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Journal of Biomedical Science
|
October 8, 2022
Delivering genes with human immunodeficiency virus-derived vehicles: still state-of-the-art after 25 years
Jonas Holst Wolff, Jacob Giehm Mikkelsen
Frontiers in Genome Editing
|
March 27, 2023
Prime editing in hematopoietic stem cells-From <i>ex vivo</i> to <i>in vivo</i> CRISPR-based treatment of blood disorders
Jonas Holst Wolff, Jacob Giehm Mikkelsen
Frontiers in Genome Editing
|
December 6, 2021
piggyPrime: High-Efficacy Prime Editing in Human Cells Using piggyBac-Based DNA Transposition
Jonas Holst Wolff, Jakob Haldrup, Emil Aagaard Thomsen, et al.
Nucleic Acids Research
|
June 1, 2021
pegIT - a web-based design tool for prime editing
Mads Valdemar Anderson, Jakob Haldrup, Emil Aagaard Thomsen, et al.
Nucleic Acids Research
|
August 14, 2025
Gene editing in hematopoietic stem cells by co-delivery of Cas9/sgRNA ribonucleoprotein and templates for homology-directed repair in 'all-in-one' lentivirus-derived nanoparticles
Sofie Andersen, Jonas Holst Wolff, Thomas Wisbech Skov, et al.
Nucleic Acids Research
|
September 7, 2023
Engineered lentivirus-derived nanoparticles (LVNPs) for delivery of CRISPR/Cas ribonucleoprotein complexes supporting base editing, prime editing and in vivo gene modification
Jakob Haldrup, Sofie Andersen, Alexander Rafael LaVilla Labial, et al.
Nature Communications
|
August 12, 2025
Targeted gene editing and near-universal cDNA insertion of CYBA and CYBB as a treatment for chronic granulomatous disease
Jonas Holst Wolff, Thomas Wisbech Skov, Didde Haslund, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 31, 2025
Treatment of GATA2 deficiency by allele-specific CRISPR-Cas9-directed gene correction in hematopoietic stem cells
Thomas Wisbech Skov, Jonas Holst Wolff, Didde Haslund, et al.
Molecular Therapy. Advances
|
July 13, 2026
AAV vector production in suspension cells using PEI transfection and sodium butyrate with orthogonal assessment of function and quality
Sujan Ravendran, Simon Fammé, Maya Graham Noer, et al.
The Journal of Experimental Medicine
|
October 29, 2025
Genetically heterozygous - transcriptionally homozygous IRF7 deficiency underlies herpesvirus CNS infections in humans
Marvin Werner, Jonas Holst Wolff, Justin Taft, et al.
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Search research articles
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Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Journal of Biomedical Science
|
October 8, 2022
Delivering genes with human immunodeficiency virus-derived vehicles: still state-of-the-art after 25 years
Jonas Holst Wolff, Jacob Giehm Mikkelsen
Frontiers in Genome Editing
|
March 27, 2023
Prime editing in hematopoietic stem cells-From <i>ex vivo</i> to <i>in vivo</i> CRISPR-based treatment of blood disorders
Jonas Holst Wolff, Jacob Giehm Mikkelsen
Frontiers in Genome Editing
|
December 6, 2021
piggyPrime: High-Efficacy Prime Editing in Human Cells Using piggyBac-Based DNA Transposition
Jonas Holst Wolff, Jakob Haldrup, Emil Aagaard Thomsen, et al.
Nucleic Acids Research
|
June 1, 2021
pegIT - a web-based design tool for prime editing
Mads Valdemar Anderson, Jakob Haldrup, Emil Aagaard Thomsen, et al.
Nucleic Acids Research
|
August 14, 2025
Gene editing in hematopoietic stem cells by co-delivery of Cas9/sgRNA ribonucleoprotein and templates for homology-directed repair in 'all-in-one' lentivirus-derived nanoparticles
Sofie Andersen, Jonas Holst Wolff, Thomas Wisbech Skov, et al.
Nucleic Acids Research
|
September 7, 2023
Engineered lentivirus-derived nanoparticles (LVNPs) for delivery of CRISPR/Cas ribonucleoprotein complexes supporting base editing, prime editing and in vivo gene modification
Jakob Haldrup, Sofie Andersen, Alexander Rafael LaVilla Labial, et al.
Nature Communications
|
August 12, 2025
Targeted gene editing and near-universal cDNA insertion of CYBA and CYBB as a treatment for chronic granulomatous disease
Jonas Holst Wolff, Thomas Wisbech Skov, Didde Haslund, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 31, 2025
Treatment of GATA2 deficiency by allele-specific CRISPR-Cas9-directed gene correction in hematopoietic stem cells
Thomas Wisbech Skov, Jonas Holst Wolff, Didde Haslund, et al.
Molecular Therapy. Advances
|
July 13, 2026
AAV vector production in suspension cells using PEI transfection and sodium butyrate with orthogonal assessment of function and quality
Sujan Ravendran, Simon Fammé, Maya Graham Noer, et al.
The Journal of Experimental Medicine
|
October 29, 2025
Genetically heterozygous - transcriptionally homozygous IRF7 deficiency underlies herpesvirus CNS infections in humans
Marvin Werner, Jonas Holst Wolff, Justin Taft, et al.
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