Lust and Tanaka demonstrated for the first time that adeno-associated viral vectors (AAVs) can efficiently deliver transgenes into axolotl neurons. By testing different AAV serotypes—variants ...

Figure 1: Strategy for packaging a large gene by the split AAV vectors through heterodimerization. Figure 3: Characterization of the split AAV vector heterodimerization by RT–PCR and DNA-PCR.

Unlock key insights into the Adeno-Associated Virus Vectors in Gene Therapy Market! Download DelveInsight’s comprehensive report to explore market trends, pipeline analysis, and emerging ...

ChromaTan Inc. and Landmark Bio PBLLC have been awarded a grant from the National Institute for Innovation in Manufacturing ...

Scientists developed a promising gene replacement therapy for Dravet syndrome in mice. The therapy alleviated symptoms ...

Viral vectors introduce genes and gene editing sequences into cells, and are a popular platform for gene therapy due to their safety and efficacy features. Adeno-associated viral (AAV) vectors in ...

The Adeno Associated Virus Vector Manufacturing market, valued at USD 1,148.4 million in 2024, is expected to register robust revenue CAGR of 19.6%.Request free copy of this report:  March 14, 2025 - ...

The Adeno-Associated Virus (AAV) Vectors in Gene Therapy pipeline signifies a promising field of medical research poised for considerable advancements by 2025. With diligent therapeutic and ...

Immunotherapy has emerged as one of the major options for cancer treatment in the past decade. With the successful application of immune checkpoint inhibitors and the introduction of immune regulatory ...

The authors have demonstrated the use of adenine base editors delivered via adeno-associated viruses to introduce edits in the mitochondrial genome. The manuscript describes the methodology well, and ...

A young man with Duchenne MD and treated with Elevidys has died of acute liver failure, Sarepta reports; it's working with ...