News

A Ph.D. student in biomolecular engineering at the University of California, Santa Cruz, has built a software program ...
Rare genetic diseases are challenging for patients and their families—made all the more overwhelming because symptoms tend to ...
The field of biotechnology has made significant strides in enhancing agricultural productivity by developing crops that can ...
Remember "Baby KJ"? Now CRISPR pioneers have partnered with the Chan Zuckerberg Initiative to launch center for curing rare ...
Trisomy is a genetic condition characterized by the presence of an extra chromosome. This means that the affected person has ...
The global CRISPR gene editing market size is calculated at USD 4.77 billion in 2025 and is expected to reach around USD ...
Personalized CRISPR cures for children born with rare genetic diseases are now a step closer to being more widely available.
CRISPR is revolutionizing medicine by enabling precise DNA edits, treating genetic diseases like sickle cell anemia and ...
New research has found a novel target with therapeutic potential for metastatic eye melanoma—an aggressive eye cancer—with ...
Personalized CRISPR cures for children born with rare genetic diseases are now a step closer to being more widely available.
The Byers Award recognizes outstanding research by faculty members in the middle of their careers. Martin Kampman’s honorary 2025 lecture is titled “A CRISPR approach to neurodegenerative diseases.” ...
Scientists have created a near-copy of the long-extinct dire wolf. Using advanced CRISPR gene editing tech, it now looks ...