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8d
TwistedSifter on MSNScientists Have Successfully Used CRISPR Gene Editing Technology To Create A Spider With Glowing Red SilkIn addition, some species of spider are able to create silk that is the stronger than Kevlar and has many practical uses ...
Crispr Therapeutics' current revenue from CASGEVY is limited by high costs, profit-sharing, and logistical hurdles. Click ...
A newly discovered bacterial defense protein named Cat1 reveals an extraordinary method of viral neutralization. All living ...
For the past eight years, though, AstraZeneca has been making a concerted effort to address that, and success rates have risen dramatically to 19% in 2012–2016.
The CRISPR gene editing technology has transformed the research lab, and this powerful tool is now making its way into the clinic... | Cell And Molecular Biology ...
Researchers have completed a first-in-human clinical trial testing a CRISPR/Cas9 gene-editing technique ... which has never been done before. While the results are promising, the process remains ...
RNA gene scissors (CRISPR-Cas13) are gaining significant attention as a next-generation gene therapy with fewer side effects.
18d
ScienceAlert on MSNWorld's First CRISPR-Edited Spiders Shoot Fluoro Red Silk From Their ButtBeginning a chain of events that will presumably lead to the origin of our universe's Spider-Man, researchers in Germany have created the world's first spiders to be genetically modified using CRISPR ...
For years, the CRISPR-Cas9 genome technology has been reshaping genetic engineering ... and biodegradability. This successful experiment could open the door to enhanced silk functionalities ...
After spending over 300 days at CHOP, KJ Muldoon has been released from the hospital after receiving personalized CRISPR gene ...
Delve into what the new CRISPR tool, CAST, has to offer. CRISPR-associated transposases are already gaining traction in ...
Drs. Musunuru and Ahrens-Nicklas (wearing masks) posed with KJ’s family after the baby’s successful CRISPR treatment. Developing CRISPR cures for rare disease has been part of the IGI’s mission since ...
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