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Gene Therapy|June 15, 2001
A simplified system for constructing recombinant adenoviral vectors containing heterologous peptides in the HI loop of their fiber knobH Mizuguchi, N Koizumi, T Hosono, et al.Cold Spring Harbor Symposia on Quantitative Biology|July 28, 2006
Genomic progression in mouse models for liver tumorsA D Tward, K D Jones, S Yant, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|March 29, 2001
Linear DNAs concatemerize in vivo and result in sustained transgene expression in mouse liverZ Y Chen, S R Yant, C Y He, et al.Journal of Virology|December 1, 1996
Elimination of hepatitis C virus RNA in infected human hepatocytes by adenovirus-mediated expression of ribozymesA Lieber, C Y He, S J Polyak, et al.Journal of Virology|October 29, 1997
The role of Kupffer cell activation and viral gene expression in early liver toxicity after infusion of recombinant adenovirus vectorsA Lieber, C Y He, L Meuse, et al.Gene Therapy|June 17, 2003
Sustainable correction of junctional epidermolysis bullosa via transposon-mediated nonviral gene transferS Ortiz-Urda, Q Lin, S R Yant, et al.The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
IMAGe, a new clinical association of intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaliesE Vilain, M Le Merrer, C Lecointre, et al.Human Gene Therapy|December 1, 1992
Hepatic gene therapy: persistent expression of human alpha 1-antitrypsin in mice after direct gene delivery in vivoM A Kay, Q Li, T J Liu, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|August 3, 2001
Epstein-Barr virus/human vector provides high-level, long-term expression of alpha1-antitrypsin in miceS M Stoll, C R Sclimenti, E J Baba, et al.Gene Therapy|March 1, 1995
Strain related variations in adenovirally mediated transgene expression from mouse hepatocytes in vivo: comparisons between immunocompetent and immunodeficient inbred strainsD Barr, J Tubb, D Ferguson, et al.Pageof 11