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Showing results (91-100 of 221) with videos related to

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Molecular Therapy : the Journal of the American Society of Gene Therapy|August 27, 2021
Flies in the ointment: AAV vector preparations and tumor riskJunping Zhang, Xiangping Yu, Roland W Herzog, et al.
Journal of Virology|August 26, 2016
Heparan Sulfate Binding Promotes Accumulation of Intravitreally Delivered Adeno-associated Viral Vectors at the Retina for Enhanced Transduction but Weakly Influences TropismKenton T Woodard, Katharine J Liang, William C Bennett, et al.
Molecular Therapy. Methods & Clinical Development|March 4, 2024
Rationally engineered novel AAV capsids for intra-articular gene deliveryWenjun Li, Susi Liu Feng, Lizette Herrschaft, et al.
Scientific Reports|July 30, 2014
Adeno-associated viral vectors show serotype specific transduction of equine joint tissue explants and cultured monolayersDaniel D Hemphill, C Wayne McIlwraith, R Jude Samulski, et al.
Human Gene Therapy|June 6, 2017
AAV Gene Therapy for Alcoholism: Inhibition of Mitochondrial Aldehyde Dehydrogenase Enzyme Expression in Hepatoma CellsAnamaria C Sanchez, Chengwen Li, Barbara Andrews, 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.
Journal of Virology|November 12, 2003
Development and characterization of novel empty adenovirus capsids and their impact on cellular gene expressionJackie L Stilwell, Douglas M McCarty, Atsuko Negishi, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 17, 2011
Combination therapy utilizing shRNA knockdown and an optimized resistant transgene for rescue of diseases caused by misfolded proteinsChengwen Li, Pingjie Xiao, Steven James Gray, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 4, 2011
Systemic gene transfer to skeletal muscle using reengineered AAV vectorsJana L Phillips, Julia Hegge, Jon A Wolff, et al.
Journal of Virology|May 6, 2016
Identification and Validation of Small Molecules That Enhance Recombinant Adeno-associated Virus Transduction following High-Throughput ScreensSarah C Nicolson, Chengwen Li, Matthew L Hirsch, et al.
Pageof 23

Showing results (91-100 of 221) with videos related to

Sort By:
Pageof 23
Molecular Therapy : the Journal of the American Society of Gene Therapy|August 27, 2021
Flies in the ointment: AAV vector preparations and tumor riskJunping Zhang, Xiangping Yu, Roland W Herzog, et al.
Journal of Virology|August 26, 2016
Heparan Sulfate Binding Promotes Accumulation of Intravitreally Delivered Adeno-associated Viral Vectors at the Retina for Enhanced Transduction but Weakly Influences TropismKenton T Woodard, Katharine J Liang, William C Bennett, et al.
Molecular Therapy. Methods & Clinical Development|March 4, 2024
Rationally engineered novel AAV capsids for intra-articular gene deliveryWenjun Li, Susi Liu Feng, Lizette Herrschaft, et al.
Scientific Reports|July 30, 2014
Adeno-associated viral vectors show serotype specific transduction of equine joint tissue explants and cultured monolayersDaniel D Hemphill, C Wayne McIlwraith, R Jude Samulski, et al.
Human Gene Therapy|June 6, 2017
AAV Gene Therapy for Alcoholism: Inhibition of Mitochondrial Aldehyde Dehydrogenase Enzyme Expression in Hepatoma CellsAnamaria C Sanchez, Chengwen Li, Barbara Andrews, 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.
Journal of Virology|November 12, 2003
Development and characterization of novel empty adenovirus capsids and their impact on cellular gene expressionJackie L Stilwell, Douglas M McCarty, Atsuko Negishi, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 17, 2011
Combination therapy utilizing shRNA knockdown and an optimized resistant transgene for rescue of diseases caused by misfolded proteinsChengwen Li, Pingjie Xiao, Steven James Gray, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 4, 2011
Systemic gene transfer to skeletal muscle using reengineered AAV vectorsJana L Phillips, Julia Hegge, Jon A Wolff, et al.
Journal of Virology|May 6, 2016
Identification and Validation of Small Molecules That Enhance Recombinant Adeno-associated Virus Transduction following High-Throughput ScreensSarah C Nicolson, Chengwen Li, Matthew L Hirsch, et al.
Pageof 23