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Josephine M Janssen

Showing results (11-20 of 26) with videos related to

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Nucleic Acids Research|June 10, 2016
Probing the impact of chromatin conformation on genome editing toolsXiaoyu Chen, Marrit Rinsma, Josephine M Janssen, et al.
The Journal of Gene Medicine|December 11, 2012
Development of an AdEasy-based system to produce first- and second-generation adenoviral vectors with tropism for CAR- or CD46-positive cellsJosephine M Janssen, Jin Liu, Jaroslav Skokan, et al.
Trends in Biotechnology|April 4, 2026
Selector adeno-associated viral vectors facilitate on-target precise genome editing and purge off-target chromosomal insertionsZhen Li, Xiaoling Wang, Jin Liu, et al.
Nucleic Acids Research|January 15, 2016
Selection-free gene repair after adenoviral vector transduction of designer nucleases: rescue of dystrophin synthesis in DMD muscle cell populationsIgnazio Maggio, Luca Stefanucci, Josephine M Janssen, et al.
Nature Methods|August 26, 2014
Adenoviral vector DNA for accurate genome editing with engineered nucleasesMaarten Holkers, Ignazio Maggio, Sara F D Henriques, et al.
Nucleic Acids Research|July 1, 2022
Large-scale genome editing based on high-capacity adenovectors and CRISPR-Cas9 nucleases rescues full-length dystrophin synthesis in DMD muscle cellsFrancesca Tasca, Marcella Brescia, Qian Wang, et al.
Nucleic Acids Research|January 5, 2021
Precise and broad scope genome editing based on high-specificity Cas9 nickasesQian Wang, Jin Liu, Josephine M Janssen, et al.
Nucleic Acids Research|December 10, 2024
Precision genome editing using combinatorial viral vector delivery of CRISPR-Cas9 nucleases and donor DNA constructsZhen Li, Xiaoling Wang, Josephine M Janssen, et al.
Nucleic Acids Research|January 1, 2013
Differential integrity of TALE nuclease genes following adenoviral and lentiviral vector gene transfer into human cellsMaarten Holkers, Ignazio Maggio, Jin Liu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 27, 2011
Transcription factor rational design improves directed differentiation of human mesenchymal stem cells into skeletal myocytesManuel A F V Gonçalves, Josephine M Janssen, Quynh G Nguyen, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Nucleic Acids Research|June 10, 2016
Probing the impact of chromatin conformation on genome editing toolsXiaoyu Chen, Marrit Rinsma, Josephine M Janssen, et al.
The Journal of Gene Medicine|December 11, 2012
Development of an AdEasy-based system to produce first- and second-generation adenoviral vectors with tropism for CAR- or CD46-positive cellsJosephine M Janssen, Jin Liu, Jaroslav Skokan, et al.
Trends in Biotechnology|April 4, 2026
Selector adeno-associated viral vectors facilitate on-target precise genome editing and purge off-target chromosomal insertionsZhen Li, Xiaoling Wang, Jin Liu, et al.
Nucleic Acids Research|January 15, 2016
Selection-free gene repair after adenoviral vector transduction of designer nucleases: rescue of dystrophin synthesis in DMD muscle cell populationsIgnazio Maggio, Luca Stefanucci, Josephine M Janssen, et al.
Nature Methods|August 26, 2014
Adenoviral vector DNA for accurate genome editing with engineered nucleasesMaarten Holkers, Ignazio Maggio, Sara F D Henriques, et al.
Nucleic Acids Research|July 1, 2022
Large-scale genome editing based on high-capacity adenovectors and CRISPR-Cas9 nucleases rescues full-length dystrophin synthesis in DMD muscle cellsFrancesca Tasca, Marcella Brescia, Qian Wang, et al.
Nucleic Acids Research|January 5, 2021
Precise and broad scope genome editing based on high-specificity Cas9 nickasesQian Wang, Jin Liu, Josephine M Janssen, et al.
Nucleic Acids Research|December 10, 2024
Precision genome editing using combinatorial viral vector delivery of CRISPR-Cas9 nucleases and donor DNA constructsZhen Li, Xiaoling Wang, Josephine M Janssen, et al.
Nucleic Acids Research|January 1, 2013
Differential integrity of TALE nuclease genes following adenoviral and lentiviral vector gene transfer into human cellsMaarten Holkers, Ignazio Maggio, Jin Liu, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 27, 2011
Transcription factor rational design improves directed differentiation of human mesenchymal stem cells into skeletal myocytesManuel A F V Gonçalves, Josephine M Janssen, Quynh G Nguyen, et al.
Pageof 3