Researchers identify a shared RNA-protein interaction that could lead to broad-spectrum antiviral treatments for enteroviruses ...

This study offers important insight into the pathogenic basis of intragenic frameshift deletions in the carboxy-terminal domain of MECP2, which account for some Rett syndrome cases, yet similar ...

Rapid advances in sequencing technologies have transformed our ability to diagnose human genetic disorders, yet many patients still lack a molecular ...

It has been claimed that because most of our DNA is active, it must be important, but now human-plant hybrid cells have been ...

The research represents a major step forward in revealing how the three dimensional form of DNA shapes the way human biology functions. In a major step toward understanding how the physical form of ...

Researchers have discovered how cells activate a last-resort DNA repair system when severe damage strikes. When genetic ...

A game-changining achievement in genome science has identified over 140,000 distinct DNA loops in our cells, providing chromosome fold resolution that is among the best ever created. In this ongoing ...

These sequences are extremely prone to mutations and rank among the most functionally important regions in the entire human ...

New 3D genome maps reveal how DNA folding controls gene activity, offering fresh clues into disease and cell function.

These genes are part of the non-coding genome, which makes up about 98% of our DNA and was long dismissed as “junk.” This new ...

What keeps our cells the right size? Scientists have long puzzled over this fundamental question, since cells that are too ...

Large-scale human genetics studies have shown that many risk variants for common and complex diseases sit in the non-coding genome, where they can alter ...