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.
Research now shows that the countermeasure viruses came up with — inhibitory proteins referred to as 
Jennifer Doudna, Crispr and a great scientific breakthrough. 
The Wall Street Journal 
Intellia Therapeutics received notice from China's State Intellectual Property Office (SIPO) that it will grant the company a broad patent covering CRISPR/Cas9 single-guide gene-editing methods and compositions. "SIPO's decision further expands our IP portfolio and is further global recognition that Jennifer Doudna, Emmanuelle Charpentier, and their team are the pioneers...
Alexandra East-Seletsky, Jennifer Doudna, and fellow researchers have described 10 new CRISPR enzymes that, once activated, behave like Pac-Man to chew up RNA in a way that could be used as sensitive detectors of infectious viruses.
The 2017 Japan Prize in the life sciences was 
The University of California, the University of Vienna and Emmanuelle Charpentier (collectively UC) on Wednesday, April 12, - « first View: Taxonomy term
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