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Base Editing Cures Sickle Cell Disease in Clinical Trial
A single infusion of base-edited cells eliminates symptoms in 12 patients, marking a new era for genetic medicine.
CRISPR, base editing, prime editing, and breakthrough gene therapies
Scientists at UNSW Sydney have developed a gentler form of CRISPR that can turn genes back on by removing chemical...
UNSW Sydney researchers develop CRISPR technique that activates silenced genes by removing methyl groups, avoiding the...
Researchers announce CRISPR 3.0, a next-generation gene editing platform with 100-fold improved precision that could...