The study links aging organisms' inability to sustain production of key proteins to impaired translation and increased ...

These soluble protein agonists can replicate Notch activation in suspension culture, opening the door to scalable T-cell therapies.

The Waltham Innovation Center will complement Aldevron’s established scientific teams in Fargo, ND, and Madison, WI.

Stem cells differentiated into brain and neural organoids may help scientists understand both brain development and ...

DEK will provide essential infrastructure and expertise to support Bio Usawa's market entry and expansion across West Africa.

The data shows that RORDEP-proteins boost the production of hormones like GLP-1 and PYY, which help regulate appetite and ...

Targeted rewriting of the epigenome promises to overcome several challenges in direct gene editing in patient therapies.

They’ve developed an AI-driven “Virtual Lab,” through which a team of AI agents, each equipped with varied scientific ...

Improved understanding of how bacterial defense mechanisms operate may help scientists select phages with the best chance of ...

OpenCRISPR-1, an AI-generated custom gene editor capable of precision editing of the human genome. is just the beginning of ...

The remainder of 2025 will be busy for Vir Biotechnology as it strives to successfully pivot to developing cancer and infectious disease therapies.

The primary safety risks associated with gene therapy include immune reactions and off-target effects in unintended organs, such as the liver, lungs, and spleen. Nevertheless, Ali and Townsend note ...