Optimized genome-editing method opens the door to more effective treatment of genetic diseases
CRISPR-Cas9 is widely used to edit the genome by studying genes of interest and modifying disease-associated genes.
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CRISPR-Cas9 is widely used to edit the genome by studying genes of interest and modifying disease-associated genes.
Professor Itaru Hamachi, Lecturer Tomonori Tamura, and Assistant Professor Masaki Tsuchiya of Kyoto University have developed a new technology called O-ClickFC (Organelle-selective click labeling with flow cytometry), which can, at a very high speed, analyze the metabolic state of lipids in cells.
Genome editing is a type of genetic engineering that involves making precise changes to the DNA of an organism. This technology allows scientists to
A new UCLA-led study suggests that advanced genome editing technology could be used as a one-time treatment for the rare and deadly genetic disease CD3 delta severe combined immunodeficiency.
Researchers in China have successfully restored the vision of mice with retinitis pigmentosa, one of the major causes of blindness in humans.