Our experiences leave traces in the brain, stored in small groups of cells called engrams. Engrams are thought to hold the ...
On June 28, 2012, the most significant scientific breakthrough of the first quarter of the 21st century was announced to the ...
The goal of gene therapy is to permanently cure hereditary diseases. One of the most promising technologies for this is the ...
Despite setbacks and funding cuts — and a quieting of the hype blaring its arrival — multiple CRISPR-based trials are ...
Explore how oligonucleotides are reshaping therapeutics, diagnostics and CRISPR with rapid, scalable and personalized ...
Both CRSP and NTLA are advancing in vivo gene editing therapies targeting large markets, with financial stability supporting ...
One of the most revolutionary tools in cutting-edge medicine is a molecular scalpel so precise that it can modify defective DNA and fix genetic diseases like sickle cell anemia, and chronic disorders ...
A new study has revealed that the gene HMGN1 is a key driver of congenital heart defects (CHDs) in Down syndrome. Using ...
A lthough still in its early days, CRISPR has already been called the most powerful scientific tool of the century. Using ...
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