Find uplifting stories about heroes, innovations, and solutions
8008 results for "gene drive"
Scientists are developing genetically modified mosquitoes that can't spread avian malaria, offering hope for Hawaii's disappearing honeycreepers. Eleven of 17 remaining species face extinction without urgent intervention.
Scientists have begun testing a breakthrough gene therapy that could restore hearing for people with the most common genetic cause of deafness. Skylark Bio just dosed their first patient, marking a major step toward helping millions born with this genetic mutation.
Autonomous trucks just got smart enough to drive 24/7, navigating construction zones and dark highways while moving real freight across Texas. This breakthrough could reshape how America moves goods while making roads safer.
Chinese automaker BYD just became the only car company in the world with complete control over its self-driving technology, launching China's first homegrown 4nm smart driving chip. The breakthrough puts advanced autonomous driving within reach while slashing costs.
Children born completely deaf are hearing whispers for the first time thanks to an experimental gene therapy that has shown remarkable success in the largest study of its kind. The treatment could become the first FDA-approved gene therapy for deafness within months.
A parasitic fly that causes immense suffering to livestock and humans could become the first species intentionally driven to extinction using breakthrough genetic technology. MIT researcher Kevin Esvelt believes the screwworm will be the pioneering target for this controversial but potentially life-saving tool.
Melbourne researchers developed an AI tool that creates molecular "off switches" for CRISPR gene editing in just 8 weeks. The breakthrough could help make gene therapy treatments safer and more accessible for patients with genetic diseases.
Australian researchers developed an AI system that makes gene editing safer by protecting healthy genes during treatment. The breakthrough could transform how doctors treat genetic diseases like cystic fibrosis.
After decades of skepticism, researchers have perfected a gentler way to control genes using epigenetic editing. This breakthrough lets them dial gene expression up or down without changing DNA itself, opening doors to safer treatments and smarter crops.
Scientists used AlphaFold AI to redesign gene-editing proteins, making them dramatically safer by nearly eliminating unwanted DNA changes. This breakthrough could help life-saving gene therapies reach more patients with fewer risks.
Scientists built an AI that designs synthetic DNA switches capable of turning genes on and off in specific cells, potentially transforming how we treat diseases like leukemia. In lab tests, these AI-generated sequences actually outperformed natural DNA at reactivating a protective gene in leukemia cells.
Chinese automaker BYD is doing something no car company has ever done: paying for every single expense when its autonomous driving system causes an accident, with no limits and no fine print. The move could change how the entire industry handles self-driving technology.
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 cutting-edge self-driving system just achieved an unprecedented six-win streak in China's toughest autonomous driving competition. The victory marks a major milestone in making fully automated cars safe and reliable for everyday drivers.
Israel just greenlit Tesla's autonomous driving system for real-world road trials, marking a major step toward integrating self-driving technology into everyday life. The carefully monitored pilot program will help shape the future of transportation in the region.
A groundbreaking partnership between Canadian and Japanese biotech companies could slash the cost of life-saving gene therapies. With government support, they're creating technology to produce treatments faster and cheaper than ever before. --- ##
Scientists who created gene therapies that cure inherited blindness and blood disorders just won six $3 million prizes. Their discoveries are transforming devastating diseases from hopeless diagnoses into treatable conditions.
Chinese scientists successfully treated children born deaf by delivering a missing gene directly into their inner ear cells. All patients under age 3 can now hear everyday conversations after a single treatment.
A safer gene therapy for Duchenne muscular dystrophy just hit a major milestone, bringing hope to families facing this fatal muscle disease. The treatment could offer a better option than current therapies linked to serious side effects.
%2Fhttps%3A%2F%2Ftf-cmsv2-smithsonianmag-media.s3.amazonaws.com%2Ffiler_public%2Fcf%2Fcd%2Fcfcd970f-b205-4a58-b5c2-3c656d99b432%2Fbaby-hearing-test.jpg)
A groundbreaking gene therapy now offers hope to children born with a rare form of deafness, with 80% of trial participants gaining significant hearing within a year. Even better, the maker plans to provide it free to U.S. patients.
Showing 20 of 8008