Nanobody-Enhanced Targeting of AAV Gene Therapy Vectors
A limiting factor for the use of adeno-associated viruses (AAVs) as vectors in gene therapy is the broad tropism of AAV serotypes, i.e., the parallel infection of several cell types. Nanobodies are single immunoglobulin variable domains from heavy chain antibodies that naturally occur in camelids. T...
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| Principais autores: | , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2019-12-01
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| coleção: | Molecular Therapy: Methods & Clinical Development |
| Acesso em linha: | http://www.sciencedirect.com/science/article/pii/S2329050119301019 |
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