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US08846387B2 Targeted gene modification by parvoviral vectors 有权
通过细小病毒载体靶向基因修饰

Targeted gene modification by parvoviral vectors
Abstract:
This invention provides methods for obtaining targeted gene modification in vertebrate cells using parvoviral vectors, including adeno-associated virus (AAV). The parvoviral vectors used in the methods of the invention are capable of targeting a specific genetic modification to a preselected target locus in a cellular genome by homologous pairing.
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