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Gene Therapy
Citations 251-260 of 434 total displayed.
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Past content
(since Aug 1998):
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AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B
- Catherine S. Manno, Amy J. Chew, Sylvia Hutchison, Peter J. Larson, Roland W. Herzog, Valder R. Arruda, Shing Jen Tai, Margaret V. Ragni, Arthur Thompson, Margareth Ozelo, Linda B. Couto, Debra G. B. Leonard, Frederick A. Johnson, Alan McClelland, Ciaran Scallan, Erik Skarsgard, Alan W. Flake, Mark A. Kay, Katherine A. High, and Bertil Glader
Blood 2003; 101: 2963-2972.
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Mesenchymal stem cells distribute to a wide range of tissues following systemic infusion into nonhuman primates
- Steven M. Devine, Carrington Cobbs, Matt Jennings, Amelia Bartholomew, and Ron Hoffman
Blood 2003; 101: 2999-3001.
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Coincident expression of the chemokine receptors CCR6 and CCR7 by pathologic Langerhans cells in Langerhans cell histiocytosis
- Mark D. Fleming, Jack L. Pinkus, Sarah W. Alexander, Carmen Tam, Massimo Loda, Stephen E. Sallan, Kim E. Nichols, David F. Carpentieri, Geraldine S. Pinkus, and Barrett J. Rollins
Blood 2003; 101: 2473-2475.
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Humoral immune response in mice against a circulating antigen induced by adenoviral transfer is strictly dependent on expression in antigen-presenting cells
- Bart R. De Geest, Sophie A. Van Linthout, and Désiré Collen
Blood 2003; 101: 2551-2556.
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Oncolytic measles viruses displaying a single-chain antibody against CD38, a myeloma cell marker
- Kah-Whye Peng, Kathleen A. Donovan, Urs Schneider, Roberto Cattaneo, John A. Lust, and Stephen J. Russell
Blood 2003; 101: 2557-2562.
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Persistence and expression of the adenosine deaminase gene for 12 years and immune reaction to gene transfer components: long-term results of the first clinical gene therapy trial
- Linda Mesler Muul, Laura M. Tuschong, Sherry Lau Soenen, G. Jayashree Jagadeesh, W. Jay Ramsey, Zhifeng Long, Charles S. Carter, Elizabeth K. Garabedian, Melinna Alleyne, Margaret Brown, Wendy Bernstein, Shepherd H. Schurman, Thomas A. Fleisher, Susan F. Leitman, Cynthia E. Dunbar, R. Michael Blaese, and Fabio Candotti
Blood 2003; 101: 2563-2569.
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Gene therapy for Wiskott-Aldrich syndrome: rescue of T-cell signaling and amelioration of colitis upon transplantation of retrovirally transduced hematopoietic stem cells in mice
- Christoph Klein, Deanna Nguyen, Ching-Hui Liu, Atsushi Mizoguchi, Atul K. Bhan, Hiroaki Miki, Tadaomi Takenawa, Fred S. Rosen, Fred W. Alt, Richard C. Mulligan, and Scott B. Snapper
Blood 2003; 101: 2159-2166.
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IL-7 surface-engineered lentiviral vectors promote survival and efficient gene transfer in resting primary T lymphocytes
- Els Verhoeyen, Valerie Dardalhon, Odile Ducrey-Rundquist, Didier Trono, Naomi Taylor, and François-Loïc Cosset
Blood 2003; 101: 2167-2174.
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The degree of phenotypic correction of murine  -thalassemia intermedia following lentiviral-mediated transfer of a human  -globin gene is influenced by chromosomal position effects and vector copy number
- Derek A. Persons, Phillip W. Hargrove, Esther R. Allay, Hideki Hanawa, and Arthur W. Nienhuis
Blood 2003; 101: 2175-2183.
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Retrovirus-mediated IL-7 expression in leukemic dendritic cells generated from primary acute myelogenous leukemias enhances their functional properties
- Concha Bello-Fernández, Jana Stasakova, Alexander Renner, Nicole Carballido-Perrig, Margit Koening, Martina Waclavicek, Otto Madjic, Leopold Oehler, Oskar Haas, José M. Carballido, Michael Buschle, and Walter Knapp
Blood 2003; 101: 2184-2190.
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