Crispr’s ability to cut genetic code like scissors has just started to turn into medicines. Now, gene editing pioneer ...
Eli Lilly (NYSE:LLY) reached a second milestone in its CRISPR gene editing collaboration with Scribe Therapeutics, advancing programs in neurological and neuromuscular diseases. The company reported ...
News Medical on MSN
New gene editing approach offers hope for cystic fibrosis patients
UCLA researchers have developed a lipid nanoparticle-based gene-editing approach capable of inserting an entire healthy gene ...
A research team has successfully demonstrated the world's first gene-editing treatment for Leber's hereditary optic ...
UCLA researchers have developed a lipid nanoparticle-based gene-editing approach capable of inserting an entire healthy gene into human airway cells, restoring key biological function in a laboratory ...
Scientists are testing an entirely new way to fight heart disease: a gene-editing treatment that might offer a one-time fix ...
In this webinar, researchers discuss using and improving next-generation gene editing approaches for targeted, accurate, and ...
Faced with a life-threatening metabolic disease, KJ’s doctors at Children’s Hospital of Philadelphia sprinted to create a ...
Urnov is a professor of molecular therapeutics at the University of California, Berkeley, and a director at its Innovative Genomics Institute. In May, news broke of a biomedical first: the on-demand ...
Extracellular vesicles (EVs) are tiny membrane-bound particles released by cells to transport proteins and other molecules to neighboring cells. Because of this natural delivery ability, EVs have ...
The Canadian government's recent approval of the first gene-edited animal to enter the food system has reignited debates over ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results