL.
Jiang W; Zhang J; Tian Z
Cytotherapy; 2008; 10(3):265-74. PubMed ID: 18418772
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]