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CRISPR gene editing is a breakthrough that has been used to treat diseases such as sickle cell anemia, leukemia and genetic disorders, but it has challenges that limit its broad utility. Let's take a look.

CRISPR gene editing is a breakthrough that has been used to treat diseases such as sickle cell anemia, leukemia and genetic disorders, but it has challenges that limit its broad utility.

CRISPR Researchers from Aarhus University and University of Copenhagen have developed a new method, which makes CRISPR gene editing more precise than conventional methods.

Researchers from Aarhus University and University of Copenhagen have developed a new method, which makes CRISPR gene editing more precise than conventional methods. The method selects the molecules best suited for helping the CRISPR-Cas9 protein with high-precision editing at the correct location in our DNA, the researchers explain.

Washington [US], June 10 (ANI): While researchers had first engineered CRISPR as a gene-editing technology for bacterial, plant, animal and human cells it eventually became a Nobel prize-winning revolution. The technology's potential spans from curing genetically disposed diseases to applications in agricultural and industrial biotechnology, but there are challenges.