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Gene Therapy
Citations 101-110 of 434 total displayed.
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Past content
(since Aug 1998):
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Phenotypic correction of von Willebrand disease type 3 blood-derived endothelial cells with lentiviral vectors expressing von Willebrand factor
- Simon F. De Meyer, Karen Vanhoorelbeke, Marinee K. Chuah, Inge Pareyn, Veerle Gillijns, Robert P. Hebbel, Désiré Collen, Hans Deckmyn, and Thierry VandenDriessche
Blood 2006; 107: 4728-4736.
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Endoglin expression in the endothelium is regulated by Fli-1, Erg, and Elf-1 acting on the promoter and a –8-kb enhancer
- John E. Pimanda, W.Y. Iris Chan, Ian J. Donaldson, Mark Bowen, Anthony R. Green, and Berthold Göttgens
Blood 2006; 107: 4737-4745.
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Proteasome activity restricts lentiviral gene transfer into hematopoietic stem cells and is down-regulated by cytokines that enhance transduction
- Francesca Romana Santoni de Sio, Paolo Cascio, Anna Zingale, Mauro Gasparini, and Luigi Naldini
Blood 2006; 107: 4257-4265.
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High-level expression of porcine factor VIII from genetically modified bone marrow–derived stem cells
- Bagirath Gangadharan, Ernest T. Parker, Lucienne M. Ide, H. Trent Spencer, and Christopher B. Doering
Blood 2006; 107: 3859-3864.
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Acute myeloid leukemia is associated with retroviral gene transfer to hematopoietic progenitor cells in a rhesus macaque
- Ruth Seggewiss, Stefania Pittaluga, Rima L. Adler, F. Javier Guenaga, Cole Ferguson, Ingo H. Pilz, Byoung Ryu, Brian P. Sorrentino, W. Scott Young, III, Robert E. Donahue, Christof von Kalle, Arthur W. Nienhuis, and Cynthia E. Dunbar
Blood 2006; 107: 3865-3867.
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Natural gene therapy in monozygotic twins with Fanconi anemia
- Anuj Mankad, Toshiyasu Taniguchi, Barbara Cox, Yassmine Akkari, R. Keaney Rathbun, Lora Lucas, Grover Bagby, Susan Olson, Alan D'Andrea, and Markus Grompe
Blood 2006; 107: 3084-3090.
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Correction of canine X-linked severe combined immunodeficiency by in vivo retroviral gene therapy
- Suk See Ting–De Ravin, Douglas R. Kennedy, Nora Naumann, Jeffrey S. Kennedy, Uimook Choi, Brian J. Hartnett, Gilda F. Linton, Narda L. Whiting-Theobald, Peter F. Moore, William Vernau, Harry L. Malech, and Peter J. Felsburg
Blood 2006; 107: 3091-3097.
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Differentiation of naive cord-blood T cells into CD19-specific cytolytic effectors for posttransplantation adoptive immunotherapy
- Lisa Marie Serrano, Timothy Pfeiffer, Simon Olivares, Tontanai Numbenjapon, Jennifer Bennitt, Daniel Kim, David Smith, George McNamara, Zaid Al-Kadhimi, Joseph Rosenthal, Stephen J. Forman, Michael C. Jensen, and Laurence J. N. Cooper
Blood 2006; 107: 2643-2652.
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Self-complementary adeno-associated virus vectors containing a novel liver-specific human factor IX expression cassette enable highly efficient transduction of murine and nonhuman primate liver
- Amit C. Nathwani, John T. Gray, Catherine Y. C. Ng, Junfang Zhou, Yunyu Spence, Simon N. Waddington, Edward G. D. Tuddenham, Geoffrey Kemball-Cook, Jenny McIntosh, Mariette Boon-Spijker, Koen Mertens, and Andrew M. Davidoff
Blood 2006; 107: 2653-2661.
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Enhanced engraftment of hematopoietic stem/progenitor cells by the transient inhibition of an adaptor protein, Lnk
- Hitoshi Takizawa, Chiyomi Kubo-Akashi, Ikuo Nobuhisa, Sang-Mo Kwon, Masanori Iseki, Tetsuya Taga, Kiyoshi Takatsu, and Satoshi Takaki
Blood 2006; 107: 2968-2975.
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