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Human Gene Therapy|June 10, 1996
Gene targeting to the centromeric DNA of a human minichromosomeE Raimondi, M Balzaretti, D Moralli, et al.Human Gene Therapy|June 10, 1996
In vitro and in vivo liposome-mediated gene transfer leads to human MDR1 expression in mouse bone marrow progenitor cellsI Aksentijevich, I Pastan, Y Lunardi-Iskandar, et al.Human Gene Therapy|June 10, 1996
Molecular analysis of T lymphocyte-directed gene therapy for adenosine deaminase deficiency: long-term expression in vivo of genes introduced with a retroviral vectorC A Mullen, K Snitzer, K W Culver, et al.Human Gene Therapy|June 10, 1996
Gene therapy: socioeconomic and ethical issues. A roundtable discussionA L Hillman, M K Brenner, A L Caplan, et al.Human Gene Therapy|June 20, 1996
High-efficiency transduction of freshly isolated human tumor cells using adenoviral interleukin-2 vectorsT Leimig, M Brenner, J Ramsey, et al.Human Gene Therapy|September 1, 1995
Retroviral gene transfer into the intestinal epitheliumC Lau, H E Soriano, F D Ledley, et al.Human Gene Therapy|September 1, 1995
In vivo delivery of human alpha-L-iduronidase in mice implanted with neo-organsA Salvetti, P Moullier, V Cornet, et al.Human Gene Therapy|September 1, 1995
Regenerating cells in human airway surface epithelium represent preferential targets for recombinant adenovirusF Dupuit, J M Zahm, D Pierrot, et al.Human Gene Therapy|September 1, 1995
In vivo marking of spontaneous or vaccine-induced fibrosarcomas in the domestic house cat, using an adenoviral vector containing a bifunctional fusion protein, GAL-TEKF C Marini, J P Cannon, J W Belmont, et al.Pageof 414