GENE ONLINE|News &
Opinion
Blog

2021-02-17| R&DStartups

George Church’s New Startup Engineers AAV Vectors that Evades Host Immune Responses

by Rajaneesh K. Gopinath
Share To
Adeno-associated viral (AAV) vectors are widely used in vivo therapeutic gene delivery vehicles. The many advantages they provide, including safety, broad tissue tropism, lack of pathogenicity, and efficient and persistent gene transfer, have made them the "gold standard" for gene therapies.

GO Prime with only $1.49 now

LATEST
Kaiser’s Data Breach: 13.4 Million Affected in Healthcare Conglomerates Privacy Crisis
2024-04-26
Mechanisms of Allograft Rejection: Insights from Behind the Scenes
2024-04-25
ImmunityBio’s ANKTIVA® Granted FDA Approval: Breakthrough IL-15 Receptor Agonist First-in-Class for BCG-Unresponsive Non-Muscle Invasive Bladder Cancer
2024-04-24
Takeda, Astellas, and Sumitomo Mitsui Banking Declare Agreement For Early Drug Discovery Program Incubation in Joint Venture
2024-04-23
Ochre Bio Announces Partnership with Boehringer Ingelheim to Develop Novel Regenerative Treatments for Patients with Advanced Liver Disease
2024-04-22
Earth Day Awareness: Hospitals Embrace Sustainability Efforts
2024-04-22
WHO Raises Alarm: Bird Flu Threat to Humans an ‘Enormous Concern’
2024-04-19
EVENT
Scroll to Top