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Improving adeno-associated viral vector for hematopoietic stem cells gene therapy
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Characterizing and manipulating homology-directed gene editing in human cells
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Site-directed spin labeling studies of target DNA recognition by a CRISPR nuclease
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Rational selection of CRISPR/Cas9 guide RNAs for homology directed genome editing and its utility in the development of gene therapies
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Genome-scale screening in mammalian cells using CRISPR-Cas9 system
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Promoters and insulators: creating a safer integrating vector
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Current models of non-homologous end joining and their implications in gene therapy
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