The epigenetic state of chromatin, gene activity, and chromosomal positions are interrelated. A research team from the IPK ...

In 2019, the first CRISPR clinical trials were conducted to treat sickle cell diseases and in 2020, this treatment was ...

It’s a new way to create “bi-paternal” mice that can survive to adulthood—but human applications are still a long way off.

Complementary discoveries have the potential to enhance treatment options for antibiotic-resistant infections. Researchers at ...

Vertex Pharmaceuticals won approval from the U.S. Food and Drug Administration for a non-opioid pain drug, clearing the way for the rollout of a product that has simultaneously sparked high hopes and ...

Australian cancer researchers are the first to establish a next-generation gene-editing tool for modeling and interrogating human disease.

RFK Jr.'s comments about the gene-editing technology raise a question about how he would regulate it as head of HHS.

Researchers use CRISPR to overcome seemingly insurmontable reproductive barriers — but that doesn't mean this could work for ...

The most complex engineering of human cell lines ever has been achieved by scientists, revealing that our genomes are more ...

A £1.65 million treatment has been approved for use for some NHS patients, offering some with an inherited blood disorder ...

Around 1,700 people could be eligible for the one-time treatment, which is seen as a less risky alternative to a donor stem ...