Adeno-associated viruses (AAV) engineered to target specific cells in the retina can be injected directly into the vitreous of the eye to deliver genes more precisely than can be done with wild ...

The nano-complexes released the loaded-AAV intracellularly and exhibited efficient gene transduction into cells. When intravenously injected, AAV ternary complexes successfully evade NAbs.

For decades, the Amphibious Assault Vehicle (AAV) has been a cornerstone of the U.S. Marine Corps, transporting troops and cargo from ship to shore. With its 29-ton combat weight, armored ...

Safe and effective gene therapy strategies depend on robust and reliable adeno-associated virus (AAV) mediated therapeutic gene delivery. However, scaling up AAV manufacturing to obtain sufficient ...