Japanese researchers have successfully eliminated the extra chromosome responsible for Down syndrome using CRISPR gene ...

For decades, scientists have studied how to control DNA—the molecule that holds the instructions for all life. One of the ...

A newly discovered bacterial defense protein named Cat1 reveals an extraordinary method of viral neutralization. All living ...

Crispr Therapeutics' current revenue from CASGEVY is limited by high costs, profit-sharing, and logistical hurdles. Click ...

Precision gene editing is crucial for treating genetic diseases, as it enables targeted correction of specific mutations. A ...

By uncovering RNA’s previously unknown function to repair DNA damage, our findings show how RNA may directly contribute to the stability and evolution of the genome. It’s not merely a passive ...

Victoria Gray, the first person cured of sickle cell using CRISPR gene editing therapies, spoke in Fargo about her journey ...

A team from McGill University has successfully used CRISPR-Cas9 technology to edit oat DNA for the first time, enhancing key ...

Caszyme’s origin story begins in the lab, not the boardroom. It was built on groundbreaking research by renowned Lithuanian ...

Gene editing’s real value is not in re-creating copies of long-extinct species like dire wolves, but instead using it to ...

目前主流载体是AAV病毒，但它的设计就像iPhone的Lightning接口——贵、容量小、兼容性差（生产成本高，还容易引发免疫反应）。