
The research team created CRISPR guides that would cause green fluorescent protein to be expressed in only certain cellular locations and structures.
Credit: Alex Marson’s Lab.
With faster, cheaper, more precise technique, authors say it’s ‘off to the races’ toward new cell therapies. In an achievement that has significant implications for research, medicine, and industry, UC San Francisco scientists have genetically reprogrammed the human T cells without using viruses to insert DNA...
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