The CRISPR tool is capable of repairing the genetic defect responsible for the immune disease chronic granulomatous disease.
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In recent years, scientists have created a range of new methods based on CRISPR-Cas technology for precisely editing the genetic material of living organisms. One application is in cell therapy: a patient’s immune cells can be specifically reprogrammed to fight cancer more effectively. Researchers in the Department of Biosystems Science and Engineering at ETH Zurich [...]
The CRISPR tool is capable of repairing the genetic defect responsible for the immune disease chronic granulomatous disease.
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In a breakthrough study published in Cell Reports, researchers from Professor Idit Shachar’s laboratory at the Weizmann Institute of Science have...
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CRISPR Therapeutics reports mixed third-quarter results. The commercial launch of the first CRISPR-based gene therapy, Casgevy, is progressing well.
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