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Gene Therapy
Citations 351-360 of 434 total displayed.
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Past content
(since Aug 1998):
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Adenovirus-mediated expression of a mutant I B kinase 2 inhibits the response of endothelial cells to inflammatory stimuli
- Wolfgang Oitzinger, Renate Hofer-Warbinek, Johannes A. Schmid, Yuri Koshelnick, Bernd R. Binder, and Rainer de Martin
Blood 2001; 97: 1611-1617.
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Lack of dominant-negative effects of a truncated c on retroviral-mediated gene correction of immunodeficient mice
- Makoto Otsu, Kazuo Sugamura, and Fabio Candotti
Blood 2001; 97: 1618-1624.
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In utero transplantation of fetal liver cells in the mucopolysaccharidosis type VII mouse results in low-level chimerism, but overexpression of -glucuronidase can delay onset of clinical signs
- Margret L. Casal and John H. Wolfe
Blood 2001; 97: 1625-1634.
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The effect of multidrug-resistance 1 gene versus neo transduction on ex vivo and in vivo expansion of rhesus macaque hematopoietic repopulating cells
- Stephanie E. Sellers, John F. Tisdale, Brian A. Agricola, Mark E. Metzger, Robert E. Donahue, Cynthia E. Dunbar, and Brian P. Sorrentino
Blood 2001; 97: 1888-1891.
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A Fas-based suicide switch in human T cells for the treatment of graft-versus-host disease
- Daniel C. Thomis, Sarah Marktel, Chiara Bonini, Catia Traversari, Michael Gilman, Claudio Bordignon, and Tim Clackson
Blood 2001; 97: 1249-1257.
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Factors influencing in vivo transduction by recombinant adeno-associated viral vectors expressing the human factor IX cDNA
- Amit C. Nathwani, Andrew Davidoff, Hideki Hanawa, Jun-Fang Zhou, Elio F. Vanin, and Arthur W. Nienhuis
Blood 2001; 97: 1258-1265.
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Idiotype-encoding recombinant adenoviruses provide protective immunity against murine B-cell lymphomas
- John M. Timmerman, Clemens B. Caspar, Stacie L. Lambert, Athanasia D. Syrengelas, and Ronald Levy
Blood 2001; 97: 1370-1377.
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A gene therapy approach for treating T-cell-mediated autoimmune diseases
- Chiann-Chyi Chen, Amariliz Rivera, Naomi Ron, Joseph P. Dougherty, and Yacov Ron
Blood 2001; 97: 886-894.
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Second generation knockout sickle mice: the effect of HbF
- Mary E. Fabry, Sandra M. Suzuka, Rona S. Weinberg, Christine Lawrence, Stephen M. Factor, John G. Gilman, Frank Costantini, and Ronald L. Nagel
Blood 2001; 97: 410-418.
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Systemic delivery of an adenoviral vector encoding canine factor VIII results in short-term phenotypic correction, inhibitor development, and biphasic liver toxicity in hemophilia A dogs
- Angela M. Gallo-Penn, Pamela S. Shirley, Julie L. Andrews, Shawn Tinlin, Sandy Webster, Cherie Cameron, Christine Hough, Colleen Notley, David Lillicrap, Michael Kaleko, and Sheila Connelly
Blood 2001; 97: 107-113.
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