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Efficient gene delivery to photoreceptors using AAV2/rh10 and rescue of the Rho(–/–) mouse
As gene therapies for various forms of retinal degeneration progress toward human clinical trial, it will be essential to have a repertoire of safe and efficient vectors for gene delivery to the target cells. Recombinant adeno-associated virus (AAV) serotype 2/2 has been shown to be well tolerated i...
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| Foilsithe in: | Mol Ther Methods Clin Dev |
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| Main Authors: | , , , , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Nature Publishing Group
2015
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4444994/ https://ncbi.nlm.nih.gov/pubmed/26029727 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/mtm.2015.16 |
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