Recombinant AAV-mediated gene delivery to the CNS can be performed either by direct delivery at the target site or from the periphery, using intramuscular injections and retrograde transport along motor neuron projections or intravenous injections and blood-brain barrier crossing.In this chapter, we describe: 1. Methods for recombinant virus administration, including stereotactic surgery, intramuscular, and intravenous administration. 2. Methods to evaluate the number and biodistribution of brain and spinal cord cells expressing the transgene by immunohistochemisty as well as the amount of transgene product by ELISA in the target region. 3. Methods to characterize the cellular specificity of transgene expression by double immunofluorescence...
In this paper a detailed protocol is presented for neuroscientists planning to start work on first g...
Recombinant gene delivery vehicles based on the replication-defective AAV have gained a preeminent p...
In the context of motoneuron diseases, gene delivery as an experimental or therapeutic approach is h...
Recombinant AAV-mediated gene delivery to the CNS can be performed either by direct delivery at the ...
Various regions of the brain have been successfully transduced by recombinant adeno-associated virus...
Recombinant adeno-associated virus (rAAV) vectors are great tools for gene transfer due to their abi...
Recombinant adeno-associated viral (AAV) vectors are one of the most promising therapeutic delivery ...
The use of viral vectors as agents for gene delivery provides a direct approach to manipulate gene e...
The lack of methods to deliver transgene expression in spinal cord has hampered investigation of gen...
International audienceAdeno-associated virus (AAV)-mediated gene delivery has emerged as an effectiv...
The use of viral vectors as agents for gene delivery provides a direct approach to manipulate gene e...
Recombinant adeno-associated viruses (rAAVs) are commonly used as gene delivery vehicles in biomedic...
Adeno-associated virus (AAV) vectors delivered at the axonal terminals can be retrogradely transport...
Global gene delivery to the CNS has therapeutic importance for the treatment of neurological disorde...
Various administration routes of adeno-associated virus (AAV)-based gene therapy have been examined ...
In this paper a detailed protocol is presented for neuroscientists planning to start work on first g...
Recombinant gene delivery vehicles based on the replication-defective AAV have gained a preeminent p...
In the context of motoneuron diseases, gene delivery as an experimental or therapeutic approach is h...
Recombinant AAV-mediated gene delivery to the CNS can be performed either by direct delivery at the ...
Various regions of the brain have been successfully transduced by recombinant adeno-associated virus...
Recombinant adeno-associated virus (rAAV) vectors are great tools for gene transfer due to their abi...
Recombinant adeno-associated viral (AAV) vectors are one of the most promising therapeutic delivery ...
The use of viral vectors as agents for gene delivery provides a direct approach to manipulate gene e...
The lack of methods to deliver transgene expression in spinal cord has hampered investigation of gen...
International audienceAdeno-associated virus (AAV)-mediated gene delivery has emerged as an effectiv...
The use of viral vectors as agents for gene delivery provides a direct approach to manipulate gene e...
Recombinant adeno-associated viruses (rAAVs) are commonly used as gene delivery vehicles in biomedic...
Adeno-associated virus (AAV) vectors delivered at the axonal terminals can be retrogradely transport...
Global gene delivery to the CNS has therapeutic importance for the treatment of neurological disorde...
Various administration routes of adeno-associated virus (AAV)-based gene therapy have been examined ...
In this paper a detailed protocol is presented for neuroscientists planning to start work on first g...
Recombinant gene delivery vehicles based on the replication-defective AAV have gained a preeminent p...
In the context of motoneuron diseases, gene delivery as an experimental or therapeutic approach is h...