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Josephine M Janssen

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Human Gene Therapy|November 13, 2012
Histone deacetylase inhibition activates transgene expression from integration-defective lentiviral vectors in dividing and non-dividing cellsLaetitia P L Pelascini, Josephine M Janssen, Manuel A F V Gonçalves
Molecular Therapy. Nucleic Acids|March 19, 2019
The Chromatin Structure of CRISPR-Cas9 Target DNA Controls the Balance between Mutagenic and Homology-Directed Gene-Editing EventsJosephine M Janssen, Xiaoyu Chen, Jin Liu, et al.
Cells|April 8, 2020
High-Capacity Adenoviral Vectors Permit Robust and Versatile Testing of <i>DMD</i> Gene Repair Tools and Strategies in Human CellsMarcella Brescia, Josephine M Janssen, Jin Liu, et al.
Nucleic Acids Research|March 17, 2023
Precise homology-directed installation of large genomic edits in human cells with cleaving and nicking high-specificity Cas9 variantsQian Wang, Jin Liu, Josephine M Janssen, et al.
Scientific Reports|November 16, 2016
Adenoviral vectors encoding CRISPR/Cas9 multiplexes rescue dystrophin synthesis in unselected populations of DMD muscle cellsIgnazio Maggio, Jin Liu, Josephine M Janssen, et al.
Nucleic Acids Research|February 7, 2024
Selection-free precise gene repair using high-capacity adenovector delivery of advanced prime editing systems rescues dystrophin synthesis in DMD muscle cellsQian Wang, Sabrina Capelletti, Jin Liu, et al.
Plos One|June 10, 2010
Rapid and sensitive lentivirus vector-based conditional gene expression assay to monitor and quantify cell fusion activityManuel A F V Gonçalves, Josephine M Janssen, Maarten Holkers, et al.
Molecular Therapy. Nucleic Acids|March 20, 2023
High-capacity adenovector delivery of forced CRISPR-Cas9 heterodimers fosters precise chromosomal deletions in human cellsFrancesca Tasca, Marcella Brescia, Jin Liu, et al.
Nucleic Acids Research|October 20, 2021
Broadening the reach and investigating the potential of prime editors through fully viral gene-deleted adenoviral vector deliveryQian Wang, Jin Liu, Josephine M Janssen, et al.
Scientific Reports|May 30, 2014
Adenoviral vector delivery of RNA-guided CRISPR/Cas9 nuclease complexes induces targeted mutagenesis in a diverse array of human cellsIgnazio Maggio, Maarten Holkers, Jin Liu, et al.
Pageof 3

Showing results (1-10 of 26) with videos related to

Sort By:
Pageof 3
Human Gene Therapy|November 13, 2012
Histone deacetylase inhibition activates transgene expression from integration-defective lentiviral vectors in dividing and non-dividing cellsLaetitia P L Pelascini, Josephine M Janssen, Manuel A F V Gonçalves
Molecular Therapy. Nucleic Acids|March 19, 2019
The Chromatin Structure of CRISPR-Cas9 Target DNA Controls the Balance between Mutagenic and Homology-Directed Gene-Editing EventsJosephine M Janssen, Xiaoyu Chen, Jin Liu, et al.
Cells|April 8, 2020
High-Capacity Adenoviral Vectors Permit Robust and Versatile Testing of <i>DMD</i> Gene Repair Tools and Strategies in Human CellsMarcella Brescia, Josephine M Janssen, Jin Liu, et al.
Nucleic Acids Research|March 17, 2023
Precise homology-directed installation of large genomic edits in human cells with cleaving and nicking high-specificity Cas9 variantsQian Wang, Jin Liu, Josephine M Janssen, et al.
Scientific Reports|November 16, 2016
Adenoviral vectors encoding CRISPR/Cas9 multiplexes rescue dystrophin synthesis in unselected populations of DMD muscle cellsIgnazio Maggio, Jin Liu, Josephine M Janssen, et al.
Nucleic Acids Research|February 7, 2024
Selection-free precise gene repair using high-capacity adenovector delivery of advanced prime editing systems rescues dystrophin synthesis in DMD muscle cellsQian Wang, Sabrina Capelletti, Jin Liu, et al.
Plos One|June 10, 2010
Rapid and sensitive lentivirus vector-based conditional gene expression assay to monitor and quantify cell fusion activityManuel A F V Gonçalves, Josephine M Janssen, Maarten Holkers, et al.
Molecular Therapy. Nucleic Acids|March 20, 2023
High-capacity adenovector delivery of forced CRISPR-Cas9 heterodimers fosters precise chromosomal deletions in human cellsFrancesca Tasca, Marcella Brescia, Jin Liu, et al.
Nucleic Acids Research|October 20, 2021
Broadening the reach and investigating the potential of prime editors through fully viral gene-deleted adenoviral vector deliveryQian Wang, Jin Liu, Josephine M Janssen, et al.
Scientific Reports|May 30, 2014
Adenoviral vector delivery of RNA-guided CRISPR/Cas9 nuclease complexes induces targeted mutagenesis in a diverse array of human cellsIgnazio Maggio, Maarten Holkers, Jin Liu, et al.
Pageof 3