This year, gene-editing technology was customized to fix mutations in a single patient’s genes for the first time.

Programmable CRISPR tools are turning stem cell biology into something closer to software engineering, shrinking ...

A year of new treatments, new technologies, new ways to stay safe during disasters and new insights on the mysteries of the ...

Every face is unique. Genetics helps to determine our features, but sometimes genes have errors which, in early fetal ...

According to Precedence Research, the global gRNA market size is expected to grow from USD 708.92 million in 2025 to nearly ...

Syntax Bio, a synthetic biology company programming the next generation of cell therapies, has published new research in ...

Syntax Bio, a synthetic biology company programming the next generation of cell therapies, today announced it has received an award of up to $856,250 from Breakthrough T1D, the leading global type 1 ...

A team of researchers at the Icahn School of Medicine at Mount Sinai has uncovered why children with the same ...

Today's biomedical researchers are relentlessly searching for genes that drive disease, with the goal of creating therapies that target those genes to ...

Researchers used CRISPR to change the number of chromosomes in Arabidopsis by fusing chromosome arms, reducing the genome ...