CRISPR is one of the most revolutionary technologies of the modern era, and now it's being used to bring back long-lost genes ...
Morning Overview on MSN
CRISPR researchers revived an ancient gene that could block disease
Researchers have used CRISPR to switch back on a gene that vanished from the human lineage roughly 20 million years ago, ...
Climate Compass on MSN
CRISPR and the future: Can we edit out genetic diseases?
We're living in a moment where science fiction is becoming medical reality. Imagine a world where doctors can simply rewrite ...
Inside cells, DNA twists and coils itself into a variety of different secondary structures—including i-motifs (iMs) and ...
News-Medical.Net on MSN
Study identifies TAK1 gene as a key brake on cancer immunotherapy
Australian researchers have discovered that the TAK1 gene helps cancer cells survive attack from the immune system, revealing a mechanism that may limit the effectiveness of immunotherapy treatments.
Australian researchers have discovered that the TAK1 gene helps cancer cells survive attack from the immune system, revealing ...
This year saw notable progress in head and neck cancers, Huntington's disease, personalized genetic therapy, and heart ...
What keeps our cells the right size? Scientists have long puzzled over this fundamental question, since cells that are too ...
Interesting Engineering on MSN
Scientists identify a non-coding gene that directly controls how big cells grow
Scientists identify the first non-coding gene that directly controls cell size, reshaping how biology explains growth and ...
Researchers used miniature human brains grown in the lab to uncover why certain genetic mutations lead to abnormally small ...
News-Medical.Net on MSN
Advances in hemophilia gene therapy bring hope for pediatric patients
In the past three years, gene therapy has reshaped what's possible in hemophilia treatment for patients 18 and older. But a ...
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