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Gene Therapy
Citations 81-90 of 434 total displayed.
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Past content
(since Aug 1998):
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Lentivirus vectors expressing short hairpin RNAs against the U3-overlapping region of HIV nef inhibit HIV replication and infectivity in primary macrophages
- Takuya Yamamoto, Hiroyuki Miyoshi, Norio Yamamoto, Naoki Yamamoto, Jun-ichiro Inoue, and Yasuko Tsunetsugu-Yokota
Blood 2006; 108: 3305-3312.
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Correction of the disease phenotype in canine leukocyte adhesion deficiency using ex vivo hematopoietic stem cell gene therapy
- Thomas R. Bauer, Jr, Mehreen Hai, Laura M. Tuschong, Tanya H. Burkholder, Yu-chen Gu, Robert A. Sokolic, Cole Ferguson, Cynthia E. Dunbar, and Dennis D. Hickstein
Blood 2006; 108: 3313-3320.
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Effects of transient immunosuppression on adenoassociated, virus-mediated, liver-directed gene transfer in rhesus macaques and implications for human gene therapy
- Haiyan Jiang, Linda B. Couto, Susannah Patarroyo-White, Tongyao Liu, Dea Nagy, Joseph A. Vargas, Shangzhen Zhou, Ciaran D. Scallan, Jurg Sommer, Sharmila Vijay, Federico Mingozzi, Katherine A. High, and Glenn F. Pierce
Blood 2006; 108: 3321-3328.
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Gene transfer of cytidine deaminase protects myelopoiesis from cytidine analogs in an in vivo murine transplant model
- Ina Rattmann, Veronika Kleff, Ursula R. Sorg, Walter Bardenheuer, Annette Brueckner, Ralf A. Hilger, Bertram Opalka, Siegfried Seeber, Michael Flasshove, and Thomas Moritz
Blood 2006; 108: 2965-2971.
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Induction of antigen-specific tolerance by intrathymic injection of lentiviral vectors
- Gilles Marodon, Sylvain Fisson, Béatrice Levacher, Monique Fabre, Benoît L. Salomon, and David Klatzmann
Blood 2006; 108: 2972-2978.
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Ex vivo gene therapy with lentiviral vectors rescues adenosine deaminase (ADA)deficient mice and corrects their immune and metabolic defects
- Alessandra Mortellaro, Raisa Jofra Hernandez, Matteo M. Guerrini, Filippo Carlucci, Antonella Tabucchi, Maurilio Ponzoni, Francesca Sanvito, Claudio Doglioni, Clelia Di Serio, Luca Biasco, Antonia Follenzi, Luigi Naldini, Claudio Bordignon, Maria Grazia Roncarolo, and Alessandro Aiuti
Blood 2006; 108: 2979-2988.
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MicroRNAs modulate the angiogenic properties of HUVECs
- Laura Poliseno, Andrea Tuccoli, Laura Mariani, Monica Evangelista, Lorenzo Citti, Keith Woods, Alberto Mercatanti, Scott Hammond, and Giuseppe Rainaldi
Blood 2006; 108: 3068-3071.
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Cell-culture assays reveal the importance of retroviral vector design for insertional genotoxicity
- Ute Modlich, Jens Bohne, Manfred Schmidt, Christof von Kalle, Sabine Knöss, Axel Schambach, and Christopher Baum
Blood 2006; 108: 2545-2553.
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Multiple vitamin K-dependent coagulation zymogens promote adenovirus-mediated gene delivery to hepatocytes
- Alan L. Parker, Simon N. Waddington, Campbell G. Nicol, Dmitry M. Shayakhmetov, Suzanne M. Buckley, Laura Denby, Geoffrey Kemball-Cook, Shaoheng Ni, Andre Lieber, John H. McVey, Stuart A. Nicklin, and Andrew H. Baker
Blood 2006; 108: 2554-2561.
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Simple conditioning with monospecific CD4+CD25+ regulatory T cells for bone marrow engraftment and tolerance to multiple gene products
- David-Alexandre Gross, Pascal Chappert, Marylene Leboeuf, Virginie Monteilhet, Laetitia Van Wittenberghe, Olivier Danos, and Jean Davoust
Blood 2006; 108: 1841-1848.
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