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Human Gene Therapy|November 11, 2014
Aerosol-mediated delivery of AAV2/6-IκBα attenuates lipopolysaccharide-induced acute lung injury in ratsRonan J MacLoughlin, Brendan D Higgins, James Devaney, et al.Human Gene Therapy|November 25, 2014
Intravenous administration of retroviral replicating vector, Toca 511, demonstrates therapeutic efficacy in orthotopic immune-competent mouse glioma modelTiffany T Huang, Shraddha Parab, Ryan Burnett, et al.Human Gene Therapy|June 15, 2016
Naturally Existing Oncolytic Virus M1 Is Nonpathogenic for the Nonhuman Primates After Multiple Rounds of Repeated Intravenous InjectionsHaipeng Zhang, Yuan Lin, Kai Li, et al.Human Gene Therapy|March 5, 2016
Disruption of Microtubules Post-Virus Entry Enhances Adeno-Associated Virus Vector TransductionPing-Jie Xiao, Angela M Mitchell, Lu Huang, et al.Human Gene Therapy|March 27, 2013
Hepatic stellate cell-targeted delivery of hepatocyte growth factor transgene via bile duct infusion enhances its expression at fibrotic foci to regress dimethylnitrosamine-induced liver fibrosisBalakrishnan Chakrapani Narmada, Yuzhan Kang, Lakshmi Venkatraman, et al.Human Gene Therapy|December 30, 2014
Fanconi anemia gene editing by the CRISPR/Cas9 systemMark J Osborn, Richard Gabriel, Beau R Webber, et al.Human Gene Therapy|January 6, 2015
Immunological effects of a tumor necrosis factor alpha-armed oncolytic adenovirusMari Hirvinen, Maria Rajecki, Mika Kapanen, et al.Human Gene Therapy|June 8, 2012
Recent progress in gene therapy for hemophiliaMarinee K Chuah, Nisha Nair, Thierry VandenDriesscheHuman Gene Therapy|March 23, 2013
Strong cortical and spinal cord transduction after AAV7 and AAV9 delivery into the cerebrospinal fluid of nonhuman primatesLluis Samaranch, Ernesto A Salegio, Waldy San Sebastian, et al.Human Gene Therapy|March 23, 2013
Gene therapy for rare diseases: summary of a National Institutes of Health workshop, September 13, 2012Marina O'Reilly, Donald B Kohn, Jeffrey Bartlett, et al.Pageof 413