Scientists have developed a CRISPR-Cas9-based ‘gene drive’ platform to create diploid strains of the pathogen in which both gene copies could be efficiently deleted. The technique may lead the way toward a better understanding of drug resistance and biofilm-forming mechanisms, and through future research, it could help pinpoint new drug targets and combination therapies.
from Top Health News – ScienceDaily http://ift.tt/2iNLw9p
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