541 related articles for article (PubMed ID: 14722277)
21. 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]
22. Retargeting vesicular stomatitis virus glycoprotein pseudotyped lentiviral vectors with enhanced stability by in situ synthesized polymer shell.
Liang M; Yan M; Lu Y; Chen IS
Hum Gene Ther Methods; 2013 Feb; 24(1):11-8. PubMed ID: 23327104
[TBL] [Abstract][Full Text] [Related]
23. Characterization of HIV-1 vectors with gammaretrovirus envelope glycoproteins produced from stable packaging cells.
Strang BL; Ikeda Y; Cosset FL; Collins MK; Takeuchi Y
Gene Ther; 2004 Apr; 11(7):591-8. PubMed ID: 14724689
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Enhanced central nervous system transduction with lentiviral vectors pseudotyped with RVG/HIV-1gp41 chimeric envelope glycoproteins.
Trabalza A; Eleftheriadou I; Sgourou A; Liao TY; Patsali P; Lee H; Mazarakis ND
J Virol; 2014 Mar; 88(5):2877-90. PubMed ID: 24371049
[TBL] [Abstract][Full Text] [Related]
26. High-efficiency gene transfer into CD34+ cells with a human immunodeficiency virus type 1-based retroviral vector pseudotyped with vesicular stomatitis virus envelope glycoprotein G.
Akkina RK; Walton RM; Chen ML; Li QX; Planelles V; Chen IS
J Virol; 1996 Apr; 70(4):2581-5. PubMed ID: 8642689
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Vesicular stomatitis virus G-pseudotyped lentivirus vectors mediate efficient apical transduction of polarized quiescent primary alveolar epithelial cells.
Borok Z; Harboe-Schmidt JE; Brody SL; You Y; Zhou B; Li X; Cannon PM; Kim KJ; Crandall ED; Kasahara N
J Virol; 2001 Dec; 75(23):11747-54. PubMed ID: 11689655
[TBL] [Abstract][Full Text] [Related]
29. Development of Third-generation Cocal Envelope Producer Cell Lines for Robust Lentiviral Gene Transfer into Hematopoietic Stem Cells and T-cells.
Humbert O; Gisch DW; Wohlfahrt ME; Adams AB; Greenberg PD; Schmitt TM; Trobridge GD; Kiem HP
Mol Ther; 2016 Aug; 24(7):1237-46. PubMed ID: 27058824
[TBL] [Abstract][Full Text] [Related]
30. Introducing a cleavable signal peptide enhances the packaging efficiency of lentiviral vectors pseudotyped with Japanese encephalitis virus envelope proteins.
Liu H; Wu R; Yuan L; Tian G; Huang X; Wen Y; Ma X; Huang Y; Yan Q; Zhao Q; Cao S; Wen X
Virus Res; 2017 Feb; 229():9-16. PubMed ID: 27993624
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Amphotropic and VSV-G-pseudotyped retroviral vectors transduce human hematopoietic progenitor cells with similar efficiency.
von Laer D; Corovic A; Vogt B; Herwig U; Roscher S; Fehse B; Baum C
Bone Marrow Transplant; 2000 May; 25 Suppl 2():S75-9. PubMed ID: 10933195
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Lentiviral Vector Pseudotypes: Precious Tools to Improve Gene Modification of Hematopoietic Cells for Research and Gene Therapy.
Gutierrez-Guerrero A; Cosset FL; Verhoeyen E
Viruses; 2020 Sep; 12(9):. PubMed ID: 32933033
[TBL] [Abstract][Full Text] [Related]
35. Altering the tropism of lentiviral vectors through pseudotyping.
Cronin J; Zhang XY; Reiser J
Curr Gene Ther; 2005 Aug; 5(4):387-98. PubMed ID: 16101513
[TBL] [Abstract][Full Text] [Related]
36. Production and concentration of pseudotyped HIV-1-based gene transfer vectors.
Reiser J
Gene Ther; 2000 Jun; 7(11):910-3. PubMed ID: 10849549
[TBL] [Abstract][Full Text] [Related]
37. High-titer human immunodeficiency virus type 1-based vector systems for gene delivery into nondividing cells.
Mochizuki H; Schwartz JP; Tanaka K; Brady RO; Reiser J
J Virol; 1998 Nov; 72(11):8873-83. PubMed ID: 9765432
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Optimized large-scale production of high titer lentivirus vector pseudotypes.
Sena-Esteves M; Tebbets JC; Steffens S; Crombleholme T; Flake AW
J Virol Methods; 2004 Dec; 122(2):131-9. PubMed ID: 15542136
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]