Gene editing is already being used to treat a handful of rare genetic diseases; however, most therapies involve breaking or ...

In a landmark achievement for both Uganda and the global medical community, the United States Patent and Trademark Office ...

Northwestern Medicine investigators have developed a new avenue to reprogram compromised immune cells to act against tumors, ...

New gene therapy modalities, such as CRISPR guide RNA (single guide ribonucleic acid [sgRNA]) and messenger RNA (mRNA), ...

CRISPR technology has radically transformed genetic research, and at the forefront of this transformation is CRISPR screening ...

Akribion Therapeutics emerges from stealth with €8 million in seed funding to develop a novel cancer RNA-guided approach ...

In our five years of testing for this guide, we’ve found that online flower delivery services are spotty. Think shipping delays and cargo jostling, extreme temperatures, and inconsistent crops.

Potent in vivo gene editing in skeletal muscle of non-human primates by a novel, ultracompact CRISPR system delivered via a single AAV vector.

NanoCas, an ultracompact nuclease, enables efficient muscle editing in NHPs using a single AAV - advancing gene editing for hard-to-target tissues.

Every time a shuttle docks with the International Space Station (ISS), a delicate dance unfolds between the shuttle's docking system and its counterpart on the station. Thanks to international ...