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Frontiers in Genome Editing
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April 4, 2022
CRISPR/Cas-Based Gene Editing Strategies for DOCK8 Immunodeficiency Syndrome
Sujan Ravendran, Sabina Sánchez Hernández, Saskia König, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 28, 2025
Orthogonal CRISPR systems for targeted integration and multiplex base editing enable nonviral engineering of allogeneic CAR T cells
Nanna S Mikkelsen, Sujan Ravendran, Amalie D Broksø, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 9, 2022
A truncated reverse transcriptase enhances prime editing by split AAV vectors
Zongliang Gao, Sujan Ravendran, Nanna S Mikkelsen, 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.
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of 1
Search research articles
Search
Showing results (1-10 of 4) with videos related to
Sort By:
Page
of 1
Frontiers in Genome Editing
|
April 4, 2022
CRISPR/Cas-Based Gene Editing Strategies for DOCK8 Immunodeficiency Syndrome
Sujan Ravendran, Sabina Sánchez Hernández, Saskia König, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
August 28, 2025
Orthogonal CRISPR systems for targeted integration and multiplex base editing enable nonviral engineering of allogeneic CAR T cells
Nanna S Mikkelsen, Sujan Ravendran, Amalie D Broksø, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
July 9, 2022
A truncated reverse transcriptase enhances prime editing by split AAV vectors
Zongliang Gao, Sujan Ravendran, Nanna S Mikkelsen, 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.
Page
of 1