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Intravenous And Intra Arterial Infusion Articles & Analysis

1 articles found

Persistent gene editing therapy using LNP-delivered mRNAs   

Persistent gene editing therapy using LNP-delivered mRNAs  

Gene editing technology, represented by CRISPR/Cas9, has greatly accelerated the development of gene therapy, bringing hope to many genetic diseases that otherwise had no cure. In June 2021, Intellia Therapeutics' NTLA-2001, a CRISPR gene editing therapy for the treatment of transthyretin amyloidosis (ATTR) invented by Nobel Laureate Jennifer Doudna, was proven to be safe and effective in a ...

ByCreative Biolabs

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