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Human Gene Therapy
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May 12, 2017
Adeno-Associated Virus Vectors and Stem Cells: Friends or Foes?
Nolan Brown, Liujiang Song, Nageswara R Kollu, et al.
Journal of Virology
|
November 8, 2013
Promyelocytic leukemia protein is a cell-intrinsic factor inhibiting parvovirus DNA replication
Angela M Mitchell, Matthew L Hirsch, Chengwen Li, et al.
Human Molecular Genetics
|
December 23, 2017
Inhibition of antigen presentation during AAV gene therapy using virus peptides
Wenwei Shao, Xiaojing Chen, Richard J Samulski, et al.
Plos One
|
November 6, 2009
AAV recombineering with single strand oligonucleotides
Matthew L Hirsch, Francesca Storici, Chengwen Li, 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.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 21, 2017
Structure-Based Designed Nano-Dysferlin Significantly Improves Dysferlinopathy in BLA/J Mice
Telmo Llanga, Nadia Nagy, Laura Conatser, et al.
Molecular Therapy. Oncology
|
August 13, 2025
Allele-specific depletion of <i>GNAQ</i> <sup>Q209L</sup> via siRNA or an rAAV2-shRNA vector induces selective toxicity in <i>GNAQ</i> <sup>Q209L</sup> uveal melanoma cells
Trace F McCall, Emma J Sawyer, Joshua Darnell, et al.
Gene Therapy
|
August 4, 2018
Serotype survey of AAV gene delivery via subconjunctival injection in mice
Liujiang Song, Telmo Llanga, Laura M Conatser, et al.
Molecular Therapy. Methods & Clinical Development
|
June 2, 2015
A comparison of AAV strategies distinguishes overlapping vectors for efficient systemic delivery of the 6.2 kb Dysferlin coding sequence
Marina Pryadkina, William Lostal, Nathalie Bourg, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 9, 2024
A chimeric anti-vascularization immunomodulator prevents high-risk corneal transplantation rejection via ex vivo gene therapy
Brian C Gilger, Tomoko Hasegawa, R Bryan Sutton, et al.
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of 5
Search research articles
Search
Showing results (11-20 of 45) with videos related to
Sort By:
Page
of 5
Human Gene Therapy
|
May 12, 2017
Adeno-Associated Virus Vectors and Stem Cells: Friends or Foes?
Nolan Brown, Liujiang Song, Nageswara R Kollu, et al.
Journal of Virology
|
November 8, 2013
Promyelocytic leukemia protein is a cell-intrinsic factor inhibiting parvovirus DNA replication
Angela M Mitchell, Matthew L Hirsch, Chengwen Li, et al.
Human Molecular Genetics
|
December 23, 2017
Inhibition of antigen presentation during AAV gene therapy using virus peptides
Wenwei Shao, Xiaojing Chen, Richard J Samulski, et al.
Plos One
|
November 6, 2009
AAV recombineering with single strand oligonucleotides
Matthew L Hirsch, Francesca Storici, Chengwen Li, 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.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 21, 2017
Structure-Based Designed Nano-Dysferlin Significantly Improves Dysferlinopathy in BLA/J Mice
Telmo Llanga, Nadia Nagy, Laura Conatser, et al.
Molecular Therapy. Oncology
|
August 13, 2025
Allele-specific depletion of <i>GNAQ</i> <sup>Q209L</sup> via siRNA or an rAAV2-shRNA vector induces selective toxicity in <i>GNAQ</i> <sup>Q209L</sup> uveal melanoma cells
Trace F McCall, Emma J Sawyer, Joshua Darnell, et al.
Gene Therapy
|
August 4, 2018
Serotype survey of AAV gene delivery via subconjunctival injection in mice
Liujiang Song, Telmo Llanga, Laura M Conatser, et al.
Molecular Therapy. Methods & Clinical Development
|
June 2, 2015
A comparison of AAV strategies distinguishes overlapping vectors for efficient systemic delivery of the 6.2 kb Dysferlin coding sequence
Marina Pryadkina, William Lostal, Nathalie Bourg, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 9, 2024
A chimeric anti-vascularization immunomodulator prevents high-risk corneal transplantation rejection via ex vivo gene therapy
Brian C Gilger, Tomoko Hasegawa, R Bryan Sutton, et al.
Page
of 5