Recent data published in NEJM demonstrates that CRISPR gene-editing therapy achieves complete clinical efficacy endpoints in ...
Amy Scott, host of the podcast "How We Survive," reports on a company that's working on de-extinction innovation to try and ...
Researchers have spent decades-and billions of dollars-sequencing animal and crop genomes, but fungi have historically been the forgotten middle child of genomics, only noticed when they're ruining ...
Daniel Cressy, 23, has become the first person in the Gulf South to become functionally cured of sickle cell disease using ...
Gene editing has delivered remarkable results against sickle cell disease. Now researchers are working to make these ...
Researchers led by developmental biologist Kathy Niakan at the University of Cambridge have used base editing in human embryos to learn more about human embryonic development. By deactivating a gene ...
Genome editing lets scientists rewrite DNA, the instruction manual inside every living cell, with a precision that was ...
An experimental gene-editing therapy that aims to lower bad cholesterol for the long-term after a single infusion is off to a positive start in an early clinical trial. Researchers running a Phase I ...
MIT scientists have found a way to make gene editing far safer and more accurate — a breakthrough that could reshape how we treat hundreds of genetic diseases. By fine-tuning the tiny molecular “tools ...
Cardiovascular diseases could be among the world’s first medical conditions to be treated by changing a patient’s genes. If ongoing phase 3 trials succeed, gene editing will offer a novel therapy for ...
Please provide your email address to receive an email when new articles are posted on . Two studies highlight the potential of gene editing for sickle cell disease treatment. Despite increasing ...
Intellia Therapeutics said its Crispr-based treatment for a rare swelling condition succeeded in a Phase 3 trial, a landmark for gene editing. The treatment uses Nobel Prize-winning Crispr technology ...
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