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Journal of Virology
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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.
Journal of Virology
|
March 28, 2008
Surface loop dynamics in adeno-associated virus capsid assembly
Nina DiPrimio, Aravind Asokan, Lakshmanan Govindasamy, et al.
Current Gene Therapy
|
August 18, 2010
AAV's anatomy: roadmap for optimizing vectors for translational success
Angela M Mitchell, Sarah C Nicolson, Jayme K Warischalk, et al.
Human Gene Therapy
|
April 23, 2021
Mavis Agbandje-McKenna's Lifelong Commitment to Teaching and Research
Barry J Byrne, Angela L McCall, Beverly L Davidson, et al.
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.
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.
Page
of 17
Search research articles
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Showing results (51-60 of 163) with videos related to
Sort By:
Page
of 17
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.
Journal of Virology
|
March 28, 2008
Surface loop dynamics in adeno-associated virus capsid assembly
Nina DiPrimio, Aravind Asokan, Lakshmanan Govindasamy, et al.
Current Gene Therapy
|
August 18, 2010
AAV's anatomy: roadmap for optimizing vectors for translational success
Angela M Mitchell, Sarah C Nicolson, Jayme K Warischalk, et al.
Human Gene Therapy
|
April 23, 2021
Mavis Agbandje-McKenna's Lifelong Commitment to Teaching and Research
Barry J Byrne, Angela L McCall, Beverly L Davidson, et al.
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.
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.
Page
of 17