Researchers use generative AI to design synthetic enhancers that can effectively control gene expression in healthy mammalian ...

Gene therapy (introducing genetic material into living cells to fix, replace, enhance, or block a faulty gene) is rapidly ...

To enhance CAR T therapies, scientists are actively studying TCR signaling and T-cell exhaustion mechanisms to improve CAR T ...

From connectors and containers to plasmids and platforms, companies work to get these treatments to patients faster and more ...

The virus likely reached humans not via bat migration but through the wildlife trade—contradicting hypotheses that it may ...

Discovery of innate immune receptor "brake" Siglec-E offers a novel therapeutic target to prevent organ transplant rejection in mice.

Late last year, the therapy developers dosed their first patient following positive preclinical data demonstrating safety and ...

Researchers headed by a team at the California Institute of Technology developed an ultrasound-guided 3D printing technique that could make it possible to fabricate medical implants in vivo and ...

There is a consistent need from researchers to manufacture a cGMP virus to support the advancement of gene therapies.

Targeting clonal antigens and circumventing dysfunctional states may be important for conferring clinical responses to TIL therapy.

Although gene-editing and other techniques can improve the production of microbe-based biologics, AI could push these drugs ...

Researchers expect LICONN technology will be broadly useful to enable high-resolution tissue analysis in other organs and ...