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Human 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.Human Gene Therapy|August 25, 2017
Advances in Gene Therapy for HemophiliaAmit C Nathwani, Andrew M Davidoff, Edward G D TuddenhamHuman Gene Therapy|January 18, 2018
In Vivo Ovarian Cancer Gene Therapy Using CRISPR-Cas9Zhi-Yao He, Ya-Guang Zhang, Yu-Han Yang, et al.Human Gene Therapy|February 1, 2018
Overexpression of Hepatocyte Growth Factor mRNA Induced by Gene Transfer Attenuates Neointimal Hyperplasia After Balloon InjuryYu He, Li Mei, Ying Jin, et al.Human Gene Therapy|January 11, 2018
Biology of the Adrenal Gland Cortex Obviates Effective Use of Adeno-Associated Virus Vectors to Treat Hereditary Adrenal DisordersSandra Markmann, Bishnu P De, Jasmine Reid, et al.Pageof 413