251 related articles for article (PubMed ID: 11090053)
1. Lentiviral gene transfer into primary and secondary NOD/SCID repopulating cells.
Woods NB; Fahlman C; Mikkola H; Hamaguchi I; Olsson K; Zufferey R; Jacobsen SE; Trono D; Karlsson S
Blood; 2000 Dec; 96(12):3725-33. PubMed ID: 11090053
[TBL] [Abstract][Full Text] [Related]
2. High levels of transgene expression following transduction of long-term NOD/SCID-repopulating human cells with a modified lentiviral vector.
Gao Z; Golob J; Tanavde VM; Civin CI; Hawley RG; Cheng L
Stem Cells; 2001; 19(3):247-59. PubMed ID: 11359950
[TBL] [Abstract][Full Text] [Related]
3. Lentiviral vector transduction of NOD/SCID repopulating cells results in multiple vector integrations per transduced cell: risk of insertional mutagenesis.
Woods NB; Muessig A; Schmidt M; Flygare J; Olsson K; Salmon P; Trono D; von Kalle C; Karlsson S
Blood; 2003 Feb; 101(4):1284-9. PubMed ID: 12393514
[TBL] [Abstract][Full Text] [Related]
4. Transduction of human hematopoietic stem cells by lentiviral vectors pseudotyped with the RD114-TR chimeric envelope glycoprotein.
Di Nunzio F; Piovani B; Cosset FL; Mavilio F; Stornaiuolo A
Hum Gene Ther; 2007 Sep; 18(9):811-20. PubMed ID: 17824830
[TBL] [Abstract][Full Text] [Related]
5. Lentiviral gene transfer and ex vivo expansion of human primitive stem cells capable of primary, secondary, and tertiary multilineage repopulation in NOD/SCID mice. Nonobese diabetic/severe combined immunodeficient.
Piacibello W; Bruno S; Sanavio F; Droetto S; Gunetti M; Ailles L; Santoni de Sio F; Viale A; Gammaitoni L; Lombardo A; Naldini L; Aglietta M
Blood; 2002 Dec; 100(13):4391-400. PubMed ID: 12453876
[TBL] [Abstract][Full Text] [Related]
6. 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; 1(6):566-73. PubMed ID: 10933981
[TBL] [Abstract][Full Text] [Related]
7. Long-term engraftment of nonobese diabetic/severe combined immunodeficient mice with human CD34+ cells transduced by a self-inactivating human immunodeficiency virus type 1 vector.
Gatlin J; Padgett A; Melkus MW; Kelly PF; Garcia JV
Hum Gene Ther; 2001 Jun; 12(9):1079-89. PubMed ID: 11399229
[TBL] [Abstract][Full Text] [Related]
8. Comparison of three retroviral vector systems for transduction of nonobese diabetic/severe combined immunodeficiency mice repopulating human CD34+ cord blood cells.
Leurs C; Jansen M; Pollok KE; Heinkelein M; Schmidt M; Wissler M; Lindemann D; Von Kalle C; Rethwilm A; Williams DA; Hanenberg H
Hum Gene Ther; 2003 Apr; 14(6):509-19. PubMed ID: 12718762
[TBL] [Abstract][Full Text] [Related]
9. High-level transduction and gene expression in hematopoietic repopulating cells using a human immunodeficiency [correction of imunodeficiency] virus type 1-based lentiviral vector containing an internal spleen focus forming virus promoter.
Demaison C; Parsley K; Brouns G; Scherr M; Battmer K; Kinnon C; Grez M; Thrasher AJ
Hum Gene Ther; 2002 May; 13(7):803-13. PubMed ID: 11975847
[TBL] [Abstract][Full Text] [Related]
10. Enhanced transgene expression in cord blood CD34(+)-derived hematopoietic cells, including developing T cells and NOD/SCID mouse repopulating cells, following transduction with modified trip lentiviral vectors.
Sirven A; Ravet E; Charneau P; Zennou V; Coulombel L; Guétard D; Pflumio F; Dubart-Kupperschmitt A
Mol Ther; 2001 Apr; 3(4):438-48. PubMed ID: 11319904
[TBL] [Abstract][Full Text] [Related]
11. Identification of parameters required for efficient lentiviral vector transduction and engraftment of human cord blood CD34(+) NOD/SCID-repopulating cells.
Liu Y; Hangoc G; Campbell TB; Goodman M; Tao W; Pollok K; Srour EF; Broxmeyer HE
Exp Hematol; 2008 Aug; 36(8):947-56. PubMed ID: 18640494
[TBL] [Abstract][Full Text] [Related]
12. Lentiviral-mediated gene transfer into haematopoietic stem cells.
Woods NB; Mikkola H; Nilsson E; Olsson K; Trono D; Karlsson S
J Intern Med; 2001 Apr; 249(4):339-43. PubMed ID: 11298854
[TBL] [Abstract][Full Text] [Related]
13. Transduction of umbilical cord blood CD34+ NOD/SCID-repopulating cells by simian foamy virus type 1 (SFV-1) vector.
Zucali JR; Ciccarone T; Kelley V; Park J; Johnson CM; Mergia A
Virology; 2002 Oct; 302(2):229-35. PubMed ID: 12441067
[TBL] [Abstract][Full Text] [Related]
14. 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; 92(11):4013-22. PubMed ID: 9834203
[TBL] [Abstract][Full Text] [Related]
15. 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; 12(1):35-44. PubMed ID: 11177540
[TBL] [Abstract][Full Text] [Related]
16. Molecular evidence of lentiviral vector-mediated gene transfer into human self-renewing, multi-potent, long-term NOD/SCID repopulating hematopoietic cells.
Ailles L; Schmidt M; Santoni de Sio FR; Glimm H; Cavalieri S; Bruno S; Piacibello W; Von Kalle C; Naldini L
Mol Ther; 2002 Nov; 6(5):615-26. PubMed ID: 12409260
[TBL] [Abstract][Full Text] [Related]
17. Efficient retroviral-mediated gene transfer to human cord blood stem cells with in vivo repopulating potential.
Conneally E; Eaves CJ; Humphries RK
Blood; 1998 May; 91(9):3487-93. PubMed ID: 9558409
[TBL] [Abstract][Full Text] [Related]
18. Targeting transgene expression to antigen-presenting cells derived from lentivirus-transduced engrafting human hematopoietic stem/progenitor cells.
Cui Y; Golob J; Kelleher E; Ye Z; Pardoll D; Cheng L
Blood; 2002 Jan; 99(2):399-408. PubMed ID: 11781219
[TBL] [Abstract][Full Text] [Related]
19. Phenotype and function of human hematopoietic cells engrafting immune-deficient CB17-severe combined immunodeficiency mice and nonobese diabetic-severe combined immunodeficiency mice after transplantation of human cord blood mononuclear cells.
Pflumio F; Izac B; Katz A; Shultz LD; Vainchenker W; Coulombel L
Blood; 1996 Nov; 88(10):3731-40. PubMed ID: 8916937
[TBL] [Abstract][Full Text] [Related]
20. Gene delivery to hematopoietic stem cells using lentiviral vectors.
Miyoshi H
Methods Mol Biol; 2004; 246():429-38. PubMed ID: 14970608
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
