Various administration routes of adeno-associated virus (AAV)-based gene therapy have been examined to target the central nervous system to answer the question what the most optimal delivery route is for treatment of the brain with certain indications. In this study, we evaluated AAV5 vector system for its capability to target the central nervous system via intrastriatal, intrathalamic or intracerebroventricular delivery routes in rats. AAV5 is an ideal candidate for gene therapy because of its relatively low level of existing neutralizing antibodies compared to other serotypes, and its broad tissue and cell tropism. Intrastriatal administration of AAV5-GFP resulted in centralized localized vector distribution and expression in the frontal ...
Adeno-associated virus (AAV) gene therapy constitutes a powerful tool for the treatment of neurodege...
The present study was designed to characterize transduction of non-human primate brain and spinal co...
Adeno-associated virus (AAV) vectors delivered at the axonal terminals can be retrogradely transport...
The use of viral vectors as agents for gene delivery provides a direct approach to manipulate gene e...
The use of viral vectors as agents for gene delivery provides a direct approach to manipulate gene e...
The present study was designed to characterize transduction of non-human primate brain and spinal co...
The present study was designed to characterize transduction of non-human primate brain and spinal co...
The present study was designed to characterize transduction of non-human primate brain and spinal co...
Intracerebral administration of recombinant adeno-associated vector (AAV) has been performed in seve...
Intracerebral administration of recombinant adeno-associated vector (AAV) has been performed in seve...
Cerebrospinal fluid administration of recombinant adeno-associated viral (rAAV) vectors has been dem...
Cerebrospinal fluid administration of recombinant adeno-associated viral (rAAV) vectors has been dem...
Recombinant adeno-associated viruses (rAAVs) are commonly used as gene delivery vehicles in biomedic...
Recombinant adeno-associated viruses (rAAVs) are commonly used as gene delivery vehicles in biomedic...
Adeno-associated virus (AAV) gene therapy constitutes a powerful tool for the treatment of neurodege...
Adeno-associated virus (AAV) gene therapy constitutes a powerful tool for the treatment of neurodege...
The present study was designed to characterize transduction of non-human primate brain and spinal co...
Adeno-associated virus (AAV) vectors delivered at the axonal terminals can be retrogradely transport...
The use of viral vectors as agents for gene delivery provides a direct approach to manipulate gene e...
The use of viral vectors as agents for gene delivery provides a direct approach to manipulate gene e...
The present study was designed to characterize transduction of non-human primate brain and spinal co...
The present study was designed to characterize transduction of non-human primate brain and spinal co...
The present study was designed to characterize transduction of non-human primate brain and spinal co...
Intracerebral administration of recombinant adeno-associated vector (AAV) has been performed in seve...
Intracerebral administration of recombinant adeno-associated vector (AAV) has been performed in seve...
Cerebrospinal fluid administration of recombinant adeno-associated viral (rAAV) vectors has been dem...
Cerebrospinal fluid administration of recombinant adeno-associated viral (rAAV) vectors has been dem...
Recombinant adeno-associated viruses (rAAVs) are commonly used as gene delivery vehicles in biomedic...
Recombinant adeno-associated viruses (rAAVs) are commonly used as gene delivery vehicles in biomedic...
Adeno-associated virus (AAV) gene therapy constitutes a powerful tool for the treatment of neurodege...
Adeno-associated virus (AAV) gene therapy constitutes a powerful tool for the treatment of neurodege...
The present study was designed to characterize transduction of non-human primate brain and spinal co...
Adeno-associated virus (AAV) vectors delivered at the axonal terminals can be retrogradely transport...