384 related articles for article (PubMed ID: 19378133)
1. GFP-lentiviral vectors targeting for neuroAIDS.
Lu Y
Methods Mol Biol; 2009; 515():177-97. PubMed ID: 19378133
[TBL] [Abstract][Full Text] [Related]
2. Efficient gene transfer into human monocyte-derived macrophages using defective lentiviral vectors.
Lu Y; Liu C; Zeng L; Lin Z; Dewhurst S; Gartner S; Planelles V
Cell Mol Biol (Noisy-le-grand); 2003 Nov; 49(7):1151-6. PubMed ID: 14682398
[TBL] [Abstract][Full Text] [Related]
3. HIV-1-based defective lentiviral vectors efficiently transduce human monocytes-derived macrophages and suppress replication of wild-type HIV-1.
Zeng L; Planelles V; Sui Z; Gartner S; Maggirwar SB; Dewhurst S; Ye L; Nerurkar VR; Yanagihara R; Lu Y
J Gene Med; 2006 Jan; 8(1):18-28. PubMed ID: 16142830
[TBL] [Abstract][Full Text] [Related]
4. Noninvasive monitoring of long-term lentiviral vector-mediated gene expression in rodent brain with bioluminescence imaging.
Deroose CM; Reumers V; Gijsbers R; Bormans G; Debyser Z; Mortelmans L; Baekelandt V
Mol Ther; 2006 Sep; 14(3):423-31. PubMed ID: 16820324
[TBL] [Abstract][Full Text] [Related]
5. Lentiviral vectors for delivery of genes into neonatal and adult ventricular cardiac myocytes in vitro and in vivo.
Zhao J; Pettigrew GJ; Thomas J; Vandenberg JI; Delriviere L; Bolton EM; Carmichael A; Martin JL; Marber MS; Lever AM
Basic Res Cardiol; 2002 Sep; 97(5):348-58. PubMed ID: 12200634
[TBL] [Abstract][Full Text] [Related]
6. Use of a macrophage-tropic GFP-tagged human immunodeficiency virus type 1 (HIV-1) to study viral reservoirs.
Brown AM
Methods Mol Biol; 2009; 515():165-75. PubMed ID: 19378134
[TBL] [Abstract][Full Text] [Related]
7. Use of GFP to analyze morphology, connectivity, and function of cells in the central nervous system.
Harvey AR; Ehlert E; de Wit J; Drummond ES; Pollett MA; Ruitenberg M; Plant GW; Verhaagen J; Levelt CN
Methods Mol Biol; 2009; 515():63-95. PubMed ID: 19378117
[TBL] [Abstract][Full Text] [Related]
8. Development of an in vitro blood-brain barrier model to study molecular neuropathogenesis and neurovirologic disorders induced by human immunodeficiency virus type 1 infection.
Mukhtar M; Pomerantz RJ
J Hum Virol; 2000; 3(6):324-34. PubMed ID: 11100913
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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
[TBL] [Abstract][Full Text] [Related]
12. An inducible Tet-Off-H2B-GFP lentiviral reporter vector for detection and in vivo isolation of label-retaining cells.
Falkowska-Hansen B; Kollar J; Grüner BM; Schanz M; Boukamp P; Siveke J; Rethwilm A; Kirschner M
Exp Cell Res; 2010 Jul; 316(11):1885-95. PubMed ID: 20171964
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. 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]
17. 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]
18. Targeting gene-modified hematopoietic cells to the central nervous system: use of green fluorescent protein uncovers microglial engraftment.
Priller J; Flügel A; Wehner T; Boentert M; Haas CA; Prinz M; Fernández-Klett F; Prass K; Bechmann I; de Boer BA; Frotscher M; Kreutzberg GW; Persons DA; Dirnagl U
Nat Med; 2001 Dec; 7(12):1356-61. PubMed ID: 11726978
[TBL] [Abstract][Full Text] [Related]
19. Global gene transfer into the CNS across the BBB after neonatal systemic delivery of single-stranded AAV vectors.
Miyake N; Miyake K; Yamamoto M; Hirai Y; Shimada T
Brain Res; 2011 May; 1389():19-26. PubMed ID: 21397590
[TBL] [Abstract][Full Text] [Related]
20. Brain engraftment of autologous macrophages transduced with a lentiviral flap vector: an approach to complement brain dysfunctions.
Mordelet E; Kissa K; Calvo CF; Lebastard M; Milon G; van der Werf S; Vidal C; Charneau P
Gene Ther; 2002 Jan; 9(1):46-52. PubMed ID: 11850722
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
