A new CRISPR breakthrough shows scientists can turn genes back on without cutting DNA, by removing chemical tags that act ...
CRISPR–Cas9-based therapies are widely investigated for their clinical applications. However, there are limitations ...
Therapeutic Potential of CRISPR–Cas3 Genome-Editing System for Transthyretin Amyloidosis. Credit: Institute of Medical ...
A new CRISPR approach can control genes without cutting DNA, opening a safer path for treating genetic diseases. A newly ...
SCD gene therapy approaches using CRISPR, gene therapy, and base editing show different stem cell outcomes in a mouse study.
Victoria Gray spent 34 years battling the debilitating pain of sickle cell disease. Then she volunteered to be the world's first "prototype" for a CRISPR therapy, based on technology invented at UC ...
Technologies at the Advanced Rodent Transgenics Laboratory include genome editing design and implementation and transgenic ...
ON MARCH 15th 2024, a dark brown, gene-edited pig was driven from its home in the Midwest to a medical facility on the outskirts of Boston, Massachusetts. It had never before been outside the clean ...
The gene-editing technique known as CRISPR is promising to revolutionize medicine. Some researchers are trying to help make it available for people with very rare genetic disorders. A gene-editing ...
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