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

New AI model takes minutes rather than days to predict how a specific DNA sequence will arrange itself in the cell nucleus.

The most complex engineering of human cell lines ever has been achieved by scientists, revealing that our genomes are more resilient to significant structural changes than was previously thought.

The global Preimplantation Genetic Testing (PGT) market is on the rise, projected to reach US$ 1.65 billion by 2033, driven ...

Introduction: Allogeneic chimeric antigen receptor T (CAR-T) therapy, also known as universal CAR-T (UCAR-T) therapy, offers broad applicability, high production efficiency, and reduced costs, ...

A Yale study finds that the Earth’s ozone layer, crucial for life’s protection from UV radiation, was delayed in stabilizing by a battle between iodine and oxygen, hindering the emergence of complex ...

The idea behind the notorious CRISPR-baby scandal, editing reproductive cells or ... together they increase a person’s risk of these complex diseases. Doctors already use technologies that screen ...

Get Instant Summarized Text (Gist) CRISPR nucleases, Cas9 and Cas12, have been engineered to evade immune detection, addressing a key challenge in CRISPR-based therapies. By identifying and ...

Despite its potential, the CRISPR/Cas9 system for genome editing is accompanied by a series of limitations and challenges. These issues include off-target effects, complex genome structures, low ...