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Sihong Song

Showing results (21-30 of 49) with videos related to

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Journal of Neurochemistry|June 23, 2017
Ischemia-responsive protein 94 is a key mediator of ischemic neuronal injury-induced microglial activationRajiv Tikamdas, Sarthak Singhal, Ping Zhang, et al.
Human Gene Therapy|June 17, 2006
Alpha1-antitrypsin gene therapy modulates cellular immunity and efficiently prevents type 1 diabetes in nonobese diabetic miceYuanqing Lu, Mei Tang, Clive Wasserfall, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 10, 2004
DNA-dependent PK inhibits adeno-associated virus DNA integrationSihong Song, Yuanqing Lu, Young-Kook Choi, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 17, 2010
Ex vivo transduction and transplantation of bone marrow cells for liver gene delivery of alpha1-antitrypsinHong Li, Yuanqing Lu, Rafal P Witek, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 4, 2002
Improved method of recombinant AAV2 delivery for systemic targeted gene therapyCathryn Mah, Thomas J Fraites, Irene Zolotukhin, et al.
The Journal of Gene Medicine|March 7, 2006
Therapeutic level of functional human alpha 1 antitrypsin (hAAT) secreted from murine muscle transduced by adeno-associated virus (rAAV1) vectorYuanqing Lu, Young-Kook Choi, Martha Campbell-Thompson, et al.
Frontiers in Physiology|October 11, 2021
Transgenic Mice Overexpressing Human Alpha-1 Antitrypsin Exhibit Low Blood Pressure and Altered Epithelial Transport Mechanisms in the Inactive and Active CyclesLauren P Liu, Mohammed F Gholam, Ahmed Samir Elshikha, et al.
The Journal of Gene Medicine|April 20, 2005
Enhancing rAAV vector expression in the lungIsabel Virella-Lowell, Benjamin Zusman, Kevin Foust, et al.
Journal of Translational Medicine|February 25, 2011
Alpha-1 antitrypsin protein and gene therapies decrease autoimmunity and delay arthritis development in mouse modelChristian Grimstein, Young-Kook Choi, Clive H Wasserfall, et al.
Hepatology (Baltimore, Md.)|September 24, 2004
Ex vivo transduced liver progenitor cells as a platform for gene therapy in miceSihong Song, Rafal P Witek, Yuanqing Lu, et al.
Pageof 5

Showing results (21-30 of 49) with videos related to

Sort By:
Pageof 5
Journal of Neurochemistry|June 23, 2017
Ischemia-responsive protein 94 is a key mediator of ischemic neuronal injury-induced microglial activationRajiv Tikamdas, Sarthak Singhal, Ping Zhang, et al.
Human Gene Therapy|June 17, 2006
Alpha1-antitrypsin gene therapy modulates cellular immunity and efficiently prevents type 1 diabetes in nonobese diabetic miceYuanqing Lu, Mei Tang, Clive Wasserfall, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 10, 2004
DNA-dependent PK inhibits adeno-associated virus DNA integrationSihong Song, Yuanqing Lu, Young-Kook Choi, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|June 17, 2010
Ex vivo transduction and transplantation of bone marrow cells for liver gene delivery of alpha1-antitrypsinHong Li, Yuanqing Lu, Rafal P Witek, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 4, 2002
Improved method of recombinant AAV2 delivery for systemic targeted gene therapyCathryn Mah, Thomas J Fraites, Irene Zolotukhin, et al.
The Journal of Gene Medicine|March 7, 2006
Therapeutic level of functional human alpha 1 antitrypsin (hAAT) secreted from murine muscle transduced by adeno-associated virus (rAAV1) vectorYuanqing Lu, Young-Kook Choi, Martha Campbell-Thompson, et al.
Frontiers in Physiology|October 11, 2021
Transgenic Mice Overexpressing Human Alpha-1 Antitrypsin Exhibit Low Blood Pressure and Altered Epithelial Transport Mechanisms in the Inactive and Active CyclesLauren P Liu, Mohammed F Gholam, Ahmed Samir Elshikha, et al.
The Journal of Gene Medicine|April 20, 2005
Enhancing rAAV vector expression in the lungIsabel Virella-Lowell, Benjamin Zusman, Kevin Foust, et al.
Journal of Translational Medicine|February 25, 2011
Alpha-1 antitrypsin protein and gene therapies decrease autoimmunity and delay arthritis development in mouse modelChristian Grimstein, Young-Kook Choi, Clive H Wasserfall, et al.
Hepatology (Baltimore, Md.)|September 24, 2004
Ex vivo transduced liver progenitor cells as a platform for gene therapy in miceSihong Song, Rafal P Witek, Yuanqing Lu, et al.
Pageof 5