One year after receiving CRISPR gene editing therapy at CHOP, a Delaware County baby is thriving, and doctors want to expand treatment to others.
Science Unbound on MSN
The road from IVF to designer babies and what’s next
Advances in gene editing tools like CRISPR‑Cas9 and pre-implantation embryo screening are turning the idea of designer babies — selecting or altering embryonic traits — into a possibility rather than ...
CNBC's Becky Quick reports on the progress of KJ Muldoon, the first patient to receive a personalized CRISPR-based gene editing therapy. Got a confidential news tip? We want to hear from you. Sign up ...
Crispr’s ability to cut genetic code like scissors has just started to turn into medicines. Now, gene editing pioneer Jennifer Doudna wants to build an entire ecosystem to bring these treatments ...
Inside the growing scientific quest to understand what creatures with the extraordinary ability to defy the ravages of time can teach us about making human aging better.
Fascinated with the mystery of aging and what animals can reveal about longevity? Explore how scientists are drawing ...
A new method for safely inserting large chunks of DNA into genomes has now measured up in mice, potentially paving the way ...
Sickle cell disease—the subject of a new Seminar in The Lancet—is one of the most prevalent and fastest-growing genetic disorders worldwide. Although its true prevalence is difficult to determine ...
Modulator pills transformed cystic fibrosis care. But the fight for a cure is not over — so long as research remains funded.
The aim of the pathway is to remove red tape for bespoke therapies designed for patients with rare diseases.
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