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Jude Samulski

Showing results (131-140 of 198) with videos related to

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Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|March 24, 2006
Minimizing oxidative stress by gene delivery of superoxide dismutase accelerates regeneration after transplantation of reduced-size livers in the ratThorsten G Lehmann, Tom Luedde, Robert F Schwabe, et al.
Human Gene Therapy Methods|October 15, 2013
K137R mutation on adeno-associated viral capsids had minimal effect on enhancing gene delivery in vivoChunping Qiao, Chengwen Li, Chunxia Zhao, et al.
Molecular Therapy. Methods & Clinical Development|February 22, 2021
Preclinical biodistribution, tropism, and efficacy of oligotropic AAV/Olig001 in a mouse model of congenital white matter diseaseJeremy S Francis, Vladimir Markov, Irenuez D Wojtas, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 31, 2009
Directed evolution of a novel adeno-associated virus (AAV) vector that crosses the seizure-compromised blood-brain barrier (BBB)Steven J Gray, Bonita L Blake, Hugh E Criswell, et al.
Plos One|March 14, 2013
In cellulo examination of a beta-alpha hybrid construct of beta-hexosaminidase A subunits, reported to interact with the GM2 activator protein and hydrolyze GM2 gangliosideIncilay Sinici, Sayuri Yonekawa, Ilona Tkachyova, et al.
Human Gene Therapy|January 10, 2020
Adeno-Associated Virus Serotype-Specific Inverted Terminal Repeat Sequence Role in Vector Transgene ExpressionLauriel F Earley, Laura M Conatser, Victoria M Lue, et al.
Plos Pathogens|June 1, 2011
AAV exploits subcellular stress associated with inflammation, endoplasmic reticulum expansion, and misfolded proteins in models of cystic fibrosisJarrod S Johnson, Martina Gentzsch, Liqun Zhang, et al.
Biomaterials|January 8, 2022
Customized blood-brain barrier shuttle peptide to increase AAV9 vector crossing the BBB and augment transduction in the brainXintao Zhang, Zheng Chai, Amanda Lee Dobbins, et al.
Molecular Therapy. Nucleic Acids|February 7, 2013
Optimization of scAAVIL-1ra In Vitro and In Vivo to Deliver High Levels of Therapeutic Protein for Treatment of OsteoarthritisLaurie R Goodrich, Jennifer N Phillips, C Wayne McIlwraith, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 6, 2003
Recombinant adeno-associated virus serotype 4 mediates unique and exclusive long-term transduction of retinal pigmented epithelium in rat, dog, and nonhuman primate after subretinal deliveryMichel Weber, Joseph Rabinowitz, Nathalie Provost, et al.
Pageof 20

Showing results (131-140 of 198) with videos related to

Sort By:
Pageof 20
Liver Transplantation : Official Publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society|March 24, 2006
Minimizing oxidative stress by gene delivery of superoxide dismutase accelerates regeneration after transplantation of reduced-size livers in the ratThorsten G Lehmann, Tom Luedde, Robert F Schwabe, et al.
Human Gene Therapy Methods|October 15, 2013
K137R mutation on adeno-associated viral capsids had minimal effect on enhancing gene delivery in vivoChunping Qiao, Chengwen Li, Chunxia Zhao, et al.
Molecular Therapy. Methods & Clinical Development|February 22, 2021
Preclinical biodistribution, tropism, and efficacy of oligotropic AAV/Olig001 in a mouse model of congenital white matter diseaseJeremy S Francis, Vladimir Markov, Irenuez D Wojtas, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 31, 2009
Directed evolution of a novel adeno-associated virus (AAV) vector that crosses the seizure-compromised blood-brain barrier (BBB)Steven J Gray, Bonita L Blake, Hugh E Criswell, et al.
Plos One|March 14, 2013
In cellulo examination of a beta-alpha hybrid construct of beta-hexosaminidase A subunits, reported to interact with the GM2 activator protein and hydrolyze GM2 gangliosideIncilay Sinici, Sayuri Yonekawa, Ilona Tkachyova, et al.
Human Gene Therapy|January 10, 2020
Adeno-Associated Virus Serotype-Specific Inverted Terminal Repeat Sequence Role in Vector Transgene ExpressionLauriel F Earley, Laura M Conatser, Victoria M Lue, et al.
Plos Pathogens|June 1, 2011
AAV exploits subcellular stress associated with inflammation, endoplasmic reticulum expansion, and misfolded proteins in models of cystic fibrosisJarrod S Johnson, Martina Gentzsch, Liqun Zhang, et al.
Biomaterials|January 8, 2022
Customized blood-brain barrier shuttle peptide to increase AAV9 vector crossing the BBB and augment transduction in the brainXintao Zhang, Zheng Chai, Amanda Lee Dobbins, et al.
Molecular Therapy. Nucleic Acids|February 7, 2013
Optimization of scAAVIL-1ra In Vitro and In Vivo to Deliver High Levels of Therapeutic Protein for Treatment of OsteoarthritisLaurie R Goodrich, Jennifer N Phillips, C Wayne McIlwraith, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 6, 2003
Recombinant adeno-associated virus serotype 4 mediates unique and exclusive long-term transduction of retinal pigmented epithelium in rat, dog, and nonhuman primate after subretinal deliveryMichel Weber, Joseph Rabinowitz, Nathalie Provost, et al.
Pageof 20