Parasitic worms are difficult to kill with current therapies, but their commensal bacteria might be their Achilles’ heel.

Download this application note to learn how a comprehensive target enrichment panel enables scientists to detect highly divergent viral strains, thereby making NGS a viable approach for viral pathogen ...

Inventia Life Science, an innovator in 3D cell culture technologies, announces the launch of RASTRUM™ Allegro, a ...

New research uncovered an alarming accumulation of plastic particles in human brains, raising concerns about their potential ...

In 2004, a research group at Peking University First Hospital discovered a mutation in the gene coding for a sodium-channel ...

Cell-cell interactions help drive tolerogenic or inflammatory responses to the maelstrom of antigens passing through the gut.

Disinfectants induce oxidative damage in bacteria, but a single mutation triggers the expression of genes that help the ...

Encasing CRISPR tools in oil droplets offers a fast-track approach to conducting extensive genetic screens in animals.

Researchers at Cellectis leveraged gene editing to create a CAR T cell that acts in an IF/THEN system. Traditional methods to develop CAR T cells that use the patient’s cells introduce challenges ...

Genetic medicines could treat certain diseases, however, the current delivery systems available—viral vectors and lipid nanoparticles (LNPs)—pose unique challenges for gene therapy applications. For ...

A single gene controls earwax and body odor, shaping one’s unique scent through microbes. In 2006, scientists identified the culprit: the ATP binding cassette subfamily C member 11 ( ABCC11) gene. 1 A ...

Both Cas9 and Cas12a cleave DNA, but they differ in how they cut the molecule.