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Journal Abstract Search

373 related items for PubMed ID: 18557700

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  • 4. Simplified retroviral vector gcsap with murine stem cell virus long terminal repeat allows high and continued expression of enhanced green fluorescent protein by human hematopoietic progenitors engrafted in nonobese diabetic/severe combined immunodeficient mice.
    Kaneko S, Onodera M, Fujiki Y, Nagasawa T, Nakauchi H.
    Hum Gene Ther; 2001 Jan 01; 12(1):35-44. PubMed ID: 11177540
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  • 6. Serial transplantations in nonobese diabetic/severe combined immunodeficiency mice of transduced human CD34+ cord blood cells: efficient oncoretroviral gene transfer and ex vivo expansion under serum-free conditions.
    Gammaitoni L, Lucchi S, Bruno S, Tesio M, Gunetti M, Pignochino Y, Migliardi G, Lazzari L, Aglietta M, Rebulla P, Piacibello W.
    Stem Cells; 2006 May 01; 24(5):1201-12. PubMed ID: 16410386
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  • 7. Highly efficient transduction of the green fluorescent protein gene in human umbilical cord blood stem cells capable of cobblestone formation in long-term cultures and multilineage engraftment of immunodeficient mice.
    van Hennik PB, Verstegen MM, Bierhuizen MF, Limón A, Wognum AW, Cancelas JA, Barquinero J, Ploemacher RE, Wagemaker G.
    Blood; 1998 Dec 01; 92(11):4013-22. PubMed ID: 9834203
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  • 9. Ex vivo culture of cord blood CD34+ cells expands progenitor cell numbers, preserves engraftment capacity in nonobese diabetic/severe combined immunodeficient mice, and enhances retroviral transduction efficiency.
    Novelli EM, Cheng L, Yang Y, Leung W, Ramírez M, Tanavde V, Enger C, Civin CI.
    Hum Gene Ther; 1999 Dec 10; 10(18):2927-40. PubMed ID: 10609654
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  • 12. Highly efficient gene transfer into preterm CD34 hematopoietic progenitor cells.
    Shields LE, Kiem HP, Andrews RG.
    Am J Obstet Gynecol; 2000 Sep 10; 183(3):732-7. PubMed ID: 10992201
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  • 14. Transduction of human CD34+ CD38- bone marrow and cord blood-derived SCID-repopulating cells with third-generation lentiviral vectors.
    Guenechea G, Gan OI, Inamitsu T, Dorrell C, Pereira DS, Kelly M, Naldini L, Dick JE.
    Mol Ther; 2000 Jun 10; 1(6):566-73. PubMed ID: 10933981
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  • 15. Sustained transgene expression by human cord blood derived CD34+ cells transduced with simian immunodeficiency virus agmTYO1-based vectors carrying the human coagulation factor VIII gene in NOD/SCID mice.
    Kikuchi J, Mimuro J, Ogata K, Tabata T, Ueda Y, Ishiwata A, Kimura K, Takano K, Madoiwa S, Mizukami H, Hanazono Y, Kume A, Hasegawa M, Ozawa K, Sakata Y.
    J Gene Med; 2004 Oct 10; 6(10):1049-60. PubMed ID: 15386735
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  • 16. Oncoretroviral gene transfer to NOD/SCID repopulating cells using three different viral envelopes.
    Relander T, Karlsson S, Richter J.
    J Gene Med; 2002 Oct 10; 4(2):122-32. PubMed ID: 11933213
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  • 17. Optimization of retroviral-mediated gene transfer to human NOD/SCID mouse repopulating cord blood cells through a systematic analysis of protocol variables.
    Hennemann B, Conneally E, Pawliuk R, Leboulch P, Rose-John S, Reid D, Chuo JY, Humphries RK, Eaves CJ.
    Exp Hematol; 1999 May 10; 27(5):817-25. PubMed ID: 10340397
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  • 18. Novel alginate three-dimensional static and rotating culture systems for effective ex vivo amplification of human cord blood hematopoietic stem cells and in vivo functional analysis of amplified cells in NOD/SCID mice.
    Yuan Y, Sin WY, Xue B, Ke Y, Tse KT, Chen Z, Xie Y, Xie Y.
    Transfusion; 2013 Sep 10; 53(9):2001-11. PubMed ID: 23384125
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