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Next-generation CRISPR tools and therapies improved by modified RNA guides Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR), a gene-editing tool, is a promising way to treat diseases by removing, adding, or altering sections of deoxyribonucleic acid (DNA) sequences. It is currently the most straightforward, most flexible, and accurate method of gene manipulation. A new type of gene-editing tool, CRISPR-Cas13, has shown promise in RNA targeting. Previous studies have shown the tool as a potential treatment method for viral diseases, including coronavirus disease (COVID-19). Researchers at the lab of Neville Sanjana at New York University (NYU) and the New York Genome Center (NYGC) have developed chemically modified guide RNAs for a CRISPR system that targets RNA instead of DNA.

New yorkUnited statesAngela betsaidab laguipoYork genome centerNeville sanjana at new york universityAngela betsaidaRegularly interspaced short palindromic repeatsNeville sanjanaNew york universityNew york genome centerCell chemical biologyபுதியது யார்க்ஒன்றுபட்டது மாநிலங்களில்யார்க் மரபணு மையம்நெவில் சஞ்சனாபுதியது யார்க் பல்கலைக்கழகம்