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Human Gene Therapy|February 9, 2008
Delivery vehicles for small interfering RNA in vivoAntonin R de FougerollesHuman Gene Therapy|April 12, 2008
Delivery of recombinant adeno-associated virus-mediated human tissue kallikrein for therapy of chronic renal failure in ratsLing Tu, Xizhen Xu, Huaibing Wan, et al.Human Gene Therapy|January 5, 1999
Tissue-specific, cell cycle-regulated chimeric transcription factors for the targeting of gene expression to tumor cellsV Jérôme, R MüllerHuman Gene Therapy|January 5, 1999
Construction, propagation, and titer estimation of recombinant adenoviruses carrying proapoptotic genesN Shinoura, M Ohashi, Y Yoshida, et al.Human Gene Therapy|January 5, 1999
Long-term genetic modification of rhesus monkey hematopoietic cells following transplantation of adenoassociated virus vector-transduced CD34+ cellsS Schimmenti, J Boesen, E A Claassen, et al.Human Gene Therapy|January 5, 1999
Herpes simplex virus type 1 DNA amplified as bacterial artificial chromosome in Escherichia coli: rescue of replication-competent virus progeny and packaging of amplicon vectorsY Saeki, T Ichikawa, A Saeki, et al.Human Gene Therapy|February 28, 2002
Adenovirus vector-induced inflammation: capsid-dependent induction of the C-C chemokine RANTES requires NF-kappa BGloria P Bowen, Stephanie L Borgland, Mindy Lam, et al.Human Gene Therapy|February 28, 2002
Immunoinhibitory DNA vaccine protects against autoimmune diabetes through cDNA encoding a selective CTLA-4 (CD152) ligandGerald J Prud'homme, Yigang Chang, Xiaoying LiHuman Gene Therapy|February 28, 2002
Self-assembly of a virus-mimicking nanostructure system for efficient tumor-targeted gene deliveryLiang Xu, Peter Frederik, Kathleen F Pirollo, et al.Human Gene Therapy|March 21, 2006
Modified adenoviral vectors ablated for coxsackievirus-adenovirus receptor, alphav integrin, and heparan sulfate binding reduce in vivo tissue transduction and toxicityNaoya Koizumi, Kenji Kawabata, Fuminori Sakurai, et al.Pageof 414