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Human Gene Therapy|June 28, 2003
Pathways of removal of free DNA vector ends in normal and DNA-PKcs-deficient SCID mouse hepatocytes transduced with rAAV vectorsHiroyuki Nakai, Theresa A Storm, Sally Fuess, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|April 3, 2017
Sequence-Modified Antibiotic Resistance Genes Provide Sustained Plasmid-Mediated Transgene Expression in MammalsJiamiao Lu, Feijie Zhang, Andrew Z Fire, et al.Human Gene Therapy|April 7, 2005
Modified infusion procedures affect recombinant adeno-associated virus vector type 2 transduction in the liverKazuo Ohashi, Hiroyuki Nakai, Linda B Couto, et al.Nature Structural & Molecular Biology|February 3, 2009
Biological basis for restriction of microRNA targets to the 3' untranslated region in mammalian mRNAsShuo Gu, Lan Jin, Feijie Zhang, et al.Journal of Virology|March 3, 2004
Rapid uncoating of vector genomes is the key to efficient liver transduction with pseudotyped adeno-associated virus vectorsClare E Thomas, Theresa A Storm, Zan Huang, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|August 30, 2003
Minicircle DNA vectors devoid of bacterial DNA result in persistent and high-level transgene expression in vivoZhi-Ying Chen, Cheng-Yi He, Anja Ehrhardt, et al.Current Biology : CB|July 17, 2012
Slicing-independent RISC activation requires the argonaute PAZ domainShuo Gu, Lan Jin, Yong Huang, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|July 31, 2008
Expression of shRNA from a tissue-specific pol II promoter is an effective and safe RNAi therapeuticJeffery C Giering, Dirk Grimm, Theresa A Storm, et al.Human Gene Therapy|March 18, 2003
Optimization of cis-acting elements for gene expression from nonviral vectors in vivoAnja Ehrhardt, Peter D Peng, Hui Xu, et al.Journal of Virology|August 10, 2007
The role of DNA-PKcs and artemis in opening viral DNA hairpin termini in various tissues in miceKatsuya Inagaki, Congrong Ma, Theresa A Storm, et al.Pageof 19