This year, gene-editing technology was customized to fix mutations in a single patient’s genes for the first time.
Biotech startup CrisprBits uses CRISPR-based techniques to change the shape of diagnostics by decoding genetic sequencing ...
Syntax Bio, a synthetic biology company programming the next generation of cell therapies, has published new research in ...
Revolutions in gene therapy are rapidly changing the landscape of modern medicine, forcing society and science alike to ...
Scientists at UCL and GOSH have used groundbreaking base-edited CAR‑T cell therapy — BE‑CAR7 — to treat aggressive T‑cell ...
Morning Overview on MSN
Programmable CRISPR cuts stem cell timing from months to weeks
Programmable CRISPR tools are turning stem cell biology into something closer to software engineering, shrinking ...
News Medical on MSN
‘Ready-made’ T-cell gene therapy tackles ‘incurable’ T-cell leukemia
A groundbreaking new treatment using genome-edited immune cells, developed by scientists at UCL (University College London) ...
A cutting-edge base-edited CAR T-cell therapy is opening a revolutionary new frontier for patients battling aggressive T-cell ...
9don MSN
Lyme disease often goes undetected when it's most treatable. These teens are working to change that.
Teens at a Georgia high school may have come up with a better way to detect and treat Lyme disease. They took their idea to ...
As global temperatures rise, Cold Spring Harbor Laboratory (CSHL) scientists work to grow stronger, more resilient crops. Yet ...
Drug resistance has long turned some of the most advanced lung cancer therapies into temporary victories, with tumors learning to shrug off chemotherapy that once held them in check. A new wave of ...
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