Tuesday, February 26, 2019

Journals on Medical Research

Abstract

Clustered regularly interspaced short #palindromicrepeat (CRISPR) and CRISPR associated protein 9 (Cas9) form a complex known as CRISPR-Cas9, which is an efficient tool for gene editing that was discovered through the study of bacterial defense mechanisms against foreign #nucleic acids. This technology allows for the knock-out or knock-in of specific DNA sequences. Therefore, CRISPR-Cas9 may provide a new method to abrogate the effects of genes that lead to disease or introduce genes that promote improvements in health. The powerful nature of these potential uses can be illustrated by considering the #geneticbases of #diseases such as cancer or #obesity. Clearly, there will be many ethical debates about the future of this technology to alter genetic function.

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