Explore how oligonucleotides are reshaping therapeutics, diagnostics and CRISPR with rapid, scalable and personalized solutions across biotech.

A new gene-editing technique enables the correction of multiple genetic mutations simultaneously, transforming the prospects ...

Understanding how cells turn genes on and off is one of biology's most enduring mysteries. Now, a new technology developed by chemist Brian Liau and his collaborators at Harvard offers an ...

Immunometabolism have advanced the understanding of dynamic interplay between metabolic pathways and immune responses.

A new study has revealed that the gene HMGN1 is a key driver of congenital heart defects (CHDs) in Down syndrome. Using CRISPR activation in human stem cells and mouse models, scientists showed that ...

Using the CRISPR-Cas9 tool, the researchers edited the toad eggs to turn off a gene known as tyrosinase, which is responsible ...

Cell culture plates in the Roeder lab where scientists recently studied gene expression in breast cancer. (Credit: Lori ...

Smith, a microbiologist whose discovery revolutionize the field of genetic engineering, was a Johns Hopkins School of ...

A new gene therapy shows promise in controlling cholesterol by lowering bad LDL levels, potentially reducing the risk of ...

A research team from the University of Osaka, in collaboration with the Massachusetts Institute of Technology, has uncovered ...

As we approach the anticipated artificial intelligence singularity and the strain builds, showing the fault lines in our systems, different aspects emerge and begin to converge.

We have written about the promise of gene therapy to correct genetic disease many times. An exciting development happened ...