Innovative research into the gene-editing tool targets influenza’s ability to replicate—stopping it in its tracks.
At the height of the COVID-19 pandemic in 2020, Marvin Collins ’22, a bioengineering student, was balancing their Stanford classes from home in Alabama while also helping bioengineering professor ...
Abu Dhabi successfully completes its first gene therapy for genetic blood disorders, revolutionizing treatment approaches for ...
CRSP’s main value driver is Casgevy, which was approved for sickle cell disease and β-thalassemia. It’s a one-time ex vivo CRISPR/Cas9 stem‐cell therapy. Unfortunately, Casgevy’s rollout has been slow ...
12don MSN
Contrarius Global Equity Fund’s thoughts on CRISPR Therapeutics’ (CRSP) gene editing therapy
Contrarius Investment Management, an investment management company, released its third-quarter investor letter for the ...
AZoLifeSciences on MSN
CRISPR for Christmas? The year’s biggest gene editing breakthroughs, unwrapped
In 2025, CRISPR advanced gene editing with safe, effective therapies and AI tools, marking a shift towards real-world ...
CRISPR is a gene-editing tool that acts like “molecular scissors,” but using it on cancer is complex. The technology’s biggest impact so far is in research labs, helping scientists understand how ...
Cathie Wood’s Ark Invest increased exposure to gene-editing names and autonomous mobility companies while further cutting ...
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