Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector
The development of methods for efficient gene transfer to terminally differentiated retinal cells is important to study the function of the retina as well as for gene therapy of retinal diseases. We have developed a lentiviral vector system based on the HIV that can transduce terminally differentiat...
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| Publicado en: | Proc Natl Acad Sci U S A |
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| Autores principales: | , , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
National Academy of Sciences
1997
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC23360/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9294208/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.94.19.10319 |
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