CRISPR-based pharmacogenomic screening is used ... For now, Kampmann’s work is aimed at understanding the basic biology of neurodegeneration. But the techniques he has helped to pioneer are ...

自从基因编辑策略CRISPR出现以来，它遇到了一个很大的限制：经典的CRISPR系统太笨重了，无法进入人体的许多组织并进行切片和切割。现在，加州大学伯克利分校的Jennifer Doudna因帮助开发CRISPR而获得2020年诺贝尔奖，她与人共同创立了一家公司，该公司的研究人员 ...

CRISPR is a technology that can be used to edit genes and, as such, will likely change the world. The essence of CRISPR is simple: it’s a way of finding a specific bit of DNA inside a cell.

Doctors harvest stem cells from the patient’s bone marrow and then send them off to a lab, where CRISPR is used to turn up the production of another, functional version of haemoglobin.

Widely used as a genome editing tool, the CRISPR-Cas9 system allows researchers to precisely induce frameshift mutations in specific genes or insert foreign nucleic acid sequences into a cell’s DNA.

Suffering on such an immense scale can appear hopeless. However, a technique called CRISPR gene editing promises to help deal with these issues and many more—and wise regulation can spur it on.

"These cells co-develop together, just like they would in an actual embryo, and establish that history of being neighbors," ...

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 ...

India has the chance to lead in CRISPR technology by driving ethical gene editing innovations in healthcare, agriculture, and ...

Researchers at Kumamoto University have successfully executed a practical trial of a new genome-editing technique that allows ...