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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 risk
Junping 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 Tropism
Kenton 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 delivery
Wenjun 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 monolayers
Daniel 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 Cells
Anamaria 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 Transduction
Ping-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 expression
Jackie 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 proteins
Chengwen 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 vectors
Jana 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 Screens
Sarah C Nicolson, Chengwen Li, Matthew L Hirsch, et al.
Page
of 23
Search research articles
Search
Showing results (91-100 of 221) with videos related to
Sort By:
Page
of 23
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 27, 2021
Flies in the ointment: AAV vector preparations and tumor risk
Junping 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 Tropism
Kenton 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 delivery
Wenjun 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 monolayers
Daniel 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 Cells
Anamaria 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 Transduction
Ping-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 expression
Jackie 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 proteins
Chengwen 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 vectors
Jana 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 Screens
Sarah C Nicolson, Chengwen Li, Matthew L Hirsch, et al.
Page
of 23