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As seen in: Oxford University Press (OUP)
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Articles

An engineered baculoviral protein and DNA co-delivery system for CRISPR-based mammalian genome editing

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By Sathish K. N, Cantock's Close, Newby G.A, GIGA Proteomics Facility
| Oxford University Press (OUP)
CRISPR technologies have revolutionized gene editing over the past decade, providing highly promising avenues for the treatment of genetic disorders (1–6). Commonly used viral vectors, such as adeno-associated virus (AAV), lentivirus (LV) and adenovirus (AdV) have been largely adopted for the delivery of CRISPR-based genome editing components (7–9).
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