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Tracing the fate of AAV vectors in the body
A study of AAV gene therapy in monkeys proposes that integrated vectors may drive long-term transgene expression.
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Encapsulated stem cell–derived β cells exert glucose control in patients with type 1 diabetes
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The world’s first CRISPR therapy is approved: who will receive it?
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CRISPR therapies march into clinic, but genotoxicity concerns linger
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A prevascularized subcutaneous device-less site for islet and cellular transplantation