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Human Gene Therapy|June 2, 2001
Long-term efficacy after [E1-, polymerase-] adenovirus-mediated transfer of human acid-alpha-glucosidase gene into glycogen storage disease type II knockout miceE Y Ding, B L Hodges, H Hu, et al.Human Gene Therapy|June 2, 2001
A new-generation stable inducible packaging cell line for lentiviral vectorsD Farson, R Witt, R McGuinness, et al.Human Gene Therapy|June 2, 2001
Preclinical safety evaluation of G207, a replication-competent herpes simplex virus type 1, inoculated intraprostatically in mice and nonhuman primatesS Varghese, J T Newsome, S D Rabkin, et al.Human Gene Therapy|March 10, 2001
Modulating the fibrinolytic system of peripheral blood mononuclear cells with adenovirusR R Schleef, M A Olman, L A Miles, et al.Human Gene Therapy|March 27, 2001
EGTA enhancement of adenovirus-mediated gene transfer to mouse tracheal epithelium in vivoQ Chu, J A St George, M Lukason, et al.Human Gene Therapy|March 27, 2001
Cochlear gene delivery through an intact round window membrane in mouseJ Jero, A N Mhatre, C J Tseng, et al.Human Gene Therapy|December 19, 2000
Effects of preexisting immunity on the response to herpes simplex-based oncolytic viral therapyK A Delman, J J Bennett, J S Zager, et al.Human Gene Therapy|December 19, 2000
Analysis of testes and semen from rabbits treated by intravenous injection with a retroviral vector encoding the human factor VIII gene: no evidence of germ line transductionH H Roehl, M E Leibbrandt, J S Greengard, et al.Human Gene Therapy|March 28, 2003
Ultrasound-guided percutaneous delivery of adenoviral vectors encoding the beta-galactosidase and human factor IX genes to early gestation fetal sheep in uteroAnna David, Terry Cook, Simon Waddington, et al.Human Gene Therapy|March 28, 2003
High-efficiency lentiviral vector-mediated gene transfer into murine macrophages and activated splenic B lymphocytesGabriela R Rossi, Mario R Mautino, Richard A MorganPageof 413