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Danielle N. Clark

University of California, Los Angeles

7

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92

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Gene delivery using AAV8 in vivo for disease stabilization in a bimodal gene therapy approach for the treatment of ADA-deficient SCID

2021 Molecular therapy. Methods & clinical development
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Citations (1)
Global and Local Manipulation of DNA Repair Mechanisms to Alter Site-Specific Gene Editing Outcomes in Hematopoietic Stem Cells

2020
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Editing the Sickle Cell Disease Mutation in Primary Human Hematopoietic Stem Cells: Comparison of Endonucleases and Homologous Donor Templates

2019 Molecular Therapy
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Dosing and re-administration of intravenous lentiviral vector for in vivo gene therapy: Studies in rhesus monkeys and ADA-deficient mice

2019 Molecular therapy. Methods & clinical development
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Improving Gene Editing Outcomes in Human Hematopoietic Stem and Progenitor Cells by Temporal Control of DNA Repair

2019 Stem Cells
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764. Dosing and Re-Administration of Intravenous Lentiviral Vector for Liver-Directed Gene Transfer in Young Rhesus Monkeys and ADA-Deficient Mice

2016 Molecular Therapy
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442. Decreased Survival and Engraftment in Adult ADA-Deficient Mice Co-Transplanted With Uncorrected Lineage-Positive Bone Marrow Cells Combined With Gene-Corrected Lineage-Negative Bone Marrow Cells

2015 Molecular Therapy
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