BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 11753362)

  • 1. Production of human clotting Factor IX without toxicity in mice after vascular delivery of a lentiviral vector.
    Tsui LV; Kelly M; Zayek N; Rojas V; Ho K; Ge Y; Moskalenko M; Mondesire J; Davis J; Roey MV; Dull T; McArthur JG
    Nat Biotechnol; 2002 Jan; 20(1):53-7. PubMed ID: 11753362
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Efficient delivery of human clotting factor IX after injection of lentiviral vectors in utero.
    Chen XG; Zhu HZ; Gong JL; Li F; Xue JL
    Acta Pharmacol Sin; 2004 Jun; 25(6):789-93. PubMed ID: 15169633
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. The application of a lentiviral vector for gene transfer in fetal human hepatocytes.
    Zahler MH; Irani A; Malhi H; Reutens AT; Albanese C; Bouzahzah B; Joyce D; Gupta S; Pestell RG
    J Gene Med; 2000; 2(3):186-93. PubMed ID: 10894264
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Epstein-Barr virus vectors provide prolonged robust factor IX expression in mice.
    Sclimenti CR; Neviaser AS; Baba EJ; Meuse L; Kay MA; Calos MP
    Biotechnol Prog; 2003; 19(1):144-51. PubMed ID: 12573017
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Involvement of glycosaminoglycans in vesicular stomatitis virus G glycoprotein pseudotyped lentiviral vector-mediated gene transfer into airway epithelial cells.
    Copreni E; Castellani S; Palmieri L; Penzo M; Conese M
    J Gene Med; 2008 Dec; 10(12):1294-302. PubMed ID: 18816484
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Gene transfer in ovarian cancer cells: a comparison between retroviral and lentiviral vectors.
    Indraccolo S; Habeler W; Tisato V; Stievano L; Piovan E; Tosello V; Esposito G; Wagner R; Uberla K; Chieco-Bianchi L; Amadori A
    Cancer Res; 2002 Nov; 62(21):6099-107. PubMed ID: 12414634
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Targeted transgene expression in rat brain using lentiviral vectors.
    Jakobsson J; Ericson C; Jansson M; Björk E; Lundberg C
    J Neurosci Res; 2003 Sep; 73(6):876-85. PubMed ID: 12949915
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Highly efficient lentiviral gene transfer in CD34+ and CD34+/38-/lin- cells from mobilized peripheral blood after cytokine prestimulation.
    Géronimi F; Richard E; Redonnet-Vernhet I; Lamrissi-Garcia I; Lalanne M; Ged C; Moreau-Gaudry F; De Verneuil H
    Stem Cells; 2003; 21(4):472-80. PubMed ID: 12832700
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Efficient gene delivery and targeted expression to hepatocytes in vivo by improved lentiviral vectors.
    Follenzi A; Sabatino G; Lombardo A; Boccaccio C; Naldini L
    Hum Gene Ther; 2002 Jan; 13(2):243-60. PubMed ID: 11812281
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Repopulation of rat liver by fetal hepatoblasts and adult hepatocytes transduced ex vivo with lentiviral vectors.
    Oertel M; Rosencrantz R; Chen YQ; Thota PN; Sandhu JS; Dabeva MD; Pacchia AL; Adelson ME; Dougherty JP; Shafritz DA
    Hepatology; 2003 May; 37(5):994-1005. PubMed ID: 12717380
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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. PubMed ID: 11273773
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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. PubMed ID: 15693055
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Anticancer effect of a lentiviral vector capable of expressing HIV-1 Vpr.
    Pang S; Kang MK; Kung S; Yu D; Lee A; Poon B; Chen IS; Lindemann B; Park NH
    Clin Cancer Res; 2001 Nov; 7(11):3567-73. PubMed ID: 11705878
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Transgenesis by lentiviral vectors: lack of gene silencing in mammalian embryonic stem cells and preimplantation embryos.
    Pfeifer A; Ikawa M; Dayn Y; Verma IM
    Proc Natl Acad Sci U S A; 2002 Feb; 99(4):2140-5. PubMed ID: 11854510
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A lentiviral vector with novel multiple cloning sites: stable transgene expression in vitro and in vivo.
    Santhosh CV; Tamhane MC; Kamat RH; Patel VV; Mukhopadhyaya R
    Biochem Biophys Res Commun; 2008 Jul; 371(3):546-50. PubMed ID: 18448070
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Restricted transgene persistence after lentiviral vector-mediated fetal gene transfer in the pregnant rabbit model.
    Moreno R; Rosal M; Martinez I; Vilardell F; Gonzalez JR; Petriz J; Hernandez-Andrade E; Gratacós E; Aran JM
    J Gene Med; 2008 Sep; 10(9):951-64. PubMed ID: 18613266
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A highly efficient, stable, and rapid approach for ex vivo human liver gene therapy via a FLAP lentiviral vector.
    Giannini C; Morosan S; Tralhao JG; Guidotti JE; Battaglia S; Mollier K; Hannoun L; Kremsdorf D; Gilgenkrantz H; Charneau P
    Hepatology; 2003 Jul; 38(1):114-22. PubMed ID: 12829993
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.