试图了解CRISPR-Cas9系统起源的研究人员发现了一类由转座子编码的RNA引导的核酸酶，他们称其为“OMEGA”，后者可在人类细胞中用于基因组编辑。

CRISPR-Cas9 genome editing exploits the CRISPR-Cas system to modify a genome in a targeted manner. Guided by RNA, the Cas9 endonuclease breaks DNA at a target sequence. Imprecise repair of the ...

This protein can easily be programmed to find and bind to almost any desired target sequence, simply by giving it a piece of RNA to guide it in its search. When the CRISPR Cas9 protein is added to ...

But as it turns out, CRISPR/Cas9 gene editing is a completely natural ... The last one, RNA interference, is the process by which RNA handles gene regulation. It’s also known as RNA silencing.

CRISPR Therapeutics AG is a gene editing company, which engages in the development of transformative gene-based medicines for serious diseases using its proprietary CRISPR/Cas9 platform.