Stripecke R - Search Results

1

The use of lentiviral vectors in gene therapy of leukemia: combinatorial gene delivery of immunomodulators into leukemia cells by state-of-the-art vectors.

Stripecke R, Koya RC, Ta HQ, Kasahara N, Levine AM. Stripecke R, et al. Blood Cells Mol Dis. 2003 Jul-Aug;31(1):28-37. doi: 10.1016/s1079-9796(03)00062-7. Blood Cells Mol Dis. 2003. PMID: 12850480

2

Potent maturation of monocyte-derived dendritic cells after CD40L lentiviral gene delivery.

Koya RC, Kasahara N, Favaro PM, Lau R, Ta HQ, Weber JS, Stripecke R. Koya RC, et al. Among authors: stripecke r. J Immunother. 2003 Sep-Oct;26(5):451-60. doi: 10.1097/00002371-200309000-00008. J Immunother. 2003. PMID: 12973034

3

Making dendritic cells from the inside out: lentiviral vector-mediated gene delivery of granulocyte-macrophage colony-stimulating factor and interleukin 4 into CD14+ monocytes generates dendritic cells in vitro.

Koya RC, Weber JS, Kasahara N, Lau R, Villacres MC, Levine AM, Stripecke R. Koya RC, et al. Among authors: stripecke r. Hum Gene Ther. 2004 Aug;15(8):733-48. doi: 10.1089/1043034041648381. Hum Gene Ther. 2004. PMID: 15319031

4

Transduction of acute myeloid leukemia cells with third generation self-inactivating lentiviral vectors expressing CD80 and GM-CSF: effects on proliferation, differentiation, and stimulation of allogeneic and autologous anti-leukemia immune responses.

Koya RC, Kasahara N, Pullarkat V, Levine AM, Stripecke R. Koya RC, et al. Among authors: stripecke r. Leukemia. 2002 Sep;16(9):1645-54. doi: 10.1038/sj.leu.2402582. Leukemia. 2002. PMID: 12200676

5

Lentiviral vector-mediated autonomous differentiation of mouse bone marrow cells into immunologically potent dendritic cell vaccines.

Koya RC, Kimura T, Ribas A, Rozengurt N, Lawson GW, Faure-Kumar E, Wang HJ, Herschman H, Kasahara N, Stripecke R. Koya RC, et al. Among authors: stripecke r. Mol Ther. 2007 May;15(5):971-80. doi: 10.1038/mt.sj.6300126. Epub 2007 Mar 20. Mol Ther. 2007. PMID: 17375074 Free article.

6

Lentiviral vectors with CMV or MHCII promoters administered in vivo: immune reactivity versus persistence of expression.

Kimura T, Koya RC, Anselmi L, Sternini C, Wang HJ, Comin-Anduix B, Prins RM, Faure-Kumar E, Rozengurt N, Cui Y, Kasahara N, Stripecke R. Kimura T, et al. Among authors: stripecke r. Mol Ther. 2007 Jul;15(7):1390-9. doi: 10.1038/sj.mt.6300180. Epub 2007 May 1. Mol Ther. 2007. PMID: 17505480 Free article.

7

Immunotherapy with acute leukemia cells modified into antigen-presenting cells: ex vivo culture and gene transfer methods.

Stripecke R, Levine AM, Pullarkat V, Cardoso AA. Stripecke R, et al. Leukemia. 2002 Oct;16(10):1974-83. doi: 10.1038/sj.leu.2402701. Leukemia. 2002. PMID: 12357348 Review.

8

Lentiviral vectors for efficient delivery of CD80 and granulocyte-macrophage- colony-stimulating factor in human acute lymphoblastic leukemia and acute myeloid leukemia cells to induce antileukemic immune responses.

Stripecke R, Cardoso AA, Pepper KA, Skelton DC, Yu XJ, Mascarenhas L, Weinberg KI, Nadler LM, Kohn DB. Stripecke R, et al. Blood. 2000 Aug 15;96(4):1317-26. Blood. 2000. PMID: 10942373 Free article.

9

Receptor-specific targeting mediated by the coexpression of a targeted murine leukemia virus envelope protein and a binding-defective influenza hemagglutinin protein.

Lin AH, Kasahara N, Wu W, Stripecke R, Empig CL, Anderson WF, Cannon PM. Lin AH, et al. Among authors: stripecke r. Hum Gene Ther. 2001 Mar 1;12(4):323-32. doi: 10.1089/10430340150503957. Hum Gene Ther. 2001. PMID: 11242525

10

Permanent, lowered HLA class I expression using lentivirus vectors with shRNA constructs: Averting cytotoxicity by alloreactive T lymphocytes.

Haga K, Lemp NA, Logg CR, Nagashima J, Faure-Kumar E, Gomez GG, Kruse CA, Mendez R, Stripecke R, Kasahara N, Cicciarelli JC. Haga K, et al. Among authors: stripecke r. Transplant Proc. 2006 Dec;38(10):3184-8. doi: 10.1016/j.transproceed.2006.10.158. Transplant Proc. 2006. PMID: 17175217 Free PMC article.

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