AAV

Slowly and cautiously, Ali's group and others have been trying out an AAV-based gene therapy in people with an inherited form of blindness.

The company used an adeno-associated virus (AAV) to deliver a gene with the aim of suppressing inflammation.

This may be assessed by means of the aggregate abrasion value (AAV) test.

These results suggested that the existence of AAV ITRs played an active role for long-term transgene expression even without tans elements.

Coker and her colleagues hope to conduct a prospective study that would follow women over time to determine the precise role of AAV.

Conclusion: PCA from AAV is a favorable protein C-activating reagent that has high potency and produces less influence on the experiment.

Different AAV structures have different therapeutic properties.

The gene can be delivered to the eye using a virus called Adeno-Associated Virus (AAV).

We intend to construct recombinant AAV vector, so that BDNF can be expressed in CNS for the treatment of AD.

Guangping and his team have tirelessly pursued this avenue, and they continue to add to the repertoire of AAV serotype vectors.

Objective To construct a recombinant AAV reporter virus expressing GFP and observe its expression in NIH 3T3 cell.

AAV doesn't always insert in this particular spot, however, even when it still has its site-specific preference.

AAV vectors will be promising gene therapy vectors.

Osteogenic induction of rabbit's bone marrow stromal cells and transfection of AAV-EGFP in vitro

Effect of recombinant AAV vector on tumor gene therapy