To help achieve more precise control of gene therapy, engineers have designed a new control circuit that can keep gene expression levels within a target range. The method could be used to deliver ...

India has launched its first human gene therapy for hemophilia, showing progress in biotech-led healthcare innovation.

Three oral and 12 poster presentations demonstrate breadth and progress of AskBio’s gene therapy research and development ...

A study published in The New England Journal of Medicine looks at a new CRISPR gene therapy for children with a rare genetic disease. Dr Alena Pance, Senior Lecturer in Genetics, University of ...

It's like writing software but for biology, giving us new ways of giving instructions ... The study could lead to new ways ...

In this op-ed, Charles Gersbach explores how genetic tuning is emerging as a next-generation approach to modulating gene ...

Researchers at the Paul Scherrer Institute PSI have developed an AI that could open up a new, cost-effective approach to ...

The interaction between RNA-binding proteins (RBPs) and circular RNAs (circRNAs) has emerged as a key area of interest in ...

It’s like writing software but for biology ... a gene on individually could effectively shut that gene down when they occur together. The results could provide a new tool for gene-therapy ...

Odylia Therapeutics, a nonprofit (501(c)3) biotechnology company dedicated to advancing treatments for rare diseases, today announced its latest pipeline project: a unique and innovative ...

A new publication shines a spotlight on HER3, a long-overlooked member of the ErbB receptor family, revealing its critical ...