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Human Gene Therapy|October 25, 2000
Packaging cell line characteristics and optimizing retroviral vector titer: the National Gene Vector Laboratory experienceL Reeves, P Smucker, K CornettaHuman Gene Therapy|October 25, 2000
Efficient transformation of primary human amniocytes by E1 functions of Ad5: generation of new cell lines for adenoviral vector productionG Schiedner, S Hertel, S KochanekHuman Gene Therapy|October 25, 2000
Treatment of a lysosomal storage disease, mucopolysaccharidosis VII, with microencapsulated recombinant cellsC J Ross, L Bastedo, S A Maier, et al.Human Gene Therapy|November 24, 1999
A high-efficiency Cre/loxP-based system for construction of adenoviral vectorsP Ng, R J Parks, D T Cummings, et al.Human Gene Therapy|October 9, 1999
Engraftment of hematopoietic progenitor cells transduced with the Fanconi anemia group C gene (FANCC)J M Liu, S Kim, E J Read, et al.Human Gene Therapy|October 9, 1999
A pressure-mediated nonviral method for efficient arterial gene and oligonucleotide transferH E von der Leyen, R Braun-Dullaeus, M J Mann, et al.Human Gene Therapy|October 9, 1999
In vivo transfer of bacterial marker genes results in differing levels of gene expression and tumor progression in immunocompetent and immunodeficient miceK V Lukacs, C D Porter, O E Pardo, et al.Human Gene Therapy|October 9, 1999
Conferral of an antiviral state to CD4+ cells by a zipper motif envelope mutant of the human immunodeficiency virus type 1 transmembrane protein gp41C K Chuang, S F Lee, S S ChenHuman Gene Therapy|December 28, 1999
Solvoplex: a new type of synthetic vector for intrapulmonary gene deliveryK Schughart, R Bischoff, U B Rasmussen, et al.Human Gene Therapy|December 28, 1999
Intravenous cytokine gene delivery by lipid-DNA complexes controls the growth of established lung metastasesS W Dow, R E Elmslie, L G Fradkin, et al.Pageof 413