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Items: 1 to 20 of 84

1.

In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector.

Naldini L, Blömer U, Gallay P, Ory D, Mulligan R, Gage FH, Verma IM, Trono D.

Science. 1996 Apr 12;272(5259):263-7.

PMID:
8602510
2.

Efficacy and safety analyses of a recombinant human immunodeficiency virus type 1 derived vector system.

Chang LJ, Urlacher V, Iwakuma T, Cui Y, Zucali J.

Gene Ther. 1999 May;6(5):715-28.

3.

The efficiency of simian foamy virus vector type-1 (SFV-1) in nondividing cells and in human PBLs.

Mergia A, Chari S, Kolson DL, Goodenow MM, Ciccarone T.

Virology. 2001 Feb 15;280(2):243-52.

4.

Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo.

Zufferey R, Nagy D, Mandel RJ, Naldini L, Trono D.

Nat Biotechnol. 1997 Sep;15(9):871-5.

PMID:
9306402
5.

Stable integration of human immunodeficiency virus-based retroviral vectors into the chromosomes of nondividing cells.

Miyake K, Suzuki N, Matsuoka H, Tohyama T, Shimada T.

Hum Gene Ther. 1998 Mar 1;9(4):467-75.

PMID:
9525308
6.

Efficient transduction of nondividing human cells by feline immunodeficiency virus lentiviral vectors.

Poeschla EM, Wong-Staal F, Looney DJ.

Nat Med. 1998 Mar;4(3):354-7.

PMID:
9500613
7.

Lentiviral-mediated gene transfer into human lymphocytes: role of HIV-1 accessory proteins.

Chinnasamy D, Chinnasamy N, Enriquez MJ, Otsu M, Morgan RA, Candotti F.

Blood. 2000 Aug 15;96(4):1309-16.

8.

Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors.

Kafri T, Blömer U, Peterson DA, Gage FH, Verma IM.

Nat Genet. 1997 Nov;17(3):314-7.

PMID:
9354796
10.

Hybrid HIV/MSCV LTR enhances transgene expression of lentiviral vectors in human CD34(+) hematopoietic cells.

Choi JK, Hoang N, Vilardi AM, Conrad P, Emerson SG, Gewirtz AM.

Stem Cells. 2001;19(3):236-46.

11.

Stable transduction of primary human monocytes by simian lentiviral vector PBj.

Mühlebach MD, Wolfrum N, Schüle S, Tschulena U, Sanzenbacher R, Flory E, Cichutek K, Schweizer M.

Mol Ther. 2005 Dec;12(6):1206-16. Epub 2005 Sep 16.

12.

Development of HIV vectors for anti-HIV gene therapy.

Poeschla E, Corbeau P, Wong-Staal F.

Proc Natl Acad Sci U S A. 1996 Oct 15;93(21):11395-9. Review.

13.

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. Erratum in: J Gene Med. 2005 Jun;7(6):835.

PMID:
15693055
14.

Murine and HIV-based retroviral vectors for in vitro and in vivo gene transfer.

Alfa RW, Blesch A.

Methods Mol Med. 2006;129:241-54.

PMID:
17085815
15.

Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector.

Miyoshi H, Takahashi M, Gage FH, Verma IM.

Proc Natl Acad Sci U S A. 1997 Sep 16;94(19):10319-23.

16.

Transduction of liver cells by lentiviral vectors: analysis in living animals by fluorescence imaging.

Pfeifer A, Kessler T, Yang M, Baranov E, Kootstra N, Cheresh DA, Hoffman RM, Verma IM.

Mol Ther. 2001 Mar;3(3):319-22.

17.

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.

PMID:
10835599
18.
20.

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. Epub 2006 Jun 3.

PMID:
16872845

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