Single residue AAV capsid mutation improves transduction of photoreceptors in the Abca4(-/-) mouse and bipolar cells in the rd1 mouse and human retina ex-vivo

Gene therapy using adeno-associated viral vectors (AAV) for the treatment of retinal degenerations has shown safety and efficacy in clinical trials. However, very high levels of vector expression may be necessary for the treatment of conditions such as Stargardt disease where a dual vector approach...

Descripción completa

Detalles Bibliográficos
Autores principales: De Silva, Samantha R., Charbel Issa, Peter, Singh, Mandeep S., Lipinski, Daniel M., Barnea-Cramer, Alona O., Walker, Nathan J., Barnard, Alun R., Hankins, Mark W., MacLaren, Robert E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5097463/
https://www.ncbi.nlm.nih.gov/pubmed/27416076
http://dx.doi.org/10.1038/gt.2016.54

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5097463/
https://www.ncbi.nlm.nih.gov/pubmed/27416076
http://dx.doi.org/10.1038/gt.2016.54

Ejemplares similares