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Human Gene Therapy|March 21, 1998
Plasmid DNA encoding targeted naturally processed peptides generates protective cytotoxic T lymphocyte responses in immunized animalsM L Hedley, J L Strominger, R G UrbanHuman Gene Therapy|March 21, 1998
Bone marrow stromal cells as targets for gene therapy of hemophilia AM K Chuah, H Brems, V Vanslembrouck, et al.Human Gene Therapy|March 21, 1998
Fluorescent virions: dynamic tracking of the pathway of adenoviral gene transfer vectors in living cellsP L Leopold, B Ferris, I Grinberg, et al.Human Gene Therapy|August 10, 1997
LacZ and interleukin-3 expression in vivo after retroviral transduction of marrow-derived human osteogenic mesenchymal progenitorsJ A Allay, J E Dennis, S E Haynesworth, et al.Human Gene Therapy|August 10, 1997
Replicative potential and telomere length in human skeletal muscle: implications for satellite cell-mediated gene therapyS Decary, V Mouly, C B Hamida, et al.Human Gene Therapy|August 10, 1997
Highly efficient retrovirus-mediated gene transfer into rat hepatocytes in vivoO Kitten, F L Cosset, N FerryHuman Gene Therapy|July 20, 1997
Use of the cosmid adenoviral vector cloning system for the in vitro construction of recombinant adenoviral vectorsS Fu, A B DeisserothHuman Gene Therapy|June 13, 1998
Quantitation of host cell DNA contaminate in pharmaceutical-grade plasmid DNA using competitive polymerase chain reaction and enzyme-linked immunosorbent assayR Lahijani, M Duhon, E Lusby, et al.Human Gene Therapy|June 13, 1998
Long-term expression of human clotting factor IX from retrovirally transduced primary human keratinocytes in vivoS J White, S M Page, P Margaritis, et al.Human Gene Therapy|June 13, 1998
Internal ribosomal entry site-containing retroviral vectors with green fluorescent protein and drug resistance markersV V Levenson, E D Transue, I B RoninsonPageof 414