Delivery of drugs, molecules or cellsDrug and cell deliveryEpigeneticsGenetic engineeringGenomic engineeringGenomicsMolecular and cell engineeringNucleic acid therapiesProtein engineeringTissue engineeringTranslational medicine
Recombinant AAV vectors are becoming more popular for therapeutic genome editing. We describe a clinically relevant approach to enhance insertion a therapeutic sequence into almost any site in the host genome.
Customise your preferences for any tracking technology
The following allows you to customize your consent preferences for any tracking technology used
to help us achieve the features and activities described below. To learn more about how these trackers help us