Gene editing tool CRISPR-Cas9 has made it possible to isolate RNA in living cells for the first time. The cures for some of the world's most perplexing diseases might be closer than we think.
According to a study published in Cell, researchers have determined how to isolate and edit messenger RNA that carries genetic instructions from the cell's nucleus to make new proteins for the first time using gene-editing tool Clustered Regularly Interspaced Short Palindromic Repeats, also known as CRISPR-Cas9.
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http://www.usnews.com/news/articles/2016-03-23/gene-tool-shows-promise-in-curing-hiv-cancer-and-autism
http://www.usnews.com/news/articles/2016-03-23/gene-tool-shows-promise-in-curing-hiv-cancer-and-autism