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Human Gene Therapy|August 16, 2017
Evaluation of Intrathecal Routes of Administration for Adeno-Associated Viral Vectors in Large AnimalsChristian Hinderer, Peter Bell, Nathan Katz, et al.Human Gene Therapy|August 17, 2017
Advances and Challenges in Cardiovascular Gene TherapyJohanna Lähteenvuo, Seppo Ylä-HerttualaHuman Gene Therapy|August 18, 2017
Improved Hematopoietic Gene Therapy in a Mouse Model of Fanconi Anemia Mediated by Mesenchymal Stromal CellsMaría Fernández-García, Maria Luisa Lamana, Miriam Hernando-Rodríguez, et al.Human Gene Therapy|August 22, 2017
The Future Looks Brighter After 25 Years of Retinal Gene TherapyAlberto Auricchio, Alexander J Smith, Robin R AliHuman Gene Therapy|August 22, 2017
Lentiviral Vector Promoter is Decisive for Aberrant Transcript FormationSimone J Scholz, Raffaele Fronza, Cynthia C Bartholomä, et al.Human Gene Therapy|August 23, 2017
Minicircle Versus Plasmid DNA Delivery by Receptor-Targeted PolyplexesAna Krhac Levacic, Stephan Morys, Susanne Kempter, et al.Human Gene Therapy|August 23, 2017
Plasmid DNA Manufacturing for Indirect and Direct Clinical ApplicationsMarco Schmeer, Tatjana Buchholz, Martin SchleefHuman Gene Therapy|February 9, 2019
Preclinical Assessment of Suitable Natural Killer Cell Sources for Chimeric Antigen Receptor Natural Killer-Based "Off-the-Shelf" Acute Myeloid Leukemia ImmunotherapiesStephan Kloess, Olaf Oberschmidt, Julia Dahlke, et al.Human Gene Therapy|February 9, 2019
A "Hibernating-Like" Viable State Induced by Lentiviral Vector-Mediated Pigment Epithelium-Derived Factor Overexpression in Rat Acute Ischemic MyocardiumYanliang Yuan, Bing Huang, Haoran Miao, et al.Human Gene Therapy|January 26, 2018
Gene Therapy for Hemophilia and Duchenne Muscular Dystrophy in ChinaXionghao Liu, Mujun Liu, Lingqian Wu, et al.Pageof 414