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

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

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

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

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

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

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.

Careful planning can make a substantial difference on your path to commercial success. Here we delve into key considerations ...

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

Single-cell biology has transformed how we decode cellular heterogeneity, but a new frontier is emerging: understanding what ...