Authors: George Rajna
Selecting the most effective molecules for drug delivery is often a trial-and-error process, but Cornell engineers are providing some precision thanks to a technique that reveals the performance of those molecules inside living cells.  Now, researchers at MIT and elsewhere have developed a system to deliver medical treatments that can be released at precise times, minimally-invasively, and that ultimately could also deliver those drugs to specifically targeted areas such as a specific group of neurons in the brain.  Gene editing technology is a technology that eliminates the underlying causes of and treats diseases by removing specific genesor editing genes to restore their normal function. In particular, CRISPR gene editing technology is now commonly used for immunotherapy by correcting the genes of immune cells to induce them to attack cancer cells selectively. 
Comments: 68 Pages.
[v1] 2019-11-04 03:31:28
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