All known genetic diseases could be cured within the next decade thanks to major advances in gene editing, a leading ...
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A 'genetic master key': creating a therapy capable of treating thousands of rare diseases in one go
Scientists from MIT and Harvard present a new strategy called PERT in 'Nature'. Instead of correcting gene by gene, they use ...
A team of researchers at the Broad Institute, led by gene-editing pioneer David Liu, has developed a new genome-editing ...
CRISPR gene-editing technology lets scientists make precise changes to an organism’s DNA. Invented in 2012 by Jennifer Doudna and Emmanuelle Charpentier, biochemists who went on to win the Nobel prize ...
Instead of fixing one of the many genes that can be mutated, the technique addresses a type of mutation they share, a stop ...
Hosts David and Gina explore how scientists over the centuries unlocked the ability to edit our genes ...
Instead of requiring personalized gene edits for each patient, the new approach could create a standardized method to use for ...
Opal Sandy underwent a gene therapy injection to her right ear in 2023. A 3-year-old girl who underwent a breakthrough gene therapy treatment to treat profound hearing loss can hear on her own, two ...
An experimental genetic therapy can cure most cases of the 'Bubble Boy' disease, ADA-SCID In the rare disorder, children are born without a functioning immune system due to genetic mutations The ...
Clinical setbacks and controversial pricing may have put a dampener on the gene therapy sector, but one of the industry’s pioneers is looking for a way forward. GEMMA Biotherapeutics, the biotech ...
In September 2025, the Food and Drug Administration (FDA) issued three draft guidance documents designed to facilitate the continued development of novel cell and gene therapies. The recommendations ...
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