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1335 results for "gene-editing"
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.
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.
Scientists have developed a new gene editing approach that spreads healing changes from cell to cell, dramatically increasing its reach in the body. This breakthrough could transform treatment for countless genetic diseases that were previously too difficult to address.
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.
Scientists are developing a breakthrough gene editing approach that spreads between cells like neighbors sharing flyers. This could treat far more diseases by reaching dramatically more cells in the body.
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After a deadly fungus wiped out billions of American chestnut trees, scientists are using gene editing to bring them back. Three new approaches could also save coral reefs, black-footed ferrets, and other threatened species.
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.
A new biotech company just launched with $230 million to develop a one-time cure for a genetic disease affecting thousands. Serapha Bio aims to fix the root cause of Alpha-1 Antitrypsin Deficiency using cutting-edge gene editing.
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.
Scientists from Harvard, MIT, and Case Western used CRISPR gene editing to extend the lives of mice with deadly prion diseases by 60%. While the treatment isn't ready for humans yet, it marks a breakthrough against diseases that currently have no cure.
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 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 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.
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.
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.
A one-time gene-editing treatment just became the first to succeed in a major clinical trial, reducing dangerous swelling attacks by 87% for people with a rare genetic condition. The breakthrough could change what's possible for treating 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.
Israeli researchers used CRISPR technology to remove the gene that makes grapefruit taste bitter, potentially opening the door for kids and picky eaters to enjoy this nutritious fruit. The breakthrough could expand the market for grapefruit and help more people access its health benefits without the pucker.
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.
Scientists tested a one-time gene therapy that lowered cholesterol up to 62% in patients, potentially replacing daily pills and injections with a single treatment. The breakthrough could transform how millions manage heart disease risk.
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