Find uplifting stories about heroes, innovations, and solutions
39 results for "gene editing"
Researchers discovered how to supercharge immune cells used in cancer treatment by turning off a single gene, making them fight tumors longer and stronger. The breakthrough could help millions of patients whose cancers don't respond to current therapies.
A one-time gene-editing treatment slashed bad cholesterol by 62% in early human trials, offering hope for millions who struggle with heart disease prevention. Eli Lilly's breakthrough therapy showed no serious side effects in the study.
A groundbreaking study from Ghana shows how honest reporting about agricultural innovations builds more public trust than hype. Researchers found that including diverse voices, not just experts, helps people make better decisions about new farming technologies.
A single-dose CRISPR treatment freed patients from a painful genetic disorder that causes life-threatening swelling attacks. The breakthrough marks the first Phase 3 success for in vivo gene editing and could launch in 2027.
A new FDA pathway could cut the time to get personalized CRISPR treatments from four years to just three months, making life-saving gene editing accessible to thousands of children born with rare genetic diseases. Baby KJ Muldoon became the first person to receive this revolutionary treatment in February 2025.
Scientists are calling new gene editing treatments a potential "functional cure" for sickle cell disease, offering hope to millions. Early results show patients living pain-free after a single treatment.
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.
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