There are currently four clinical-stage gene-editing candidates in clinical trials for sickle cell disease, which affects millions of people worldwide...
Professor Stephanie Cherqui of University of California San Diego’s School of Medicine recently received a prestigious grant from the Californian...
Extended survival times and inhibited growth of patient-derived glioblastoma brain tumours have been achieved in mice with CRISPR-Cas9 mediated...
Researchers at Ulsan National Institute of Science and Technology in South Korea have developed a CRISPR-Cas9-based method to eliminate tumour cells....
Folding DNA into compact structures allows for efficient integration of large genes, and this might lead to new therapies for genetic diseases with...
For years, Dr. Yan Zhang at the University of Michigan wondered why scientists were struggling to adapt certain type I CRISPR systems for gene editing...
At a Danish hospital, researchers have integrated CRISPR gene editing into a clinical scale workflow for immunotherapy. Gene editing releases a brake...
A combination of genes either knocked out or activated by CRISPR promises to be a general and straightforward way to obtain high-yielding crops fully...
