Gene Editing for Cardiac Protection
CRISPR-Cas9 gene editing has shown promise as a therapeutic approach to treating rare hereditary diseases.
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CRISPR-Cas9 gene editing has shown promise as a therapeutic approach to treating rare hereditary diseases.
In this interview, News Medical speaks to Assitant Professor Ryan Jackson about his latest work, published in tandem Nature papers, detailing the discovery of a new CRISPR immune system.
In this free infographic, find out how your CRISPR gene editing experiments can benefit from Cas9 proteins.
In a first for the genetic toolset known as CRISPR, a recently discovered protein has been found to act as a kind of multipurpose self-destruct system for bacteria, capable of degrading single-stranded RNA, single-stranded DNA and double-stranded DNA.
In a rare feat, Utah State University biochemists Thomson Hallmark and Ryan Jackson, along with collaborators, published not one, but two seminal papers in a top-tier, peer-reviewed journal this week.