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Rising global temperatures are threatening rice, a staple food that nourishes billions of people around the world. But researchers ... a temperature-sensitive gene found in some common rice ...
They would use a technology known as CRISPR, a personalized gene-editing therapy ... He became the first known patient in the world to be treated using CRISPR personalized just for him, according ...
Brylie St Clair, who the media has dubbed “the world’s hottest softball player,” just might be the Olivia Dunne of baseball. She has it all: the looks, the body, and the athletic ability to ...
ST. LUCIE COUNTY — How do you create a balsa ... Now, along with a team from Morningside Elementary, they are going to the world competition on the Michigan State University campus in East ...
The St. Louis Cardinals have found a blueprint for success this year. St. Louis has performed well above expectations. In fact, there likely isn’t a team out there right now that has ...
Researchers at the University of Bayreuth have recently successfully bred the world’s first CRISPR-Cas9 ... a novel CRISPR solution containing the gene sequence for a red fluorescent silk ...
At some point in your running life, it will hit you—wherever you turn, it will seem like everyone is talking about marathons. A lot. Your real-world and online running friends will share weekly ...
Which is how their son became the world’s first recipient of a personalized gene-editing therapy in what has been hailed as a medical milestone. Ahrens-Nicklas teamed up with Kiran Musunuru ...
A baby born with a rare and dangerous genetic disease is growing and thriving after getting an experimental gene editing treatment made just for him. Researchers described the case in a new study ...
Gene and cell therapies (GCTs) can target the kidney to treat congenital, acute or chronic diseases affecting this organ. However, its complex structure poses a challenge for these technologies. To be ...
This is real life. This is not hypothetical.” DR. KIRAN MUSUNURU, a gene-editing researcher at the University of Pennsylvania, who in months helped develop a targeted treatment to heal an ...
In a global first, scientists have used advanced base editing to repair a deadly gene mutation in a newborn, marking a major leap forward in the treatment of rare inherited metabolic diseases.
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