237 related articles for article (PubMed ID: 16522168)
1. Specific and stable gene transfer to human embryonic stem cells using pseudotyped lentiviral vectors.
Jang JE; Shaw K; Yu XJ; Petersen D; Pepper K; Lutzko C; Kohn DB
Stem Cells Dev; 2006 Feb; 15(1):109-17. PubMed ID: 16522168
[TBL] [Abstract][Full Text] [Related]
2. Transduction of human hematopoietic stem cells by lentiviral vectors pseudotyped with the RD114-TR chimeric envelope glycoprotein.
Di Nunzio F; Piovani B; Cosset FL; Mavilio F; Stornaiuolo A
Hum Gene Ther; 2007 Sep; 18(9):811-20. PubMed ID: 17824830
[TBL] [Abstract][Full Text] [Related]
3. Lentiviral vectors pseudotyped with a modified RD114 envelope glycoprotein show increased stability in sera and augmented transduction of primary lymphocytes and CD34+ cells derived from human and nonhuman primates.
Sandrin V; Boson B; Salmon P; Gay W; Nègre D; Le Grand R; Trono D; Cosset FL
Blood; 2002 Aug; 100(3):823-32. PubMed ID: 12130492
[TBL] [Abstract][Full Text] [Related]
4. Improved lentiviral gene transfer into human embryonic stem cells grown in co-culture with murine feeder and stroma cells.
Wurm M; Gross B; Sgodda M; Ständker L; Müller T; Forssmann WG; Horn PA; Blasczyk R; Cantz T
Biol Chem; 2011 Oct; 392(10):887-95. PubMed ID: 21812756
[TBL] [Abstract][Full Text] [Related]
5. RD114 envelope proteins provide an effective and versatile approach to pseudotype lentiviral vectors.
Bell AJ; Fegen D; Ward M; Bank A
Exp Biol Med (Maywood); 2010 Oct; 235(10):1269-76. PubMed ID: 20876083
[TBL] [Abstract][Full Text] [Related]
6. Lentiviral vectors pseudotyped with glycoproteins from Ross River and vesicular stomatitis viruses: variable transduction related to cell type and culture conditions.
Kahl CA; Pollok K; Haneline LS; Cornetta K
Mol Ther; 2005 Mar; 11(3):470-82. PubMed ID: 15727944
[TBL] [Abstract][Full Text] [Related]
7. Targeted transduction patterns in the mouse brain by lentivirus vectors pseudotyped with VSV, Ebola, Mokola, LCMV, or MuLV envelope proteins.
Watson DJ; Kobinger GP; Passini MA; Wilson JM; Wolfe JH
Mol Ther; 2002 May; 5(5 Pt 1):528-37. PubMed ID: 11991743
[TBL] [Abstract][Full Text] [Related]
8. Improved transduction of human sheep repopulating cells by retrovirus vectors pseudotyped with feline leukemia virus type C or RD114 envelopes.
Lucas ML; Seidel NE; Porada CD; Quigley JG; Anderson SM; Malech HL; Abkowitz JL; Zanjani ED; Bodine DM
Blood; 2005 Jul; 106(1):51-8. PubMed ID: 15774617
[TBL] [Abstract][Full Text] [Related]
9. RD114-pseudotyped oncoretroviral vectors. Biological and physical properties.
Kelly PF; Carrington J; Nathwani A; Vanin EF
Ann N Y Acad Sci; 2001 Jun; 938():262-76; discussion 276-7. PubMed ID: 11458516
[TBL] [Abstract][Full Text] [Related]
10. Transduction of bone-marrow-derived mesenchymal stem cells by using lentivirus vectors pseudotyped with modified RD114 envelope glycoproteins.
Zhang XY; La Russa VF; Reiser J
J Virol; 2004 Feb; 78(3):1219-29. PubMed ID: 14722277
[TBL] [Abstract][Full Text] [Related]
11. Critical factors influencing stable transduction of human CD34(+) cells with HIV-1-derived lentiviral vectors.
Haas DL; Case SS; Crooks GM; Kohn DB
Mol Ther; 2000 Jul; 2(1):71-80. PubMed ID: 10899830
[TBL] [Abstract][Full Text] [Related]
12. Cocal-pseudotyped lentiviral vectors resist inactivation by human serum and efficiently transduce primate hematopoietic repopulating cells.
Trobridge GD; Wu RA; Hansen M; Ironside C; Watts KL; Olsen P; Beard BC; Kiem HP
Mol Ther; 2010 Apr; 18(4):725-33. PubMed ID: 19997089
[TBL] [Abstract][Full Text] [Related]
13. Lentiviral vectors pseudotyped with baculovirus gp64 efficiently transduce mouse cells in vivo and show tropism restriction against hematopoietic cell types in vitro.
Schauber CA; Tuerk MJ; Pacheco CD; Escarpe PA; Veres G
Gene Ther; 2004 Feb; 11(3):266-75. PubMed ID: 14737086
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Transduction of human primitive repopulating hematopoietic cells with lentiviral vectors pseudotyped with various envelope proteins.
Kim YS; Wielgosz MM; Hargrove P; Kepes S; Gray J; Persons DA; Nienhuis AW
Mol Ther; 2010 Jul; 18(7):1310-7. PubMed ID: 20372106
[TBL] [Abstract][Full Text] [Related]
16. Efficient gene transfer to human peripheral blood monocyte-derived dendritic cells using human immunodeficiency virus type 1-based lentiviral vectors.
Chinnasamy N; Chinnasamy D; Toso JF; Lapointe R; Candotti F; Morgan RA; Hwu P
Hum Gene Ther; 2000 Sep; 11(13):1901-9. PubMed ID: 10986562
[TBL] [Abstract][Full Text] [Related]
17. Comparison of various envelope proteins for their ability to pseudotype lentiviral vectors and transduce primitive hematopoietic cells from human blood.
Hanawa H; Kelly PF; Nathwani AC; Persons DA; Vandergriff JA; Hargrove P; Vanin EF; Nienhuis AW
Mol Ther; 2002 Mar; 5(3):242-51. PubMed ID: 11863413
[TBL] [Abstract][Full Text] [Related]
18. Human mesenchymal stem cells (hMSCs) expressing truncated soluble vascular endothelial growth factor receptor (tsFlk-1) following lentiviral-mediated gene transfer inhibit growth of Burkitt's lymphoma in a murine model.
Kyriakou CA; Yong KL; Benjamin R; Pizzey A; Dogan A; Singh N; Davidoff AM; Nathwani AC
J Gene Med; 2006 Mar; 8(3):253-64. PubMed ID: 16288493
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Gene transfer to repopulating human CD34+ cells using amphotropic-, GALV-, or RD114-pseudotyped HIV-1-based vectors from stable producer cells.
Relander T; Johansson M; Olsson K; Ikeda Y; Takeuchi Y; Collins M; Richter J
Mol Ther; 2005 Mar; 11(3):452-9. PubMed ID: 15727942
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]