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Journal Abstract Search
302 related items for PubMed ID: 11592842
1. Multigene lentiviral vectors based on differential splicing and translational control. Zhu Y, Feuer G, Day SL, Wrzesinski S, Planelles V. Mol Ther; 2001 Oct; 4(4):375-82. PubMed ID: 11592842 [Abstract] [Full Text] [Related]
2. Modified HIV-1 based lentiviral vectors have an effect on viral transduction efficiency and gene expression in vitro and in vivo. Park F, Kay MA. Mol Ther; 2001 Sep; 4(3):164-73. PubMed ID: 11545606 [Abstract] [Full Text] [Related]
3. Generation of a packaging cell line for prolonged large-scale production of high-titer HIV-1-based lentiviral vector. Ni Y, Sun S, Oparaocha I, Humeau L, Davis B, Cohen R, Binder G, Chang YN, Slepushkin V, Dropulic B. J Gene Med; 2005 Jun; 7(6):818-34. PubMed ID: 15693055 [Abstract] [Full Text] [Related]
4. Production of multicistronic HIV-1 based lentiviral vectors. Chinnasamy N, Shaffer J, Chinnasamy D. Methods Mol Biol; 2009 Jun; 515():137-50. PubMed ID: 19378113 [Abstract] [Full Text] [Related]
5. Lentiviral transduction of human hematopoietic cells by HIV-1- and SIV-based vectors containing a bicistronic cassette driven by various internal promoters. Dupuy FP, Mouly E, Mesel-Lemoine M, Morel C, Abriol J, Cherai M, Baillou C, Nègre D, Cosset FL, Klatzmann D, Lemoine FM. J Gene Med; 2005 Sep; 7(9):1158-71. PubMed ID: 15880619 [Abstract] [Full Text] [Related]
6. An inducible packaging cell system for safe, efficient lentiviral vector production in the absence of HIV-1 accessory proteins. Pacchia AL, Adelson ME, Kaul M, Ron Y, Dougherty JP. Virology; 2001 Mar 30; 282(1):77-86. PubMed ID: 11259192 [Abstract] [Full Text] [Related]
7. Lentiviral vectors that carry anti-HIV shRNAs: problems and solutions. ter Brake O, Berkhout B. J Gene Med; 2007 Sep 30; 9(9):743-50. PubMed ID: 17628029 [Abstract] [Full Text] [Related]
8. Influence of the small leader exons 2 and 3 on human immunodeficiency virus type 1 gene expression. Krummheuer J, Lenz C, Kammler S, Scheid A, Schaal H. Virology; 2001 Aug 01; 286(2):276-89. PubMed ID: 11485396 [Abstract] [Full Text] [Related]
9. Inhibition of simian/human immunodeficiency virus replication in CD4+ T cells derived from lentiviral-transduced CD34+ hematopoietic cells. Braun SE, Wong FE, Connole M, Qiu G, Lee L, Gillis J, Lu X, Humeau L, Slepushkin V, Binder GK, Dropulic B, Johnson RP. Mol Ther; 2005 Dec 01; 12(6):1157-67. PubMed ID: 16168713 [Abstract] [Full Text] [Related]
10. Comparative analysis of molecular strategies attenuating positional effects in lentiviral vectors carrying multiple genes. Osti D, Marras E, Ceriani I, Grassini G, Rubino T, Viganò D, Parolaro D, Perletti G. J Virol Methods; 2006 Sep 01; 136(1-2):93-101. PubMed ID: 16690138 [Abstract] [Full Text] [Related]
11. Inhibition of human immunodeficiency virus type 1 (HIV-1) replication by HIV-1-based lentivirus vectors expressing transdominant Rev. Mautino MR, Keiser N, Morgan RA. J Virol; 2001 Apr 01; 75(8):3590-9. PubMed ID: 11264348 [Abstract] [Full Text] [Related]
12. Multiply attenuated, self-inactivating lentiviral vectors efficiently transduce human coronary artery cells in vitro and rat arteries in vivo. Céfaï D, Simeoni E, Ludunge KM, Driscoll R, von Segesser LK, Kappenberger L, Vassalli G. J Mol Cell Cardiol; 2005 Feb 01; 38(2):333-44. PubMed ID: 15698840 [Abstract] [Full Text] [Related]
13. Defective lentiviral vectors are efficiently trafficked by HIV-1 and inhibit its replication. Klimatcheva E, Planelles V, Day SL, Fulreader F, Renda MJ, Rosenblatt J. Mol Ther; 2001 Jun 01; 3(6):928-39. PubMed ID: 11407907 [Abstract] [Full Text] [Related]
15. Titering lentiviral vectors: comparison of DNA, RNA and marker expression methods. Sastry L, Johnson T, Hobson MJ, Smucker B, Cornetta K. Gene Ther; 2002 Sep 01; 9(17):1155-62. PubMed ID: 12170379 [Abstract] [Full Text] [Related]
16. Lentiviral siRNAs targeting multiple highly conserved RNA sequences of human immunodeficiency virus type 1. Chang LJ, Liu X, He J. Gene Ther; 2005 Jul 01; 12(14):1133-44. PubMed ID: 15750613 [Abstract] [Full Text] [Related]
17. Use of cis- and trans-acting viral regulatory sequences to improve expression of human immunodeficiency virus vectors in human lymphocytes. Parolin C, Taddeo B, Palú G, Sodroski J. Virology; 1996 Aug 15; 222(2):415-22. PubMed ID: 8806525 [Abstract] [Full Text] [Related]
18. Lentiviral vectors harboring a dual-gene system allow high and homogeneous transgene expression in selected polyclonal human embryonic stem cells. Ben-Dor I, Itsykson P, Goldenberg D, Galun E, Reubinoff BE. Mol Ther; 2006 Aug 15; 14(2):255-67. PubMed ID: 16632408 [Abstract] [Full Text] [Related]
19. Efficient gene transfer in skeletal muscle with AAV-derived bicistronic vector using the FGF-1 IRES. Delluc-Clavières A, Le Bec C, Van den Berghe L, Conte C, Allo V, Danos O, Prats AC. Gene Ther; 2008 Aug 15; 15(15):1090-8. PubMed ID: 18369321 [Abstract] [Full Text] [Related]