173 related articles for article (PubMed ID: 15994284)
1. In vivo gene transfer into rat bone marrow progenitor cells using rSV40 viral vectors.
Liu B; Daviau J; Nichols CN; Strayer DS
Blood; 2005 Oct; 106(8):2655-62. PubMed ID: 15994284
[TBL] [Abstract][Full Text] [Related]
2. Gene transfer using recombinant simian virus 40 viral vectors into mice bone marrow progenitor cells depressed the immunogenicity of keratinocyte stem cells.
Li W; Xu T; Wang JF; Wu XF; Li M; Lu PY
Transplant Proc; 2008 Dec; 40(10):3656-9. PubMed ID: 19100460
[TBL] [Abstract][Full Text] [Related]
3. Efficient gene transfer to hematopoietic progenitor cells using SV40-derived vectors.
Strayer DS; Pomerantz RJ; Yu M; Rosenzweig M; BouHamdan M; Yurasov S; Johnson RP; Goldstein H
Gene Ther; 2000 May; 7(10):886-95. PubMed ID: 10845727
[TBL] [Abstract][Full Text] [Related]
4. Delivering genes to the organ-localized immune system: long-term results of direct intramarrow transduction.
Louboutin JP; Liu B; Chekmasova AA; Reyes BA; van Bockstaele EJ; Strayer DS
J Gene Med; 2007 Oct; 9(10):843-51. PubMed ID: 17694566
[TBL] [Abstract][Full Text] [Related]
5. Rat bone marrow progenitor cells transduced in situ by rSV40 vectors differentiate into multiple central nervous system cell lineages.
Louboutin JP; Liu B; Reyes BA; Van Bockstaele EJ; Strayer DS
Stem Cells; 2006 Dec; 24(12):2801-9. PubMed ID: 16960137
[TBL] [Abstract][Full Text] [Related]
6. Evaluation of primitive murine hematopoietic stem and progenitor cell transduction in vitro and in vivo by recombinant adeno-associated virus vector serotypes 1 through 5.
Zhong L; Li W; Li Y; Zhao W; Wu J; Li B; Maina N; Bischof D; Qing K; Weigel-Kelley KA; Zolotukhin I; Warrington KH; Li X; Slayton WB; Yoder MC; Srivastava A
Hum Gene Ther; 2006 Mar; 17(3):321-33. PubMed ID: 16544981
[TBL] [Abstract][Full Text] [Related]
7. In vivo gene transfer to the CNS using recombinant SV40-derived vectors.
Louboutin JP; Agrawal L; Liu B; Strayer DS
Expert Opin Biol Ther; 2008 Sep; 8(9):1319-35. PubMed ID: 18694352
[TBL] [Abstract][Full Text] [Related]
8. Strategies for CNS-directed gene delivery: in vivo gene transfer to the brain using SV40-derived vectors.
Louboutin JP; Reyes BA; Agrawal L; Van Bockstaele E; Strayer DS
Gene Ther; 2007 Jun; 14(12):939-49. PubMed ID: 17443215
[TBL] [Abstract][Full Text] [Related]
9. In vivo gene transfer into adult stem cells in unconditioned mice by in situ delivery of a lentiviral vector.
Worsham DN; Schuesler T; von Kalle C; Pan D
Mol Ther; 2006 Oct; 14(4):514-24. PubMed ID: 16893684
[TBL] [Abstract][Full Text] [Related]
10. Simian virus-40 as a gene therapy vector.
Vera M; Fortes P
DNA Cell Biol; 2004 May; 23(5):271-82. PubMed ID: 15169607
[TBL] [Abstract][Full Text] [Related]
11. Gene transfer to the cerebellum.
Louboutin JP; Reyes BA; Van Bockstaele EJ; Strayer DS
Cerebellum; 2010 Dec; 9(4):587-97. PubMed ID: 20700772
[TBL] [Abstract][Full Text] [Related]
12. In Vivo Hematopoietic Stem Cell Transduction.
Richter M; Stone D; Miao C; Humbert O; Kiem HP; Papayannopoulou T; Lieber A
Hematol Oncol Clin North Am; 2017 Oct; 31(5):771-785. PubMed ID: 28895846
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Recombinant self-complementary adeno-associated virus serotype vector-mediated hematopoietic stem cell transduction and lineage-restricted, long-term transgene expression in a murine serial bone marrow transplantation model.
Maina N; Han Z; Li X; Hu Z; Zhong L; Bischof D; Weigel-Van Aken KA; Slayton WB; Yoder MC; Srivastava A
Hum Gene Ther; 2008 Apr; 19(4):376-83. PubMed ID: 18370591
[TBL] [Abstract][Full Text] [Related]
15. Durability of transgene expression and vector integration: recombinant SV40-derived gene therapy vectors.
Strayer D; Branco F; Zern MA; Yam P; Calarota SA; Nichols CN; Zaia JA; Rossi J; Li H; Parashar B; Ghosh S; Chowdhury JR
Mol Ther; 2002 Aug; 6(2):227-37. PubMed ID: 12161189
[TBL] [Abstract][Full Text] [Related]
16. Hematologic recovery in mice transplanted with bone marrow stem cells expressing anti-human immunodeficiency virus genes.
Morel F; Salimi S; Markovits J; Austin TW; Plavec I
Hum Gene Ther; 1999 Nov; 10(17):2779-87. PubMed ID: 10584924
[TBL] [Abstract][Full Text] [Related]
17. HIV, but not murine leukemia virus, vectors mediate high efficiency gene transfer into freshly isolated G0/G1 human hematopoietic stem cells.
Uchida N; Sutton RE; Friera AM; He D; Reitsma MJ; Chang WC; Veres G; Scollay R; Weissman IL
Proc Natl Acad Sci U S A; 1998 Sep; 95(20):11939-44. PubMed ID: 9751769
[TBL] [Abstract][Full Text] [Related]
18. Highly efficient gene transfer into baboon marrow repopulating cells using GALV-pseudotype oncoretroviral vectors produced by human packaging cells.
Horn PA; Topp MS; Morris JC; Riddell SR; Kiem HP
Blood; 2002 Dec; 100(12):3960-7. PubMed ID: 12393453
[TBL] [Abstract][Full Text] [Related]
19. Comparison of retroviral-mediated gene transfer into cultured human CD34+ hematopoietic progenitor cells derived from peripheral blood, bone marrow, and fetal umbilical cord blood.
Campain JA; Terrell KL; Tomczak JA; Shpall EJ; Hami LS; Harrison GS
Biol Blood Marrow Transplant; 1997 Nov; 3(5):273-81. PubMed ID: 9450923
[TBL] [Abstract][Full Text] [Related]
20. Introduction of the green fluorescent protein gene into hematopoietic stem cells results in prolonged discrepancy of in vivo transduction levels between bone marrow progenitors and peripheral blood cells in nonhuman primates.
Hanazono Y; Terao K; Shibata H; Nagashima T; Ageyama N; Asano T; Ueda Y; Kato I; Kume A; Hasegawa M; Ozawa K
J Gene Med; 2002; 4(5):470-7. PubMed ID: 12221639
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
