In an unprecedented medical achievement, a child with a rare genetic disorder receives a customized CRISPR gene therapy, paving the way for future treatments of similar conditions.
Scientists have uncovered that our sensitive teeth evolved from the 'body armor' of ancient fish, revealing a fascinating link between extinct species and modern human anatomy.
Researchers have developed a groundbreaking method for inserting large genes into specific locations in human cells, potentially transforming the field of gene therapy and opening new avenues in medical research.
In a surprising turn of events, Regeneron has announced its acquisition of 23andMe for $256 million following the company's bankruptcy. The pharma giant aims to leverage 23andMe's vast customer data for drug discovery while prioritizing privacy and security.
In a groundbreaking case, a 6-month-old baby boy named KJ was treated with a personalized CRISPR gene-editing therapy, correcting a dangerous mutation before it could threaten his life. This innovative approach promises hope for similar cases.
A groundbreaking study reveals that human intelligence may stem from sudden changes in gene regulation, challenging the notion of gradual evolution. Discover how these genetic shifts distinguish us from our closest relatives.
A baby diagnosed with a rare genetic disorder has shown remarkable improvement after receiving an experimental gene editing treatment tailored just for him. This groundbreaking therapy offers hope for others with similar conditions.
After decades of research, scientists from Kyushu University have pinpointed the gene responsible for orange fur in domestic cats, explaining the prevalence of orange males and the unique patterns in females. This groundbreaking discovery may impact more than just fur color.
A new study reveals that prolonged sitting can harm your brain, even if you exercise regularly. Discover how sitting impacts memory and brain health, especially for those at genetic risk.
KJ Muldoon, born with a deadly genetic disorder, received a groundbreaking CRISPR treatment just six months after birth. His remarkable progress showcases the future of personalized medicine for rare diseases.
