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33 results for "gene editing"
Japan just became the latest nation to outlaw gene editing for designer babies, backing its ban with serious consequences. The new law protects against unproven technology while keeping the door open for legitimate medical research.
Chinese researchers just proved that a safer, more precise gene editing tool can cure β-Thalassaemia, a life-threatening blood disorder affecting millions worldwide. Unlike earlier methods, this new system made zero mistakes while editing patient cells.
A breakthrough gene editing treatment has achieved what doctors call a "functional cure" for sickle cell disease, with 27 out of 28 patients experiencing zero painful crises after receiving the therapy. The one-time treatment edits patients' own blood cells to correct the genetic mutation, offering new hope for 100,000 Americans living with this painful disease.
Scientists created wheat that produces up to 93% less of a toxic compound when toasted, potentially making your morning toast much safer. The breakthrough uses precise gene editing without reducing crop yields.
University of Virginia researchers used gene editing to fix the DNA mutation causing a deadly form of epilepsy, potentially opening the door to cures for inherited brain disorders. The technique eliminated seizures in lab mice and improved their movement and cognitive function.
A groundbreaking gene therapy trial has achieved what doctors call a "functional cure" for sickle cell disease, eliminating painful crises in 27 out of 28 patients. The one-time treatment uses gene editing to fix the blood disorder that has killed patients decades too soon.
A bacterial defense system discovered in 2012 has transformed into life-saving treatments for cancer and rare diseases. Scientists refined CRISPR gene editing from crude molecular scissors into precision medicine that's curing patients today.
Twenty-seven out of 28 patients with severe sickle cell disease are now living pain-free after a groundbreaking gene editing treatment. The one-time therapy is offering new hope to people living with a genetic disorder that typically shortens life expectancy to the mid-40s.
Researchers have developed a method to engineer cancer-fighting immune cells directly in the bloodstream, eliminating the need for expensive lab processing. Early tests show tumors disappearing in two weeks.
Scientists just cleared tumors in mice by creating cancer-fighting cells directly inside their bodies, skipping the costly lab process. This breakthrough could make one of medicine's most powerful cancer treatments faster and more accessible.
Scientists just cleared tumors in mice without removing their cells from their bodies first. This breakthrough could transform how we fight cancer.
Scientists have genetically modified a common probiotic supplement to make it 100% safe for people with weakened immune systems. The breakthrough could finally allow cancer patients, babies, and elderly people to use probiotics without risk of dangerous infections.
An 18-year-old patient with a once-incurable immune disease now shows no symptoms after Montreal doctors used groundbreaking "prime editing" gene therapy. A year after treatment, he's living a normal life with three-quarters of his diseased cells permanently corrected.
A 19-year-old from Kelowna, B.C., became the first Canadian cured of a life-threatening immune disease using groundbreaking gene editing technology. His doctor says he no longer needs to worry about deadly infections sneaking past his weakened immune system.
A 1989 Nobel Prize-winning discovery revealed RNA could perform chemistry, not just carry instructions. That breakthrough now enables mRNA vaccines, CRISPR gene editing, and treatments for diseases once thought incurable.
A 19-year-old from British Columbia became the first person ever cured using "prime editing," a breakthrough gene therapy that fixed a fatal immune disorder. The treatment freed him from daily medication and the constant fear of life-threatening infections.
Ty Sperle, 18, became the first person in the world cured of chronic granulomatous disease through groundbreaking gene editing treatment. His success opens the door for curing countless other rare genetic diseases affecting children everywhere.
The FDA just announced a new pathway that could bring life-saving gene editing treatments to patients with rare diseases in record time. For families battling conditions once considered untreatable, this could change everything.
Scientists have created a precise gene-editing tool that could offer permanent treatment for cystic fibrosis patients, potentially replacing daily medications that cost hundreds of thousands of dollars per year. The breakthrough could transform care for people living with this and other genetic diseases.
A 9½-month-old baby became the first person ever to receive a custom gene-editing treatment designed specifically for his unique mutation. The breakthrough offers hope for thousands of rare genetic diseases that were once considered unreachable.
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