The big biotech, which has made genetic medicine a focus in recent years, is paying Tessera $150 million for rights to a ...
If approved, Regeneron and Tessera's TSRA-196 could become the first curative therapy to reach patients with AATD, who have ...
A new FDA pathway could speed bespoke gene therapies, but key questions over scope and commercial viability remain.
Lyme disease often goes undetected when it's most treatable. These teens are working to change that.
Teens at a Georgia high school may have come up with a better way to detect and treat Lyme disease. They took their idea to ...
Soy Nómada on MSN
One-Time' Injection Could End High Cholesterol; New Study Stuns
A groundbreaking new study reveals a gene-editing therapy that dramatically lowered 'bad' cholesterol in monkeys, offering ...
But sometimes, this top investor who focuses on innovation does see eye-to-eye with analysts, and the perfect example of this ...
Following the weekend data presentation, Citizens voiced optimism regarding CRISPR’s in-vivo projects. The firm noted some ...
Key breakthrough for the return of the dodo: viable cells have been obtained and genetically modified birds have been prepared.
The Minister noted that with the development and transfer of India's first indigenous CRISPR-based gene therapy, the nation ...
A New Way of Stopping High Cholesterol Sounds Like Sci-Fi. Doctors Call it the "Future of Medicine."
New research breaks down how scientists use CRISPR technology to lower cholesterol. The cholesterol-lowering effects could be permanent.
Oppenheimer emphasized the advancements in CRISPR’s in vivo initiatives, highlighting the comprehensive findings from the ...
Nearly 40% of respondents identified AI-based frameworks as their top priority for reducing cyber risk over the next three ...
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