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Gene Therapy
Citations 161-170 of 434 total displayed.
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Past content
(since Aug 1998):
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Noninvasive MR imaging of magnetically labeled stem cells to directly identify neovasculature in a glioma model
- Stasia A. Anderson, John Glod, Ali S. Arbab, Martha Noel, Parwana Ashari, Howard A. Fine, and Joseph A. Frank
Blood 2005; 105: 420-425.
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Monitoring the effect of gene silencing by RNA interference in human CD34+ cells injected into newborn RAG2-/-  c-/- mice: functional inactivation of p53 in developing T cells
- Ramon Gimeno, Kees Weijer, Arie Voordouw, Christel H. Uittenbogaart, Nicolas Legrand, Nuno L. Alves, Erwin Wijnands, Bianca Blom, and Hergen Spits
Blood 2004; 104: 3886-3893.
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Successful correction of the human  -thalassemia major phenotype using a lentiviral vector
- Geetha Puthenveetil, Jessica Scholes, Denysha Carbonell, Naveen Qureshi, Ping Xia, Licheng Zeng, Shulian Li, Ying Yu, Alan L Hiti, Jiing-Kuan Yee, and Punam Malik
Blood 2004; 104: 3445-3453.
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Tumor cells escape suicide gene therapy by genetic and epigenetic instability
- Oliver Frank, Cornelia Rudolph, Christoph Heberlein, Nils von Neuhoff, Evelin Schröck, Axel Schambach, Brigitte Schlegelberger, Boris Fehse, Wolfram Ostertag, Carol Stocking, and Christopher Baum
Blood 2004; 104: 3543-3549.
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Targeted retroviral transduction of c-kit+ hematopoietic cells using novel ligand display technology
- Anil Chandrashekran, Myrtle Y. Gordon, and Colin Casimir
Blood 2004; 104: 2697-2703.
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Multistep process through which adenoviral vector vaccine overcomes anergy to tumor-associated antigens
- Yucheng Tang, Lixin Zhang, Jing Yuan, Hakan Akbulut, Jonathan Maynard, Phyllis-Jean Linton, and Albert Deisseroth
Blood 2004; 104: 2704-2713.
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Permanent phenotypic correction of hemophilia B in immunocompetent mice by prenatal gene therapy
- Simon N. Waddington, Megha S. Nivsarkar, Ajay R. Mistry, Suzanne M. K. Buckley, Geoffrey Kemball-Cook, Karen L. Mosley, Kyriacos Mitrophanous, Pippa Radcliffe, Maxine V. Holder, Mairi Brittan, Anastasios Georgiadis, Faisal Al-Allaf, Brian W. Bigger, Lisa G. Gregory, H. Terence Cook, Robin R. Ali, Adrian Thrasher, Edward G. D. Tuddenham, Mike Themis, and Charles Coutelle
Blood 2004; 104: 2714-2721.
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Targeted delivery of adenoviral vectors by cytotoxic T cells
- Patricia Yotnda, Barbara Savoldo, Nicolas Charlet-Berguerand, Cliona Rooney, and Malcolm Brenner
Blood 2004; 104: 2272-2280.
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Extended -globin locus control region elements promote consistent therapeutic expression of a -globin lentiviral vector in murine -thalassemia
- Hideki Hanawa, Phillip W. Hargrove, Steven Kepes, Deo K. Srivastava, Arthur W. Nienhuis, and Derek A. Persons
Blood 2004; 104: 2281-2290.
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Conserved CTL epitopes on the adenovirus hexon protein expand subgroup cross-reactive and subgroup-specific CD8+ T cells
- Ann M. Leen, Uluhan Sili, Elio F. Vanin, Alan M. Jewell, Weidong Xie, Dario Vignali, Pedro A. Piedra, Malcolm K. Brenner, and Cliona M. Rooney
Blood 2004; 104: 2432-2440.
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