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The American Journal of Pathology
|
August 1, 2006
Rapid growth of invasive metastatic melanoma in carcinogen-treated hepatocyte growth factor/scatter factor-transgenic mice carrying an oncogenic CDK4 mutation
Damia Tormo, Aleix Ferrer, Evelyn Gaffal, et al.
Blood
|
June 10, 2009
AAV-1-mediated gene transfer to skeletal muscle in humans results in dose-dependent activation of capsid-specific T cells
Federico Mingozzi, Janneke J Meulenberg, Daniel J Hui, et al.
Blood
|
July 5, 2007
Modulation of tolerance to the transgene product in a nonhuman primate model of AAV-mediated gene transfer to liver
Federico Mingozzi, Nicole C Hasbrouck, Etiena Basner-Tschakarjan, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
March 30, 2016
Superior In vivo Transduction of Human Hepatocytes Using Engineered AAV3 Capsid
Koen Vercauteren, Brad E Hoffman, Irene Zolotukhin, et al.
The Journal of Clinical Investigation
|
May 14, 2009
Capsid antigen presentation flags human hepatocytes for destruction after transduction by adeno-associated viral vectors
Gary C Pien, Etiena Basner-Tschakarjan, Daniel J Hui, et al.
Blood
|
January 18, 2013
Engineered AAV vector minimizes in vivo targeting of transduced hepatocytes by capsid-specific CD8+ T cells
Ashley T Martino, Etiena Basner-Tschakarjan, David M Markusic, et al.
Blood
|
May 5, 2017
Plasmacytoid and conventional dendritic cells cooperate in crosspriming AAV capsid-specific CD8<sup>+</sup> T cells
Geoffrey L Rogers, Jamie L Shirley, Irene Zolotukhin, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
April 29, 2010
Safety of AAV factor IX peripheral transvenular gene delivery to muscle in hemophilia B dogs
Virginia Haurigot, Federico Mingozzi, George Buchlis, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 17, 2013
Modulation of CD8+ T cell responses to AAV vectors with IgG-derived MHC class II epitopes
Daniel J Hui, Etiena Basner-Tschakarjan, Yifeng Chen, et al.
Plos One
|
May 14, 2013
AAV-mediated gene therapy for choroideremia: preclinical studies in personalized models
Vidyullatha Vasireddy, Jason A Mills, Rajashekhar Gaddameedi, et al.
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Search research articles
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Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
The American Journal of Pathology
|
August 1, 2006
Rapid growth of invasive metastatic melanoma in carcinogen-treated hepatocyte growth factor/scatter factor-transgenic mice carrying an oncogenic CDK4 mutation
Damia Tormo, Aleix Ferrer, Evelyn Gaffal, et al.
Blood
|
June 10, 2009
AAV-1-mediated gene transfer to skeletal muscle in humans results in dose-dependent activation of capsid-specific T cells
Federico Mingozzi, Janneke J Meulenberg, Daniel J Hui, et al.
Blood
|
July 5, 2007
Modulation of tolerance to the transgene product in a nonhuman primate model of AAV-mediated gene transfer to liver
Federico Mingozzi, Nicole C Hasbrouck, Etiena Basner-Tschakarjan, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
March 30, 2016
Superior In vivo Transduction of Human Hepatocytes Using Engineered AAV3 Capsid
Koen Vercauteren, Brad E Hoffman, Irene Zolotukhin, et al.
The Journal of Clinical Investigation
|
May 14, 2009
Capsid antigen presentation flags human hepatocytes for destruction after transduction by adeno-associated viral vectors
Gary C Pien, Etiena Basner-Tschakarjan, Daniel J Hui, et al.
Blood
|
January 18, 2013
Engineered AAV vector minimizes in vivo targeting of transduced hepatocytes by capsid-specific CD8+ T cells
Ashley T Martino, Etiena Basner-Tschakarjan, David M Markusic, et al.
Blood
|
May 5, 2017
Plasmacytoid and conventional dendritic cells cooperate in crosspriming AAV capsid-specific CD8<sup>+</sup> T cells
Geoffrey L Rogers, Jamie L Shirley, Irene Zolotukhin, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
April 29, 2010
Safety of AAV factor IX peripheral transvenular gene delivery to muscle in hemophilia B dogs
Virginia Haurigot, Federico Mingozzi, George Buchlis, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 17, 2013
Modulation of CD8+ T cell responses to AAV vectors with IgG-derived MHC class II epitopes
Daniel J Hui, Etiena Basner-Tschakarjan, Yifeng Chen, et al.
Plos One
|
May 14, 2013
AAV-mediated gene therapy for choroideremia: preclinical studies in personalized models
Vidyullatha Vasireddy, Jason A Mills, Rajashekhar Gaddameedi, et al.
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of 3