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Human Gene Therapy|December 1, 1994
Inhibition of human immunodeficiency virus type-1 by retroviral vectors expressing antisense-TARM K Chuah, T VandenDriessche, H K Chang, et al.Human Gene Therapy|December 1, 1994
Gene expression following direct injection of DNA into liverM A Hickman, R W Malone, K Lehmann-Bruinsma, et al.Human Gene Therapy|December 1, 1994
Emergence of early region 1-containing replication-competent adenovirus in stocks of replication-defective adenovirus recombinants (delta E1 + delta E3) during multiple passages in 293 cellsH Lochmüller, A Jani, J Huard, et al.Human Gene Therapy|June 1, 1993
Evaluation of expression of transferred genes in differentiating myeloid cells: expression of human glucocerebrosidase in murine macrophagesD L Freas, P H Correll, S F Dougherty, et al.Human Gene Therapy|March 28, 2002
Effective gene transfer to human melanomas via integrin-targeted adenoviral vectorsTakafumi Nakamura, Kenzo Sato, Hirofumi HamadaHuman Gene Therapy|March 28, 2002
Replication-selective herpes simplex virus type 1 mutant therapy of cervical cancer is enhanced by low-dose radiationStephanie V Blank, Stephen C Rubin, George Coukos, et al.Human Gene Therapy|March 5, 2002
Gene therapy of murine solid tumors with T cells transduced with a retroviral vascular endothelial growth factor--immunotoxin target geneNi Jin, Wei Chen, Bruce R Blazar, et al.Human Gene Therapy|October 1, 1994
Gene transfer in baboons using prosthetic vascular grafts seeded with retrovirally transduced smooth muscle cells: a model for local and systemic gene therapyR L Geary, A W Clowes, S Lau, et al.Human Gene Therapy|October 1, 1994
Systemic delivery of secreted protein by grafts of epidermal keratinocytes: prospects for keratinocyte gene therapyE S Fenjves, J Smith, S Zaradic, et al.Human Gene Therapy|October 1, 1994
Adenoviral vector-mediated gene transfer into sheep arteries using a double-balloon catheterJ J Rome, V Shayani, K D Newman, et al.Pageof 413