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Hepatology (Baltimore, Md.)|July 29, 2003
A potent and specific morpholino antisense inhibitor of hepatitis C translation in miceAnton P McCaffrey, Leonard Meuse, Mobin Karimi, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 8, 2003
Free DNA ends are essential for concatemerization of synthetic double-stranded adeno-associated virus vector genomes transfected into mouse hepatocytes in vivoHiroyuki Nakai, Sally Fuess, Theresa A Storm, et al.
Gene Therapy|October 19, 2019
Distinct transduction of muscle tissue in mice after systemic delivery of AAVpo1 vectorsWarut Tulalamba, Jonas Weinmann, Quang Hong Pham, et al.
Biotechnology Journal|September 5, 2014
CRISPR/Cas9-mediated genome engineering: an adeno-associated viral (AAV) vector toolboxElena Senís, Chronis Fatouros, Stefanie Große, et al.
Human Gene Therapy|April 1, 2004
Comparison of adenoviral and adeno-associated viral vectors for pancreatic gene delivery in vivoAlfred Y Wang, Peter D Peng, Anja Ehrhardt, et al.
RNA (New York, N.Y.)|February 26, 2010
Human tRNA-derived small RNAs in the global regulation of RNA silencingDirk Haussecker, Yong Huang, Ashley Lau, et al.
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