Researchers at the Max Planck Institute for Evolutionary Anthropology have addressed a longstanding challenge in CRISPR ...

In the latest episode of Touching Base, we discuss big news in CRISPR along with updates in the business side of biotech.

Gene editing, once a theoretical ambition, has matured into a revolutionary frontier in biotechnology. Technologies like CRISPR-Cas9, TALENs, and Zinc Finger Nucleases (ZFNs) have unlocked ...

The medical promise of CRISPR gene editing can be seen most easily in current research on oral cancer, which affects more than 50,000 Americans every year. An increasing challenge in the treatment ...

CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) technology, which was developed as a gene-editing tool, has shown significant promise in biomedical applications, including ...

05. A strange thing happened weeks before the Food and Drug Administration approved the first treatment made with CRISPR gene editing, an all-but cure for certain patients with sickle cell disease.

Researchers in Lithuania present the molecular structure of a new, more-versatile CRISPR system for gene editing. When you purchase through links on our site, we may earn an affiliate commission.

Recently, herpesvirus of turkeys (HVT), which was initially employed as a vaccine against Marek’s disease (MD), has been shown to be a highly effective viral vector for producing ... Herein, we ...

For in vivo CRISPR-Cas9 delivery, cryo-inactivated non-pathogenic KRAS-mutant NSCLC cells were used as a vector. This cell vehicle allows for highly targeted lung delivery via passive trapping by ...