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Structure of the gene therapy vector, adeno-associated virus with its cell receptor, AAVR
Adeno-associated virus (AAV) vectors are preeminent in emerging clinical gene therapies. Generalizing beyond the most tractable genetic diseases will require modulation of cell specificity and immune neutralization. Interactions of AAV with its cellular receptor, AAVR, are key to understanding cell-...
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| Опубликовано в: : | eLife |
|---|---|
| Главные авторы: | , , , , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
eLife Sciences Publications, Ltd
2019
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6561701/ https://ncbi.nlm.nih.gov/pubmed/31115336 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7554/eLife.44707 |
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