CRISPR Cas9 explained. CRISPR (clustered regularly interspaced short palindromic repeats) are segments of prokaryotic DNA containing short repetitions of base sequences. is an RNA-guided gene-editing platform that makes use of a bacterially derived protein (Cas9) and a synthetic guide RNA to introduce a double strand break at a specific location within the genome.
Cas9 is an enzyme that snips DNA, and CRISPR is a collection of DNA sequences that tells Cas9 exactly where to snip.
Podcast on the development of Crispr, and the ethical questions raised by new genome editing techniques.
Researchers have discovered how 
Jennifer Doudna and Emmanuelle Charpentier were awarded the Japan Prize today for their invention of the revolutionary gene-editing technology known as CRISPR-Cas9, which has swept into research labs around the world and is already yielding new therapies for cancer and hereditary diseases.
The Verge talks with Jennifer Doudna to discuss just what CRISPR might mean for the future of science, and disease research.
The cancer moonshot aims to end cancer as it is known today. One of the key discoveries in that effort is CRISPR/Cas9 pioneered by Jennifer Doudna.
Scientists at the University of California, Berkeley, have engineered a new way to deliver CRISPR-Cas9 gene-editing technology inside cells and have demonstrated in mice that the - « first View: Taxonomy term
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