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About 150 people in Singapore have transthyretin amyloid cardiomyopathy. Read more at straitstimes.com. Read more at ...
16h
MedPage Today on MSNIn a First, CRISPR Used to Treat Infant With Ultra-Rare DiseaseA tailored CRISPR base-editing therapy was given for the first time to an infant who was born with a rare genetic disease, ...
Scientists at the McGovern Institute and the Broad Institute of MIT and Harvard have reengineered a compact RNA-guided enzyme ...
The researchers have conducted a first-in-human clinical trial testing a CRISPR/Cas9 gene-editing technique aimed at ...
A federal appeals court said the patent office made legal errors in awarding foundational patents for CRISPR-Cas9 to the ...
Those hoping the Court of Appeals for the Federal Circuit would finally resolve priority in the long-pending dispute between the University ...
17h
inews.co.uk on MSNBreakthrough for children with rare diseases as ‘miracle’ gene editing saves babyA desperately sick baby with a rare disease has been treated using personalised gene-editing therapy in what has been ...
CRISPR Therapeutics benefits from Casgevy’s approval and a deep pipeline, despite early rollout hurdles and cost challenges.
Base-editing technologies along with AAV engineering not only help reduce costs but can also accelerate preclinical ...
In a precedential opinion issued on Monday, the U.S. Court of Appeals for the Federal Circuit (CAFC) vacated and remanded a ...
Nkure Therapeutics and Crispr Therapeutics partner to develop off-the-shelf CAR T therapy for oncology in India.
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