To date, CRISPR has been the most effective method for dividing cells in large organs like the skin or the gut.
对皮肤、肠道等较大的器官来说，CRISPR是迄今为止最有效的细胞再生方法。
In the meantime, researchers and startups are moving ahead, working on advancements using the CRISPR technology.
与此同时，研究者和初创公司仍将继续借助CRISPR技术来推进自己的工作。
News of the discovery comes a day after Chinese scientists successfully tested a similar DNA-modifying technique, known as CRISPR.
该发现公布前一天，中国科学家成功测试了一种类似的DNA改造技术，被称为CRISPR。
They also found that "CRISPR interference," as this phenomenon is known, involves the targeting of the incoming plasmid or virus DNA directly.
他们也发现了CRISPR干扰作用，正如被认识的一样，该作用包括间接将进入的质粒或者病毒DNA作为目标。
Researchers have developed a method to cut the viral DNA from a person's infected cells. It is called CRISPR/Cas9 and it means the person could be virus-free.
研究人员已经找到了一种从人体感染细胞中剔除病毒DNA的办法，它被称之为CRISPR/Cas9基因剪辑技术，这意味着这个人可以摆脱病毒。
The CRISPR elements are part of a prokaryotic defence system directed against external attacks by e. g. viruses and may be viewed as a simple immune system of microorganisms.
CRISPR是原核生物免疫防御系统的组成部分，能帮助原核生物抵抗入侵的病毒，可看作是一个简单的微生物免疫系统。
The potential treatments and USES that may stem from the CRISPR method still remain a few years off-hopefully long enough to solve who gets the final ownership on the core technology.
而源于这项技术的潜在治疗手段和应用，估计仍需要几年时间才会成为现实，但愿在此期间，我们能够解决这项核心技术的归属问题。
But CRISPR is very real, with the potential, one day, to cure genetically-linked diseases like sickle cell anemia, produce better crops, and create a huge supply of organs for transplant.
不过，CRISPR这种基因编辑技术可是货真价实的。它有可能在未来的某一天治愈细胞性贫血等与基因相关的疾病，种出更好的庄稼，或者带来大量可供移植的器官。
The Northwestern researchers have discovered that a special DNA sequence found in certain bacteria, called a CRISPR locus, can impede the spread of antibiotic resistance in pathogenic staphylococci.
西北大学研究人员在一种细菌中发现了一个叫做CRISPR位点的特殊DNA序列，该位点可以阻止抗生素抗性在致病性金黄色葡萄球菌中的传播。
The researchers' experiments show that the CRISPR locus limits the ability of the S. epidermidis strain to act as a plasmid recipient, essentially denying entry to the genes carrying the resistance.
研究者的实验表明，CRISPR位点限制了s。epidermidis菌株作为一个质粒接受体的能力，从本质上阻断了能引起抗性基因的进入。
This mode of gene regulation is not restricted to eukaryotes; bacteria utilize small RNAs, notably those made from CRISPR loci that silence the expression of bacteriophages, transposons and plasmids.
这种基因调控模式不仅限于真核生物，细菌利用小分子rna，尤其是那些从CRISPR位点沉默的噬菌体，转座子和质粒表达。
This mode of gene regulation is not restricted to eukaryotes; bacteria utilize small RNAs, notably those made from CRISPR loci that silence the expression of bacteriophages, transposons and plasmids.
这种基因调控模式不仅限于真核生物，细菌利用小分子rna，尤其是那些从CRISPR位点沉默的噬菌体，转座子和质粒表达。
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