Researchers are enhancing the best features of AAV capsids and overcoming their limitations to accelerate gene-based therapies.

International collaborations, refined gene-editing protocols, and targeted immunologic maneuvers keep the cancer gene therapy ...

In addition, delivery via the vascular route could be exploited to access primary or metastatic lung tumors. These practical considerations favor the development of gene therapy strategies for ...

The study did not draw conclusions about past, ongoing or future gene therapy research that relied upon these methods for measuring AAV vectors. It also did not make any policy or regulatory ...

Gene therapy could potentially cure ... cells safely and effectively. Existing methods of engineering one of the most commonly used gene-delivery vehicles, adeno-associated viruses (AAV), are ...

NIS gene delivery into medullary and follicular ... which allows the clinician to pursue therapeutic strategies, including gene therapy, that might ablate normal as well as malignant thyroid ...

BENGALURU: Bengaluru-based Narayana Nethralaya is developing gene therapy solutions that could drastically reduce the cost of ...

In two new papers, researchers from The Jackson Laboratory (JAX) report the successful use of two approaches -- gene therapy ...

Dyno’s platform applies AI and high-throughput in vivo data to solve the most critical challenge facing gene therapy developers: gene delivery ... and sequence design methods for the treatment ...

The global gene transfer technologies market, valued at US$3.63 billion in 2023, is forecasted to grow at a robust CAGR of ...