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MicroRNA-Restricted Transgene Expression in the Retina
BACKGROUND: Gene transfer using adeno-associated viral (AAV) vectors has been successfully applied in the retina for the treatment of inherited retinal dystrophies. Recently, microRNAs have been exploited to fine-tune transgene expression improving therapeutic outcomes. Here we evaluated the ability...
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| Hlavní autoři: | , , , , , , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Public Library of Science
2011
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3144214/ https://ncbi.nlm.nih.gov/pubmed/21818300 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0022166 |
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