A cutting-edge base-edited CAR T-cell therapy is opening a revolutionary new frontier for patients battling aggressive T-cell leukemia.
A new treatment using genome-edited immune cells, developed by scientists at UCL (University College London) and Great Ormond ...
CRISPR, the gene-editing technology which won its creators the 2020 Nobel Prize for Chemistry, is most well-known for its ...
The genetically engineered food is also protein packed and sustainable, say scientists. Chinese researchers used gene-editing ...
This year, gene-editing technology was customized to fix mutations in a single patient’s genes for the first time.
Syntax Bio, a synthetic biology company programming the next generation of cell therapies, today announced the publication of ...
Goldenberries taste like a cross between pineapple and mango, pack the nutritional punch of a superfood, and are increasingly ...
Casgevy, now a "national priority" drug, helped kids with sickle cell and thalassemia, results which may help toward a label ...
Syntax Bio, a synthetic biology company programming the next generation of cell therapies, today announced the publication of new research in Science Advances detailing the company’s CRISPR-based ...
Syntax Bio, a synthetic biology company programming the next generation of cell therapies, has published new research in ...
Biotech startup CrisprBits uses CRISPR-based techniques to change the shape of diagnostics by decoding genetic sequencing ...
A bespoke CRISPR base-editing therapy designed for a single infant with CPS1 deficiency has produced encouraging early ...
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