177 related articles for article (PubMed ID: 16150648)
21. Efficient transduction of neurons using Ross River glycoprotein-pseudotyped lentiviral vectors.
Jakobsson J; Nielsen TT; Staflin K; Georgievska B; Lundberg C
Gene Ther; 2006 Jun; 13(12):966-73. PubMed ID: 16511527
[TBL] [Abstract][Full Text] [Related]
22. Functional HIV-2- and SIVsmmPBj- derived lentiviral vectors generated by a novel polymerase chain reaction-based approach.
Kloke BP; Schüle S; Mühlebach MD; Wolfrum N; Cichutek K; Schweizer M
J Gene Med; 2010 May; 12(5):446-52. PubMed ID: 20440755
[TBL] [Abstract][Full Text] [Related]
23. G2 cell cycle arrest and cyclophilin A in lentiviral gene transfer.
Zhang S; Joseph G; Pollok K; Berthoux L; Sastry L; Luban J; Cornetta K
Mol Ther; 2006 Oct; 14(4):546-54. PubMed ID: 16901758
[TBL] [Abstract][Full Text] [Related]
24. [Construction of a lentiviral vector for RNA interference of PRL-3 gene and its stable expression in SW480 cells].
Liu YH; Li JM; Zhou J; Ding YQ
Nan Fang Yi Ke Da Xue Xue Bao; 2008 Apr; 28(4):509-12. PubMed ID: 18495578
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Reversible immortalization of human primary cells by lentivector-mediated transfer of specific genes.
Salmon P; Oberholzer J; Occhiodoro T; Morel P; Lou J; Trono D
Mol Ther; 2000 Oct; 2(4):404-14. PubMed ID: 11020357
[TBL] [Abstract][Full Text] [Related]
27. Efficient lentiviral transduction of Herpesvirus saimiri immortalized T cells as a model for gene therapy in primary immunodeficiencies.
Toscano MG; Frecha C; Ortega C; Santamaría M; Martín F; Molina IJ
Gene Ther; 2004 Jun; 11(12):956-61. PubMed ID: 15029233
[TBL] [Abstract][Full Text] [Related]
28. Shuttle of lentiviral vectors via transplanted cells in vivo.
Blömer U; Gruh I; Witschel H; Haverich A; Martin U
Gene Ther; 2005 Jan; 12(1):67-74. PubMed ID: 15385952
[TBL] [Abstract][Full Text] [Related]
29. [*OPCML gene transferred by recombinant lentiviruses in vitro and its inhibition to ovarian cancer cells].
Yao DS; Li L; Garson K; Vanderhyden BC
Zhonghua Fu Chan Ke Za Zhi; 2006 May; 41(5):333-8. PubMed ID: 16762191
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Suspension packaging cell lines for the simplified generation of T-cell receptor encoding retrovirus vector particles.
Reuss S; Biese P; Cosset FL; Takeuchi Y; Uckert W
Gene Ther; 2007 Apr; 14(7):595-603. PubMed ID: 17235289
[TBL] [Abstract][Full Text] [Related]
32. Gene transfer systems derived from Visna virus: analysis of virus production and infectivity.
Berkowitz RD; Ilves H; Plavec I; Veres G
Virology; 2001 Jan; 279(1):116-29. PubMed ID: 11145895
[TBL] [Abstract][Full Text] [Related]
33. Spleen necrosis virus-derived C-type retroviral vectors for gene transfer to quiescent cells.
Parveen Z; Krupetsky A; Engelstädter M; Cichutek K; Pomerantz RJ; Dornburg R
Nat Biotechnol; 2000 Jun; 18(6):623-9. PubMed ID: 10835599
[TBL] [Abstract][Full Text] [Related]
34. Transient gene expression by nonintegrating lentiviral vectors.
Nightingale SJ; Hollis RP; Pepper KA; Petersen D; Yu XJ; Yang C; Bahner I; Kohn DB
Mol Ther; 2006 Jun; 13(6):1121-32. PubMed ID: 16556511
[TBL] [Abstract][Full Text] [Related]
35. A packaging cell line generating CD4-specific retroviral vectors for efficient gene transfer into primary human T-helper lymphocytes.
Thaler S; Schnierle BS
Mol Ther; 2001 Sep; 4(3):273-9. PubMed ID: 11545619
[TBL] [Abstract][Full Text] [Related]
36. Lentiviral vector-mediated siRNA knockdown of SR-PSOX inhibits foam cell formation in vitro.
Zhang L; Liu HJ; Li TJ; Yang Y; Guo XL; Wu MC; Rui YC; Wei LX
Acta Pharmacol Sin; 2008 Jul; 29(7):847-52. PubMed ID: 18565283
[TBL] [Abstract][Full Text] [Related]
37. DNA transposons for modification of human primary T lymphocytes.
Huang X; Wilber A; McIvor RS; Zhou X
Methods Mol Biol; 2009; 506():115-26. PubMed ID: 19110623
[TBL] [Abstract][Full Text] [Related]
38. Safe two-plasmid production for the first clinical lentivirus vector that achieves >99% transduction in primary cells using a one-step protocol.
Lu X; Humeau L; Slepushkin V; Binder G; Yu Q; Slepushkina T; Chen Z; Merling R; Davis B; Chang YN; Dropulic B
J Gene Med; 2004 Sep; 6(9):963-73. PubMed ID: 15352069
[TBL] [Abstract][Full Text] [Related]
39. Gene delivery into primary cerebral cortical neurons by lentiviral vector.
Zhang Y; Wang H; Pan H; Bao X; Li M; Jin J; Wu X
Cell Biol Int; 2006 Oct; 30(10):777-83. PubMed ID: 16872845
[TBL] [Abstract][Full Text] [Related]
40. Gene therapy in skin: choosing the optimal viral vector.
Teo EH; Cross KJ; Bomsztyk ED; Lyden DC; Spector JA
Ann Plast Surg; 2009 May; 62(5):576-80. PubMed ID: 19387165
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]