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Human Gene Therapy|June 13, 1998
A method of limited replication for the efficient in vivo delivery of adenovirus to cancer cellsJ S Han, D Qian, M S Wicha, et al.Human Gene Therapy|June 13, 1998
Adenovirus-mediated in vivo gene transfer in guinea pig middle ear mucosaM Mondain, S Restituito, V Vincenti, et al.Human Gene Therapy|April 29, 1998
In vitro selection for K562 cells with higher retrovirally mediated copy number of aldehyde dehydrogenase class-1 and higher resistance to 4-hydroperoxycyclophosphamideJ S Moreb, M Schweder, B Gray, et al.Human Gene Therapy|April 29, 1998
High-level dystrophin expression after adenovirus-mediated dystrophin minigene transfer to skeletal muscle of dystrophic dogs: prolongation of expression with immunosuppressionJ M Howell, H Lochmüller, A O'Hara, et al.Human Gene Therapy|April 29, 1998
Vector-specific complementation profiles of two independent primary defects in cystic fibrosis airwaysY Zhang, Q Jiang, L Dudus, et al.Human Gene Therapy|April 29, 1998
Combination therapy with interleukin-2 and wild-type p53 expressed by adenoviral vectors potentiates tumor regression in a murine model of breast cancerB M Pützer, J L Bramson, C L Addison, et al.Human Gene Therapy|April 29, 1998
Cancer gene therapy by direct tumor injections of a nonviral T7 vector encoding a thymidine kinase geneX Chen, Y Li, K Xiong, et al.Human Gene Therapy|March 21, 1998
Repetitive adenovirus administration to the parotid gland: role of immunological barriers and induction of oral toleranceH Kagami, J C Atkinson, S M Michalek, et al.Human Gene Therapy|April 3, 1998
Construction of vectors expressing bioactive heterodimeric and single-chain murine interleukin-12 for gene therapyY L Lee, M H Tao, Y H Chow, et al.Human Gene Therapy|April 3, 1998
Inhibition of human immunodeficiency virus replication and growth advantage of CD4+ T cells from HIV-infected individuals that express intracellular antibodies against HIV-1 gp120 or TatM C Poznansky, R Foxall, A Mhashilkar, et al.Pageof 414