Cargando…
Next-generation sequencing of mitochondrial targeted AAV transfer of human ND4 in mice
PURPOSE: To determine the effects of mitochondrial targeting sequence (MTS) modified AAV gene delivery of wild-type human NADH dehydrogenase subunit 4 (ND4), mutated in most cases of the blinding disease Leber hereditary optic neuropathy (LHON), on the host mouse mitochondrial genome. METHODS: We in...
Autores principales: | Yu, Hong, Mehta, Arpit, Wang, Gaofeng, Hauswirth, William W., Chiodo, Vince, Boye, Sanford L., Guy, John |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Vision
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3712668/ https://www.ncbi.nlm.nih.gov/pubmed/23869167 |
Ejemplares similares
-
rAAV2/5 gene-targeting to rods: dose-dependent efficiency and complications associated with different promoters
por: Beltran, William A., et al.
Publicado: (2010) -
Recombinant AAV-Mediated BEST1 Transfer to the Retinal Pigment Epithelium: Analysis of Serotype-Dependent Retinal Effects
por: Guziewicz, Karina E., et al.
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., et al.
Publicado: (2009) -
Mutant NADH dehydrogenase subunit 4 gene delivery to mitochondria by targeting sequence-modified adeno-associated virus induces visual loss and optic atrophy in mice
por: Yu, Hong, et al.
Publicado: (2012) -
Intraocular route of AAV2 vector administration defines humoral immune response and therapeutic potential
por: Li, Qiuhong, et al.
Publicado: (2008)