Scientists are testing CRISPR gene editing as a potential HIV cure after successfully removing the virus from infected cells ...

PHILADELPHIA (WPVI) -- Researchers at Temple University's School of Medicine and a team at the University of Nebraska Medical Center say they have, for the first time, eliminated the DNA of HIV-1, the ...

Clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated (Cas) proteins are core components of fast-evolving therapeutic gene editing tools. Scientists have used CRISPR ...

CRISPR Therapeutics’ gene-editing treatments are highly customized and shockingly expensive. The market is watching to see if the underlying science can be applied to treat many diseases. The company ...

CRISPR Therapeutics is the first company to secure an FDA approval of a gene-editing drug. That drug's underlying science, however, could be used to create treatments for any number of genetically ...

CRISPR has the power to correct genetic mutations, but current delivery methods are either unsafe or inefficient, keeping the technology from reaching its full medical potential. With the power to ...