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Human Gene Therapy|December 17, 2010
Corneal endothelial cells are protected from apoptosis by gene therapyThomas A Fuchsluger, Ula Jurkunas, Andrius Kazlauskas, et al.
Human Gene Therapy|December 4, 2010
AAV delivery of wild-type rhodopsin preserves retinal function in a mouse model of autosomal dominant retinitis pigmentosaHaoyu Mao, Thomas James, Alison Schwein, et al.
Human Gene Therapy|February 1, 2011
Gene therapy for canine leukocyte adhesion deficiency with lentiviral vectors using the murine stem cell virus and human phosphoglycerate kinase promotersMichael J Hunter, Huifen Zhao, Laura M Tuschong, et al.
Human Gene Therapy|January 13, 2011
Mycophenolate mofetil impairs transduction of single-stranded adeno-associated viral vectorsPaula S Montenegro-Miranda, Lysbeth ten Bloemendaal, Cindy Kunne, et al.
Human Gene Therapy|July 29, 2010
Rapid production of clinical-grade gammaretroviral vectors in expanded surface roller bottles using a "modified" step-filtration process for clearance of packaging cellsSteven A Feldman, Stephanie L Goff, Hui Xu, et al.
Human Gene Therapy|April 22, 2011
p53 inhibits adeno-associated viral vector integrationJeana Zacharias, Liudmila G Romanova, Jeremiah Menk, et al.
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.
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