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Researchers engineered and screened dozens of base editors to precisely target a single mutation without editing other portions of the DNA.
Cas9 is directed to its target within the DNA sequence through the use of the guide RNA. A specific sequence of DNA that is between two and five nucleotides in length must align with the 3’ end of the ...
When scientists discovered how bacteria protect themselves against viral invaders, called phages, in the early 2000s, little ...
Sign up for CNN’s Wonder Theory science newsletter. Explore the universe with news on fascinating discoveries, scientific advancements and more. The United Kingdom ...
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News-Medical.Net on MSNCRISPR-based therapeutic approach designed to treat fatal pediatric disease
Multisystemic smooth muscle dysfunction syndrome (MSMDS) is a rare condition associated with stroke, aortic dissection ...
This story is part of a series on the current progression in Regenerative Medicine. This piece is part of a series dedicated to the eye and improvements in restoring vision. In 1999, I defined ...
Scientists study a molecular machine that moves jumping genes in DNA, paving the way for a new gene editing tool beyond ...
First-mover advantages are a big deal in the world of pharmaceuticals. CRISPR Therapeutics scored the first-ever regulatory approval for a CRISPR/Cas9 treatment this month. While logistical challenges ...
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