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Journal Abstract Search

657 related items for PubMed ID: 8875226

  • 1. Analysis of the relative level of gene expression from different retroviral vectors used for gene therapy.
    Byun J, Kim SH, Kim JM, Yu SS, Robbins PD, Yim J, Kim S.
    Gene Ther; 1996 Sep; 3(9):780-8. PubMed ID: 8875226
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  • 6. Use of bicistronic retroviral vectors encoding the LacZ gene together with a gene of interest: a method to select producer cells and follow transduced target cells.
    Staal FJ, Bakker AQ, Verkuijlen M, van Oort E, Spits H.
    Cancer Gene Ther; 1996 Sep; 3(5):345-51. PubMed ID: 8894254
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  • 9. The selectable marker neo gene down-regulates gene expression from retroviral vectors containing an internal ribosome entry site.
    Byun J, Kim JM, Robbins PD, Kim S.
    Gene Ther; 1998 Oct; 5(10):1441-4. PubMed ID: 9930351
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  • 10. Stable integration of retrovirally transduced genes into human umbilical cord blood high-proliferative potential colony-forming cells (HPP-CFC) as assessed after multiple HPP-CFC colony replatings in vitro.
    Lu L, Xiao M, Clapp DW, Li ZH, Broxmeyer HE.
    Blood Cells; 1994 Oct; 20(2-3):525-30. PubMed ID: 7749119
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  • 11. A comparative evaluation of gene transfer into blood cells using the same retroviral backbone for independent expression of the EGFP and deltaLNGFR marker genes.
    Giaretta I, Madeo D, Bonaguro R, Cappellari A, Rodeghiero F, Giorgio P.
    Haematologica; 2000 Jul; 85(7):680-9. PubMed ID: 10897118
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  • 12. In situ generation of pseudotyped retroviral progeny by adenovirus-mediated transduction of tumor cells enhances the killing effect of HSV-tk suicide gene therapy in vitro and in vivo.
    Okada T, Caplen NJ, Ramsey WJ, Onodera M, Shimazaki K, Nomoto T, Ajalli R, Wildner O, Morris J, Kume A, Hamada H, Blaese RM, Ozawa K.
    J Gene Med; 2004 Mar; 6(3):288-99. PubMed ID: 15026990
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  • 13. Congenital erythropoietic porphyria: prolonged high-level expression and correction of the heme biosynthetic defect by retroviral-mediated gene transfer into porphyric and erythroid cells.
    Kauppinen R, Glass IA, Aizencang G, Astrin KH, Atweh GF, Desnick RJ.
    Mol Genet Metab; 1998 Sep; 65(1):10-7. PubMed ID: 9787090
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  • 14. Increased gene transfer into human CD34+ progenitor cells using retroviral vectors produced by a canine packaging cell line.
    Bauer G, Sauter S, Ibanez C, Rice CR, Valdez P, Jolly D, Kohn DB.
    Biol Blood Marrow Transplant; 1998 Sep; 4(3):119-27. PubMed ID: 9923409
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  • 15. Adenovirus vectors as transcomplementing templates for the production of replication defective retroviral vectors.
    Ramsey WJ, Caplen NJ, Li Q, Higginbotham JN, Shah M, Blaese RM.
    Biochem Biophys Res Commun; 1998 May 29; 246(3):912-9. PubMed ID: 9618311
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  • 16. An improved method for generating retroviral producer clones for vectors lacking a selectable marker gene.
    Persons DA, Mehaffey MG, Kaleko M, Nienhuis AW, Vanin EF.
    Blood Cells Mol Dis; 1998 Jun 29; 24(2):167-82. PubMed ID: 9642098
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  • 17. Adenovirus and retrovirus mediated interferon alpha gene transfer into CD34+ cells maintains regeneration capacity and enhances adhesion molecules in K562 cells.
    Seiter K, Kancherla R, Yang L, Quan S, Farley TJ, Abraham NG, Ahmed T.
    J Investig Med; 1999 Sep 29; 47(8):414-24. PubMed ID: 10510594
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  • 18. Generation of high-titer retroviral vectors following receptor-mediated, adenovirus-augmented transfection.
    von Rüden T, Stingl L, Cotten M, Wagner E, Zatloukal K.
    Biotechniques; 1995 Mar 29; 18(3):484-9. PubMed ID: 7779400
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  • 19. Construction of a high efficiency retroviral vector for gene therapy of Hunter's syndrome.
    Hong Y, Yu SS, Kim JM, Lee K, Na YS, Whitley CB, Sugimoto Y, Kim S.
    J Gene Med; 2003 Jan 29; 5(1):18-29. PubMed ID: 12516048
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  • 20. [Recombinant human GM-CSF retroviral vector construction and expression in human breast cancer cells].
    Zhao M, Mao N, Ba D.
    Zhonghua Zhong Liu Za Zhi; 1997 Jan 29; 19(1):42-4. PubMed ID: 10743054
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