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Items: 1 to 20 of 214

1.

Advances in lentiviral vector design for gene-modification of hematopoietic stem cells.

Logan AC, Lutzko C, Kohn DB.

Curr Opin Biotechnol. 2002 Oct;13(5):429-36. Review.

PMID:
12459333
2.

Gene transfer into hematopoietic stem cells using lentiviral vectors.

Scherr M, Eder M.

Curr Gene Ther. 2002 Feb;2(1):45-55. Review.

PMID:
12108973
3.

Lentivirus-mediated gene transfer into hematopoietic repopulating cells in baboons.

Horn PA, Morris JC, Bukovsky AA, Andrews RG, Naldini L, Kurre P, Kiem HP.

Gene Ther. 2002 Nov;9(21):1464-71.

4.

No false start for novel pseudotyped vectors.

Sanders DA.

Curr Opin Biotechnol. 2002 Oct;13(5):437-42. Review.

PMID:
12459334
5.

Efficient transduction of pigtailed macaque hematopoietic repopulating cells with HIV-based lentiviral vectors.

Trobridge GD, Beard BC, Gooch C, Wohlfahrt M, Olsen P, Fletcher J, Malik P, Kiem HP.

Blood. 2008 Jun 15;111(12):5537-43. doi: 10.1182/blood-2007-09-115022. Epub 2008 Apr 3.

6.

Equal potency of gammaretroviral and lentiviral SIN vectors for expression of O6-methylguanine-DNA methyltransferase in hematopoietic cells.

Schambach A, Bohne J, Chandra S, Will E, Margison GP, Williams DA, Baum C.

Mol Ther. 2006 Feb;13(2):391-400. Epub 2005 Oct 12.

7.
8.

ABC transporter inhibitors that are substrates enhance lentiviral vector transduction into primitive hematopoietic progenitor cells.

Davis BM, Humeau L, Slepushkin V, Binder G, Korshalla L, Ni Y, Ogunjimi EO, Chang LF, Lu X, Dropulic B.

Blood. 2004 Jul 15;104(2):364-73. Epub 2004 Apr 1.

10.

Specific transgene expression in human and mouse CD4+ cells using lentiviral vectors with regulatory sequences from the CD4 gene.

Marodon G, Mouly E, Blair EJ, Frisen C, Lemoine FM, Klatzmann D.

Blood. 2003 May 1;101(9):3416-23. Epub 2003 Jan 2.

11.

Production of clinical-grade recombinant adeno-associated virus vectors.

Snyder RO, Flotte TR.

Curr Opin Biotechnol. 2002 Oct;13(5):418-23. Review.

PMID:
12459331
12.

Expression and recombination of the EGFP and EYFP genes in lentiviral vectors carrying two heterologous promoters.

Dijon M, Torne-Celer C, Moreau T, Tonnelle C, Chabannon C.

Cytotherapy. 2005;7(5):417-26.

PMID:
16236631
13.

A roadmap to safe, efficient, and stable lentivirus-mediated gene therapy with hematopoietic cell transplantation.

Neschadim A, McCart JA, Keating A, Medin JA.

Biol Blood Marrow Transplant. 2007 Dec;13(12):1407-16. Review.

14.

In vivo gene delivery into hCD34+ cells in a humanized mouse model.

Frecha C, Fusil F, Cosset FL, Verhoeyen E.

Methods Mol Biol. 2011;737:367-90. doi: 10.1007/978-1-61779-095-9_15.

PMID:
21590405
15.

Gene delivery to hematopoietic stem cells using lentiviral vectors.

Miyoshi H.

Methods Mol Biol. 2004;246:429-38.

PMID:
14970608
16.

Glycoprotein Ibalpha promoter drives megakaryocytic lineage-restricted expression after hematopoietic stem cell transduction using a self-inactivating lentiviral vector.

Lavenu-Bombled C, Izac B, Legrand F, Cambot M, Vigier A, Massé JM, Dubart-Kupperschmitt A.

Stem Cells. 2007 Jun;25(6):1571-7. Epub 2007 Mar 22.

17.

High-level beta-globin expression and preferred intragenic integration after lentiviral transduction of human cord blood stem cells.

Imren S, Fabry ME, Westerman KA, Pawliuk R, Tang P, Rosten PM, Nagel RL, Leboulch P, Eaves CJ, Humphries RK.

J Clin Invest. 2004 Oct;114(7):953-62.

19.

The use of a recombinant lentiviral vector for ex vivo gene transfer into the rat CNS.

Englund U, Ericson C, Rosenblad C, Mandel RJ, Trono D, Wictorin K, Lundberg C.

Neuroreport. 2000 Dec 18;11(18):3973-7.

PMID:
11192612
20.

Lentiviral vectors: are they the future of animal transgenesis?

Park F.

Physiol Genomics. 2007 Oct 22;31(2):159-73. Epub 2007 Aug 7. Review.

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