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Gene Therapy
Citations 371-380 of 434 total displayed.
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Past content
(since Aug 1998):
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Induction of B-cell tolerance by retroviral gene therapy
- Jennifer L. Bracy and John Iacomini
Blood 2000; 96: 3008-3015.
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Efficient retrovirus-mediated gene transfer to transplantable human bone marrow cells in the absence of fibronectin
- Burkhard Hennemann, Il-Hoan Oh, Jean Y. Chuo, Christian P. Kalberer, Patricia D. Schley, Stefan Rose-John, R. Keith Humphries, and Connie J. Eaves
Blood 2000; 96: 2432-2439.
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Highly efficient gene transfer into cord blood nonobese diabetic/severe combined immunodeficiency repopulating cells by oncoretroviral vector particles pseudotyped with the feline endogenous retrovirus (RD114) envelope protein
- Patrick F. Kelly, Jody Vandergriff, Amit Nathwani, Arthur W. Nienhuis, and Elio F. Vanin
Blood 2000; 96: 1206-1214.
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Lentiviral-mediated gene transfer into human lymphocytes: role of HIV-1 accessory proteins
- Dhanalakshmi Chinnasamy, Nachimuthu Chinnasamy, Melissa J. Enriquez, Makoto Otsu, Richard A. Morgan, and Fabio Candotti
Blood 2000; 96: 1309-1316.
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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
- Renata Stripecke, Angelo A. Cardoso, Karen A. Pepper, Dianne C. Skelton, Xiao-Jin Yu, Leo Mascarenhas, Kenneth I. Weinberg, Lee M. Nadler, and Donald B. Kohn
Blood 2000; 96: 1317-1326.
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Dendritic cells transduced by multiply deleted HIV-1 vectors exhibit normal phenotypes and functions and elicit an HIV-specific cytotoxic T-lymphocyte response in vitro
- Andreas Gruber, June Kan-Mitchell, Kelli L. Kuhen, Tetsu Mukai, and Flossie Wong-Staal
Blood 2000; 96: 1327-1333.
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Mild preconditioning and low-level engraftment confer methotrexate resistance in mice transplanted with marrow expressing drug-resistant dihydrofolate reductase activity
- Rohaizah I. James, Christopher A. Warlick, Miechaleen D. Diers, Roland Gunther, and R. Scott McIvor
Blood 2000; 96: 1334-1341.
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Prolonged survival and tissue trafficking following adoptive transfer of CD4 gene-modified autologous CD4+ and CD8+ T cells in human immunodeficiency virus-infected subjects
- Ronald T. Mitsuyasu, Peter A. Anton, Steven G. Deeks, David T. Scadden, Elizabeth Connick, Matthew T. Downs, Andreas Bakker, Margo R. Roberts, Carl H. June, Sayeh Jalali, Andy A. Lin, Rukmini Pennathur-Das, and Kristen M. Hege
Blood 2000; 96: 785-793.
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Highly efficient gene transfer in naive human T cells with a murine leukemia virus-based vector
- Valérie Dardalhon, Sara Jaleco, Cosette Rebouissou, Christophe Ferrand, Nadia Skander, Louise Swainson, Pierre Tiberghien, Hergen Spits, Nelly Noraz, and Naomi Taylor
Blood 2000; 96: 885-893.
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Inactivation of a GFP retrovirus occurs at multiple levels in long-term repopulating stem cells and their differentiated progeny
- Christopher A. Klug, Samuel Cheshier, and Irving L. Weissman
Blood 2000; 96: 894-901.
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