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Nucleic Acids Research
|
June 10, 2016
Probing the impact of chromatin conformation on genome editing tools
Xiaoyu 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 cells
Josephine 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 insertions
Zhen 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 populations
Ignazio Maggio, Luca Stefanucci, Josephine M Janssen, et al.
Nature Methods
|
August 26, 2014
Adenoviral vector DNA for accurate genome editing with engineered nucleases
Maarten 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 cells
Francesca Tasca, Marcella Brescia, Qian Wang, et al.
Nucleic Acids Research
|
January 5, 2021
Precise and broad scope genome editing based on high-specificity Cas9 nickases
Qian 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 constructs
Zhen 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 cells
Maarten 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 myocytes
Manuel A F V Gonçalves, Josephine M Janssen, Quynh G Nguyen, et al.
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of 3
Search research articles
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Showing results (11-20 of 26) with videos related to
Sort By:
Page
of 3
Nucleic Acids Research
|
June 10, 2016
Probing the impact of chromatin conformation on genome editing tools
Xiaoyu 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 cells
Josephine 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 insertions
Zhen 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 populations
Ignazio Maggio, Luca Stefanucci, Josephine M Janssen, et al.
Nature Methods
|
August 26, 2014
Adenoviral vector DNA for accurate genome editing with engineered nucleases
Maarten 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 cells
Francesca Tasca, Marcella Brescia, Qian Wang, et al.
Nucleic Acids Research
|
January 5, 2021
Precise and broad scope genome editing based on high-specificity Cas9 nickases
Qian 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 constructs
Zhen 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 cells
Maarten 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 myocytes
Manuel A F V Gonçalves, Josephine M Janssen, Quynh G Nguyen, et al.
Page
of 3