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Human Gene Therapy|May 6, 2011
Cardiac gene transfer of short hairpin RNA directed against phospholamban effectively knocks down gene expression but causes cellular toxicity in caninesLawrence T Bish, Meg M Sleeper, Caryn Reynolds, et al.Human Gene Therapy|May 11, 2011
Intravesical interleukin-15 gene therapy in an orthotopic bladder cancer modelKazuhiro Matsumoto, Eiji Kikuchi, Minoru Horinaga, et al.Human Gene Therapy|April 2, 2011
Delivery of AAV2/9-microdystrophin genes incorporating helix 1 of the coiled-coil motif in the C-terminal domain of dystrophin improves muscle pathology and restores the level of α1-syntrophin and α-dystrobrevin in skeletal muscles of mdx miceTaeyoung Koo, Alberto Malerba, Takis Athanasopoulos, et al.Human Gene Therapy|March 24, 2011
Human embryonic stem cell-derived mesenchymal stem cells as cellular delivery vehicles for prodrug gene therapy of glioblastomaXiao Ying Bak, Dang Hoang Lam, Jingye Yang, et al.Human Gene Therapy|April 14, 2011
Lentiviral vectors: their molecular design, safety, and use in laboratory and preclinical researchBoro DropulićHuman Gene Therapy|April 5, 2011
A foamy virus vector system for stable and efficient RNAi expression in mammalian cellsMagdalini Papadaki, Elena Konstantina Siapati, George VassilopoulosHuman Gene Therapy|October 26, 2018
Somatic Gene Editing of GUCY2D by AAV-CRISPR/Cas9 Alters Retinal Structure and Function in Mouse and MacaqueK Tyler McCullough, Sanford L Boye, Diego Fajardo, et al.Human Gene Therapy|July 16, 2019
Gene Therapy for Methylmalonic Acidemia: Past, Present, and FutureRandy J Chandler, Charles P VendittiHuman Gene Therapy|October 19, 2013
Gene therapy with beta-defensin 2 induces antitumor immunity and enhances local antitumor effectsDan Li, Wei Wang, Hua-shan Shi, et al.Human Gene Therapy|October 25, 2013
Mouse regenerating myofibers detected as false-positive donor myofibers with anti-human spectrinAnete Rozkalne, Carl Adkin, Jinhong Meng, et al.Pageof 414