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Human Gene Therapy|November 26, 1998
Targeting bacteriophage to mammalian cell surface receptors for gene deliveryD Larocca, A Witte, W Johnson, et al.
Human Gene Therapy|November 26, 1998
Characterization of diverse viral vector preparations, using a simple and rapid whole-virion dot-blot methodD M Nelson, J J Wahlfors, L Chen, et al.
Human Gene Therapy|January 18, 2006
Adeno-associated virus types 5 and 6 use distinct receptors for cell entryMichael P Seiler, A Dusty Miller, Joseph Zabner, et al.
Human Gene Therapy|January 18, 2006
Intravenous and isolated limb perfusion delivery of wild type and a tumor-selective replicating mutant vaccinia virus in nonhuman primatesArpana M Naik, Sricharan Chalikonda, J Andrea McCart, et al.
Human Gene Therapy|January 18, 2006
Efficient AAV1-AAV2 hybrid vector for gene therapy of hemophiliaBernd Hauck, Ray Ruian Xu, Jing Xie, et al.
Human Gene Therapy|January 18, 2006
Tumor-targeting nanoimmunoliposome complex for short interfering RNA deliveryKathleen F Pirollo, Gerald Zon, Antonina Rait, et al.
Human Gene Therapy|October 30, 1998
Genetically engineered antibodies in gene transfer and gene therapyM Pelegrin, M Marin, D Noël, et al.
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