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Gene Therapy
Citations 41-50 of 434 total displayed.
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Past content
(since Aug 1998):
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Overnight transduction with foamyviral vectors restores the long-term repopulating activity of Fancc–/– stem cells
- Yue Si, Anna C. Pulliam, Yvonne Linka, Samantha Ciccone, Cordula Leurs, Jin Yuan, Olaf Eckermann, Stefan Fruehauf, Sean Mooney, Helmut Hanenberg, and D. Wade Clapp
Blood 2008; 112: 4458-4465.
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Intraarticular factor IX protein or gene replacement protects against development of hemophilic synovitis in the absence of circulating factor IX
- Junjiang Sun, Narine Hakobyan, Leonard A. Valentino, Brian L. Feldman, R. Jude Samulski, and Paul E. Monahan
Blood 2008; 112: 4532-4541.
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Prophylactic infusion of cytomegalovirus-specific cytotoxic T lymphocytes stimulated with Ad5f35pp65 gene-modified dendritic cells after allogeneic hemopoietic stem cell transplantation
- Kenneth P. Micklethwaite, Leighton Clancy, Upinder Sandher, Anna M. Hansen, Emily Blyth, Vicki Antonenas, Mary M. Sartor, Kenneth F. Bradstock, and David J. Gottlieb
Blood 2008; 112: 3974-3981.
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Unaltered repopulation properties of mouse hematopoietic stem cells transduced with lentiviral vectors
- Africa Gonzalez-Murillo, M. Luz Lozano, Eugenio Montini, Juan A. Bueren, and Guillermo Guenechea
Blood 2008; 112: 3138-3147.
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Syngeneic transplantation of hematopoietic stem cells that are genetically modified to express factor VIII in platelets restores hemostasis to hemophilia A mice with preexisting FVIII immunity
- Qizhen Shi, Scot A. Fahs, David A. Wilcox, Erin L. Kuether, Patricia A. Morateck, Nicole Mareno, Hartmut Weiler, and Robert R. Montgomery
Blood 2008; 112: 2713-2721.
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Adoptive immunotherapy for indolent non-Hodgkin lymphoma and mantle cell lymphoma using genetically modified autologous CD20-specific T cells
- Brian G. Till, Michael C. Jensen, Jinjuan Wang, Eric Y. Chen, Brent L. Wood, Harvey A. Greisman, Xiaojun Qian, Scott E. James, Andrew Raubitschek, Stephen J. Forman, Ajay K. Gopal, John M. Pagel, Catherine G. Lindgren, Philip D. Greenberg, Stanley R. Riddell, and Oliver W. Press
Blood 2008; 112: 2261-2271.
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Resistance of mature T cells to oncogene transformation
- Sebastian Newrzela, Kerstin Cornils, Zhixiong Li, Christopher Baum, Martijn H. Brugman, Marianne Hartmann, Johann Meyer, Sylvia Hartmann, Martin-Leo Hansmann, Boris Fehse, and Dorothee von Laer
Blood 2008; 112: 2278-2286.
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Transient blockade of the inducible costimulator pathway generates long-term tolerance to factor VIII after nonviral gene transfer into hemophilia A mice
- Baowei Peng, Peiqing Ye, Bruce R. Blazar, Gordon J. Freeman, David J. Rawlings, Hans D. Ochs, and Carol H. Miao
Blood 2008; 112: 1662-1672.
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Efficient transduction of pigtailed macaque hematopoietic repopulating cells with HIV-based lentiviral vectors
- Grant D. Trobridge, Brian C. Beard, Christina Gooch, Martin Wohlfahrt, Philip Olsen, James Fletcher, Punam Malik, and Hans-Peter Kiem
Blood 2008; 111: 5537-5543.
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Development of gene therapy for blood disorders
- Arthur W. Nienhuis
Blood 2008; 111: 4431-4444.
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