Human extracellular matrices can be edited in their composition using the CRISPR/Cas9 system, leading to materials exhibiting tailored regenerative capacities.

Efficient disruption of tyrb resulted in albino phenotype in F0 grass carp mutants. FAYETTEVILLE, GA, UNITED STATES, March 27, 2025 /EINPre ...

A team of researchers at Karolinska Institutet has developed a novel tool for genetic research. The study, published in ...

An R75W mutation in the gap junction β2 (GJB2) gene causes severe fragmentation of gap junction plaques, connecting adjacent ...

Glioblastoma (GBM), one of the most aggressive types of brain cancer, is one of the greatest challenges for medicine, both ...

Many physicians and scientists are now searching for the best clinical applications for this promising technology. Cas9: CRISPR-associated protein 9, an endonuclease from bacteria that forms a ...

The Cas9 protein is the most widely used by scientists. This protein can easily be programmed to find and bind to almost any desired target sequence, simply by giving it a piece of RNA to guide it ...

Advances in the gene-editing technology known as CRISPR-Cas9 over the past 15 years have yielded important new insights into ...