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Federico Mingozzi

Showing results (31-40 of 138) with videos related to

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Blood|April 24, 2004
Induction of antigen-specific CD4+ T-cell anergy and deletion by in vivo viral gene transferEric Dobrzynski, Federico Mingozzi, Yi-Lin Liu, et al.
Frontiers in Immunology|October 4, 2016
Induction of Hematopoietic Microchimerism by Gene-Modified BMT Elicits Antigen-Specific B and T Cell Unresponsiveness toward Gene Therapy ProductsJérémie Martinet, Gwladys Bourdenet, Amine Meliani, et al.
Human Gene Therapy|September 6, 2023
Understanding and Tackling Immune Responses to Adeno-Associated Viral VectorsHelena Costa-Verdera, Carmen Unzu, Erika Valeri, et al.
Blood|January 25, 2012
Factor IX expression in skeletal muscle of a severe hemophilia B patient 10 years after AAV-mediated gene transferGeorge Buchlis, Gregory M Podsakoff, Antonetta Radu, et al.
Molecular Therapy. Nucleic Acids|November 30, 2016
Transposon-mediated Generation of Cellular and Mouse Models of Splicing Mutations to Assess the Efficacy of snRNA-based TherapeuticsElena Barbon, Mattia Ferrarese, Laetitia van Wittenberghe, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|November 3, 2005
Identification of mouse AAV capsid-specific CD8+ T cell epitopesDenise E Sabatino, Federico Mingozzi, Daniel J Hui, et al.
Journal of Medical Virology|November 26, 2008
Diverse IgG subclass responses to adeno-associated virus infection and vector administrationSamuel L Murphy, Hojun Li, Federico Mingozzi, et al.
Journal of Virology|September 20, 2002
Improved hepatic gene transfer by using an adeno-associated virus serotype 5 vectorFederico Mingozzi, Jörg Schüttrumpf, Valder R Arruda, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 17, 2019
The Effect of CpG Sequences on Capsid-Specific CD8<sup>+</sup> T Cell Responses to AAV Vector Gene TransferZhiQuan Xiang, Raj K Kurupati, Yan Li, et al.
Human Gene Therapy|August 23, 2012
Correction of pathological accumulation of glycosaminoglycans in central nervous system and peripheral tissues of MPSIIIA mice through systemic AAV9 gene transferAlbert Ruzo, Sara Marcó, Miquel García, et al.
Pageof 14

Showing results (31-40 of 138) with videos related to

Sort By:
Pageof 14
Blood|April 24, 2004
Induction of antigen-specific CD4+ T-cell anergy and deletion by in vivo viral gene transferEric Dobrzynski, Federico Mingozzi, Yi-Lin Liu, et al.
Frontiers in Immunology|October 4, 2016
Induction of Hematopoietic Microchimerism by Gene-Modified BMT Elicits Antigen-Specific B and T Cell Unresponsiveness toward Gene Therapy ProductsJérémie Martinet, Gwladys Bourdenet, Amine Meliani, et al.
Human Gene Therapy|September 6, 2023
Understanding and Tackling Immune Responses to Adeno-Associated Viral VectorsHelena Costa-Verdera, Carmen Unzu, Erika Valeri, et al.
Blood|January 25, 2012
Factor IX expression in skeletal muscle of a severe hemophilia B patient 10 years after AAV-mediated gene transferGeorge Buchlis, Gregory M Podsakoff, Antonetta Radu, et al.
Molecular Therapy. Nucleic Acids|November 30, 2016
Transposon-mediated Generation of Cellular and Mouse Models of Splicing Mutations to Assess the Efficacy of snRNA-based TherapeuticsElena Barbon, Mattia Ferrarese, Laetitia van Wittenberghe, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|November 3, 2005
Identification of mouse AAV capsid-specific CD8+ T cell epitopesDenise E Sabatino, Federico Mingozzi, Daniel J Hui, et al.
Journal of Medical Virology|November 26, 2008
Diverse IgG subclass responses to adeno-associated virus infection and vector administrationSamuel L Murphy, Hojun Li, Federico Mingozzi, et al.
Journal of Virology|September 20, 2002
Improved hepatic gene transfer by using an adeno-associated virus serotype 5 vectorFederico Mingozzi, Jörg Schüttrumpf, Valder R Arruda, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 17, 2019
The Effect of CpG Sequences on Capsid-Specific CD8<sup>+</sup> T Cell Responses to AAV Vector Gene TransferZhiQuan Xiang, Raj K Kurupati, Yan Li, et al.
Human Gene Therapy|August 23, 2012
Correction of pathological accumulation of glycosaminoglycans in central nervous system and peripheral tissues of MPSIIIA mice through systemic AAV9 gene transferAlbert Ruzo, Sara Marcó, Miquel García, et al.
Pageof 14