Cargando…
Toward Development of Neuron Specific Transduction After Systemic Delivery of Viral Vectors
Widespread transduction of the CNS with a single, non-invasive systemic injection of adeno-associated virus is now possible due to the creation of blood-brain barrier-permeable capsids. However, as these capsids are mutants of AAV9, they do not have specific neuronal tropism. Therefore, it is necess...
Autores principales: | Finneran, Dylan J., Njoku, Ikenna P., Flores-Pazarin, Diego, Ranabothu, Meghana R., Nash, Kevin R., Morgan, David, Gordon, Marcia N. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8426581/ https://www.ncbi.nlm.nih.gov/pubmed/34512509 http://dx.doi.org/10.3389/fneur.2021.685802 |
Ejemplares similares
-
CNS-Wide over Expression of Fractalkine Improves Cognitive Functioning in a Tauopathy Model
por: Finneran, Dylan J., et al.
Publicado: (2018) -
Efficient gene delivery and selective transduction of astrocytes in the mammalian brain using viral vectors
por: Merienne, Nicolas, et al.
Publicado: (2013) -
GABAergic Gene Regulatory Elements Used in Adeno-Associated Viral Vectors
por: Duba-Kiss, Robert, et al.
Publicado: (2021) -
Retinal transduction profiles by high-capacity viral vectors
por: Puppo, Agostina, et al.
Publicado: (2014) -
Efficient delivery of Cre-recombinase to neurons in vivo and stable transduction of neurons using adeno-associated and lentiviral vectors
por: Ahmed, Bushra Y, et al.
Publicado: (2004)