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CRISPR is a highly precise gene editing tool that is changing cancer research and treatment.
A panel of Hutch scientists talked gene therapy, big data and financial toxicity to reporters at the annual AAAS meeting.
Edited T cells survive and thrive in three patients in the first U.S. trial using this approach.
The new method may increase gene editing efficiency and safety for future use in human cells.
Scientists are preparing to bring DNA-editing tools to the clinic.
Scientists have discovered a swifter and more precise way to edit the genome of immune cells, opening doors for cancer and HIV therapies.
New immunotherapy approach could make engineering immune cells faster and cheaper.
How the idea for synthetic cells took Silicon Valley by storm
Feng Zhang, PhD, is recognized for his groundbreaking work in the field of CRISPR genome editing.
Fred Hutch experts lend their predictions for the coming year’s advances
New CRISPR-based genetic diagnostic tool that may make it faster and easier to diagnose acute and chronic diseases.
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