Tyrosine capsid-mutant AAV vectors for gene delivery to the canine retina from a subretinal or intravitreal approach

por Mowat, FM, Gornik, KR, Dinculescu, A, Boye, SL, Hauswirth, WW, Petersen-Jones, SM, Bartoe, JT
Publicado 2013

AAV retinal transduction in a large animal model species: Comparison of a self-complementary AAV2/5 with a single-stranded AAV2/5 vector

por Petersen-Jones, S.M., Bartoe, J.T., Fischer, A.J., Scott, M., Boye, S.L., Chiodo, V., Hauswirth, W.W.
Publicado 2009

Different tropism of adenoviruses and adeno-associated viruses to corneal cells: implications for corneal gene therapy

por Liu, J., Saghizadeh, M., Tuli, S.S., Kramerov, A.A., Lewin, A.S., Bloom, D.C., Hauswirth, W.W., Castro, M.G., Schultz, G.S., Ljubimov, A.V.
Publicado 2008